Ascentage Pharma to Participate in Two Upcoming Investor Conferences in November 2025

Ascentage Pharma to Participate in Two Upcoming Investor Conferences in November 2025




Ascentage Pharma to Participate in Two Upcoming Investor Conferences in November 2025

ROCKVILLE, Md. and SUZHOU, China, Oct. 29, 2025 (GLOBE NEWSWIRE) — Ascentage Pharma Group International (NASDAQ: AAPG; HKEX: 6855) (“Ascentage Pharma” or the “Company”), a global, commercial stage, integrated biopharmaceutical company engaged in the discovery, development and commercialization of novel, differentiated therapies to address unmet medical needs in cancer, announced today that the Company’s management is scheduled to participate in the following investor conferences in November 2025.

  • Goldman Sachs APAC Healthcare Corporate Day 2025: One-on-one and group investor meetings on November 5
  • Stifel 2025 Healthcare Conference: Presentation on November 13 at 2:40 pm EST

About Ascentage Pharma Group International

Ascentage Pharma Group International (NASDAQ: AAPG; HKEX: 6855) (“Ascentage Pharma” or the “Company”) is a global, commercial stage, integrated biopharmaceutical company engaged in the discovery, development and commercialization of novel, differentiated therapies to address unmet medical needs in cancer. The company has built a rich pipeline of innovative drug products and candidates that include inhibitors targeting key apoptotic pathway proteins, such as Bcl-2, MDM2, p53 as well as next-generation kinase inhibitors.

The Company’s first approved product, Olverembatinib, is the first novel third-generation BCR-ABL1 inhibitor approved in China for the treatment of patients with chronic myelogenous leukemia (CML) in chronic phase (CML-CP) with T315I mutations, CML in accelerated phase (CML-AP) with T315I mutations, and CML-CP that is resistant or intolerant to first and second-generation TKIs. All indications are covered by the China National Reimbursement Drug List (NRDL). Ascentage Pharma is currently conducting an FDA-cleared registrational Phase III trial, called POLARIS-2, of Olverembatinib for CML, as well as registrational Phase III trials for patients with newly diagnosed philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ALL), called POLARIS-1, and succinate dehydrogenase (SDH)-deficient gastrointestinal stromal tumor (GIST) patients, called POLARIS-3.

The Company’s second approved product, Lisaftoclax, is a novel Bcl-2 inhibitor for the treatment of various hematologic malignancies. Lisaftoclax has been approved by China’s National Medical Products Administration (NMPA) for the treatment of adult patients with chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL) who have previously received at least one systemic therapy including Bruton’s tyrosine kinase (BTK) inhibitors. The Company is currently conducting four global registrational Phase III trials: the FDA-cleared GLORA study of Lisaftoclax in combination with BTK inhibitors in patients with CLL/SLL previously treated with BTK inhibitors for more than 12 months with suboptimal response; the GLORA-2 study in patients with newly diagnosed CLL/SLL; the GLORA-3 study in newly diagnosed, elderly and unfit patients with acute myeloid leukemia ( AML); and the FDA-cleared GLORA-4 study in patients with newly diagnosed higher-risk myelodysplastic syndrome (HR MDS).

Leveraging its robust R&D capabilities, Ascentage Pharma has built a portfolio of global intellectual property rights and entered into global partnerships and other relationships with numerous leading biotechnology and pharmaceutical companies, such as Takeda, AstraZeneca, Merck, Pfizer, and Innovent, in addition to research and development relationships with leading research institutions, such as Dana-Farber Cancer Institute, Mayo Clinic, National Cancer Institute and the University of Michigan. For more information, visit https://ascentage.com/

Forward-Looking Statements

This press release includes forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995 and Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. All statements, other than statements of historical facts, contained in this press release may be forward-looking statements, including statements that express Ascentage Pharma’s opinions, expectations, beliefs, plans, objectives, assumptions or projections regarding future events or future results of operations or financial condition. These forward-looking statements are subject to a number of risks and uncertainties as discussed in Ascentage Pharma’s filings with the SEC, including those set forth in the sections titled “Risk factors” and “Cautionary note regarding forward-looking statements” in its Annual Report on Form 20-F for the year ended December 31, 2024, filed with the SEC on April 16, 2025, the sections headed “Forward-looking Statements” and “Risk Factors” in the prospectus of the Company for its Hong Kong initial public offering dated October 16, 2019, and other filings with the SEC and/or The Stock Exchange of Hong Kong Limited it has made or it makes from time to time that may cause actual results, levels of activity, performance or achievements to be materially different from the information expressed or implied by these forward-looking statements. The forward-looking statements contained in this press release do not constitute profit forecast by the Company’s management.

As a result of these factors, you should not rely on these forward-looking statements as predictions of future events. The forward-looking statements contained in this press release are based on Ascentage Pharma’s current expectations and beliefs concerning future developments and their potential effects and speak only as of the date of such statements. Ascentage Pharma does not undertake any obligation to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise.

Contacts
Investor Relations:
Hogan Wan, Head of IR and Strategy
Ascentage Pharma
Hogan.Wan@ascentage.com
+86 512 85557777

Stephanie Carrington
ICR Healthcare
AscentageIR@icrhealthcare.com
+1 (646) 277-1282

Media Relations:
Jon Yu
ICR Healthcare
AscentagePR@icrhealthcare.com
+1 (646) 677-1855

Vaxil Announces Non-Brokered Private Placement

Vaxil Announces Non-Brokered Private Placement




Vaxil Announces Non-Brokered Private Placement

Not for distribution by US newswire or in United States

NESS-ZIONA, ISRAEL, Oct. 29, 2025 (GLOBE NEWSWIRE) — VAXIL BIO LTD. (“Vaxil” or the “Company”) (TSX VENTURE: VXL), is pleased to announce that the Company intends to complete a non-brokered private placement on a commercially reasonable efforts basis (the “Offering“) of up to 2,456,140 units (“Units“) of the Company at a price of $0.1425 per Unit to raise gross proceeds of up to $350,000. Each Unit will consist of one common share of the Company (“Shares”) and one common share purchase warrant of the Company (“Warrants“). Each Warrant will entitle the holder to acquire one Share at a price of $0.19 per Share for a period of five years following the closing of the Offering.

Net proceeds from the Offering will be used by the Company to support general corporate purposes.

The closing of the Offering is subject to a number of conditions, including but not limited to, approval by the TSX Venture Exchange of the Offering

The Company expects the Offering to close on or around November 14, 2025.

On the closing of the Offering, the Company has agreed to pay certain finders a cash commission of up to 8% of the gross proceeds of the Offering and non-transferrable Warrants (the “Finders‘ Warrants“) of up to 8% of the aggregate number of Units issued pursuant to the Offering.

The Units, the Shares and Warrants comprising the Units and the Finders’ Warrants will be subject to a hold period of four months and one day from their date of issue in accordance with applicable securities laws.

ABOUT VAXIL

Vaxil was an immunotherapy biotech company focused on targeting prominent cancer markers and infectious diseases. Its lead product was ImMucin™ for which it had received orphan drug status from the FDA and EMA. The Company is presently evaluating the pursuit other business, which may or may not be in the biotechnology industry, in order to enhance shareholder value.

Neither TSX Venture Exchange nor its Regulation Services Provider (as that term is defined in the policies of the TSX Venture Exchange) accepts responsibility for the adequacy or accuracy of this release.

Disclaimer: The TSX Venture Exchange Inc. has in no way passed upon the merits of the Company and has neither approved nor disapproved the contents of this press release. This news release contains forward-looking information, which involves known and unknown risks, uncertainties and other factors that may cause actual events to differ materially from current expectation. Important factors – including the availability of funds, the results of financing efforts, the results of exploration activities — that could cause actual results to differ materially from the Company’s expectations are disclosed in the Company’s documents filed from time to time on SEDAR (see www.sedar.com). Readers are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date of this press release. The company disclaims any intention or obligation, except to the extent required by law, to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise. This press release does not constitute an offer to sell or a solicitation of an offer to sell any of the securities described herein in the United States or elsewhere. These securities have not been, and will not be, registered in the United States Securities Act of 1933, as amended, or any state securities laws, and may not be offered or sold in the United States or to U.S. persons unless registered or exempt therefrom.

Contact Information

For further information please visit https://vaxil-bio.com/ or contact:

Gadi Levin, CEO
info@vaxil-bio.com
647-558-5564

Vaxil Announces Non-Brokered Private Placement

Vaxil Announces Non-Brokered Private Placement




Vaxil Announces Non-Brokered Private Placement

Not for distribution by US newswire or in United States

NESS-ZIONA, ISRAEL, Oct. 29, 2025 (GLOBE NEWSWIRE) — VAXIL BIO LTD. (“Vaxil” or the “Company”) (TSX VENTURE: VXL), is pleased to announce that the Company intends to complete a non-brokered private placement on a commercially reasonable efforts basis (the “Offering“) of up to 2,456,140 units (“Units“) of the Company at a price of $0.1425 per Unit to raise gross proceeds of up to $350,000. Each Unit will consist of one common share of the Company (“Shares”) and one common share purchase warrant of the Company (“Warrants“). Each Warrant will entitle the holder to acquire one Share at a price of $0.19 per Share for a period of five years following the closing of the Offering.

Net proceeds from the Offering will be used by the Company to support general corporate purposes.

The closing of the Offering is subject to a number of conditions, including but not limited to, approval by the TSX Venture Exchange of the Offering

The Company expects the Offering to close on or around November 14, 2025.

On the closing of the Offering, the Company has agreed to pay certain finders a cash commission of up to 8% of the gross proceeds of the Offering and non-transferrable Warrants (the “Finders‘ Warrants“) of up to 8% of the aggregate number of Units issued pursuant to the Offering.

The Units, the Shares and Warrants comprising the Units and the Finders’ Warrants will be subject to a hold period of four months and one day from their date of issue in accordance with applicable securities laws.

ABOUT VAXIL

Vaxil was an immunotherapy biotech company focused on targeting prominent cancer markers and infectious diseases. Its lead product was ImMucin™ for which it had received orphan drug status from the FDA and EMA. The Company is presently evaluating the pursuit other business, which may or may not be in the biotechnology industry, in order to enhance shareholder value.

Neither TSX Venture Exchange nor its Regulation Services Provider (as that term is defined in the policies of the TSX Venture Exchange) accepts responsibility for the adequacy or accuracy of this release.

Disclaimer: The TSX Venture Exchange Inc. has in no way passed upon the merits of the Company and has neither approved nor disapproved the contents of this press release. This news release contains forward-looking information, which involves known and unknown risks, uncertainties and other factors that may cause actual events to differ materially from current expectation. Important factors – including the availability of funds, the results of financing efforts, the results of exploration activities — that could cause actual results to differ materially from the Company’s expectations are disclosed in the Company’s documents filed from time to time on SEDAR (see www.sedar.com). Readers are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date of this press release. The company disclaims any intention or obligation, except to the extent required by law, to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise. This press release does not constitute an offer to sell or a solicitation of an offer to sell any of the securities described herein in the United States or elsewhere. These securities have not been, and will not be, registered in the United States Securities Act of 1933, as amended, or any state securities laws, and may not be offered or sold in the United States or to U.S. persons unless registered or exempt therefrom.

Contact Information

For further information please visit https://vaxil-bio.com/ or contact:

Gadi Levin, CEO
info@vaxil-bio.com
647-558-5564

Cytek® Biosciences Deepens Commitment to Expanding Access to Flow Cytometry

Cytek® Biosciences Deepens Commitment to Expanding Access to Flow Cytometry




Cytek® Biosciences Deepens Commitment to Expanding Access to Flow Cytometry

Supports ISAC in Mission to Extend Flow Cytometry Reach Worldwide; Unveils Programs Offering Instrument Award and Research Grants

FREMONT, Calif., Oct. 29, 2025 (GLOBE NEWSWIRE) — Amid the reduction of various government grant programs and global economic challenges that have tightened research funding, Cytek Biosciences, Inc. (Nasdaq: CTKB) is taking steps to ensure critical scientific research can continue. Joining the International Society for Advancement of Cytometry’s (ISAC) mission to advance global availability and adoption of cytometry technology and empower scientists, Cytek has launched a two-part research support initiative to make cell analysis more accessible.

ISAC President Jessica P. Houston commended these initiatives. “Cytek’s commitment to expanding access to advanced cytometry is a vital contribution to global public health. By supporting under-resourced labs, they’re helping ensure that essential research can continue – regardless of geography or funding. I applaud this meaningful step toward greater scientific equity.”

As the first phase of this initiative, Cytek is awarding a three-laser Cytek Northern Lights™ flow cytometer. This easy-to-use, flexible, and affordable full spectrum flow cytometer incorporates Cytek’s powerful Full Spectrum Profiling™ (FSP®) technology, enabling a wide array of assays on one instrument. The Cytek Northern Lights™ system delivers high-quality data quickly, making advanced performance attainable for everyday research applications.

“What sets Cytek apart is not just the instruments we build, but how we engage with the scientific community,” said Wenbin Jiang, Ph.D., CEO of Cytek Biosciences. “Our employees share a passion for advancing discovery, and that inspires us to support research through initiatives like this. Together, we are helping shape an industry where innovation is measured not only by patents or features but by the real impact on science worldwide.”

In the second phase of the initiative, Cytek plans to launch a grant program to fund eligible research projects, with applications assessed through a transparent, merit-based process overseen by the company’s scientific advisory board. The grant program is expected to debut in conjunction with CYTO 2026, with full details to be shared at that time.

These initiatives build on an ongoing collaboration between Cytek and ISAC to expand access to advanced cytometry tools worldwide. Earlier this year, the organizations partnered to donate a Cytek Northern Lights™ flow cytometer to the Laboratory of Molecular Biology and Cytogenetics at Hospital Dr. Arturo Oñativia in Salta, Argentina. With support from both ISAC and Cytek, the instrument is enabling high-parameter immune monitoring and translational research, strengthening scientific capabilities in the region. The donation exemplifies how collaboration can empower scientists in underserved communities and advance the field of cytometry globally.

Cytek is committed to democratizing access to flow cytometry, empowering every lab, regardless of budget, size, or location, with the tools and support to unlock cellular insights that drive progress in health, science, and society.

“By pairing world-class instrumentation with community engagement and support programs, Cytek is helping to ensure that the benefits of innovation reach the entire scientific community,” Jiang added. “We are committed to supporting research that advances science for everyone.”

To enter for a chance to win the Cytek Northern Lights™ three-laser system, please visit https://cytekbio.com/pages/expanding-access.1

For more information, please visit https://cytekbio.com/.

About the International Society for Advancement of Cytometry (ISAC)
The International Society for Advancement of Cytometry (ISAC) is a global scientific society with a mission to foster an inclusive, multidisciplinary, international community in the field of single-cell analysis. Focusing on flow and image cytometry, automated microscopy, and high-content screening, ISAC champions technological innovation and the development of professionals in these domains. With a vision centered on advancing cytometry, ISAC addresses key challenges in single-bioparticle analysis. As a collaborative hub, ISAC facilitates the exchange of cutting-edge ideas and educational opportunities, uniting academicians, industry professionals, researchers, and students. To discover more about ISAC’s contributions to the world of cytometry or to explore the benefits of membership, please visit www.isac-net.org.

About Cytek Biosciences, Inc.
Cytek Biosciences (Nasdaq: CTKB) is a leading cell analysis solutions company advancing the next generation of cell analysis tools by delivering high-resolution, high-content and high-sensitivity cell analysis utilizing its patented Full Spectrum Profiling™ (FSP®) technology. Cytek’s novel approach harnesses the power of information within the entire spectrum of a fluorescent signal to achieve a higher level of multiplexing with precision and sensitivity. Cytek’s platform includes: its core FSP instruments, the Cytek Aurora™, Northern Lights™, Cytek Aurora™ CS and Cytek Aurora™ Evo systems; the Cytek Orion™ reagent cocktail preparation system; the Enhanced Small Particle™ (ESP™) detection technology; the flow cytometers and imaging products under the Amnis® and Guava® brands; and reagents, software and services to provide a comprehensive and integrated suite of solutions for its customers. Cytek is headquartered in Fremont, California with offices and distribution channels across the globe. More information about the company and its products is available at www.cytekbio.com.

Cytek’s products are for research use only and not for use in diagnostic procedures (other than Cytek’s Northern Lights-CLC system and certain reagents, which are available for clinical use only in China and the European Union).

Cytek, Full Spectrum Profiling, FSP, Cytek Aurora, Northern Lights, Enhanced Small Particle, ESP, Cytek Orion, Amnis and Guava are trademarks of Cytek Biosciences, Inc.

In addition to filings with the Securities and Exchange Commission (SEC), press releases, public conference calls and webcasts, Cytek uses its website (www.cytekbio.com), LinkedIn page and X account as channels of distribution of information about its company, products, planned financial and other announcements, attendance at upcoming investor and industry conferences and other matters. Such information may be deemed material information and Cytek may use these channels to comply with its disclosure obligations under Regulation FD. Therefore, investors should monitor Cytek’s website, LinkedIn page, and X account in addition to following its SEC filings, news releases, public conference calls and webcasts.

Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995 as contained in Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended, which are subject to the “safe harbor” created by those sections. All statements other than statements of historical facts are forward-looking statements. In some cases, you can identify forward-looking statements because they contain words such as “anticipate,” “believe,” “contemplate,” “continue,” “could,” “estimate,” “expect,” “intend,” “may,” “plan,” “potential,” “predict,” “project,” “should,” “target,” “will,” or “would” or the negative of these words or other similar terms or expressions. These forward-looking statements include statements regarding Cytek’s future initiatives to expand access to advanced cytometry tools worldwide. These statements are based on management’s current expectations, forecasts, beliefs, assumptions and information currently available to management. These statements also deal with future events and involve known and unknown risks, uncertainties and other factors that may cause actual results, performance or achievements to be materially different from the information expressed or implied by these forward-looking statements. Factors that could cause actual results to differ materially include global geopolitical, economic and market conditions; Cytek’s ability to manage the impacts of recent and future export controls and licensing requirements, tariffs and NIH funding policies on its business; Cytek’s ability to evaluate its prospects for future viability and predict future performance; Cytek’s ability to accurately forecast customer demand and adoption of its products; Cytek’s ability to recognize the anticipated benefits of collaborations; Cytek’s dependence on certain sole and single source suppliers; competition; market acceptance of Cytek’s current and potential products; Cytek’s ability to manage the growth and complexity of its organization, maintain relationships with customers and suppliers and hire and retain key employees; Cytek’s ability to manufacture its products in high-quality commercial quantities successfully and consistently to meet demand; Cytek’s ability to increase penetration in its existing markets and expand into adjacent markets; Cytek’s ability to secure additional distributors or maintain good relationships with its existing distributors; Cytek’s ability to successfully develop and introduce new products; Cytek’s ability to maintain, protect and enhance its intellectual property; Cytek’s ability to continue to stay in compliance with its material contractual obligations, applicable laws and regulations; and foreign currency exchange impacts. You should refer to the section entitled “Risk Factors” set forth in Cytek’s Quarterly Report on Form 10-Q filed on August 6, 2025 with the SEC, and other filings Cytek makes with the SEC from time to time for a discussion of important factors that may cause actual results to differ materially from those expressed or implied by Cytek’s forward-looking statements. Although Cytek believes that the expectations reflected in the forward-looking statements are reasonable, it cannot provide any assurance that these expectations will prove to be correct nor can it guarantee that the events and circumstances reflected in the forward-looking statements will occur. The forward-looking statements in this press release are based on information available to Cytek as of the date hereof, and Cytek disclaims any obligation to update any forward-looking statements provided to reflect any change in its expectations or any change in events, conditions, or circumstances on which any such statement is based, except as required by law. These forward-looking statements should not be relied upon as representing Cytek’s as of any date subsequent to the date of this press release.

Media Contact:
Stephanie Olsen
Lages & Associates
(949) 453-8080
stephanie@lages.com

Investor Contact:
Paul Goodson
Head of Investor Relations
Cytek Biosciences
pgoodson@cytekbio.com


1 No purchase necessary to enter or win. The instrument award is open only to institutions, organizations, and business entities that are eligible to participate through an authorized representative over the age of 18 who is a legal resident of the United States or Canada. Please read the Official Rules and Privacy Notice for more information.

A photo accompanying this announcement is available at https://www.globenewswire.com/NewsRoom/AttachmentNg/c39ad800-c0ca-41fd-8cf0-f5e80c4156e6

STERIS Announces Dividend of $0.63 per share

STERIS Announces Dividend of $0.63 per share




STERIS Announces Dividend of $0.63 per share

DUBLIN, IRELAND, Oct. 29, 2025 (GLOBE NEWSWIRE) — STERIS plc (NYSE: STE) (“STERIS” or the “Company”) announced today that the Company will distribute a quarterly dividend of $0.63 per share. The dividend is payable on December 18, 2025, to shareholders of record at the close of business on November 18, 2025.  

Additional information about the U.S. tax treatment of dividends, including required Forms 8937, is available at www.steris-ir.com.

STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention. WE HELP OUR CUSTOMERS CREATE A HEALTHIER AND SAFER WORLD by providing innovative healthcare and life science products and services around the globe.

Company Contact:

Julie Winter, Vice President, Investor Relations and Corporate Communications

Julie_Winter@steris.com

440.392.7245

CAUTIONARY STATEMENT REGARDING FORWARD-LOOKING INFORMATION

This release may contain statements concerning certain trends, expectations, forecasts, estimates, or other forward-looking information affecting or relating to STERIS or its industry, products or activities that are intended to qualify for the protections afforded “forward-looking statements” under the Private Securities Litigation Reform Act of 1995 and other laws and regulations. Forward-looking statements speak only as to the date the statement is made and may be identified by the use of forward-looking terms such as “may,” “will,” “expects,” “believes,” “anticipates,” “plans,” “estimates,” “projects,” “targets,” “forecasts,” “outlook,” “impact,” “potential,” “confidence,” “improve,” “optimistic,” “deliver,” “orders,” “backlog,” “comfortable,” “trend,” and “seeks,” or the negative of such terms or other variations on such terms or comparable terminology.

Many factors could cause actual results to differ materially from those in the forward-looking statements including, without limitation, those identified in STERIS’s recent Annual Report on Form 10-K and other filings with the Securities and Exchange Commission. Other potential risks and uncertainties that could cause actual results to differ materially from those in the forward-looking statements include, without limitation: (a) operating costs, pressure on pricing (including, without limitation, as a result of inflation), Customer loss and business disruption (including, without limitation, difficulties in maintaining relationships with employees, Customers, clients or suppliers) being greater than expected and leading to erosion of profit margins; (b) STERIS’s ability to successfully integrate acquired businesses into its existing businesses, including unknown or inestimable liabilities, impairments, or increases in expected integration costs or difficulties in connection with the integration of such businesses; (c) changes in tax laws or interpretations or the adoption of certain income tax treaties in jurisdictions where we operate that could increase our consolidated tax liabilities, including changes in tax laws that would result in STERIS being treated as a domestic corporation for United States federal tax purposes, or tariffs and/or other trade barriers; (d) the possibility that compliance with laws, court rulings, certifications, regulations, or other regulatory actions, or the outcome of any pending or threatened litigation, including the Isomedix litigation, may delay, limit or prevent new product or service introductions, impact production, supply and/or marketing of existing products or services, result in uncovered costs, or otherwise affect STERIS’s performance, results, prospects or value; (e) the potential of international unrest, including military conflicts, economic downturn and effects of currency fluctuations; (f) the possibility of delays in receipt of orders, order cancellations, or the manufacture or shipment of ordered products; (g) the possibility that anticipated growth, performance or other results may not be achieved, or that timing, execution, impairments, or other issues associated with STERIS’s businesses, industry or initiatives may adversely impact STERIS’s performance, results, prospects or value; (h) the impact on STERIS and its operations of any legislation, regulations or orders, including but not limited to any new trade, regulations or orders, that may be implemented by the U.S. administration or Congress, or of any responses thereto by non-U.S. governments; (i) the possibility that anticipated financial results, anticipated revenue, productivity improvements, cost savings, growth synergies, and other anticipated benefits of acquisitions, restructuring efforts, and divestitures will not be realized or will be less than anticipated; (j) the level of STERIS’s indebtedness limiting financial flexibility or increasing future borrowing costs; (k) the effects of changes in credit availability and pricing, as well as the ability of STERIS and STERIS’s Customers and suppliers to adequately access the credit markets, on favorable terms or at all, when needed; (l) the impacts of increasing competition within our industry, which may exert pressure on our pricing strategy or lead to decreasing demand for our products and services; (m) the effects on our operations resulting from labor-related issues, such as strikes, unsuccessful union negotiations and other workforce disruptions; (n) the possibility of economic downturns and recessions, which could negatively impact our business by reducing consumer and Customer spending. Unless legally required, STERIS does not undertake to update or revise any forward-looking statements even if events make clear that any projected results, express or implied, will not be realized.

STERIS Announces Dividend of $0.63 per share

STERIS Announces Dividend of $0.63 per share




STERIS Announces Dividend of $0.63 per share

DUBLIN, IRELAND, Oct. 29, 2025 (GLOBE NEWSWIRE) — STERIS plc (NYSE: STE) (“STERIS” or the “Company”) announced today that the Company will distribute a quarterly dividend of $0.63 per share. The dividend is payable on December 18, 2025, to shareholders of record at the close of business on November 18, 2025.  

Additional information about the U.S. tax treatment of dividends, including required Forms 8937, is available at www.steris-ir.com.

STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention. WE HELP OUR CUSTOMERS CREATE A HEALTHIER AND SAFER WORLD by providing innovative healthcare and life science products and services around the globe.

Company Contact:

Julie Winter, Vice President, Investor Relations and Corporate Communications

Julie_Winter@steris.com

440.392.7245

CAUTIONARY STATEMENT REGARDING FORWARD-LOOKING INFORMATION

This release may contain statements concerning certain trends, expectations, forecasts, estimates, or other forward-looking information affecting or relating to STERIS or its industry, products or activities that are intended to qualify for the protections afforded “forward-looking statements” under the Private Securities Litigation Reform Act of 1995 and other laws and regulations. Forward-looking statements speak only as to the date the statement is made and may be identified by the use of forward-looking terms such as “may,” “will,” “expects,” “believes,” “anticipates,” “plans,” “estimates,” “projects,” “targets,” “forecasts,” “outlook,” “impact,” “potential,” “confidence,” “improve,” “optimistic,” “deliver,” “orders,” “backlog,” “comfortable,” “trend,” and “seeks,” or the negative of such terms or other variations on such terms or comparable terminology.

Many factors could cause actual results to differ materially from those in the forward-looking statements including, without limitation, those identified in STERIS’s recent Annual Report on Form 10-K and other filings with the Securities and Exchange Commission. Other potential risks and uncertainties that could cause actual results to differ materially from those in the forward-looking statements include, without limitation: (a) operating costs, pressure on pricing (including, without limitation, as a result of inflation), Customer loss and business disruption (including, without limitation, difficulties in maintaining relationships with employees, Customers, clients or suppliers) being greater than expected and leading to erosion of profit margins; (b) STERIS’s ability to successfully integrate acquired businesses into its existing businesses, including unknown or inestimable liabilities, impairments, or increases in expected integration costs or difficulties in connection with the integration of such businesses; (c) changes in tax laws or interpretations or the adoption of certain income tax treaties in jurisdictions where we operate that could increase our consolidated tax liabilities, including changes in tax laws that would result in STERIS being treated as a domestic corporation for United States federal tax purposes, or tariffs and/or other trade barriers; (d) the possibility that compliance with laws, court rulings, certifications, regulations, or other regulatory actions, or the outcome of any pending or threatened litigation, including the Isomedix litigation, may delay, limit or prevent new product or service introductions, impact production, supply and/or marketing of existing products or services, result in uncovered costs, or otherwise affect STERIS’s performance, results, prospects or value; (e) the potential of international unrest, including military conflicts, economic downturn and effects of currency fluctuations; (f) the possibility of delays in receipt of orders, order cancellations, or the manufacture or shipment of ordered products; (g) the possibility that anticipated growth, performance or other results may not be achieved, or that timing, execution, impairments, or other issues associated with STERIS’s businesses, industry or initiatives may adversely impact STERIS’s performance, results, prospects or value; (h) the impact on STERIS and its operations of any legislation, regulations or orders, including but not limited to any new trade, regulations or orders, that may be implemented by the U.S. administration or Congress, or of any responses thereto by non-U.S. governments; (i) the possibility that anticipated financial results, anticipated revenue, productivity improvements, cost savings, growth synergies, and other anticipated benefits of acquisitions, restructuring efforts, and divestitures will not be realized or will be less than anticipated; (j) the level of STERIS’s indebtedness limiting financial flexibility or increasing future borrowing costs; (k) the effects of changes in credit availability and pricing, as well as the ability of STERIS and STERIS’s Customers and suppliers to adequately access the credit markets, on favorable terms or at all, when needed; (l) the impacts of increasing competition within our industry, which may exert pressure on our pricing strategy or lead to decreasing demand for our products and services; (m) the effects on our operations resulting from labor-related issues, such as strikes, unsuccessful union negotiations and other workforce disruptions; (n) the possibility of economic downturns and recessions, which could negatively impact our business by reducing consumer and Customer spending. Unless legally required, STERIS does not undertake to update or revise any forward-looking statements even if events make clear that any projected results, express or implied, will not be realized.

Cytek® Biosciences Deepens Commitment to Expanding Access to Flow Cytometry

Cytek® Biosciences Deepens Commitment to Expanding Access to Flow Cytometry




Cytek® Biosciences Deepens Commitment to Expanding Access to Flow Cytometry

Supports ISAC in Mission to Extend Flow Cytometry Reach Worldwide; Unveils Programs Offering Instrument Award and Research Grants

FREMONT, Calif., Oct. 29, 2025 (GLOBE NEWSWIRE) — Amid the reduction of various government grant programs and global economic challenges that have tightened research funding, Cytek Biosciences, Inc. (Nasdaq: CTKB) is taking steps to ensure critical scientific research can continue. Joining the International Society for Advancement of Cytometry’s (ISAC) mission to advance global availability and adoption of cytometry technology and empower scientists, Cytek has launched a two-part research support initiative to make cell analysis more accessible.

ISAC President Jessica P. Houston commended these initiatives. “Cytek’s commitment to expanding access to advanced cytometry is a vital contribution to global public health. By supporting under-resourced labs, they’re helping ensure that essential research can continue – regardless of geography or funding. I applaud this meaningful step toward greater scientific equity.”

As the first phase of this initiative, Cytek is awarding a three-laser Cytek Northern Lights™ flow cytometer. This easy-to-use, flexible, and affordable full spectrum flow cytometer incorporates Cytek’s powerful Full Spectrum Profiling™ (FSP®) technology, enabling a wide array of assays on one instrument. The Cytek Northern Lights™ system delivers high-quality data quickly, making advanced performance attainable for everyday research applications.

“What sets Cytek apart is not just the instruments we build, but how we engage with the scientific community,” said Wenbin Jiang, Ph.D., CEO of Cytek Biosciences. “Our employees share a passion for advancing discovery, and that inspires us to support research through initiatives like this. Together, we are helping shape an industry where innovation is measured not only by patents or features but by the real impact on science worldwide.”

In the second phase of the initiative, Cytek plans to launch a grant program to fund eligible research projects, with applications assessed through a transparent, merit-based process overseen by the company’s scientific advisory board. The grant program is expected to debut in conjunction with CYTO 2026, with full details to be shared at that time.

These initiatives build on an ongoing collaboration between Cytek and ISAC to expand access to advanced cytometry tools worldwide. Earlier this year, the organizations partnered to donate a Cytek Northern Lights™ flow cytometer to the Laboratory of Molecular Biology and Cytogenetics at Hospital Dr. Arturo Oñativia in Salta, Argentina. With support from both ISAC and Cytek, the instrument is enabling high-parameter immune monitoring and translational research, strengthening scientific capabilities in the region. The donation exemplifies how collaboration can empower scientists in underserved communities and advance the field of cytometry globally.

Cytek is committed to democratizing access to flow cytometry, empowering every lab, regardless of budget, size, or location, with the tools and support to unlock cellular insights that drive progress in health, science, and society.

“By pairing world-class instrumentation with community engagement and support programs, Cytek is helping to ensure that the benefits of innovation reach the entire scientific community,” Jiang added. “We are committed to supporting research that advances science for everyone.”

To enter for a chance to win the Cytek Northern Lights™ three-laser system, please visit https://cytekbio.com/pages/expanding-access.1

For more information, please visit https://cytekbio.com/.

About the International Society for Advancement of Cytometry (ISAC)
The International Society for Advancement of Cytometry (ISAC) is a global scientific society with a mission to foster an inclusive, multidisciplinary, international community in the field of single-cell analysis. Focusing on flow and image cytometry, automated microscopy, and high-content screening, ISAC champions technological innovation and the development of professionals in these domains. With a vision centered on advancing cytometry, ISAC addresses key challenges in single-bioparticle analysis. As a collaborative hub, ISAC facilitates the exchange of cutting-edge ideas and educational opportunities, uniting academicians, industry professionals, researchers, and students. To discover more about ISAC’s contributions to the world of cytometry or to explore the benefits of membership, please visit www.isac-net.org.

About Cytek Biosciences, Inc.
Cytek Biosciences (Nasdaq: CTKB) is a leading cell analysis solutions company advancing the next generation of cell analysis tools by delivering high-resolution, high-content and high-sensitivity cell analysis utilizing its patented Full Spectrum Profiling™ (FSP®) technology. Cytek’s novel approach harnesses the power of information within the entire spectrum of a fluorescent signal to achieve a higher level of multiplexing with precision and sensitivity. Cytek’s platform includes: its core FSP instruments, the Cytek Aurora™, Northern Lights™, Cytek Aurora™ CS and Cytek Aurora™ Evo systems; the Cytek Orion™ reagent cocktail preparation system; the Enhanced Small Particle™ (ESP™) detection technology; the flow cytometers and imaging products under the Amnis® and Guava® brands; and reagents, software and services to provide a comprehensive and integrated suite of solutions for its customers. Cytek is headquartered in Fremont, California with offices and distribution channels across the globe. More information about the company and its products is available at www.cytekbio.com.

Cytek’s products are for research use only and not for use in diagnostic procedures (other than Cytek’s Northern Lights-CLC system and certain reagents, which are available for clinical use only in China and the European Union).

Cytek, Full Spectrum Profiling, FSP, Cytek Aurora, Northern Lights, Enhanced Small Particle, ESP, Cytek Orion, Amnis and Guava are trademarks of Cytek Biosciences, Inc.

In addition to filings with the Securities and Exchange Commission (SEC), press releases, public conference calls and webcasts, Cytek uses its website (www.cytekbio.com), LinkedIn page and X account as channels of distribution of information about its company, products, planned financial and other announcements, attendance at upcoming investor and industry conferences and other matters. Such information may be deemed material information and Cytek may use these channels to comply with its disclosure obligations under Regulation FD. Therefore, investors should monitor Cytek’s website, LinkedIn page, and X account in addition to following its SEC filings, news releases, public conference calls and webcasts.

Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995 as contained in Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended, which are subject to the “safe harbor” created by those sections. All statements other than statements of historical facts are forward-looking statements. In some cases, you can identify forward-looking statements because they contain words such as “anticipate,” “believe,” “contemplate,” “continue,” “could,” “estimate,” “expect,” “intend,” “may,” “plan,” “potential,” “predict,” “project,” “should,” “target,” “will,” or “would” or the negative of these words or other similar terms or expressions. These forward-looking statements include statements regarding Cytek’s future initiatives to expand access to advanced cytometry tools worldwide. These statements are based on management’s current expectations, forecasts, beliefs, assumptions and information currently available to management. These statements also deal with future events and involve known and unknown risks, uncertainties and other factors that may cause actual results, performance or achievements to be materially different from the information expressed or implied by these forward-looking statements. Factors that could cause actual results to differ materially include global geopolitical, economic and market conditions; Cytek’s ability to manage the impacts of recent and future export controls and licensing requirements, tariffs and NIH funding policies on its business; Cytek’s ability to evaluate its prospects for future viability and predict future performance; Cytek’s ability to accurately forecast customer demand and adoption of its products; Cytek’s ability to recognize the anticipated benefits of collaborations; Cytek’s dependence on certain sole and single source suppliers; competition; market acceptance of Cytek’s current and potential products; Cytek’s ability to manage the growth and complexity of its organization, maintain relationships with customers and suppliers and hire and retain key employees; Cytek’s ability to manufacture its products in high-quality commercial quantities successfully and consistently to meet demand; Cytek’s ability to increase penetration in its existing markets and expand into adjacent markets; Cytek’s ability to secure additional distributors or maintain good relationships with its existing distributors; Cytek’s ability to successfully develop and introduce new products; Cytek’s ability to maintain, protect and enhance its intellectual property; Cytek’s ability to continue to stay in compliance with its material contractual obligations, applicable laws and regulations; and foreign currency exchange impacts. You should refer to the section entitled “Risk Factors” set forth in Cytek’s Quarterly Report on Form 10-Q filed on August 6, 2025 with the SEC, and other filings Cytek makes with the SEC from time to time for a discussion of important factors that may cause actual results to differ materially from those expressed or implied by Cytek’s forward-looking statements. Although Cytek believes that the expectations reflected in the forward-looking statements are reasonable, it cannot provide any assurance that these expectations will prove to be correct nor can it guarantee that the events and circumstances reflected in the forward-looking statements will occur. The forward-looking statements in this press release are based on information available to Cytek as of the date hereof, and Cytek disclaims any obligation to update any forward-looking statements provided to reflect any change in its expectations or any change in events, conditions, or circumstances on which any such statement is based, except as required by law. These forward-looking statements should not be relied upon as representing Cytek’s as of any date subsequent to the date of this press release.

Media Contact:
Stephanie Olsen
Lages & Associates
(949) 453-8080
stephanie@lages.com

Investor Contact:
Paul Goodson
Head of Investor Relations
Cytek Biosciences
pgoodson@cytekbio.com


1 No purchase necessary to enter or win. The instrument award is open only to institutions, organizations, and business entities that are eligible to participate through an authorized representative over the age of 18 who is a legal resident of the United States or Canada. Please read the Official Rules and Privacy Notice for more information.

A photo accompanying this announcement is available at https://www.globenewswire.com/NewsRoom/AttachmentNg/c39ad800-c0ca-41fd-8cf0-f5e80c4156e6

Wave Life Sciences Announced Positive Target Engagement Data from INLIGHT Clinical Trial of WVE-007 for Obesity During Annual Research Day

Wave Life Sciences Announced Positive Target Engagement Data from INLIGHT Clinical Trial of WVE-007 for Obesity During Annual Research Day




Wave Life Sciences Announced Positive Target Engagement Data from INLIGHT Clinical Trial of WVE-007 for Obesity During Annual Research Day

Dose-dependent mean reductions of Activin E of up to 85% one month post single dose of WVE-007 in INLIGHT clinical trial, exceeding levels that led to weight loss in preclinical models; WVE-007 is generally safe and well tolerated to date

Activin E reduction in lowest dose cohort of INLIGHT was sustained through 6 months, supporting once or twice a year dosing

Multiple clinical data updates from INLIGHT, including body composition and body weight, are anticipated starting in 4Q 2025

Additional updates included announcement of WVE-008, PNPLA3 RNA editing candidate for liver disease, with CTA submission anticipated in 2026

Preclinical data supports Wave’s emerging pipeline of hepatic and extra-hepatic RNA editing and siRNA programs; emerging modality adds capability to simultaneously edit and silence two unique targets with a single oligonucleotide construct

CAMBRIDGE, Mass., Oct. 29, 2025 (GLOBE NEWSWIRE) — Wave Life Sciences Ltd. (Nasdaq: WVE), a clinical-stage biotechnology company focused on unlocking the broad potential of RNA medicines to transform human health, today announced Activin E target engagement data from its INLIGHT clinical trial of WVE-007, a GalNAc-siRNA, for the treatment of obesity during the company’s annual analyst and investor Research Day.

“We are incredibly excited to be observing potent, durable, and dose-dependent Activin E reductions with just single doses of WVE-007 in the first three cohorts of our INLIGHT clinical trial for obesity. This indicates our preclinical data are translating and affirms we have a potential best-in-class RNAi modality enabled by our proprietary chemistry, including PN,” said Paul Bolno, MD, MBA, President and Chief Executive Officer of Wave Life Sciences. “We also continue to lead the field in RNA editing. With the successful clinical translation of WVE-006 for AATD, we are further expanding our editing pipeline and have now selected WVE-008 as our PNPLA3 RNA editing clinical candidate for liver disease. WVE-008 is on track to enter clinical development next year with the filing of a CTA. In addition to that, we are pioneering a new modality by uniting editing and silencing in a single oligonucleotide construct. With multiple planned clinical updates across our RNA editing and RNAi programs, Wave is in a unique position to unlock tremendous value from our robust RNA medicines pipeline.”

INLIGHT clinical study and target engagement update:

WVE-007 (GalNAc-siRNA): INHBE silencing approach designed to reduce fat while preserving muscle mass

  • Wave’s INHBE program has a strong foundation in human genetics. People living with naturally low levels of INHBE have lower levels of unhealthy visceral fat, lower fasting glucose and triglycerides, and a lower risk of type 2 diabetes and cardiovascular disease. Silencing INHBE mRNA aims to reduce Activin E levels, thereby inducing fat loss without impacting muscle mass.
  • In Wave’s preclinical studies of mice with diet-induced obesity (DIO), single doses of GalNAc INHBE-siRNA led to potent and durable Activin E reductions of greater than 70%, and weight loss driven by reduction in visceral fat, without affecting muscle mass. Preclinical studies also support the use of INHBE GalNAc-siRNA as an add-on to GLP-1s or to curtail weight regain following cessation of GLP-1s. These reduced Activin E levels led to adipocyte shrinkage, fewer pro-inflammatory macrophages, less fibrosis, and improved insulin sensitivity in visceral adipose tissue, linking increased lipolysis to lower cardiometabolic risk.
  • Today, Wave announced highly significant, dose-dependent Activin E reductions were observed in the first three cohorts of its ongoing INLIGHT clinical trial evaluating WVE-007 (3:1 active: placebo). The trial is designed to address safety and tolerability as well as target engagement (Activin E reduction). One-month follow-up was available from Cohort 2 (240 mg) and Cohort 3 (400 mg), and six-month follow-up from Cohort 1.
  • At day 29 (one month post single dose), mean Activin E reductions from baseline were all highly significant (p<0.0001 for all doses):
    • Cohort 3 (400 mg): 85% reduction
    • Cohort 2 (240 mg): 75% reduction
    • Cohort 1 (75 mg): 56% reduction
  • The one-month reductions of Activin E observed in the 240 mg and 400 mg cohorts exceed levels that led to fat loss in preclinical models.
  • In Cohort 1 (75 mg), Activin E reductions were durable throughout the 6-month follow-up, supporting WVE-007’s potential for once or twice yearly doing.
  • WVE-007 is safe and well tolerated to date. An independent data monitoring committee supported dose expansion of the 600 mg cohort and dose escalation beyond that.
  • WVE-007 aims to achieve fat loss on par with semaglutide by six months of follow up post-single WVE-007 dose.
  • Next steps: Wave expects to deliver multiple clinical data updates from INLIGHT, including body composition and body weight:
    • 4Q 2025: semaglutide three-month follow-up data from the expanded Cohort 2 (240 mg), as well as data from Cohort 1 (75 mg).
    • 1Q 2026: anticipated six-month follow-up data from Cohort 2 and three-month follow-up data from Cohort 3.
    • 2Q 2026: anticipated six-month follow-up data from Cohort 3 and three-month follow-up data from Cohort 4.

Additional details can be found in the company’s Research Day presentation.

Additional updates from today’s presentation:

WVE-006 (RNA Editing): potential first- and best-in-class therapy for AATD that addresses both lung and liver manifestations of the disease

  • The ongoing Phase 1b/2a RestorAATion-2 study is evaluating WVE-006, a GalNAc-conjugated RNA editing oligonucleotide, as a treatment for alpha-1 antitrypsin deficiency (AATD). The multidose portion of Cohort 2 is currently ongoing with monthly doses of 400 mg. Today, Wave announced Cohort 3 is now underway at doses of 600 mg of WVE-006.
  • In September 2025, Wave announced WVE-006 has already achieved key treatment goals by restoring protein levels associated with lower risk of AATD liver and lung diseases. Total AAT levels reached 13 µM, wild type M-AAT protein accounted for 64% of circulating total AAT after treatment, with a corresponding reduction in Z AATD. Notably, WVE-006 restored the ability to dynamically produce therapeutically relevant levels of AAT protein during an acute phase response, with an individual reaching over 20 µM AAT protein.
  • Next steps: 400 mg multidose cohort data expected in the first quarter of 2026; 600 mg single dosing is underway in the third and final cohort, with single and multi-dose data expected in 2026.

WVE-008 (RNA Editing): potential first-in-class, disease modifying therapy for PNPLA3-I148M liver disease

  • Building on the successful clinical translation of Wave’s RNA editing capability, the company has selected WVE-008 as its clinical candidate for PNPLA3-I148M liver disease.
  • There are an estimated 9 million homozygous PNPLA3-I148M individuals with liver disease in the U.S. and Europe. These homozygous carriers have a significantly higher risk of liver-related death compared to heterozygous carriers. Wave’s RNA editing approach aims to achieve at least 50% correction to restore the heterozygous phenotype with low risk of liver disease, similar to the approach with WVE-006.
  • Next steps: Wave expects to file a Clinical Trial Application (CTA) for WVE-008 in 2026.

Wave’s platform innovations: extra-hepatic delivery and an emerging new modality

  • Through chemistry optimization tailored to target and cell type, Wave is expanding its emerging pipeline of siRNAs (SpiNAs) and RNA editing oligonucleotides (AIMers) to both hepatic and extrahepatic tissues, including skeletal muscle, heart, adipose, and kidney.
  • Emerging modality adds capability to simultaneously edit and silence two unique targets with a single oligonucleotide construct. Wave presented preclinical data demonstrating that a single GalNAc-oligonucleotide construct upregulated LDLR protein and silenced PCSK9 mRNA.

An archived webcast of the event can be accessed by visiting “Investor Events” on the investor relations section of the Wave Life Sciences website: https://ir.wavelifesciences.com/events-publications/events.

About Wave Life Sciences
Wave Life Sciences (Nasdaq: WVE) is a biotechnology company focused on unlocking the broad potential of RNA medicines to transform human health. Wave’s RNA medicines platform, PRISM®, combines multiple modalities, chemistry innovation and deep insights in human genetics to deliver scientific breakthroughs that treat both rare and common disorders. Its toolkit of RNA-targeting modalities includes editing, splicing, RNA interference and antisense silencing, providing Wave with unmatched capabilities for designing and sustainably delivering candidates that optimally address disease biology. Wave’s diversified pipeline includes clinical programs in alpha-1 antitrypsin deficiency, obesity, Duchenne muscular dystrophy, and Huntington’s disease, as well as several preclinical programs utilizing the company’s broad RNA therapeutics toolkit. Driven by the calling to “Reimagine Possible,” Wave is leading the charge toward a world in which human potential is no longer hindered by the burden of disease. Wave is headquartered in Cambridge, MA. For more information on Wave’s science, pipeline and people, please visit www.wavelifesciences.com and follow Wave on X and LinkedIn.

Forward-Looking Statements
This press release contains forward-looking statements concerning our goals, beliefs, expectations, strategies, objectives and plans, and other statements that are not necessarily based on historical facts, including statements regarding the following, among others: the anticipated initiation, site activation, patient recruitment, patient enrollment, dosing, generation and reporting of data and completion of our clinical trials, including interactions with regulators and any potential registration based on these data, and the timing and announcement of such events; our understanding of the dose levels and dosing frequency of our therapeutic candidates; our understanding of the safety profile of our therapeutic candidates; our expectations for our clinical candidates and the anticipated therapeutic benefits thereof; the potential of WVE-007’s mechanism (INHBE) as a novel and unique obesity treatment to induce fat loss, preserve muscle, and drive weight loss; the anticipated therapeutic benefits of WVE-006 as a therapy for AATD and the potential to address both lung and liver manifestations of the disease; our understanding of the anticipated therapeutic benefits of WVE-008 as a therapy for PNPLA3-I148M liver disease; regulatory submissions and timing for regulatory feedback; the protocol, design and endpoints of our clinical trials; the future performance and results of our programs in clinical trials; our expectations with respect to how our preclinical and clinical data successes to date may predict success for our future therapeutic candidates, future clinical data readouts and further validate of our platform; the potential of our preclinical data to predict the behavior of our compounds in humans; our identification and expected timing of future product candidates and clinical-stage programs and their therapeutic potential; the anticipated benefits of our therapeutic candidates and pipeline compared to our competitors; patient population estimates related to our therapeutic candidates and the potential addressable market that our therapeutics may address; our ability to design compounds using various modalities and the anticipated benefits of that approach; the breadth and versatility of our PRISM drug discovery and development platform; the expected benefits of our stereopure oligonucleotides compared with stereorandom oligonucleotides; the potential benefits of our RNA editing capability, including our AIMers, compared to others; the potential benefits of our emerging pipeline of siRNAs (SpiNAs) compared to others; the benefits of RNA medicines generally; the potential for certain of our programs to be best-in-class or first-in-class; our ability to translate genetic insights into high impact medicines; the status and progress of our programs relative to potential competitors; the progress and potential benefits of our collaborations; our expectations on the company’s future growth; and the anticipated duration of our cash runway and our ability to fund future operations. The words “may,” “will,” “could,” “would,” “should,” “expect,” “plan,” “anticipate,” “intend,” “believe,” “estimate,” “predict,” “project,” “potential,” “continue,” “target” and similar expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. Any forward-looking statements in this press release are based on management’s current expectations and beliefs and are subject to a number of risks, uncertainties and important factors that may cause actual results to differ materially from those indicated by these forward-looking statements as a result of these risks, uncertainties and important factors, including, without limitation, the risks and uncertainties described in the section entitled “Risk Factors” in Wave’s most recent Annual Report on Form 10-K filed with the Securities and Exchange Commission (SEC), as amended, and in other filings Wave makes with the SEC from time to time. Wave undertakes no obligation to update the information contained in this press release to reflect subsequently occurring events or circumstances.

Contact:
Kate Rausch
VP, Corporate Affairs and Investor Relations
+1 617-949-4827

Investors:
James Salierno
Director, Investor Relations
+1 617-949-4043
InvestorRelations@wavelifesci.com

Media:
Katie Sullivan
Senior Director, Corporate Communications
+1 617-949-2936
MediaRelations@wavelifesci.com

Wave Life Sciences Announced Positive Target Engagement Data from INLIGHT Clinical Trial of WVE-007 for Obesity During Annual Research Day

Wave Life Sciences Announced Positive Target Engagement Data from INLIGHT Clinical Trial of WVE-007 for Obesity During Annual Research Day




Wave Life Sciences Announced Positive Target Engagement Data from INLIGHT Clinical Trial of WVE-007 for Obesity During Annual Research Day

Dose-dependent mean reductions of Activin E of up to 85% one month post single dose of WVE-007 in INLIGHT clinical trial, exceeding levels that led to weight loss in preclinical models; WVE-007 is generally safe and well tolerated to date

Activin E reduction in lowest dose cohort of INLIGHT was sustained through 6 months, supporting once or twice a year dosing

Multiple clinical data updates from INLIGHT, including body composition and body weight, are anticipated starting in 4Q 2025

Additional updates included announcement of WVE-008, PNPLA3 RNA editing candidate for liver disease, with CTA submission anticipated in 2026

Preclinical data supports Wave’s emerging pipeline of hepatic and extra-hepatic RNA editing and siRNA programs; emerging modality adds capability to simultaneously edit and silence two unique targets with a single oligonucleotide construct

CAMBRIDGE, Mass., Oct. 29, 2025 (GLOBE NEWSWIRE) — Wave Life Sciences Ltd. (Nasdaq: WVE), a clinical-stage biotechnology company focused on unlocking the broad potential of RNA medicines to transform human health, today announced Activin E target engagement data from its INLIGHT clinical trial of WVE-007, a GalNAc-siRNA, for the treatment of obesity during the company’s annual analyst and investor Research Day.

“We are incredibly excited to be observing potent, durable, and dose-dependent Activin E reductions with just single doses of WVE-007 in the first three cohorts of our INLIGHT clinical trial for obesity. This indicates our preclinical data are translating and affirms we have a potential best-in-class RNAi modality enabled by our proprietary chemistry, including PN,” said Paul Bolno, MD, MBA, President and Chief Executive Officer of Wave Life Sciences. “We also continue to lead the field in RNA editing. With the successful clinical translation of WVE-006 for AATD, we are further expanding our editing pipeline and have now selected WVE-008 as our PNPLA3 RNA editing clinical candidate for liver disease. WVE-008 is on track to enter clinical development next year with the filing of a CTA. In addition to that, we are pioneering a new modality by uniting editing and silencing in a single oligonucleotide construct. With multiple planned clinical updates across our RNA editing and RNAi programs, Wave is in a unique position to unlock tremendous value from our robust RNA medicines pipeline.”

INLIGHT clinical study and target engagement update:

WVE-007 (GalNAc-siRNA): INHBE silencing approach designed to reduce fat while preserving muscle mass

  • Wave’s INHBE program has a strong foundation in human genetics. People living with naturally low levels of INHBE have lower levels of unhealthy visceral fat, lower fasting glucose and triglycerides, and a lower risk of type 2 diabetes and cardiovascular disease. Silencing INHBE mRNA aims to reduce Activin E levels, thereby inducing fat loss without impacting muscle mass.
  • In Wave’s preclinical studies of mice with diet-induced obesity (DIO), single doses of GalNAc INHBE-siRNA led to potent and durable Activin E reductions of greater than 70%, and weight loss driven by reduction in visceral fat, without affecting muscle mass. Preclinical studies also support the use of INHBE GalNAc-siRNA as an add-on to GLP-1s or to curtail weight regain following cessation of GLP-1s. These reduced Activin E levels led to adipocyte shrinkage, fewer pro-inflammatory macrophages, less fibrosis, and improved insulin sensitivity in visceral adipose tissue, linking increased lipolysis to lower cardiometabolic risk.
  • Today, Wave announced highly significant, dose-dependent Activin E reductions were observed in the first three cohorts of its ongoing INLIGHT clinical trial evaluating WVE-007 (3:1 active: placebo). The trial is designed to address safety and tolerability as well as target engagement (Activin E reduction). One-month follow-up was available from Cohort 2 (240 mg) and Cohort 3 (400 mg), and six-month follow-up from Cohort 1.
  • At day 29 (one month post single dose), mean Activin E reductions from baseline were all highly significant (p<0.0001 for all doses):
    • Cohort 3 (400 mg): 85% reduction
    • Cohort 2 (240 mg): 75% reduction
    • Cohort 1 (75 mg): 56% reduction
  • The one-month reductions of Activin E observed in the 240 mg and 400 mg cohorts exceed levels that led to fat loss in preclinical models.
  • In Cohort 1 (75 mg), Activin E reductions were durable throughout the 6-month follow-up, supporting WVE-007’s potential for once or twice yearly doing.
  • WVE-007 is safe and well tolerated to date. An independent data monitoring committee supported dose expansion of the 600 mg cohort and dose escalation beyond that.
  • WVE-007 aims to achieve fat loss on par with semaglutide by six months of follow up post-single WVE-007 dose.
  • Next steps: Wave expects to deliver multiple clinical data updates from INLIGHT, including body composition and body weight:
    • 4Q 2025: semaglutide three-month follow-up data from the expanded Cohort 2 (240 mg), as well as data from Cohort 1 (75 mg).
    • 1Q 2026: anticipated six-month follow-up data from Cohort 2 and three-month follow-up data from Cohort 3.
    • 2Q 2026: anticipated six-month follow-up data from Cohort 3 and three-month follow-up data from Cohort 4.

Additional details can be found in the company’s Research Day presentation.

Additional updates from today’s presentation:

WVE-006 (RNA Editing): potential first- and best-in-class therapy for AATD that addresses both lung and liver manifestations of the disease

  • The ongoing Phase 1b/2a RestorAATion-2 study is evaluating WVE-006, a GalNAc-conjugated RNA editing oligonucleotide, as a treatment for alpha-1 antitrypsin deficiency (AATD). The multidose portion of Cohort 2 is currently ongoing with monthly doses of 400 mg. Today, Wave announced Cohort 3 is now underway at doses of 600 mg of WVE-006.
  • In September 2025, Wave announced WVE-006 has already achieved key treatment goals by restoring protein levels associated with lower risk of AATD liver and lung diseases. Total AAT levels reached 13 µM, wild type M-AAT protein accounted for 64% of circulating total AAT after treatment, with a corresponding reduction in Z AATD. Notably, WVE-006 restored the ability to dynamically produce therapeutically relevant levels of AAT protein during an acute phase response, with an individual reaching over 20 µM AAT protein.
  • Next steps: 400 mg multidose cohort data expected in the first quarter of 2026; 600 mg single dosing is underway in the third and final cohort, with single and multi-dose data expected in 2026.

WVE-008 (RNA Editing): potential first-in-class, disease modifying therapy for PNPLA3-I148M liver disease

  • Building on the successful clinical translation of Wave’s RNA editing capability, the company has selected WVE-008 as its clinical candidate for PNPLA3-I148M liver disease.
  • There are an estimated 9 million homozygous PNPLA3-I148M individuals with liver disease in the U.S. and Europe. These homozygous carriers have a significantly higher risk of liver-related death compared to heterozygous carriers. Wave’s RNA editing approach aims to achieve at least 50% correction to restore the heterozygous phenotype with low risk of liver disease, similar to the approach with WVE-006.
  • Next steps: Wave expects to file a Clinical Trial Application (CTA) for WVE-008 in 2026.

Wave’s platform innovations: extra-hepatic delivery and an emerging new modality

  • Through chemistry optimization tailored to target and cell type, Wave is expanding its emerging pipeline of siRNAs (SpiNAs) and RNA editing oligonucleotides (AIMers) to both hepatic and extrahepatic tissues, including skeletal muscle, heart, adipose, and kidney.
  • Emerging modality adds capability to simultaneously edit and silence two unique targets with a single oligonucleotide construct. Wave presented preclinical data demonstrating that a single GalNAc-oligonucleotide construct upregulated LDLR protein and silenced PCSK9 mRNA.

An archived webcast of the event can be accessed by visiting “Investor Events” on the investor relations section of the Wave Life Sciences website: https://ir.wavelifesciences.com/events-publications/events.

About Wave Life Sciences
Wave Life Sciences (Nasdaq: WVE) is a biotechnology company focused on unlocking the broad potential of RNA medicines to transform human health. Wave’s RNA medicines platform, PRISM®, combines multiple modalities, chemistry innovation and deep insights in human genetics to deliver scientific breakthroughs that treat both rare and common disorders. Its toolkit of RNA-targeting modalities includes editing, splicing, RNA interference and antisense silencing, providing Wave with unmatched capabilities for designing and sustainably delivering candidates that optimally address disease biology. Wave’s diversified pipeline includes clinical programs in alpha-1 antitrypsin deficiency, obesity, Duchenne muscular dystrophy, and Huntington’s disease, as well as several preclinical programs utilizing the company’s broad RNA therapeutics toolkit. Driven by the calling to “Reimagine Possible,” Wave is leading the charge toward a world in which human potential is no longer hindered by the burden of disease. Wave is headquartered in Cambridge, MA. For more information on Wave’s science, pipeline and people, please visit www.wavelifesciences.com and follow Wave on X and LinkedIn.

Forward-Looking Statements
This press release contains forward-looking statements concerning our goals, beliefs, expectations, strategies, objectives and plans, and other statements that are not necessarily based on historical facts, including statements regarding the following, among others: the anticipated initiation, site activation, patient recruitment, patient enrollment, dosing, generation and reporting of data and completion of our clinical trials, including interactions with regulators and any potential registration based on these data, and the timing and announcement of such events; our understanding of the dose levels and dosing frequency of our therapeutic candidates; our understanding of the safety profile of our therapeutic candidates; our expectations for our clinical candidates and the anticipated therapeutic benefits thereof; the potential of WVE-007’s mechanism (INHBE) as a novel and unique obesity treatment to induce fat loss, preserve muscle, and drive weight loss; the anticipated therapeutic benefits of WVE-006 as a therapy for AATD and the potential to address both lung and liver manifestations of the disease; our understanding of the anticipated therapeutic benefits of WVE-008 as a therapy for PNPLA3-I148M liver disease; regulatory submissions and timing for regulatory feedback; the protocol, design and endpoints of our clinical trials; the future performance and results of our programs in clinical trials; our expectations with respect to how our preclinical and clinical data successes to date may predict success for our future therapeutic candidates, future clinical data readouts and further validate of our platform; the potential of our preclinical data to predict the behavior of our compounds in humans; our identification and expected timing of future product candidates and clinical-stage programs and their therapeutic potential; the anticipated benefits of our therapeutic candidates and pipeline compared to our competitors; patient population estimates related to our therapeutic candidates and the potential addressable market that our therapeutics may address; our ability to design compounds using various modalities and the anticipated benefits of that approach; the breadth and versatility of our PRISM drug discovery and development platform; the expected benefits of our stereopure oligonucleotides compared with stereorandom oligonucleotides; the potential benefits of our RNA editing capability, including our AIMers, compared to others; the potential benefits of our emerging pipeline of siRNAs (SpiNAs) compared to others; the benefits of RNA medicines generally; the potential for certain of our programs to be best-in-class or first-in-class; our ability to translate genetic insights into high impact medicines; the status and progress of our programs relative to potential competitors; the progress and potential benefits of our collaborations; our expectations on the company’s future growth; and the anticipated duration of our cash runway and our ability to fund future operations. The words “may,” “will,” “could,” “would,” “should,” “expect,” “plan,” “anticipate,” “intend,” “believe,” “estimate,” “predict,” “project,” “potential,” “continue,” “target” and similar expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. Any forward-looking statements in this press release are based on management’s current expectations and beliefs and are subject to a number of risks, uncertainties and important factors that may cause actual results to differ materially from those indicated by these forward-looking statements as a result of these risks, uncertainties and important factors, including, without limitation, the risks and uncertainties described in the section entitled “Risk Factors” in Wave’s most recent Annual Report on Form 10-K filed with the Securities and Exchange Commission (SEC), as amended, and in other filings Wave makes with the SEC from time to time. Wave undertakes no obligation to update the information contained in this press release to reflect subsequently occurring events or circumstances.

Contact:
Kate Rausch
VP, Corporate Affairs and Investor Relations
+1 617-949-4827

Investors:
James Salierno
Director, Investor Relations
+1 617-949-4043
InvestorRelations@wavelifesci.com

Media:
Katie Sullivan
Senior Director, Corporate Communications
+1 617-949-2936
MediaRelations@wavelifesci.com

Emergent BioSolutions Reports Third Quarter 2025 Financial Results

Emergent BioSolutions Reports Third Quarter 2025 Financial Results




Emergent BioSolutions Reports Third Quarter 2025 Financial Results

  • Third Quarter 2025 Total Revenues of $231.1 million, above the high end of Q3 guidance by $21.0 million
  • Third Quarter 2025 Net Income of $51.2 million and Net Income Margin of 22%
  • Third Quarter 2025 Gross Margin % of 54% and Adjusted Gross Margin % of 61%, an expansion of 300 bps and 200 bps, respectively, versus prior year
  • Third Quarter 2025 Adjusted EBITDA of $87.8 million and Adjusted EBITDA Margin of 38%
  • Raising the Full Year 2025 Revenue and Profitability Guidance
  • Strong Sequential Naloxone Revenue Growth, Primarily Driven by NARCAN® Nasal Spray, QoQ Through Q3 2025

GAITHERSBURG, Md., Oct. 29, 2025 (GLOBE NEWSWIRE) — Emergent BioSolutions Inc. (NYSE: EBS) today reported financial results for the third quarter ended September 30, 2025.

“Following a strong second quarter, we are proud to again beat the high end of our third quarter 2025 revenue guidance by $21 million, with continued margin expansion that gives us confidence in meeting the higher end of our adjusted EBITDA guidance for 2025,” said Joe Papa, president and CEO of Emergent. “We remain confident in our products business as evidenced by the sequential growth of our naloxone franchise, where pricing has stabilized for NARCAN® Nasal Spray, as well as continued demand from our international customers, who represent 34% of our medical countermeasures orders year to date. The Company has now secured eleven MCM contract modifications and product orders in 2025, highlighting the consistent global demand for medical countermeasures products, in a world where biological threats represent a growing risk. Our balance sheet is healthy, and we are judiciously deploying our capital to create shareholder value and build a long-term growth trajectory.”

FINANCIAL HIGHLIGHTS (1)

Q3 2025 vs. Q3 2024

($ in millions, except per share amounts) Q3 2025 Q3 2024 % Change
Total Revenues $ 231.1   $ 293.8   (21 )%
Net Income $ 51.2   $ 114.8   (55 )%
Net Income per Diluted Share $ 0.91   $ 2.06   (56 )%
Adjusted Net Income(2) $ 60.4   $ 76.2   (21 )%
Adjusted Net Income per Diluted Share(2) $ 1.06   $ 1.37   (23 )%
Adjusted EBITDA(2) $ 87.8   $ 105.3   (17 )%
Net Income Margin   22 %   39 %    
Adjusted EBITDA Margin(2)   38 %   36 %    
Gross Margin %   54 %   51 %    
Adjusted Gross Margin %(2)   61 %   59 %    


Year to Date (“YTD”) 2025
vs YTD 2024

($ in millions, except per share amounts) YTD 2025 YTD 2024 % Change
Total Revenues $ 594.2   $ 848.9   (30 )%
Net Income (Loss) $ 107.2   $ (159.3 ) 167 %
Net Income (Loss) per Diluted Share $ 1.89   $ (3.03 ) 162 %
Adjusted Net Income (Loss)(2) $ 109.6   $ (14.7 ) 846 %
Adjusted Net Income (Loss) per Diluted Share(2) $ 1.93   $ (0.28 ) 787 %
Adjusted EBITDA(2) $ 193.9   $ 162.1   20 %
Net Income (Loss) Margin   18 % (19) %  
Adjusted EBITDA Margin(2)   33 %   19 %  
Gross Margin %   48 %   26 %  
Adjusted Gross Margin %(2)   57 %   46 %  

RECENT BUSINESS UPDATES

  • Received $29 Million in MCM product orders from international government partner
  • Secured $17 Million contract modification for Oral Suspension TEMBEXA® (brincidofovir)
  • Secured $56 Million contract modification for ACAM2000® (Smallpox and Mpox (Vaccinia) Vaccine, Live)
  • Secured $30 Million contract modification for CYFENDUS® (Anthrax Vaccine Adsorbed, Adjuvanted)
  • Secured $52 Million contract modification award for CNJ-016® (Vaccinia Immune Globulin Intravenous, Human (VIGIV))
  • Updated proprietary distribution platform, NARCANDirect®, to offer KLOXXADO® Nasal Spray 8 mg and Convenience Kits
  • Recognized multiple naloxone awareness days throughout the quarter, and applauded the over-the-counter availability of naloxone in U.S. House of Representatives buildings
  • New Publication in Expert Review of Anti-infective Therapy Evaluates Brincidofovir as Potential Antiviral Treatment for Mpox

THIRD QUARTER 2025 FINANCIAL PERFORMANCE (1)

Revenues

The Company uses the following categories in discussing revenues:

  • Naloxone — comprises contributions from NARCAN® Nasal Spray and KLOXXADO® Nasal Spray
  • Anthrax MCM — comprises contributions from CYFENDUS®, previously known as AV7909, BioThrax®, Anthrasil® and Raxibacumab
  • Smallpox MCM — comprises contributions from ACAM2000®, CNJ-016® (VIGIV) and TEMBEXA®
  • Other Products — comprises contributions from BAT® and RSDL® (3)
  • All Other Revenues — comprises revenues from the Services operating segment and contracts and grants revenues
($ in millions) Q3 2025 Q3 2024 % Change
Product sales, net:(4)      
Naloxone $ 74.9 $ 95.3 (21 )%
Anthrax MCM   1.4   11.4 (88 )%
Smallpox MCM   83.6   132.7 (37 )%
Other Products   57.5   30.1 91 %
Total Product sales, net $ 217.4 $ 269.5 (19 )%
       
All other revenues $ 13.7 $ 24.3 (44 )%
       
Total revenues $ 231.1 $ 293.8 (21 )%


Product Sales, net
(4)

Naloxone

For Q3 2025, revenues from Naloxone products decreased $20.4 million, or 21%, as compared with Q3 2024. The decrease was primarily driven by lower sales of OTC NARCAN® and lower Canadian sales of branded NARCAN®, primarily driven by an unfavorable price and volume mix, partially offset by an increase in KLOXXADO® sales.

Anthrax MCM

For Q3 2025, revenues from Anthrax MCM products decreased $10.0 million, or 88%, as compared with Q3 2024. The decrease primarily reflects the impact of timing of USG sales of BioThrax® as well as timing of international sales of CYFENDUS® in the prior year period. Anthrax vaccine product sales are primarily made under annual purchase options exercised by the U.S. Government (“USG”). Fluctuations in revenues result from the timing of the exercise of annual purchase options, the timing of USG purchases, the availability of governmental funding and Company delivery of orders that follow.

Smallpox MCM

For Q3 2025, revenues from Smallpox MCM products decreased $49.1 million, or 37%, as compared with Q3 2024. The decrease was primarily due to lower USG ACAM2000® and CNJ-016® (VIGIV) sales due to timing, partially offset by an increase in international CNJ-016® (VIGIV), ACAM2000®, and TEMBEXA® sales. Fluctuations in revenues from Smallpox MCM result from the timing of the exercise of annual purchase options in the existing procurement contracts, the timing of USG purchases, the availability of governmental funding and Company delivery of orders that follow.

Other Products

For Q3 2025, revenues from Other Product sales increased $27.4 million, or 91%, as compared with Q3 2024. The increase was primarily due to higher USG BAT® sales due to timing, partially offset by a decrease in international sales orders.

All Other Revenues

Services

For Q3 2025, revenues from Services decreased $9.7 million, or 68%, as compared with Q3 2024. The decrease was primarily attributable to the decrease in revenue from the Company’s Camden facility in the current year period, which was sold to Bora Pharmaceuticals in the third quarter of 2024, partially offset by an increase in production at the Company’s Winnipeg facility.

Contracts and Grants

For Q3 2025, revenues from contracts and grants decreased $0.9 million, or 9%, as compared with Q3 2024. The decrease was due to declines in overall funded R&D projects, partially offset by an increase in development work in connection with Ebanga™.

Operating Expenses

($ in millions) Q3 2025 Q3 2024 % Change
Cost of product and services sales, net $ 85.9 $ 122.6 (30 )%
Research and development (“R&D”)   13.5   13.8 (2 )%
Selling, general and administrative (“SG&A”)   38.9   76.6 (49 )%
Amortization of intangible assets   16.3   16.3 %
Total operating expenses $ 154.6 $ 229.3 (33 )%


Cost of Product and Services Sales, Net

For Q3 2025, cost of product and services sales, net decreased $36.7 million, or 30%, as compared with Q3 2024. The decrease was driven by decreases in cost of Services of $16.2 million, cost of MCM Product sales of $15.9 million and cost of Commercial Product sales of $4.6 million.

Research and Development Expenses

For Q3 2025, R&D expenses decreased $0.3 million, or 2% as compared with Q3 2024. The decrease was primarily due to decreases in overhead and severance related costs, partially offset by an increase in unfunded R&D project spend and in Ebanga™ related development work.

Selling, General and Administrative Expenses

For Q3 2025, SG&A expenses decreased $37.7 million, or 49%, as compared with Q3 2024. The decrease was primarily due to the absence of a one-time expense of $10.0 million recognized in the prior year period and the receipt of a one-time reimbursement of $10.5 million in the current year period related to settlements of our securities and shareholder litigation matters. These non-recurring items were coupled with decreases in compensation and other employee related expenses as a result of the restructuring initiatives that began during the first quarter of 2023, and lower marketing, professional services and legal expenses.

ADDITIONAL FINANCIAL INFORMATION(1)

Capital Expenditures

($ in millions) Q3 2025 Q3 2024 % Change
Capital expenditures $ 3.4   $ 5.8   (41 )%
Capital expenditures as a % of total revenues   1 %   2 %    

For Q3 2025, capital expenditures decreased largely due to lower development activities across the Company’s facilities.

REPORTABLE SEGMENT INFORMATION

The Company manages the business with a focus on three operating segments: (1) a Commercial Products segment consisting of NARCAN® Nasal Spray and KLOXXADO® Nasal Spray, which product is currently being integrated into our distribution network, NARCANDirect®; (2) a MCM Products segment consisting of Anthrax – MCM, Smallpox – MCM and Other products and (3) a services segment consisting of our Bioservices offerings (“Services”). Commercial Products and MCM Products are our two reportable segments. In the first quarter of 2025, the Company’s determined that its Services operating segment no longer meets the quantitative thresholds of a reportable segment and did not meet the aggregation criteria set forth in Accounting Standards Codification 280, Segment Reporting, and as such is categorized within “All other revenues” along with “Contracts and Grants”. The Company evaluates the performance of these reportable segments based on revenues and segment adjusted gross margin, which is a non-GAAP financial measure. Segment revenue includes external customer sales, but does not include inter-segment services. The Company does not allocate contracts and grants revenue, R&D, SG&A, amortization of intangible assets, interest and other income (expense) or taxes to its evaluation of the performance of these segments.

THIRD QUARTER 2025 REPORTABLE SEGMENT RESULTS

($ in millions) Commercial Products
Quarter Ended September 30,
  2025     2024   $ Change % Change
Revenues $ 74.9   $ 95.3   $ (20.4 ) (21 )%
Cost of sales   42.6     47.2     (4.6 ) (10 )%
Intangible asset amortization   9.4     9.4       %
Gross margin** $ 22.9   $ 38.7   $ (15.8 ) (41 )%
Gross margin %**   31 %   41 %    
Add back:        
Intangible asset amortization $ 9.4   $ 9.4   $   %
Segment adjusted gross margin(2) $ 32.3   $ 48.1   $ (15.8 ) (33 )%
Segment adjusted gross margin %(2)   43 %   50 %    
         
         
** Gross margin is calculated as revenues less cost of sales and intangible asset amortization. Gross margin % is calculated as gross margin divided by revenues.
NM – Not Meaningful
 

Cost of Commercial Product sales decreased $4.6 million, or 10%, to $42.6 million for the quarter ended September 30, 2025. The decrease was primarily due to lower sales of OTC NARCAN® and lower Canadian sales of branded NARCAN®, partially offset by an increase in KLOXXADO® sales

Commercial Products gross margin decreased $15.8 million, or 41%, to $22.9 million for the quarter ended September 30, 2025. Commercial Products gross margin percentage decreased 10 percentage points to 31% for the quarter ended September 30, 2025. The decrease was largely due to lower sales of OTC NARCAN® and lower branded NARCAN® sales, as well as an unfavorable price and volume mix, partially offset by an increase in KLOXXADO® sales. Commercial Products segment adjusted gross margin in the current year period excludes the impact of intangible asset amortization of $9.4 million.

($ in millions) MCM Products
Quarter Ended September 30,
  2025     2024   $ Change % Change
Revenues $ 142.5   $ 174.2   $ (31.7 ) (18) %
Cost of sales   38.1     54.0     (15.9 ) (29) %
Intangible asset amortization   6.9     6.9       %
Gross margin** $ 97.5   $ 113.3   $ (15.8 ) (14) %
Gross margin %**   68 %   65 %    
Add back:        
Intangible asset amortization $ 6.9   $ 6.9   $   %
Inventory step-up provision       1.2     (1.2 ) (100) %
Restructuring costs   0.2     4.9     (4.7 ) (96) %
Segment adjusted gross margin(2) $ 104.6   $ 126.3   $ (21.7 ) (17) %
Segment adjusted gross margin %(2)   73 %   73 %    
         
         
** Gross margin is calculated as revenues less cost of sales and intangible asset amortization. Gross margin % is calculated as gross margin divided by revenues.
NM – Not Meaningful
 

Cost of MCM product sales decreased $15.9 million, or 29%, to $38.1 million for the quarter ended September 30, 2025. The decrease was primarily due to lower production costs of ACAM2000®, BioThrax®, and CNJ-016® (VIGIV), reflecting reduced volumes, combined with favorable manufacturing variances due to lower shut-down and severance costs, partially offset by an increase in costs related to higher BAT® sales volume.

MCM Product gross margin decreased $15.8 million, or 14%, to $97.5 million for the quarter ended September 30, 2025. MCM Product gross margin percentage increased 3 percentage points to 68% for the quarter ended September 30, 2025. The increase in gross margin percentage was primarily due to a favorable sales mix which was weighted more heavily towards higher margin products and a decrease in shutdown and severance related costs compared with the third quarter of 2024. MCM Product segment adjusted gross margin in the current year period excludes the impacts of intangible asset amortization of $6.9 million and restructuring costs of $0.2 million.

YTD 2025 REPORTABLE SEGMENT RESULTS

($ in millions) Commercial Products
Nine Months Ended September 30,
  2025     2024   $ Change % Change
Revenues $ 187.7   $ 333.8   $ (146.1 ) (44 )%
Cost of sales   103.5     152.7     (49.2 ) (32 )%
Intangible asset amortization   28.3     28.3       %
Gross margin** $ 55.9   $ 152.8   $ (96.9 ) (63 )%
Gross margin %**   30 %   46 %    
Add back:        
Intangible asset amortization $ 28.3   $ 28.3   $   %
Restructuring costs   0.2         0.2   NM
Segment adjusted gross margin(2) $ 84.4   $ 181.1   $ (96.7 ) (53 )%
Segment adjusted gross margin %(2)   45 %   54 %    
         
         
** Gross margin is calculated as revenues less cost of sales and intangible asset amortization. Gross margin % is calculated as gross margin divided by revenues.
NM – Not Meaningful
 

Cost of Commercial Product sales decreased $49.2 million, or 32%, to $103.5 million for the nine months ended September 30, 2025. The decrease was primarily due to lower sales of OTC NARCAN® and lower Canadian sales of branded NARCAN®, partially offset by an increase in KLOXXADO® sales.

Commercial Products gross margin decreased $96.9 million, or 63%, to $55.9 million for the nine months ended September 30, 2025. Commercial Products gross margin percentage decreased 16 percentage points to 30% for the nine months ended September 30, 2025. The decrease was largely due to lower sales of OTC NARCAN® and lower branded NARCAN® sales, as well as an unfavorable price, volume and product mix, partially offset by an increase in KLOXXADO® sales. Commercial Products segment adjusted gross margin in the current year period excludes the impact of intangible asset amortization of $28.3 million and restructuring costs of $0.2 million.

($ in millions) MCM Products
Nine Months Ended September 30,
  2025     2024   $ Change % Change
Revenues $ 357.5   $ 393.0   $ (35.5 ) (9) %
Cost of sales   114.1     147.3     (33.2 ) (23) %
Intangible asset amortization   20.5     20.5       %
Gross margin** $ 222.9   $ 225.2   $ (2.3 ) (1) %
Gross margin %**   62 %   57 %    
Add back:        
Intangible asset amortization $ 20.5   $ 20.5   $   %
Changes in fair value of financial instruments       0.6     (0.6 ) (100) %
Restructuring costs   (1.0 )   7.5     (8.5 ) (113) %
Inventory step-up provision   1.8     1.2     0.6   50 %
Segment adjusted gross margin(2) $ 244.2   $ 255.0   $ (10.8 ) (4) %
Segment adjusted gross margin %(2)   68 %   65 %    
         
         
** Gross margin is calculated as revenues less cost of sales and intangible asset amortization. Gross margin % is calculated as gross margin divided by revenues.
NM – Not Meaningful
 

Cost of MCM product sales decreased $33.2 million, or 23%, to $114.1 million for the nine months ended September 30, 2025. The decrease was primarily due to lower productions costs of CYFENDUS®, BioThrax®, and ACAM2000® reflecting reduced volumes, no RSDL® related costs in 2025 due to the sale of RSDL® to SERB in the third quarter of 2024, combined with favorable manufacturing variances mostly due to lower shut-down and severance costs and lower Raxibacumab inventory reserves. These decreases were partially offset by higher costs for Anthrasil®, TEMBEXA®, CNJ-016® (VIGIV) sales due to higher unit volume.

MCM Product gross margin decreased $2.3 million, or 1%, to $222.9 million for the nine months ended September 30, 2025. MCM Product gross margin percentage increased 5 percentage points to 62% for the nine months ended September 30, 2025. The increase in gross margin percentage was primarily due to a favorable sales mix which was weighted more heavily towards higher margin products and a decrease in shutdown and severance costs compared with the prior year period. MCM Product segment adjusted gross margin in the current year period excludes the impacts of intangible asset amortization of $20.5 million, inventory step-up provision of $1.8 million and restructuring costs of $(1.0) million.

2025 FINANCIAL FORECAST

The Company provides the following updated financial forecast for full year 2025, reflecting management’s expectations based on the most current information available.

METRIC
($ in millions)
Updated Range
(as of 10/29/2025)
Action Previous Range
(as of 08/05/2025)
Total revenues $775 – $835 REVISED $765 – $835
Net income $60 – $75 REVISED $40 – $65
Adjusted net income(2) $70 – $85 REVISED $45 – $70
Adjusted EBITDA(2) $195 – $210 REVISED $175 – $200
Adjusted gross margin %(2) 52% – 54% REVISED 50% – 52%
       
Segment Level Revenue      
MCM Products(3) $450 – $475 REVISED $440 – $475
Commercial Products(5) $265 – $300 UNCHANGED $265 – $300

Key Assumptions
($ and shares in millions)
Updated Range
(as of 10/29/2025)
Interest expense $55
R&D ~7% to 8% of Revenues
SG&A ~25% to 26% of Revenues
Weighted avg. fully diluted share count ~56
Capex ~$16
Depreciation & amortization ~$100


FOOTNOTES

(1) All financial information included in this release is unaudited.

(2) See Non-GAAP Financial Measures” and the “Reconciliation of Non-GAAP Financial Measures” tables for the definitions and reconciliations of these non-GAAP financial measures to the most closely related GAAP financial measures.

(3) Our MCM Products revenue in 2025 and forecasted revenue excludes revenues related to RSDL®, which was sold during the third quarter of 2024.

(4) Product sales, net are reported net of variable consideration including returns, rebates, wholesaler fees and prompt pay discounts in accordance with GAAP.

(5) Our Commercial Products forecast consists of revenues for NARCAN® Nasal Spray and revenues from distribution of KLOXXADO® naloxone HCl nasal spray 8 mg pursuant to an agreement with Hikma Pharmaceuticals PLC in January 2025. 

CONFERENCE CALL, PRESENTATION SUPPLEMENT AND WEBCAST INFORMATION

Company management will host a conference call at 5:00 pm eastern time today, October 29, 2025, to discuss these financial results. The conference call and presentation supplement can be accessed from the Company’s website or through the following:

By phone
Advanced registration is required.
Visit https://register-conf.media-server.com/register/BI87c9854c104a472e92d2ff019fcc47cf to register and receive an email with the dial-in number, passcode and registrant ID.

By webcast
Visit https://edge.media-server.com/mmc/p/azeu358t/
A replay of the call can be accessed from the Emergent website.

ABOUT EMERGENT BIOSOLUTIONS INC.

At Emergent, our mission is to protect and save lives. For over 25 years, we’ve been at work preparing those entrusted with protecting public health. We deliver protective and life-saving solutions for health threats like smallpox, mpox, botulism, Ebola, anthrax and opioid overdose emergencies. To learn more about how we help prepare communities around the world for today’s health challenges and tomorrow’s threats, visit our website and follow us on LinkedIn, X, Instagram, Apple Podcasts and Spotify.

NON-GAAP FINANCIAL MEASURES

In the accompanying analysis of financial information, we sometimes use information derived from consolidated and segment financial information that may not be presented in our financial statements or prepared in accordance with generally accepted accounting principles in the United States (“GAAP”). Certain of these financial measures are considered not in conformity with GAAP (“non-GAAP financial measures”) under the United States Securities and Exchange Commission (“SEC”) rules. Specifically, we have referred to the following non-GAAP financial measures:

  • Adjusted Net Income (Loss)
  • Adjusted Net Income (Loss) per Diluted Share
  • Adjusted EBITDA
  • Adjusted EBITDA Margin
  • Adjusted Gross Margin
  • Adjusted Gross Margin %
  • Segment Adjusted Gross Margin
  • Segment Adjusted Gross Margin %

We define Adjusted Net Income (Loss) and Adjusted Net Income (Loss) per Diluted Share, which are non-GAAP financial measures, as net income (loss) and net income (loss) per diluted share, respectively, excluding the impact of non-cash amortization charges, impairments, severance and restructuring costs, inventory step-up provision, acquisition and divestiture costs, exit and disposal costs, loss (gain) on sale of business and assets held for sale, settlement charges, net, contingent consideration milestones, changes in fair value of financial instruments, other expense (income) items and tax effects. We use Adjusted Net Income (Loss) for the purpose of calculating Adjusted Net Income (Loss) per Diluted Share. Management uses Adjusted Net Income (Loss) per Diluted Share to assess total Company operating performance on a consistent basis. We believe that these non-GAAP financial measures, when considered together with our GAAP financial results and GAAP financial measures, provide management and investors with an additional understanding of our business operating results, including underlying trends.

We define Adjusted EBITDA, which is a non-GAAP financial measure, as net income (loss) before depreciation and amortization, income tax provision, interest expense, net, excluding the impact of changes in fair value of financial instruments, acquisition and divestiture costs, severance and restructuring costs, loss (gain) on sale of business and assets held for sale, inventory step-up provision, contingent consideration milestones, impairments, settlement charges, net, exit and disposal costs and other expense (income) items. We define Adjusted EBITDA Margin, which is a non-GAAP financial measure, as Adjusted EBITDA divided by Total Revenues. We believe that these non-GAAP financial measures, when considered together with our GAAP financial results and GAAP financial measures, provide management and investors with a more complete understanding of our operating results, including underlying trends. In addition, EBITDA is a common alternative measure of operating performance used by many of our competitors. It is used by investors, financial analysts, rating agencies and others to value and compare the financial performance of companies in our industry, although it may be defined differently by different companies. Therefore, we also believe that this non-GAAP financial measure, considered along with corresponding GAAP financial measures, provides management and investors with additional information for comparison of our operating results with the operating results of other companies.

We define Adjusted Gross Margin, which is a non-GAAP financial measure, as Gross Margin, excluding the impact of intangible asset amortization, restructuring costs, changes in the fair value of financial instruments, settlement charges, net and inventory step-up provision. We define Adjusted Gross Margin %, which is a non-GAAP financial measure, as Adjusted Gross Margin as a percentage of Products and services sales, net.

We define Segment Adjusted Gross Margin, which is a non-GAAP financial measure, as a segment’s Gross Margin excluding the respective impact of intangible asset amortization, restructuring costs, changes in the fair value of financial instruments and inventory step-up provision. We define Segment Adjusted Gross Margin %, which is a non-GAAP financial measure, as Segment Adjusted Gross Margin as a percentage of a segment’s revenues.

Non-GAAP financial measures are not defined in the same manner by all companies and may not be comparable with other similarly titled measures of other companies. The determination of the amounts that are excluded from these non-GAAP financial measures are a matter of management judgment and depend upon, among other factors, the nature of the underlying expense or income amounts. Non-GAAP financial measures should be considered in addition to, but not as a substitute for or superior to, the information contained in our Consolidated Statements of Operations and Consolidated Statements of Cash Flows. Reconciliations of these non-GAAP financial measures to the most directly comparable GAAP financial measures are included in the financial tables accompanying this press release.

SAFE HARBOR STATEMENT

This press release includes forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, as amended. All statements, other than statements of historical fact, including statements regarding the future performance of the Company or any of our businesses, our business strategy, future operations, future financial position, future revenues and earnings, our ability to achieve the objectives of our restructuring initiatives and divestitures, including our future results, projected costs, prospects, plans and objectives of management, are forward-looking statements. We generally identify forward-looking statements by using words like “anticipate,” “believe,” “can,” “continue,” “could,” “estimate,” “expect,” “confident,” “commit,” “forecast,” “future,” “outlook,” “goal,” “intend,” “may,” “plan,” “position,” “possible,” “potential,” “predict,” “project,” “should,” “target,” “will,” “would,” and similar expressions or variations thereof, or the negative thereof, but these terms are not the exclusive means of identifying such statements. These forward-looking statements are based on our current intentions, beliefs, assumptions and expectations regarding future events based on information that is currently available. You should realize that if underlying assumptions prove inaccurate or unknown risks or uncertainties materialize, actual results could differ materially from our expectations. Readers are, therefore, cautioned not to place undue reliance on any forward-looking statement contained herein. Any such forward-looking statement speaks only as of the date of this press release, and, except as required by law, we do not undertake any obligation to update any forward-looking statement to reflect new information, events or circumstances.

There are a number of important factors that could cause our actual results to differ materially from those indicated by such forward-looking statements, including, among others, the availability of USG funding for contracts related to procurement of our medical countermeasure (“MCM”) products, including CYFENDUS® (Anthrax Vaccine Adsorbed (AVA) Adjuvanted), previously known as AV7909, ACAM2000® (Smallpox (Vaccinia) Vaccine, Live), CNJ-016® (Vaccinia Immune Globulin Intravenous (Human) (VIGIV)), BAT® (Botulism Antitoxin Heptavalent (A,B,C,D,E,F,G)-(Equine)), BioThrax® (Anthrax Vaccine Adsorbed) Ebanga™ (ansuvimab-zykl) and/or TEMBEXA® (brincidofovir) among others, as well as contracts related to development of medical countermeasures; our ability to meet our commitments to quality and compliance in all of our manufacturing operations; our ability to negotiate additional USG procurement or follow-on contracts for our MCM products that have expired or will be expiring; the commercial availability and impact of a generic and competitive marketplace on future sales of NARCAN® (naloxone HCL) Nasal Spray and over-the-counter NARCAN® Nasal Spray; our ability to perform under our contracts with the USG, including the timing of and specifications relating to deliveries; the ability of our contractors and suppliers to maintain compliance with current good manufacturing practices and other regulatory obligations; our ability to negotiate new or further commitments related to the collaboration and deployment of capacity toward future commercial manufacturing related to our bioservices and under existing Bioservices contracts; our ability to collect reimbursement for raw materials and payment of service fees from our Bioservices customers; the results of pending government investigations and their potential impact on our business; our ability to satisfy the conditions of our litigation settlement agreements, and the potential impact of such agreements, including the funds to resolve related litigation, on our business; our ability to comply with the operating and financial covenants required by (i) our term loan facility under a credit agreement, dated August 30, 2024, among the Company, the lenders from time to time party thereto and OHA Agency LLC, as administrative agent, (ii) our revolving credit facility under a credit agreement, dated September 30, 2024, among the Company, certain subsidiary borrowers, the lenders from time to time party thereto and Wells Fargo, National Association, as Agent, and (iii) our 3.875% Senior Unsecured Notes due 2028; our ability to maintain adequate internal control over financial reporting and to prepare accurate financial statements in a timely manner; our ability to maintain sufficient cash flow from our operations to pay our substantial debt, both now and in the future; our ability to invest in our business operations as a result of our current indebtedness; the impact of our share and debt repurchase programs; the procurement of our product candidates by USG entities under regulatory authorities that permit government procurement of certain medical products prior to FDA marketing authorization, and corresponding procurement by government entities outside the United States; our ability to realize the expected benefits of the sale of our travel health business to Bavarian Nordic, the sale of our Drug Product facility in Baltimore-Camden to Bora Pharmaceuticals Injectables Inc., a subsidiary of Bora Pharmaceuticals Co., Ltd., the sale of RSDL® to BTG International Inc., a subsidiary of SERB Pharmaceuticals and the sale of our Baltimore-Bayview drug substance manufacturing facility to Syngene International; our ability to realize the expected benefits from divestitures and restructuring activities; the success of our commercialization, marketing and manufacturing capabilities and strategy; our ability to identify and acquire companies, businesses, products or product candidates that satisfy our selection criteria; our ability to attract and retain qualified personnel; our ability to adequately secure and protect our intellectual property rights; our ability to realize the full benefits from our divestitures and sales of assets; the impact of cybersecurity incidents, including the risks from the unauthorized access, interruption, failure or compromise of our information systems or those of our business partners, collaborators or other third parties; and the accuracy of our estimates regarding future revenues, expenses, capital requirements and need for additional financing. The foregoing sets forth many, but not all, of the factors that could cause actual results to differ materially from our expectations in any forward-looking statement. In addition, other risks and uncertainties not presently known to us or that we currently believe to be immaterial could affect the accuracy of any forward-looking statements. Readers should consider this cautionary statement, as well as the risks identified in our periodic reports filed with the Securities and Exchange Commission, when evaluating our forward-looking statements.

Trademarks

Emergent®, BioThrax®, BaciThrax®, BAT®, Trobigard®, Anthrasil®, CNJ-016®, ACAM2000®, ​NARCAN®, CYFENDUS®, TEMBEXA® and any and all Emergent BioSolutions Inc. brands, products, services and feature names, logos and slogans are trademarks or registered trademarks of Emergent BioSolutions Inc. or its subsidiaries in the United States or other countries. All other brands, products, services and feature names or trademarks are the property of their respective owners, including KLOXXADO®, which is a registered trademark of Hikma Pharmaceuticals USA Inc.

Investor Contact
Rich Lindahl
Executive Vice President, Chief Financial Officer
lindahlr@ebsi.com
Media Contact
Assal Hellmer
Vice President, Communications
mediarelations@ebsi.com

Emergent BioSolutions Inc.
Consolidated Balance Sheets
(in millions, except per share data)
       
  September 30, 2025   December 31, 2024
  (unaudited)    
ASSETS      
Current assets:      
Cash and cash equivalents $ 245.5     $ 99.5  
Restricted cash   3.7       6.1  
Accounts receivable, net   149.5       154.5  
Inventories, net   356.3       311.7  
Prepaid expenses and other current assets   25.6       26.9  
Assets held for sale   6.3        
Total current assets   786.9       598.7  
       
Property, plant and equipment, net   209.8       270.6  
Intangible assets, net   452.7       501.5  
Other assets   11.6       18.9  
Total assets $ 1,461.0     $ 1,389.7  
       
LIABILITIES AND STOCKHOLDERS’ EQUITY      
Current liabilities:      
Accounts payable $ 57.4     $ 60.9  
Accrued expenses   13.9       17.7  
Accrued compensation   36.6       56.1  
Other current liabilities   24.1       27.7  
Liabilities held for sale   4.5        
Total current liabilities   136.5       162.4  
       
Debt   663.1       663.7  
Deferred tax liability   36.3       41.7  
Other liabilities   42.6       39.1  
Total liabilities $ 878.5     $ 906.9  
       
Stockholders’ equity:      
Preferred stock, $0.001 par value per share; 15.0 shares authorized, no shares issued and outstanding          
Common stock, $0.001 par value per share; 200.0 shares authorized, 60.6 and 59.9 shares issued; 52.7 and 54.3 shares outstanding, respectively.   0.1       0.1  
Treasury stock, at cost, 7.9 and 5.6 common shares, respectively   (243.5 )     (227.7 )
Additional paid-in capital   938.6       928.0  
Accumulated other comprehensive loss, net   (7.5 )     (5.2 )
Accumulated deficit   (105.2 )     (212.4 )
Total stockholders’ equity $ 582.5     $ 482.8  
Total liabilities and stockholders’ equity $ 1,461.0     $ 1,389.7  

Emergent BioSolutions Inc.
Consolidated Statements of Operations
(unaudited, in millions, except per share data)
       
  Three Months Ended September 30,   Nine Months Ended September 30,
    2025       2024       2025       2024  
Revenues:              
Product and services sales, net $ 222.0     $ 283.8     $ 561.4     $ 824.3  
Contracts and grants   9.1       10.0       32.8       24.6  
Total revenues   231.1       293.8       594.2       848.9  
               
Operating expenses:              
Cost of product and services sales, net(1)   85.9       122.6       241.3       563.3  
Research and development   13.5       13.8       41.1       61.6  
Selling, general and administrative   38.9       76.6       135.0       247.2  
Amortization of intangible assets   16.3       16.3       48.8       48.8  
Impairment of long-lived assets                     27.2  
Total operating expenses   154.6       229.3       466.2       948.1  
               
Income (loss) from operations   76.5       64.5       128.0       (99.2 )
               
Other income (expense):              
Interest expense   (15.2 )     (8.3 )     (44.6 )     (56.2 )
Gain (loss) on sale of business and assets held for sale         64.3       (12.2 )     24.3  
Other, net   (3.7 )     21.9       62.3       15.8  
Total other income (expense), net   (18.9 )     77.9       5.5       (16.1 )
               
Income (loss) before income taxes   57.6       142.4       133.5       (115.3 )
Income tax provision   6.4       27.6       26.3       44.0  
Net income (loss) $ 51.2     $ 114.8     $ 107.2     $ (159.3 )
               
Earnings (loss) per common share              
Basic $ 0.96     $ 2.16     $ 1.99     $ (3.03 )
Diluted $ 0.91     $ 2.06     $ 1.89     $ (3.03 )
               
Weighted average shares outstanding              
Basic   53.2       53.1       53.9       52.6  
Diluted   56.5       55.6       56.7       52.6  
               
               
(1)Exclusive of intangible asset amortization        

Emergent BioSolutions Inc.
Consolidated Statements of Cash Flows
(unaudited, in millions)
   
  Nine Months Ended September 30,
    2025       2024  
Operating Activities      
Net income (loss) $ 107.2     $ (159.3 )
Adjustments to reconcile net income (loss) to net cash provided by operating activities:      
Share-based compensation expense   10.9       13.7  
Depreciation and amortization   72.3       82.8  
Change in fair value of contingent obligations, net         0.6  
Amortization of deferred financing costs   7.2       5.2  
Deferred income taxes   (5.5 )     (5.1 )
Loss (gain) on sale of business and assets held for sale   12.2       (32.2 )
Change in fair value of warrant liability   (1.8 )     (1.1 )
Impairment of long-lived assets         27.2  
Loss on disposal of assets   3.5       28.9  
Other   (8.7 )     3.9  
Changes in operating assets and liabilities:      
Accounts receivable   (26.4 )     52.7  
Inventories   (44.5 )     (35.5 )
Prepaid expenses and other assets   27.1       146.3  
Accounts payable   (19.8 )     (22.8 )
Accrued expenses and other liabilities   (27.0 )     32.9  
Long-term incentive plan accrual   2.3       2.5  
Accrued compensation   (21.8 )     (9.9 )
Income taxes receivable and payable, net   4.6       26.6  
Contract liabilities   1.1       (18.8 )
Net cash provided by operating activities   92.9       138.6  
Investing Activities      
Purchases of property, plant and equipment   (9.9 )     (21.2 )
Proceeds from sale of property, plant and equipment   38.2       7.6  
Milestone payments from prior asset divestiture   50.0        
Proceeds from sale of business         110.2  
Purchase of convertible note receivable   (5.0 )      
Net cash provided by investing activities   73.3       96.6  
Financing Activities      
Proceeds from the issuance of debt, net of lender fees         219.0  
Proceeds allocated to warrants issued in conjunction with debt         13.4  
Proceeds allocated to common stock issued in conjunction with debt         9.3  
Principal payments on term loan facility         (198.2 )
Proceeds from revolving credit facility         65.0  
Principal payments on revolving credit facility         (284.2 )
Proceeds from issuance of common stock upon exercise of stock options   1.0        
Repurchase of debt   (6.9 )      
Purchases of treasury stock   (15.8 )      
Debt issuance costs         (14.6 )
Proceeds from share-based compensation activity         0.7  
Taxes paid for share-based compensation activity   (1.0 )     (0.9 )
Net cash used in financing activities:   (22.7 )     (190.5 )
Effect of exchange rate changes on cash, cash equivalents and restricted cash   0.1        
Net change in cash, cash equivalents and restricted cash   143.6       44.7  
Cash, cash equivalents and restricted cash, beginning of period   105.6       111.7  
Cash, cash equivalents and restricted cash, end of period $ 249.2     $ 156.4  
Supplemental cash flow disclosures:      
Cash paid for interest $ 41.7     $ 55.8  
Cash paid for income taxes, net of refunds $ 27.5     $ 35.5  
Non-cash investing and financing activities:      
Purchases of property, plant and equipment unpaid at period end $ 1.8     $ 1.6  
Gain on extinguishment of debt $ 1.1     $ 0.6  
Issuance of common stock in conjunction with debt $     $ 7.7  
Excise tax liability accrued for common stock repurchases $ 0.2     $  
Reconciliation of cash and cash equivalents and restricted cash:      
Cash and cash equivalents $ 245.5     $ 149.9  
Restricted cash   3.7       6.5  
Total $ 249.2     $ 156.4  

Emergent BioSolutions, Inc.
Reconciliation of Non-GAAP Financial Measures
Reconciliation of Net Income (Loss) and Net Income (Loss) per Diluted Share to Adjusted Net Income (Loss) and Adjusted Net Income (Loss) per Diluted Share(1)
         
  Three Months Ended September 30,   Nine Months Ended September 30,  
($ in millions, except per share data)
  2025     2024       2025     2024   Source
Net income (loss) $ 51.2   $ 114.8     $ 107.2   $ (159.3 )  
Adjustments:            
Non-cash amortization charges $ 18.8   $ 9.7     $ 56.0   $ 54.0   Amortization of intangible assets (“IA”), Other Income
Impairments                 27.2   Impairment of long-lived assets
Severance and restructuring costs       6.3       (0.8 )   22.9   Cost of product and services sales, net, SG&A and R&D
Inventory step-up provision       1.2       1.8     1.2   Cost of product and services sales, net
Acquisition and divestiture costs             0.2       SG&A
Exit and disposal costs                 13.3   R&D
Loss (gain) on sale of business and assets held for sale       (64.3 )     12.2     (24.3 ) Other Income (Expense)
Settlement charges, net   (10.5 )   10.0       (10.5 )   120.2   Cost of product and services sales, net
Contingent consideration milestones       (30.0 )     (50.0 )   (30.0 ) Other Income (Expense)
Changes in fair value of financial instruments   4.8     (1.1 )     (1.8 )   (0.5 ) Cost of product and services sales, net and Other Income (Expense)
Other expense (income), net items   (1.1 )   6.7       (4.0 )   9.8   Other Income (Expense)
Tax effect   (2.8 )   22.9       (0.7 )   (49.2 )  
Total adjustments: $ 9.2   $ (38.6 )   $ 2.4   $ 144.6    
Adjusted net income (loss) $ 60.4   $ 76.2     $ 109.6   $ (14.7 )  
Net income (loss) per diluted share $ 0.91   $ 2.06     $ 1.89   $ (3.03 )  
Adjustments:            
Non-cash amortization charges $ 0.33   $ 0.17     $ 0.99   $ 1.03   Amortization of IA, Other Income
Impairments                 0.52   Impairment of long-lived assets
Severance and restructuring costs       0.12       (0.01 )   0.44   Cost of product and services sales, net, SG&A and R&D
Inventory step-up provision       0.02       0.03     0.02   Cost of product and services sales, net
Acquisition and divestiture costs                   SG&A
Exit and disposal costs                 0.25   R&D
Loss (gain) on sale of business and assets held for sale       (1.16 )     0.22     (0.46 ) Other Income (Expense)
Settlement charges, net   (0.19 )   0.18       (0.19 )   2.29   Cost of product and services sales, net
Contingent consideration milestones       (0.54 )     (0.88 )   (0.57 ) Other Income (Expense)
Changes in fair value of financial instruments   0.08     (0.02 )     (0.03 )   (0.01 ) Cost of product and services sales, net and Other Income (Expense)
Other expense (income), net items   (0.02 )   0.12       (0.07 )   0.19   Other Income (Expense)
Tax effect   (0.05 )   0.42       (0.02 )   (0.95 )  
Total adjustments: $ 0.15   $ (0.69 )   $ 0.04   $ 2.75    
Adjusted net income (loss) per diluted share $ 1.06   $ 1.37     $ 1.93   $ (0.28 )  
Diluted shares used in computing Adjusted net income (loss) per diluted share   56.5     55.6       56.7     52.6    

Emergent BioSolutions, Inc.

Reconciliation of Net Income (Loss) and Net Income (Loss) Margin to Adjusted EBITDA and Adjusted EBITDA Margin(1)

       
($ in millions) Three Months Ended September 30,   Nine Months Ended September 30,
  2025     2024       2025     2024  
Net income (loss) $ 51.2   $ 114.8     $ 107.2   $ (159.3 )
Adjustments:          
Depreciation & amortization $ 23.4   $ 26.4     $ 72.3   $ 82.8  
Income taxes   6.4     27.6       26.3     44.0  
Total interest expense, net   13.6     7.7       41.0     54.8  
Impairments                 27.2  
Inventory step-up provision       1.2       1.8     1.2  
Changes in fair value of financial instruments   4.8     (1.1 )     (1.8 )   (0.5 )
Severance and restructuring costs       6.3       (0.8 )   22.9  
Exit and disposal costs                 13.3  
Acquisition and divestiture costs             0.2      
Loss (gain) on sale of business and assets held for sale       (64.3 )     12.2     (24.3 )
Settlement charges, net   (10.5 )   10.0       (10.5 )   120.2  
Contingent consideration milestones       (30.0 )     (50.0 )   (30.0 )
Other expense (income), net items   (1.1 )   6.7       (4.0 )   9.8  
Total adjustments $ 36.6   $ (9.5 )   $ 86.7   $ 321.4  
Adjusted EBITDA $ 87.8   $ 105.3     $ 193.9   $ 162.1  
           
Total revenues $ 231.1   $ 293.8     $ 594.2   $ 848.9  
           
Net income (loss) margin   22 %   39 %     18 % (19) %
           
Adjusted EBITDA margin   38 %   36 %     33 %   19 %


Emergent BioSolutions, Inc.

Reconciliations of Total Revenues to Product and Services Sales, Net and of Gross Margin and Gross Margin %
to Adjusted Gross Margin and Adjusted Gross Margin %(1)

       
  Three Months Ended September 30,   Nine Months Ended September 30,
($ in millions)   2025     2024       2025     2024  
Total revenues $ 231.1   $ 293.8     $ 594.2   $ 848.9  
Contracts and grants   9.1     10.0       32.8     24.6  
Product and services sales, net $ 222.0   $ 283.8     $ 561.4   $ 824.3  
           
Cost of product and services sales, net   85.9     122.6       241.3     563.3  
Intangible asset amortization   16.3     16.3       48.8     48.8  
Gross margin $ 119.8   $ 144.9     $ 271.3   $ 212.2  
Gross margin %   54 %   51 %     48 %   26 %
Add back:          
Intangible asset amortization $ 16.3   $ 16.3     $ 48.8   $ 48.8  
Inventory step-up provision       1.2       1.8     1.2  
Settlement charges, net                 110.2  
Restructuring costs   0.2     5.0       (0.8 )   7.8  
Changes in fair value of financial instruments                 0.6  
Adjusted gross margin $ 136.3   $ 167.4     $ 321.1   $ 380.8  
Adjusted gross margin %   61 %   59 %     57 %   46 %

Emergent BioSolutions, Inc.
Reconciliation of Net Income Forecast to Adjusted Net Income Forecast
     
($ in millions) 2025 Full Year Forecast Source
Net income $60 – $75  
Adjustments:    
Non-cash amortization charges $65 Amortization of IA and Other Income (Expense)
Changes in fair value of financial instruments (2) Other Income (Expense)
Severance and restructuring costs (1) Cost of products and services, net, SG&A and R&D
Inventory step-up provision 5 Cost of products and services, net
Loss (gain) on sale of business and assets held for sale 12 Other Income (Expense)
Settlement charges, net (11) SG&A
Contingent consideration milestones (50) Other Income (Expense)
Other expense (income), net items (4) Other Income (Expense)
Tax effect (4)  
Total adjustments: $10  
Adjusted net income $70 – $85  

Reconciliation of Net Income Forecast to Adjusted EBITDA Forecast
   
($ in millions) 2025 Full Year Forecast
Net income $60 – $75
Adjustments:  
Depreciation & amortization $100
Income taxes 31
Total interest expense, net 55
Inventory step-up provision 5
Changes in fair value of financial instruments (2)
Severance and restructuring costs (1)
Loss (gain) on sale of business and assets held for sale 12
Settlement charges, net (11)
Contingent consideration milestones (50)
Other expense (income), net items (4)
Total adjustments $135
Adjusted EBITDA $195 – $210


Emergent BioSolutions, Inc.

Reconciliations of Forecasted Total Revenues to Forecasted Product and Services Sales, Net and of Forecasted Gross Margin and Gross Margin % to Forecasted Adjusted Gross Margin and Adjusted Gross Margin %(1)

   

($ in millions)

2025 Full Year Forecast
Total revenues $775 – $835
Contracts & Grants (35) – (35)
Product and services sales, net $740 – $800
   
Cost of product and services sales, net $359 – $376
Intangible asset amortization 60
Gross margin $321 – $364
Gross margin % 43% – 46%
Add back:  
Intangible asset amortization $60
Inventory step-up provision 5
Restructuring costs (1)
Adjusted gross margin $385 – $428
Adjusted gross margin % 52% – 54%