SimpleTherapy Recognized as a Top 50 Healthcare Technology Company of 2025

SimpleTherapy Recognized as a Top 50 Healthcare Technology Company of 2025




SimpleTherapy Recognized as a Top 50 Healthcare Technology Company of 2025

FRESNO, Calif., Nov. 19, 2025 (GLOBE NEWSWIRE) — SimpleTherapy, a leader in virtual musculoskeletal (MSK) and behavioral health care solutions, is honored to be named one of The Healthcare Technology Report’s Top 50 Healthcare Technology Companies of 2025. This marks the company’s second consecutive year on the list, following last year’s placement in the Top 100. The recognition highlights SimpleTherapy’s ongoing dedication to providing inclusive, holistic, and accessible care tailored to each individual.

“Our inclusion in this list reflects our ongoing commitment to supporting members on their health journey through technology that’s easy to access and simple to use,” said Jeremy Oswald, President of SimpleTherapy. “We’re proud to meet people where they are, whether on their phones, tablets, laptops, or in person, while delivering care that’s truly personal and effective.”

SimpleTherapy offers five solutions that touch on an individual’s total well-being. SimpleTherapy’s solutions are:

  • SimpleMSK: Their flagship, comprehensive MSK solution, combines tech-guided and evidence-based care with virtual and in-person providers, where members can access a nationwide network of PT, OT, SLP, chiropractic, and acupuncture care, with same/next-day virtual visits and 24/7 triage.
  • SimpleBehavioral: Spanning therapy, psychiatry, substance use disorder care, and crisis care routing, SimpleTherapy delivers a complete and integrated mental health benefit administration program focusing on care and compassion at every level specific to the member’s needs.
  • SimpleConnect: SimpleTherapy’s newest solution, specific for students and families, is a 24/7, on-demand digital mental health solution that offers emotional well-being support and life-balance resources during evenings, weekends, and school breaks.
  • SimpleEAP: Available for employees by phone, web, or app, SimpleEAP provides 24/7/365 access to licensed mental health professionals for immediate, personalized support, including in-the-moment counseling, short-term therapy, work-life services, and manager consultations.
  • SimpleWellbing: In a single, integrated platform, SimpleTherapy delivers a holistic wellness experience where members can engage in evidence-based programs for stress resilience and mindfulness, sleep and energy, nutrition and weight management, activity challenges, and preventive MSK micro-sessions.

“We are constantly innovating how we can make health care more accessible for our members in our digital society” said Arpit Khemka, CEO of SimpleTherapy. “This recognition acknowledges that goal and elevates us to keep pushing forward with new technological advancements while keeping our solutions people-focused.”

For more details, read about SimpleTherapy’s recognition here.

About SimpleTherapy

SimpleTherapy is redefining care through innovative, clinically validated solutions for physical, musculoskeletal (MSK), and behavioral health. Our platform blends digital tools, virtual services, and a nationwide network of over 60,000 providers to deliver simple, personalized support. We help organizations of all sizes, including Fortune 50 companies, improve health outcomes, lower costs, and support their workforce in new, meaningful ways. Learn more at simpletherapy.com or reach out to sales@simpletherapy.com.

About The Healthcare Technology Report

The Healthcare Technology Report is a trusted resource for insights on companies transforming healthcare through technological innovation. Its annual Top 50 list highlights organizations demonstrating exceptional leadership, impact, and commitment to advancing healthcare delivery.

A photo accompanying this announcement is available at https://www.globenewswire.com/NewsRoom/AttachmentNg/1d29d75a-fa9e-4feb-8670-1a0e83c713b9

CONTACT: CONTACT Rebecca Rawl, Director of Marketing
COMPANY SimpleTherapy
PHONE 443-857-8718
EMAIL rebecca.rawl@simpletherapy.com 
WEB simpletherapy.com

Curaechoice Announces Nationwide Expansion of $0-Cost Vision Care Program

Curaechoice Announces Nationwide Expansion of $0-Cost Vision Care Program




Curaechoice Announces Nationwide Expansion of $0-Cost Vision Care Program

All Members and Their Families Gain Access to Vision Services Nationwide Beginning Jan. 1, 2026

Birmingham, Alabama, Nov. 19, 2025 (GLOBE NEWSWIRE) — Curaechoice, the nation’s #1 leader in no-cost benefits optimization solutions, today announced the nationwide expansion of its vision care program, offering comprehensive $0-cost vision services to all active members and their families starting Jan. 1, 2026.

Through this expansion, Curaechoice members will gain access to over 26,000 vision care locations, more than 12,000 vision care practitioners, and nearly 1,500 ophthalmologists — all at no out-of-pocket cost. Covered services include $0-cost annual eye exams, a broad selection of glasses and contact lenses (within employer plan limits), and treatment for advanced conditions such as glaucoma, cataracts and macular degeneration.

Harsha Hatti, president and CEO of Curaechoice, emphasized the significance of removing financial barriers to vision care.

“We know members take better care of themselves when essential services are available without financial barriers. We’ve seen this across our medical, pharmacy and dental service lines — members who once avoided care due to cost are now getting the treatment they need without fear of expense. Vision care is one of the most underused workplace benefits because of payroll deductions, copays and the high cost of glasses or contacts. Our program removes those obstacles entirely, giving members and their families the vision care they need at zero out-of-pocket cost and improving their overall health and quality of life.”

Hatti also underscored that the expansion delivers significant value to employers.

“Our vision plan removes burdensome PEPM and PMPM fees that drive up employer costs. We eliminate fixed monthly charges and give employers the flexibility to add or update plan enrollees at any time — features virtually unheard of in the benefits industry. Too many employees skip vision care due to cost and later experience preventable vision decline, which leads to measurable productivity loss. Now employers can offer a high-quality vision benefit that supports employee health, enhances productivity and strengthens overall workplace well-being.

Hatti added:

“We are proud of Curaechoice’s impact on the industry and remain unwavering in our commitment to ensuring that every stakeholder — member, employer and provider — wins using the Curaechoice program.”

The nationwide Curaechoice vision network will be available to all members beginning Jan. 1, 2026.

About Curaechoice

Curaechoice is a dynamic health benefits optimization platform serving self-insured employers and their employees nationwide. The program eliminates copays, deductibles and coinsurance across medical, dental, vision and pharmacy services—helping employees maximize their existing employer-paid benefits and access care without financial barriers. 

Press inquiries

Curaechoice
https://curaechoice.com
Curaechoice Media
media@curaechoice.com
800-646-9823
3179 Green Valley Rd PMB 634
Birmingham, AL 35243

Humber River Health 10th Anniversary Event Raises Over $2.55 Million to Power the Next Decade of Innovation and Patient-Centered Care

Humber River Health 10th Anniversary Event Raises Over $2.55 Million to Power the Next Decade of Innovation and Patient-Centered Care




Humber River Health 10th Anniversary Event Raises Over $2.55 Million to Power the Next Decade of Innovation and Patient-Centered Care

TORONTO, Nov. 19, 2025 (GLOBE NEWSWIRE) — On Friday, November 14, more than 800 guests came together to party with a purpose at The International Centre for a dazzling night of celebration, generosity, and inspiration at Humber River Health Foundation’s Sapphire Soirée, marking 10 years of innovation, compassion, and community care at Humber River Health’s Wilson Site.

The Sapphire Soirée raised over $2.55 million in support of Humber River Health, and the Foundation announced an additional $10.9 million raised in donations, helping fuel innovation across programs such as the new James B. Neill Simulation Centre, which will train over 7,000 healthcare workers annually, and the Robotic Surgery Program, which is already transforming patient outcomes through precision and minimally invasive care.

A surprise opening headliner performance by The Tenors — gifted as an Anniversary celebration — proved to be a show-stopping highlight, bringing the entire room to its feet. Cheryl Hickey lit up the stage as Emcee, while Fred Lee energized the crowd during the Fund-a-Need. Entertainment continued to build throughout the evening with a moving performance by Shanaya Patel, an electric set by the Dueling Pianos, and DJ Zorawar, who kept the dance floor full late into the night.

Culinary activations matched the energy of the entertainment. Guests enjoyed elevated food and beverage experiences from Johnnie Walker, Lavazza, and Masala Whisky, and a food truck provided by The Host, followed by gelato at the after-party, Ferrero Rocher chocolates, and panettone from Christmas Goodies. Each guest departed with stunning Bella Florist bouquets, adding a memorable finishing touch to an already exquisite evening.

Guests also heard special remarks from Premier Doug Ford about the importance of innovation in healthcare and Humber River Health’s leadership in building a more connected, compassionate system for Ontario families.

“This was truly a night to remember,” said Jennifer Stewart, President & CEO of Humber River Health Foundation. “We celebrated not only 10 years of extraordinary care, but also the people—our donors, partners, and hospital teams—who make it possible. Their generosity ensures Humber continues to light new ways in healthcare for decades to come.”

“This celebration marks more than a milestone; it’s a launchpad for the next decade of innovation. Ten years ago, Humber River Health opened North America’s first fully digital hospital, redefining the standard of modern care. This anniversary reflects our unwavering commitment to making healthcare smarter, safer, and more compassionate,” says Barbara Collins, President & CEO of Humber River Health.

The event was presented in partnership with The International Centre, whose generosity and support helped make this milestone celebration possible.

As Humber River Health looks to the future, the Foundation continues to champion innovation, technology, and patient-centered care, ensuring that every patient, today and tomorrow, has access to the best care possible, close to home.

About Humber River Health
Humber River Health is one of Canada’s largest community acute care hospitals, serving a population of more than 850,000 people in the northwest Greater Toronto Area. The multi-site hospital currently operates out of its Wilson Avenue acute care site, Finch, and Church Campus’ with over 4,000 employees, approximately 700 physicians, and over 500 volunteers. Humber River Health uses a custom combination of technology and clinical expertise to rebuild elements of care, making technology work for staff and physicians, giving them more time to spend with patients. With the support of its incredible teams, a strong will, and determination, Humber River Health is committed to Lighting New Ways in Healthcare. For more information, please visit hrh.ca.

Media Contact:

Jennifer Alavathil
Director, Marketing & Communications
Humber River Health Foundation
JAlavathil@hrh.ca

Photos accompanying this announcement are available at:
https://www.globenewswire.com/NewsRoom/AttachmentNg/7c603a55-703c-4a8e-b7b5-d3d6f4761071
https://www.globenewswire.com/NewsRoom/AttachmentNg/d2c2ca7f-5cc4-4002-9706-7ecc46f3dac8
https://www.globenewswire.com/NewsRoom/AttachmentNg/df53744a-7dda-405b-8ded-ff16bf2439fb

Catalyst Pharmaceuticals Recognized as One of North America’s Fastest-Growing Companies on the 2025 Deloitte Technology Fast 500™

Catalyst Pharmaceuticals Recognized as One of North America’s Fastest-Growing Companies on the 2025 Deloitte Technology Fast 500™




Catalyst Pharmaceuticals Recognized as One of North America’s Fastest-Growing Companies on the 2025 Deloitte Technology Fast 500™

Attributes 249% Revenue Growth to Portfolio Momentum and Focused Execution

CORAL GABLES, Fla., Nov. 19, 2025 (GLOBE NEWSWIRE) — Catalyst Pharmaceuticals, Inc. (“Catalyst” or “Company”) (Nasdaq: CPRX), a commercial-stage biopharmaceutical company focused on in-licensing, developing, and commercializing novel medicines for patients living with rare and difficult-to-treat diseases, today announced it ranked 304 on the 2025 Deloitte Technology Fast 500™, a ranking of the 500 fastest-growing technology, media, telecommunications, life sciences, fintech, and energy tech companies in North America, now in its 31st year. This achievement is based on percentage of revenue growth from fiscal year 2021 to 2024. Catalyst grew 249% during this period.

Catalyst’s President and Chief Executive Officer, Rich Daly, credits Catalyst’s best-in-class product portfolio and outstanding commercial capabilities for the Company’s 249% revenue growth. He said, “We’re proud to be recognized as one of the fastest-growing companies in North America for the second year in a row, a testament to the success of our commercial strategy, operational discipline, and talent across the organization. We remain committed to driving sustainable growth while continuing to prioritize the patients and communities we serve.”

“This year’s rankings highlight both enduring leadership and breakthrough momentum,” said Wolfe Tone, US Deloitte Private & Emerging Client Portfolio leader and partner, Deloitte Tax LLP. “More than half of the winners are prior honorees, yet the majority of the top ten are first-time entrants — demonstrating the staying power of established leaders alongside the accelerating growth of new innovators across key sectors. As in previous years, private companies continue to dominate, underscoring the agility that private enterprises bring to competitive markets, enabling the exceptional triple and quadruple digit growth reflected in these rankings.”

Catalyst previously ranked 452 as a Deloitte Technology Fast 500 award winner for 2024.

About the 2025 Deloitte Technology Fast 500

Now in its 31st year, the Deloitte Technology Fast 500 provides a ranking of the fastest-growing technology, media, telecommunications, life sciences, fintech, and energy tech companies — both public and private — in North America. Technology Fast 500 award winners are selected based on percentage fiscal year revenue growth from 2021 to 2024.

In order to be eligible for Technology Fast 500 recognition, companies must own proprietary intellectual property or proprietary technology that significantly contributes to the company’s operating revenues. Companies must have base-year operating revenues of at least US$50,000, and current-year operating revenues of at least US $5 million, with a growth rate of 50% or greater. Additionally, companies must be in business for a minimum of four years and be headquartered within North America (United States and Canada).

Please see www.deloitte.com/us/about for a detailed description of their legal structure.

About Catalyst Pharmaceuticals, Inc.

Catalyst Pharmaceuticals, Inc. (Nasdaq: CPRX), is a biopharmaceutical company committed to improving the lives of patients with rare diseases. With a proven track record of bringing life-changing treatments to the market, we focus on in-licensing, commercializing, and developing innovative therapies. Guided by our deep commitment to patient care, we prioritize accessibility, ensuring patients receive the care they need through a comprehensive suite of support services designed to provide seamless access and ongoing assistance. Catalyst maintains a well-established U.S. presence, which remains the cornerstone of our commercial strategy, while continuously evaluating strategic opportunities to expand our global footprint. Catalyst, headquartered in Coral Gables, Fla., was recognized on the Forbes 2025 list as one of America’s Most Successful Mid-Cap Companies and on the 2024 Deloitte Technology Fast 500™ list as one of North America’s Fastest-Growing Companies.

For more information, please visit Catalyst’s website at www.catalystpharma.com.

CONTACT: Investor Contact
Melissa Kendis, Catalyst Pharmaceuticals, Inc.
(305) 420-3200
IR@catalystpharma.com

Media Contact
David Schull or Olipriya Das, Russo Partners
(858) 717-2310, 646 942 5588
david.schull@russopartnersllc.com, Olipriya.das@russopartnersllc.com

Join Biovie’s Exclusive Live Investor Webinar and Q&A Session on December 9

Join Biovie’s Exclusive Live Investor Webinar and Q&A Session on December 9




Join Biovie’s Exclusive Live Investor Webinar and Q&A Session on December 9

CARSON CITY, Nev., Nov. 19, 2025 (GLOBE NEWSWIRE) — BioVie Inc. (NASDAQ: BIVI) (“BioVie” or the “Company”), a clinical-stage company developing innovative drug therapies for neurological and neurodegenerative diseases, is pleased to invite investors to a webinar on December 9, 2025, at 4:15 p.m. ET.

The exclusive event, hosted by RedChip Companies, will feature Cuong Do, President and CEO of BioVie, who will discuss bezisterim (NE3107), BioVie’s first-in-class, orally available small molecule that targets inflammation and insulin resistance, two key drivers of Alzheimer’s, Parkinson’s, and Long COVID, where it has shown encouraging signals of improved cognition, motor function, and reduced neuroinflammation across clinical studies. He will also outline progress with BIV201, BioVie’s late-stage orphan drug candidate for refractory ascites, a life-threatening complication of liver cirrhosis with no FDA-approved therapies. With multiple late-stage clinical programs advancing, strong safety data, and multi-billion-dollar market opportunities, BioVie is positioned to deliver significant value creation as it approaches pivotal milestones and potential partnerships.

A live Q&A session with management will follow the presentation.

To register for the free webinar, please visit: https://www.redchip.com/webinar/BIVI/87918761553

Questions can be pre-submitted to BIVI@redchip.com or online during the live event.

About BioVie, Inc.

BioVie Inc. (NASDAQ: BIVI) is a clinical-stage company developing innovative drug therapies for the treatment of neurological and neurodegenerative disorders (Alzheimer’s disease, Parkinson’s disease and long COVID) and advanced liver disease. In neurodegenerative disease, the Company’s drug candidate bezisterim inhibits inflammatory activation of extracellular signal-regulated kinase and the transcription factor nuclear factor-κB, and the associated neuroinflammation and insulin resistance but not ERK and NFκB homeostatic functions (e.g., insulin signaling and neuron growth and survival). Both neuroinflammation and insulin resistance are drivers of AD and PD. Persistent systematic inflammation and neuroinflammation are key features in patients with neurological symptoms of long COVID. In liver disease, the Company’s Orphan drug candidate BIV201 (continuous infusion terlipressin), with FDA Fast Track status, is being evaluated and discussed with guidance received from the FDA regarding the design of Phase 3 clinical testing of BIV201 for the reduction of further decompensation in participants with liver cirrhosis and ascites. The active agent is approved in the U.S. and in about 40 countries for related complications of advanced liver cirrhosis. For more information, visit www.bioviepharma.com.  

Forward-Looking Statements

This press release contains forward-looking statements, which may be identified by words such as “expect,” “look forward to,” “anticipate” “intend,” “plan,” “believe,” “seek,” “estimate,” “will,” “project” or words of similar meaning. Although BioVie Inc. believes such forward-looking statements are based on reasonable assumptions, it can give no assurance that its expectations will be attained. Actual results may vary materially from those expressed or implied by the statements herein due to the Company’s ability to successfully raise sufficient capital on reasonable terms or at all, available cash on hand and contractual and statutory limitations that could impair our ability to pay future dividends, our ability to complete our pre-clinical or clinical studies and to obtain approval for our product candidates, our ability to successfully defend potential future litigation, changes in local or national economic conditions as well as various additional risks, many of which are now unknown and generally out of the Company’s control, and which are detailed from time to time in reports filed by the Company with the SEC, including quarterly reports on Form 10-Q, reports on Form 8-K and annual reports on Form 10-K. BioVie Inc. does not undertake any duty to update any statements contained herein (including any forward-looking statements), except as required by law.  

Contact:
Dave Gentry
RedChip Companies, Inc.
1-407-644-4256
BIVI@redchip.com

Chuck Padala
Managing Director
LifeSci Advisors, LLC
chuck@lifesciadvisors.com

Elicio Therapeutics Appoints Veteran CMC and Technical Operations Executive Marc J. Wolfgang as Chief Technology Officer

Elicio Therapeutics Appoints Veteran CMC and Technical Operations Executive Marc J. Wolfgang as Chief Technology Officer




Elicio Therapeutics Appoints Veteran CMC and Technical Operations Executive Marc J. Wolfgang as Chief Technology Officer

Strategic Hire Strengthens Late Phase and Commercial Readiness as Elicio Advances Lymph Node-Targeted Immunotherapy Pipeline

BOSTON, Nov. 19, 2025 (GLOBE NEWSWIRE) — Elicio Therapeutics, Inc. (Nasdaq: ELTX, “Elicio” or the “Company”), a clinical-stage biotechnology company developing a pipeline of novel immunotherapies for the treatment of cancer, today announced the appointment of Marc J. Wolfgang, M.S. as Chief Technology Officer (“CTO”).

Mr. Wolfgang brings more than 30 years of biopharmaceutical leadership spanning manufacturing, CMC strategy, development, quality, and supply chain across modalities including cell therapy, biologics, nucleic-acid medicines, vaccines, and LNP platforms. He most recently served as Senior Vice President of Technical Development and Operations at Sail Biomedicines (a Flagship portfolio company), leading all development, manufacturing, analytical, and quality functions. Prior to that, he was Vice President of U.S. Manufacturing at BioNTech, where he oversaw manufacturing and supply chain operations for cell and gene therapy programs. Earlier in his career, he held senior CMC and operations roles at Cerulean Pharma, Momenta Pharmaceuticals, Millennium Pharmaceuticals, Biogen, and Boehringer Ingelheim, building and scaling manufacturing organizations, leading global tech transfers, and establishing end-to-end supply chains for clinical and commercial products.

“Marc is an exceptional CMC strategy and operations leader with deep experience guiding innovative therapeutic platforms from early development through commercial readiness,” said Robert T. Connelly, President and Chief Executive Officer of Elicio. “As we continue preparing for potential late-stage development and commercial-scale execution of ELI-002 7P and advancing our other pipeline assets, Marc’s expertise across cell therapy, RNA-based medicines, and other complex modalities aligns perfectly with our strategic priorities. We are thrilled to welcome him to the executive team at this important moment for Elicio.”

“I am delighted to join Elicio at such a pivotal time for the organization ahead of the ELI-002 7P event-driven primary disease-free survival analysis anticipated in 1H 2026,” said Mr. Wolfgang. “Elicio’s lymph node–targeted platform represents a powerful approach to enhancing and directing immune responses, and I look forward to working alongside this outstanding team to build the technical and operational infrastructure that will support the Company’s next phase of clinical development and growth.”

Mr. Wolfgang holds an M.S. in Chemistry from Montclair State University, a B.S. in Biology (Genetics) from Pennsylvania State University, and a Biopharma Executive Leadership Certificate from Babson College. He previously served as Chairman of the Nanomedicines Alliance and has collaborated extensively with the Food and Drug Administration and the National Institutes of Health working groups on nanotechnology, manufacturing, and regulatory policy.

About Elicio Therapeutics

Elicio Therapeutics, Inc. (Nasdaq: ELTX) is a clinical-stage biotechnology company advancing novel immunotherapies for the treatment of high-prevalence cancers, including mKRAS-positive pancreatic and colorectal cancers. Elicio intends to build on recent clinical successes in the personalized cancer immunotherapy space to develop effective, off-the-shelf immunotherapies. Elicio’s Amphiphile (“AMP”) technology aims to enhance the education, activation and amplification of cancer-specific T cells relative to conventional immunization strategies, with the goal of promoting durable cancer immunosurveillance in patients. Elicio’s ELI-002 lead program is an off-the-shelf immunotherapy candidate targeting the most common KRAS mutations, which drive approximately 25% of all solid tumors. Off-the-shelf immunotherapy approaches have the potential benefits of low cost, rapid commercial scale manufacturing, and rapid availability of drug to patients especially in neo-adjuvant settings and for prophylaxis in high-risk patients, contrary to personalized immunotherapy approaches. ELI-002 is being studied in an ongoing, randomized clinical trial in patients with mKRAS-positive pancreatic cancer who completed standard therapy but remain at high risk of relapse. ELI-002 also has been studied in patients with mKRAS-positive colorectal cancer (“CRC”) in Phase 1 studies. The updated AMPLIFY-201 Phase 1 data for PDAC and CRC was presented at the ESMO Immuno-Oncology Congress 2024 and included a 16.3-month median recurrence-free survival and 28.9-month median overall survival for the full study population. In the future, Elicio plans to expand ELI-002 to other indications including mKRAS positive lung cancer and other mKRAS positive cancers. Elicio’s pipeline includes additional off-the-shelf therapeutic cancer immunotherapy candidates, including ELI-007 and ELI-008, that target BRAF-driven cancers and p53 hotspot mutations, respectively. For more information, please visit www.elicio.com.

Cautionary Note on Forward-Looking Statements

Certain statements contained in this communication regarding matters that are not historical facts, are forward-looking statements within the meaning of Section 21E of the Securities Exchange Act of 1934, as amended, and the Private Securities Litigation Reform Act of 1995, known as the PSLRA. These include statements regarding Elicio’s planned clinical programs, including the timing and outcome of planned clinical trials; the timing of the anticipated event-driven primary final disease-free survival analysis of the Phase 2 AMPLIFY-7P clinical trial; the potential of Elicio’s product candidates and platform; the potential for future expansion of ELI-002 to other indications, including mKRAS positive lung cancer and other mKRAS positive cancers; the potential benefits and effectiveness of off-the-shelf immunotherapy approaches; and other statements regarding management’s intentions, plans, beliefs, expectations or forecasts for the future and, therefore, you are cautioned not to place undue reliance on them. No forward-looking statement can be guaranteed, and actual results may differ materially from those projected. Elicio undertakes no obligation to publicly update any forward-looking statement, whether as a result of new information, future events or otherwise, except to the extent required by law. Elicio uses words such as “anticipates,” “believes,” “plans,” “expects,” “projects,” “future,” “intends,” “may,” “will,” “should,” “could,” “estimates,” “predicts,” “potential,” “continue,” “guidance,” and similar expressions to identify these forward-looking statements that are intended to be covered by the safe-harbor provisions of the PSLRA. Such forward-looking statements are based on our expectations and involve risks and uncertainties; consequently, actual results may differ materially from those expressed or implied in the statements due to a number of factors, including, but not limited to, Elicio’s plans to develop and commercialize its product candidates, including ELI-002 7P; the timing of initiation of Elicio’s planned clinical trials; the timing of the availability of data from Elicio’s clinical trials, including the event-driven primary final disease-free survival analysis from the Phase 2 AMPLIFY-7P trial; the timing of any planned investigational new drug application or new drug application; Elicio’s plans to research, develop and commercialize its current and future product candidates; and Elicio’s estimates regarding future revenue, expenses, capital requirements and need for additional financing.

New factors emerge from time to time, and it is not possible for Elicio to predict all such factors, nor can Elicio assess the impact of each such factor on the business or the extent to which any factor, or combination of factors, may cause actual results to differ materially from those contained in any forward-looking statements. These risks are more fully discussed under the heading “Risk Factors” in Elicio’s Annual Report on Form 10-K for the year ended December 31, 2024, filed with the SEC on March 31, 2025, Elicio’s Quarterly Report on Form 10-Q for the quarter ended March 31, 2025, filed with the SEC on May 13, 2025, Elicio’s Quarterly Report on Form 10-Q for the quarter ended June 30, 2025, filed with the SEC on August 7, 2025, and Elicio’s Quarterly Report on Form 10-Q for the quarter ended September 30, 2025, filed with the SEC on November 13, 2025, as updated by subsequent reports and other documents filed from time to time with the SEC. Forward-looking statements included in this release are based on information available to Elicio as of the date of this release. Elicio does not undertake any obligation to update such forward-looking statements to reflect events or circumstances after the date of this release, except to the extent required by law.

Investor Relations Contact
Brian Ritchie
LifeSci Advisors
(212) 915-2578
britchie@lifesciadvisors.com 

Alignment Healthcare to Present at Piper Sandler 37th Annual Healthcare Conference

Alignment Healthcare to Present at Piper Sandler 37th Annual Healthcare Conference




Alignment Healthcare to Present at Piper Sandler 37th Annual Healthcare Conference

ORANGE, Calif., Nov. 19, 2025 (GLOBE NEWSWIRE) — Alignment Healthcare, Inc. (NASDAQ: ALHC), today announced that it will present at the Piper Sandler 37th Annual Healthcare Conference in New York on Wednesday, Dec. 3, at 10 a.m. EST.

A webcast and replay of the presentations will be available on Alignment’s investor relations website at https://ir.alignmenthealth.com/.

About Alignment Healthcare
Alignment Health is championing a new path in senior care that empowers members to age well and live their most vibrant lives. A consumer brand name of Alignment Healthcare (NASDAQ: ALHC), Alignment Health’s mission-focused team makes high-quality, low-cost care a reality for its Medicare Advantage members every day. Based in California, the company partners with nationally recognized and trusted local providers to deliver coordinated care, powered by its customized care model, 24/7 concierge care team and purpose-built technology, AVA®. As it expands its offerings and grows its national footprint, Alignment upholds its core values of leading with a serving heart and putting the senior first. For more information, visit www.alignmenthealth.com.

Investor Contact
Harrison Zhuo
hzhuo@ahcusa.com

Media Contact
Priya Shah
mPR, Inc. for Alignment Healthcare
alignment@mpublicrelations.com

DeepView™ System Featured at 2025 US Burn Conferences

DeepView™ System Featured at 2025 US Burn Conferences




DeepView™ System Featured at 2025 US Burn Conferences

DALLAS, Nov. 19, 2025 (GLOBE NEWSWIRE) — Spectral AI, Inc. (Nasdaq: MDAI) (“Spectral AI” or the “Company”), an artificial intelligence (AI) company focused on medical diagnostics for faster and more accurate treatment decisions in wound care, today announced its prominent role at the Southern Region Burn Conference, held from October 30th – November 2nd in Charleston, South Carolina. The Company was featured in multiple presentations, highlighting its contributions to advancing burn care across the country.

The DeepView System was featured across several presentation topics, including initial cost savings, AI training methodology, and clinician accuracy when following a “wait-and-see” approach. Dr. James Hwang, burn director at UAB Burn Center in Birmingham, Alabama shared, “By bringing an objective perspective to burn assessment, the field can move toward more consistent, evidence-based decisions that improve outcomes for patients and clinicians alike.”

The Company will also be highlighted at the upcoming Northeast Region Burn Conference held from November 21st – 22nd in Washington, DC. The Southern and Northeast Regional Burn Conferences both aim to advance burn care through education, research, and collaboration among multidisciplinary teams. Each conference features scientific sessions, hands-on workshops, and opportunities for continuing education, bringing together clinicians, nurses, therapists, and researchers dedicated to improving patient outcomes. Supported by the American Burn Association and regional burn societies, both conferences foster a strong professional community focused on innovation and best practices in burn treatment and recovery.

Dr. J. Michael DiMaio, Chairman of the Board of Spectral AI, expressed pride in the Company’s role at the conferences: “Our presence at both U.S. regional burn conferences demonstrates our commitment to advancing burn care. We value physician collaboration as we work to introduce this innovative burn wound assessment technology to the market.”

About Spectral AI 
Spectral AI, Inc. is a Dallas-based predictive AI company focused on medical diagnostics for faster and more accurate treatment decisions in wound care, with initial applications involving patients with burns. The Company is working to revolutionize the management of wound care by “Seeing the Unknown®” with its DeepView™ System. The DeepView System is being developed as a predictive device to offer clinicians an objective and immediate assessment of a burn wound’s healing potential prior to treatment or other medical intervention. With algorithm-driven results and a goal of exceeding the current standard of care in the future, the DeepView System is expected to provide fast and accurate treatment insight towards value care by improving patient outcomes and reducing healthcare costs. This year Spectral AI has been named on TIME’s list of World’s Top HealthTech companies 2025. For more information about the DeepView System, visit www.spectral-ai.com.

Forward-Looking Statements 
Certain statements made in this release are “forward looking statements” within the meaning of the “safe harbor” provisions of the United States Private Securities Litigation Reform Act of 1995, including statements regarding the Company’s strategy, plans, objectives, initiatives and financial outlook. When used in this press release, the words “estimates,” “projected,” “expects,” “anticipates,” “forecasts,” “plans,” “intends,” “believes,” “seeks,” “may,” “will,” “should,” “future,” “propose” and variations of these words or similar expressions (or the negative versions of such words or expressions) are intended to identify forward-looking statements. These forward-looking statements are not guarantees of future performance, conditions or results, and involve a number of known and unknown risks, uncertainties, assumptions and other important factors, many of which are outside Company’s control, that could cause actual results or outcomes to differ materially from those discussed in the forward-looking statements. As such, readers are cautioned not to place undue reliance on any forward-looking statements. 

Investors should carefully consider the foregoing factors, and the other risks and uncertainties described in the “Risk Factors” sections of the Company’s filings with the SEC, including the Registration Statement and the other documents filed by the Company. These filings identify and address other important risks and uncertainties that could cause actual events and results to differ materially from those contained in the forward-looking statements. 

Investors: 
The Equity Group 
Devin Sullivan 
Managing Director 
dsullivan@equityny.com 

Conor Rodriguez 
Analyst 
crodriguez@equityny.com

BioPorto Interim Result for the Third Quarter of 2025 – Continued progress and continued NGAL sales growth

BioPorto Interim Result for the Third Quarter of 2025 – Continued progress and continued NGAL sales growth




BioPorto Interim Result for the Third Quarter of 2025 – Continued progress and continued NGAL sales growth

November 19, 2025

Announcement no. 26

BioPorto Interim Result for the Third Quarter of 2025 – Continued progress and continued NGAL sales growth. 

Copenhagen, Denmark, November 19, 2025, (GLOBE NEWSWIRE) – BioPorto A/S (“BioPorto” or the “Company”) (CPH:BIOPOR), today announced interim financial results for the third quarter of 2025, unchanged from the pre-announced Key Financial Results that were announced on November 4, 2025.

Highlights of key strategic milestones and a renewed strategy, “Forward”

  • Delivery of the first ProNephro AKI™ (NGAL) order to the US market in August 2025, marking the first step in the commercial launch.
  • At the end of October 2025, BioPorto successfully completed patient enrollment in its clinical cut-off study. As announced previously, the Company has decided to submit a pre-submission meeting request to the US Food and Drug Administration (FDA) once the dataset has been analyzed, now expectedly in Q1 2026. The clinical validation study is scheduled to begin following feedback from FDA, allowing BioPorto to proceed with a protocol aligned with FDA feedback. Accordingly, the FDA regulatory submission is postponed from the end of 2026 and into H1 2027.
  • An updated strategy, “Forward” with focus on building market adoption, capturing high growth and expand addressable market was established. BioPorto’s purpose to “improve kidney health and quality of lives” remains intact.
  • On November 13, 2025, BioPorto announced a fully subscribed private placement of 40,438,426 new shares at market price.  The offering is expected to provide gross proceeds of approximately DKK 43 million.

Carsten Buhl, BioPorto’s Group Chief Executive Officer (CEO), comments:

“In the third quarter of 2025 we delivered the first US order of ProNephro AKI (NGAL) which marks the first step in building a commercial platform to drive broad adoption of ProNephro AKI through strategic distributors.

As we successfully completed patient enrollment and now are focusing on thorough data analysis, our commitment is to ensure the highest quality and most effective design for the validation study. While this means our FDA submission will shift into the first half of 2027, this approach derisks our design of the validation study.

Our “Forward” strategy represents a bold step in advancing our ambition to transform kidney care worldwide. By focusing our execution over the next three years, we are confident we can accelerate adoption, drive innovation, and improve outcomes for patients, all while staying true to our purpose.

Finally, on November 13, we successfully completed a share issuance, providing gross proceeds of approximately DKK 43 million. We greatly appreciate the strong support from both existing shareholders and new institutional and private investors, supplemented by a strong commitment from BioPorto’s Board and management. The proceeds are projected to cover spending throughout 2026 and thereby position the Company strongly for its journey towards positive cash flow in the second half of 2027. ”

Key Financial Results for the third quarter of 2025 and for the first nine months of 2025

  • Revenue in the third quarter of 2025 totaled DKK 10.4 million, representing a 7% increase compared to the same period last year, and a 10% increase at constant exchange rates. For the first nine months of 2025 total revenue amounted to DKK 28.7 million, representing a 1% increase compared to the same period last year. At constant exchange rates the total revenue increased by 2%.
  • For the third quarter of 2025, total NGAL sales totaled DKK 7.2 million, growing by 5% globally, and by 10% at constant exchange rates. For the first nine months of 2025, total NGAL sales rose by 5% compared to the first nine months of 2024 and by 7% at constant exchange rates.
  • Adjusted EBITDA loss in the third quarter of 2025 amounted to DKK 16.8 million as expected, compared to DKK 19.6 million in the third quarter last year. For the first nine months of 2025 Adjusted EBITDA loss amounted to DKK 63.3 million, compared to DKK 51.1 million in the same period last year.
  • As of September 30, 2025, the Company’s cash position was in line with expectations, DKK 27.6 million compared to DKK 77.1 million in the same period last year.

Guidance

Based on the results for the first 9 months of 2025, the full-year guidance for 2025 is unchanged compared to previously announcement on November 4, 2025 where the company revised the 2025 Guidance to:

  • Total revenue is expected to be in the range of DKK 40-45 million.
  • Adjusted EBITDA loss is expected to be in the range of DKK 75-80 million.

In connection with the release of the Interim Report for the third quarter of 2025, the Company will host an online investor presentation on November 19, 2025, at 11:00 CET via HC Andersen Capital. Investors interested in attending the webcast may register here: BioPorto – Presentation of Q3 2025 Interim Results

To receive BioPorto’s Company Announcements, Press Releases, Newsletters and other business relevant information, please sign up on Investor_contact.

Investor Relations Contacts

Niels Høy Nielsen, Chief Financial Officer, BioPorto A/S, investor@bioporto.com, C: +45 2551 8724

About BioPorto

BioPorto is an in vitro diagnostics company focused on saving patients’ lives and improving their quality of life with actionable kidney biomarkers – tools designed to help clinicians make changes in patient management. The Company leverages its expertise in assay development to create a pipeline of novel and compelling products that focus on conditions where there is significant unmet medical need, and where the Company’s tests can help improve clinical and economic outcomes for patients, providers, and the healthcare ecosystem.

The Company’s flagship products are based on the NGAL biomarker and designed to aid in risk assessment and management of Acute Kidney Injury (AKI), a common clinical syndrome that can have severe consequences, including significant morbidity and mortality, if not identified and treated early. With the aid of NGAL levels, physicians can identify patients at risk of AKI more rapidly than is possible with current standard of care measurements, enabling earlier intervention and more tailored patient management strategies. The Company markets NGAL tests under applicable registrations including CE mark in several countries worldwide and FDA cleared ProNephro AKITM (NGAL) in the US.

BioPorto has facilities in Copenhagen, Denmark and Boston, MA, USA. The shares of BioPorto A/S are listed on the Nasdaq Copenhagen stock exchange. For more information visit www.bioporto.com.

Forward looking statement disclaimer

Certain statements in this news release are not historical facts and may be forward-looking statements. Forward-looking statements include statements regarding the intent, belief or current expectations with respect to the Company’s expectations, intentions and projections regarding its future performance including the Company’s Guidance for 2025; currency exchange rate fluctuations; anticipated events or trends and other matters that are not historical facts, including with respect to implementation of manufacturing and quality systems, commercialization of NGAL tests, and the development of future products and new indications; concerns that may arise from additional data, analysis or results obtained during clinical trials; and, the Company’s ability to successfully market both new and existing products. These forward-looking statements, which may use words such as “aim”, “anticipate”, “believe”, “intend”, “estimate”, “expect” and words of similar meaning, include all matters that are not historical facts. These forward-looking statements involve risks, and uncertainties that could cause the actual results of operations, financial condition, liquidity, dividend policy and the development of the industry in which the Company’s business operates to differ materially from the impression created by the forward-looking statements. These statements are not guarantees of future performance and are subject to known and unknown risks, uncertainties and other factors that could cause actual results to differ materially from those expressed or implied by such forward-looking statements. Given these risks and uncertainties, prospective investors are cautioned not to place undue reliance on forward-looking statements. Forward-looking statements speak only as of the date of such statements and, except as required by applicable law, the Company undertakes no obligation to update or revise publicly any forward-looking statements, whether as a result of new information, future events or otherwise. Factors that may impact BioPorto’s success are more fully disclosed in BioPorto’s periodic financial filings, including its Annual Report for 2024, with the Danish Financial Supervisory Authority, particularly under the heading “Risk Factors”.

Attachments

Aptose Biosciences Announces Arrangement Agreement for Acquisition by Hanmi Pharmaceutical

Aptose Biosciences Announces Arrangement Agreement for Acquisition by Hanmi Pharmaceutical




Aptose Biosciences Announces Arrangement Agreement for Acquisition by Hanmi Pharmaceutical

Aptose Biosciences minority shareholders to receive C$2.41 in cash per share in a “go private” transaction

SAN DIEGO and TORONTO, Nov. 19, 2025 (GLOBE NEWSWIRE) — Aptose Biosciences Inc. (“Aptose” or the “Company”) (TSX: APS; OTC: APTOF) and Hanmi Pharmaceutical Co. Ltd. (“Hanmi”) today announced that Aptose, Hanmi and HS North America Ltd., a wholly owned subsidiary of Hanmi (“Hanmi Purchaser” and together with Hanmi, the “Hanmi Purchasers”), have entered into a definitive arrangement agreement (the “Arrangement Agreement”) pursuant to which Hanmi Purchaser will acquire all of the issued and outstanding common shares of Aptose (“Common Shares”) that are not currently owned or controlled by the Hanmi Purchasers or their respective affiliates.

Hanmi has participated in multiple financings of Aptose and owns 19.93% of all outstanding Common Shares. During the past 18 months, Hanmi has singularly supported Aptose and the continued development of tuspetinib (TUS) through debt facilities to Aptose totaling more than US$30 million. Under the terms of the Arrangement Agreement, upon the completion of the transactions contemplated under the Arrangement Agreement, Aptose shareholders, other than the Hanmi Purchasers and their respective affiliates that hold any Common Shares, will receive C$2.41 in cash per Common Share, which represents a premium of 28% over Aptose’s 30-day VWAP of C$1.88 on the Toronto Stock Exchange (TSX). 

“We are very pleased to have reached an agreement on a transaction with Hanmi,” stated William G. Rice, Ph.D., Chairman, President, and Chief Executive Officer of Aptose. “This transaction not only offers a premium value for our minority shareholders but also enables Aptose to continue the development of TUS combined with standard treatment venetoclax plus azacitidine (VEN+AZA) for acute myeloid leukemia (AML) in the TUSCANY Phase 1/2 clinical study. The TUS+VEN+AZA triplet therapy has shown promising response rates and safety in a diverse population of patients newly diagnosed with AML. We are extremely grateful for Hanmi’s ongoing support as we work toward our long-term goal of improving patient outcomes in AML.”

“We are very pleased to have reached this agreement with Aptose,” said Jae-Hyun Park of Hanmi. “With a growing body of positive data, it is important to support the uninterrupted and expanded development of tuspetinib in the TUSCANY clinical study. This step also marks Hanmi’s first beachhead and direct entry into North America, establishing a strategic foothold for future partnerships and clinical expansion in the region.”

Transaction Details

Under the terms of Arrangement Agreement, Aptose will continue from a corporation incorporated under the Canada Business Corporations Act to a corporation continued under the Business Corporations Act (Alberta) (the “Continuance”) and, following the completion of the Continuance, Hanmi Purchaser will acquire all of the issued and outstanding Common Shares that are not currently owned or controlled by the Hanmi Purchasers or their respective affiliates by way of a plan of arrangement under the Business Corporations Act (Alberta) (the “Arrangement” and, together with the Continuance, the “Transaction”).

Upon the completion of the Transaction, subject to applicable tax withholdings:

  • each Common Share (other than any Common Share owned or controlled by the Hanmi Purchasers or their respective affiliates or for which dissent rights have been validly exercised) will be transferred to Hanmi Purchaser in exchange for an amount in cash equal to C$2.41 per Common Share;
  • each Aptose option will cease to represent an option or other right to acquire any Common Share and will be deemed surrendered and exchanged for an amount in cash equal to C$2.41 per Common Share, multiplied by the number of Common Shares subject to the Aptose option, less the aggregate exercise price in respect of such Aptose option;
  • each Aptose restricted share unit will cease to represent a share unit of Aptose and will be deemed surrendered and exchanged for an amount in cash equal to C$2.41 per Common Share, multiplied by the number of Common Shares subject to the Aptose restricted share unit;
  • each Aptose warrant held by Armistice Capital Master Fund Ltd. (the “Armistice Warrants”) will cease to represent a warrant exercisable for Common Shares and will be deemed surrendered and exchanged for an amount in cash equal to an amount calculated using the “Black Scholes” valuation model in accordance with the terms of the applicable Armistice Warrant; and
  • each Aptose warrant (other than the Armistice Warrants) will cease to represent a warrant exercisable for Common Shares and will be deemed surrendered and exchanged for an amount in cash equal to C$2.41 per Common Share, multiplied by the number of Common Shares subject to the Aptose warrant, less the aggregate exercise price in respect of such Aptose warrant.

The Arrangement Agreement contains customary non-solicitation provisions prohibiting Aptose from soliciting competing acquisition proposals, as well as “right to match” provisions in favour of Hanmi Purchaser. The Arrangement Agreement provides for a C$300,000 expense fee payable to Hanmi Purchaser if the Arrangement Agreement is terminated in certain circumstances, including in the context of a change in recommendation by the board of directors of Aptose (the “Board”) or by the special committee consisting of independent members of the Board formed in connection with the Arrangement (the “Special Committee”).

The completion of the Transaction is subject to satisfaction of customary closing conditions, including court approval and approval of Aptose shareholders as further set out below. After completion of the Transaction, Aptose expects to no longer be subject to the reporting requirements of applicable Canadian securities legislation and the Common Shares will be delisted from all stock exchanges where Common Shares are currently listed, including the TSX.

Completion of the Transaction will be subject to the approval of (i) at least two-thirds (66 2/3%) of the votes cast by Aptose shareholders present in person or represented by proxy at a special meeting of Aptose shareholders to be held no later than January 16, 2026 to approve the Transaction (the “Special Meeting”), voting as a single class, and (ii) the majority of the holders of Common Shares present in person or represented by proxy at the Special Meeting, excluding the votes of the Hanmi Purchasers and their respective affiliates, and any other shareholders whose votes are required to be excluded for the purposes of “minority approval” under Multilateral Instrument 61-101 – Protection of Minority Security Holders in Special Transactions (“MI 61-101”) in the context of a “business combination” (the “Minority Shareholders”). Further details regarding the applicable voting requirements will be contained in a management information circular to be filed and mailed to Aptose shareholders in connection with the Special Meeting to approve the Transaction.

Concurrent with the execution of the Arrangement Agreement, Hanmi Purchaser entered into voting support agreements with each of the directors and officers of Aptose pursuant to which, subject to the terms of the voting support agreements, each Aptose director or officer has agreed to, among other things, vote or cause to be voted all of the Common Shares owned, controlled or directed, directly or indirectly, by them in favour of the Transaction at the Special Meeting.

Further details of the Transaction are set out in the Arrangement Agreement, which will be made available on Aptose’s SEDAR+ profile at www.sedarplus.ca.

Opinion and Formal Valuation

Locust Walk Securities, LLC (“Locust Walk”) was retained by the Special Committee to provide financial advice and prepare a formal valuation of the Common Shares, as required under MI 61-101. Locust Walk delivered a valuation that, as of November 18, 2025, and based on Locust Walk’s analysis and subject to the assumptions, limitations and qualifications to be set forth in the formal valuation that will be included in the management information circular that will be sent to Aptose shareholders in connection with the Special Meeting (the “Formal Valuation”), using multiple analyses, including DCF modeling, the fair market value of the Common Shares is in the range of C$1.00 to C$5.23 per Common Share. Locust Walk has also delivered an oral opinion (the “Fairness Opinion”) to the Special Committee that, as of November 18, 2025, and subject to the assumptions, limitations and qualifications to be set forth in Locust Walk’s written fairness opinion that will be included in the management information circular, the consideration to be received by the holders of Common Shares (other than the Hanmi Purchasers and their respective affiliates) pursuant to the Arrangement Agreement is fair, from a financial point of view, to such holders of Common Shares. The management information circular will also include factors considered by the Special Committee and the Board and other relevant information.

Unanimous Approval of Aptose Special Committee and Board of Directors

The Special Committee, after consultation with and receiving advice from its financial adviser and outside legal counsel, has unanimously recommended that the Board approve the Arrangement and that Aptose shareholders vote in favour of the Arrangement.

The Board, acting on the unanimous recommendation in favour of the Arrangement by the Special Committee and after receiving advice from its financial adviser and outside legal counsel in evaluating the Arrangement, has unanimously determined that the Arrangement is fair to Aptose shareholders (other than the Hanmi Purchasers and their respective affiliates) and that the Arrangement is in the best interests of Aptose, and resolved to unanimously recommend that Aptose shareholders vote in favour of the Arrangement.

Advisors

Locust Walk is acting as financial advisor and independent valuator to the Special Committee and the Company. McCarthy Tétrault LLP is acting as independent legal advisor to the Special Committee and the Company. Stikeman Elliott LLP is acting as independent legal advisor to Hanmi Purchaser.

About Tuspetinib

Aptose’s lead compound tuspetinib is a convenient once daily oral agent that potently targets SYK, mutated and wild type forms of FLT3, mutated KIT, JAK1/2, and RSK2 kinases, while avoiding many typical toxicity concerns observed with other agents. The ongoing TUSCANY triplet Phase 1/2 study is designed to test various doses and schedules of TUS in combination with standard dosing of azacitidine and venetoclax in newly diagnosed patients with AML who are ineligible to receive induction chemotherapy. Aptose has reported data from the first three dose cohorts that have demonstrated safety, CRs and minimal residual disease (MRD) negativity across patients with diverse mutations. The early data showed that 9 out of 10 patients responded to the TUS triplet therapy, with 100% complete remission (CR/CRh) achieved in the 80mg and 120mg cohorts. Notably, patients with difficult-to-treat mutations in TP53, RAS and FLT3 genes also achieved a 100% CR/CRh rate (press release here).

About Hanmi

Hanmi Pharmaceutical Co., Ltd., founded in 1973 in Seoul, South Korea, is a leading global biopharmaceutical company focused on developing innovative drugs in the fields of oncology, diabetes, obesity, and other metabolic diseases. The company operates GMP-compliant facilities in Hwaseong, Pyeongtaek, and Siheung, Gyeonggi-do, producing high-quality APIs and finished products exported worldwide. Renowned for pioneering R&D partnerships with Janssen, Roche, MSD, and Gilead, Hanmi drives patient-centric, first-in-class therapies as a top player in Korea’s pharmaceutical industry. For more information, please visit www.hanmipharm.com.

About Aptose

Aptose Biosciences Inc. is a clinical-stage biotechnology company committed to developing precision medicines addressing unmet medical needs in oncology, with an initial focus on hematology. The Company’s small molecule cancer therapeutics pipeline includes products designed to provide single agent efficacy and to enhance the efficacy of other anti-cancer therapies and regimens without overlapping toxicities. The Company’s lead clinical-stage compound tuspetinib (TUS), is an oral kinase inhibitor that has demonstrated activity as a monotherapy and in combination therapy in patients with relapsed or refractory acute myeloid leukemia (AML) and is being developed as a frontline triplet therapy in newly diagnosed AML. For more information, please visit www.aptose.com.

Forward Looking Statements

This news release contains “forward-looking information” and “forward-looking statements” (collectively, “forward-looking information”) within the meaning of applicable securities laws. This information includes, but is not limited to, statements concerning our objectives, our strategies to achieve those objectives, as well as statements made with respect to management’s beliefs, plans, estimates, projections and intentions, and similar statements concerning anticipated future events, results, circumstances, performance or expectations that are not historical facts. In some cases, forward-looking information can be identified by the use of forward-looking terminology such as “expects”, “estimates”, “outlook”, “forecasts”, “projection”, “prospects”, “intends”, “anticipates”, “believes”, or variations of such words and phrases or statements that certain actions, events or results “may”, “could”, “would”, “might”, “will”, “will be taken”, “occur” or “be achieved”. In addition, any statements that refer to expectations, intentions, projections or other characterizations of future events or circumstances contain forward-looking information. Statements containing forward-looking information are not historical facts but instead represent management’s expectations, estimates and projections regarding future events or circumstances. Forward-looking information in this news release include, among other things, statements relating to Aptose’s business in general; statements relating to the Transaction, the ability to complete the transactions contemplated by the Arrangement Agreement and the timing thereof, including the parties’ ability to satisfy the conditions to the completion of the Transaction, the receipt of the required Aptose shareholder approval and court approval and other customary closing conditions, the possibility of any termination of the Arrangement Agreement in accordance with its terms, and the expected benefits to the Company and its shareholders of the proposed Transaction.

Risks and uncertainties related to the transactions contemplated by the Arrangement Agreement include, but are not limited to: the possibility that the Transaction will not be completed on the terms and conditions, or on the timing, currently contemplated, and that it may not be completed at all, due to a failure to obtain or satisfy, in a timely manner or otherwise, required regulatory, shareholder and court approvals and other conditions to the completion of the Transaction or for other reasons; the risk that competing offers or acquisition proposals will be made; the negative impact that the failure to complete the Transaction for any reason could have on the price of the Common Shares or on the business of Aptose; Hanmi Purchaser’s failure to pay the cash consideration at completion of the Transaction; the business of Aptose may experience significant disruptions, including loss of employees due to transaction related uncertainty, industry conditions or other factors; risks relating to employee retention; the risk of regulatory changes that may materially impact the business or the operations of Aptose; risks related to the diversion of management’s attention from Aptose’s ongoing business operations while the Transaction is pending; and other risks and uncertainties affecting Aptose, including those described in filings and reports Aptose may make from time to time with the Canadian securities authorities. Although we have attempted to identify important risk factors that could cause actual results to differ materially from those contained in forward-looking information, there may be other risk factors not presently known to us or that we presently believe are not material that could also cause actual results or future events to differ materially from those expressed in such forward-looking information. There can be no assurance that such information will prove to be accurate, as actual results and future events could differ materially from those anticipated in such information. No forward-looking statement is a guarantee of future results. Accordingly, you should not place undue reliance on forward-looking information, which speaks only as of the date made. The forward-looking information contained in this news release represents the Company’s expectations as of the date of this news release (or as the date they are otherwise stated to be made) and are subject to change after such date. However, the Company disclaims any intention or obligation or undertaking to update or revise any forward-looking information whether as a result of new information, future events or otherwise, except as required under applicable securities laws in Canada. All of the forward-looking information contained in this news release is expressly qualified by the foregoing cautionary statements.

This announcement is for informational purposes only and does not constitute an offer to purchase or a solicitation of an offer to sell, or an offer to sell or a solicitation of an offer to buy, Common Shares.

For further information, please contact:

Aptose Biosciences Inc.                                         
Susan Pietropaolo                                                                                   
Corporate Communications & Investor Relations                        
201-923-2049
spietropaolo@aptose.com