JETRO and CIC to Showcase Promising Japanese Biotech Startups at “Japan Innovation Night” during BIO International Convention 2025 in Boston

JETRO and CIC to Showcase Promising Japanese Biotech Startups at “Japan Innovation Night” during BIO International Convention 2025 in Boston




JETRO and CIC to Showcase Promising Japanese Biotech Startups at “Japan Innovation Night” during BIO International Convention 2025 in Boston

BOSTON–(BUSINESS WIRE)–#accelerator–The Japan External Trade Organization (JETRO) and CIC Japan Desk will once again host “Japan Innovation Night: Best in Biotech” – a groundbreaking event showcasing the latest advancements in biotechnology from Japanese startups.




This exclusive gathering will take place on Wednesday, June 18th, 2025, from 5:30pm to 8pm in Venture Café at CIC Cambridge. This event provides a unique opportunity for U.S. venture capital firms and pharmaceutical companies, particularly those based in the Greater Boston Area, to explore potential partnerships and synergies with innovative Japanese biotech firms.

That same week, JETRO will also be organizing the Japan Pavilion at BIO International Convention 2025 in Boston; therefore, JETRO is pleased to bring several of the exhibiting startups to present their products in a more intimate setting at Japan Innovation Night. The event will feature ten carefully selected startups that will each be given three-minute pitches to present their latest innovations and partnering strategies and goals. A networking session will also be arranged for after the pitch session.

In 2024, the Japanese government updated its Bioeconomy Strategy, expressing its intent to step up its support for bioeconomy fields in Japan. This is on top of an already one trillion-yen budget measure enacted by the Japanese government in fiscal year 2022. The Bioeconomy Strategy underscores the Japanese government’s commitment to expanding Japan’s bioeconomy in the hopes of providing solutions to a myriad of societal and economic issues, from the environment to food to health and economic development.

In the Strategy, the Japanese government commits to enhancing the local startup ecosystem, ensuring its support aligns with the domestic biomanufacturing sector’s structure and the challenges its players face. By coordinating initiatives across government efforts, the Bioeconomy Strategy aims to establish environments that foster startup creation, growth, and R&D. JETRO will introduce innovative startups from this market at Japan Innovation Night. 

Full List of Japanese Startups:

https://www.jetro.go.jp/newsletter/SFC/2025/japan_innovation_night_2025_startup_list.pdf

Pre-Registration Here:

https://venturecafecambridge.org/event/japan-innovation-night-2025/

About JETRO

The Japan External Trade Organization (JETRO) is a Japanese government-affiliated agency that supports Japanese businesses expanding globally and international businesses entering Japan.

JETRO helps to facilitate collaboration and business alliances between Japanese and overseas companies via its business platform “J-Bridge.”

About CIC

CIC builds and operates a global network of innovation campuses where startups, scale-ups, corporations and public entities connect, work, and grow. Founded in 1999, CIC manages 1.5 million square feet of innovation-focused workspace, laboratories, and event space across North America, Europe and Asia. Additionally, CIC develops bespoke programming, builds and enables industry clusters, and provides world-class district consulting—all focused on advancing innovation.

Contacts

Ryota Hiramoto

JETRO New York

Ryota_Hiramoto@jetro.go.jp
1-212-997-0400

Tracer Biotechnologies Announces Strategic Partnership with QIAGEN to Advance Blood-Based MRD Testing for Solid Tumors

Tracer Biotechnologies Announces Strategic Partnership with QIAGEN to Advance Blood-Based MRD Testing for Solid Tumors




Tracer Biotechnologies Announces Strategic Partnership with QIAGEN to Advance Blood-Based MRD Testing for Solid Tumors

NEW YORK–(BUSINESS WIRE)–Tracer Biotechnologies, a leader in blood-based molecular diagnostics for cancer, is pleased to announce a strategic partnership with QIAGEN (NYSE: QGEN; Frankfurt Prime Standard: QIA) to co-develop and commercialize minimal residual disease (MRD) assays for solid tumors on QIAGEN’s QIAcuity digital PCR platform.


This collaboration aims to deliver highly sensitive, cost-effective, and decentralized MRD testing solutions that enable oncologists to monitor cancer recurrence and guide personalized treatment decisions using minimally invasive blood samples.

“Partnering with QIAGEN enables Tracer to bring our solid tumor MRD expertise to a broader market using a robust digital PCR platform in QIAcuity,” said Mark Kaganovich, CEO of Tracer Biotechnologies. “With QIAcuity’s sensitivity and scalability, we can deliver high-quality companion diagnostics that integrate seamlessly into clinical workflows and offer new options to oncologists and patients.”

Tracer offers two complementary MRD solutions:

  • Tracer dPCR, a tumor-informed, multiplexed digital PCR assay that allows institutions to run bespoke MRD tests internally using their own digital PCR instruments;
  • Tracer WGS, an AI-powered whole-genome ctDNA platform that enables ultra-sensitive tumor-agnostic detection and tracking with no need for prior tissue.

“This new partnership represents an important step in further establishing QIAGEN’s major role in oncology. We are bringing innovative MRD technologies into drug development through our companion diagnostic partnerships,” said Jonathan Arnold, Vice President, Head of Partnering for Precision Diagnostics at QIAGEN. “In particular, we want to strengthen our scalable, cost-effective solutions based on our QIAcuity digital PCR system and enable our pharmaceutical partners to use MRD insights for guiding personalized treatment decisions for cancer patients.”

Tracer’s mission is to turn every digital PCR machine and next-generation sequencer into a sensitive MRD assay—empowering institutions, pharmaceutical companies, and clinicians with the tools to decentralize testing, accelerate treatment decisions, and personalize cancer care.

About Tracer Biotechnologies

Tracer Biotechnologies is a molecular diagnostics company specializing in blood-based assays for cancer detection and monitoring. Our platform enables decentralized, high-performance MRD testing using either digital PCR or whole-genome sequencing—bringing precision oncology closer to the point of care. For more information visit www.tracerbio.com.

About QIAGEN

QIAGEN N.V., a Netherlands-based holding company, is the leading global provider of Sample to Insight solutions, enabling customers to extract and gain valuable molecular insights from samples containing the building blocks of life. Our Sample technologies isolate and process DNA, RNA and proteins from blood, tissue and other materials. Assay technologies prepare these biomolecules for analysis while bioinformatics software and knowledge bases can be used to interpret data to find actionable insights. Automation solutions bring these processes together into seamless and cost-effective workflows. QIAGEN serves over 500,000 customers globally in Life Sciences (academia, pharma R&D and industrial applications, primarily forensics) and Molecular Diagnostics for clinical healthcare. As of March 31, 2025, QIAGEN employed approximately 5,700 people in over 35 locations worldwide. For more information, visit www.qiagen.com.

Contacts

communications@tracerbio.com

Immunome Reports Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)

Immunome Reports Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)




Immunome Reports Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)

BOTHELL, Wash.–(BUSINESS WIRE)–Immunome, Inc. (the “Company”) (Nasdaq: IMNM), a biotechnology company focused on developing first-in-class and best-in-class targeted cancer therapies, announced today that on June 2, 2025, the Compensation Committee of the Company’s Board of Directors (the “Compensation Committee”) granted inducement awards consisting of non-statutory stock options to purchase an aggregate of 173,000 shares of common stock to 13 new employees under the Company’s 2024 Inducement Plan. The Compensation Committee approved the stock options as an inducement material to such employees’ employment in accordance with Nasdaq Listing Rule 5635(c)(4).


Each stock option has an exercise price per share equal to $9.06 per share, the Company’s closing sales price on June 2, 2025, and will vest over four years, with 25% of the underlying shares vesting on the one-year anniversary of the applicable vesting commencement date and the balance of the underlying shares vesting monthly thereafter over 36 months, subject to the new employees’ continued service relationship with the Company through the applicable vesting dates. The stock options are subject to the terms and conditions of the Company’s 2024 Inducement Plan and the terms and conditions of an applicable stock option agreement covering the grant.

About Immunome, Inc.

Immunome is a clinical-stage targeted oncology company committed to developing first-in-class and best-in-class targeted therapies designed to improve outcomes for cancer patients. We are advancing an innovative portfolio of therapeutics, drawing on leadership that previously played key roles in the design, development, and commercialization of cutting-edge targeted cancer therapies, including antibody-drug conjugate therapies (ADCs). Our most advanced pipeline programs are varegacestat (formerly AL102), a gamma secretase inhibitor which is currently in a Phase 3 trial for treatment of desmoid tumors; IM-1021, a ROR1-targeted ADC which is currently in a Phase 1 trial; and IM-3050, a FAP-targeted radioligand, which recently received IND clearance. Our pipeline also includes IM-1617, IM-1335, and IM-1340, all of which are preclinical ADCs pursuing undisclosed targets with expression in multiple solid tumors. For more information, visit www.immunome.com.

Contacts

Investor Contact
Max Rosett

Chief Financial Officer

investors@immunome.com

GlycoMimetics Stockholders Approve Proposed Merger with Crescent Biopharma and All Related Proposals

GlycoMimetics Stockholders Approve Proposed Merger with Crescent Biopharma and All Related Proposals




GlycoMimetics Stockholders Approve Proposed Merger with Crescent Biopharma and All Related Proposals

GlycoMimetics Board of Directors approves 1-for-100 reverse stock split

ROCKVILLE, Md.–(BUSINESS WIRE)–GlycoMimetics, Inc. (Nasdaq: GLYC) (“GlycoMimetics”) today announced that its stockholders have approved the proposed merger (the “Merger”) with Crescent Biopharma, Inc. (“Crescent”), along with all proposals related to the Merger. The proposals were voted upon at GlycoMimetics’ special meeting in lieu of the annual meeting of stockholders held on June 5, 2025 (the “Special Meeting”), including a reverse stock split of GlycoMimetics’ common stock to be effected at the discretion of the board of directors of GlycoMimetics (the “Board”) within the parameters approved by GlycoMimetics’ stockholders.

On June 5, 2025, following the Special Meeting, the Board approved a reverse stock split of GlycoMimetics’ common stock at a ratio of 1-for-100. Following the anticipated closing of the Merger, the combined company’s common stock is expected to begin trading on a post-reverse stock split basis on The Nasdaq Capital Market (“Nasdaq”) on June 16, 2025, under the new name “Crescent Biopharma, Inc.”, ticker symbol “CBIO”, CUSIP number 38000Q201 and ISIN number US38000Q2012.

The reverse stock split is expected to reduce the number of GlycoMimetics’ outstanding common stock from approximately 64.5 million shares to approximately 0.6 million shares. The number of shares of GlycoMimetics’ authorized common stock will not be affected by the reverse stock split. At the Special Meeting, GlycoMimetics’ stockholders approved an increase in the number of shares of GlycoMimetics’ authorized common stock from 150,000,000 shares to 175,000,000 shares in connection with the anticipated closing of the Merger. No fractional shares will be issued if, as a result of the reverse stock split, a stockholder would otherwise become entitled to a fractional share because the number of shares of GlycoMimetics common stock they hold before the reverse stock split is not evenly divisible by the split ratio. Instead, each stockholder will be entitled to receive a cash payment in lieu of such fractional share. The cash payment to be paid will be equal to the fraction of a share to which such stockholder would otherwise be entitled multiplied by the closing price per share as reported by The Nasdaq Stock Market LLC on June 12, 2025, the trading day prior to the date the charter amendment to effect the reverse stock split is expected to be filed with the Secretary of State of the State of Delaware (with such price proportionately adjusted to give effect to the reverse stock split).

As a result of the reverse stock split, proportionate adjustments will be made to the exercise prices and number of shares of GlycoMimetics’ common stock underlying GlycoMimetics’ outstanding equity awards. There will be no change to the par value per share.

Following the closing of the Merger, the combined company’s total issued and outstanding common stock is expected to be approximately 14.8 million shares, or approximately 25.3 million shares on a fully-diluted basis.

About GlycoMimetics, Inc.

GlycoMimetics is a late clinical-stage biotechnology company that was previously discovering and developing glycobiology-based therapies for cancers, including AML, and for inflammatory diseases. The company’s scientific approach was based on an understanding of the role that carbohydrates play in cell recognition. Its specialized chemistry platform can be used to discover small molecule drugs, known as glycomimetics, that alter carbohydrate-mediated recognition in diverse disease states, including cancers and inflammation. The company’s goal was to develop transformative therapies for diseases with high unmet medical need. Learn more at www.glycomimetics.com.

About Crescent Biopharma, Inc.

Crescent Biopharma, Inc. is a biotechnology company advancing novel precision-engineered molecules to advance care for patients with solid tumors. Crescent’s pipeline of three programs harnesses validated biology to accelerate the path to market for potentially best-in-class therapeutics. Crescent’s lead program is CR-001, a tetravalent PD-1 x VEGF bispecific antibody, and it is also advancing CR-002 and CR-003, antibody drug conjugates with topoisomerase inhibitor payloads for undisclosed targets. For more information, visit www.crescentbiopharma.com and follow Crescent on LinkedIn.

Forward-Looking Statements

Certain statements in this press release, other than purely historical information, may constitute “forward-looking statements” within the meaning of the federal securities laws, including for purposes of the “safe harbor” provisions under the Private Securities Litigation Reform Act of 1995, concerning GlycoMimetics, Crescent, the proposed pre-closing financing and the proposed Merger between GlycoMimetics and Crescent (collectively, the “Proposed Transactions”) and other matters. These forward-looking statements include, but are not limited to: expectations related to anticipated timing of the closing of the Merger and satisfaction (or waiver) of closing conditions under the merger agreement; the combined company’s listing on Nasdaq after the closing of the proposed Merger; the number of shares of GlycoMimetics common stock that may be outstanding as a result of the reverse stock split; and expectations regarding the ownership structure of the combined company. In addition, any statements that refer to projections, forecasts or other characterizations of future events or circumstances, including any underlying assumptions, are forward-looking statements. The words “opportunity,” “potential,” “can,” “goal,” “strategy,” “target,” “anticipate,” “achieve,” “believe,” “contemplate,” “continue,” “could,” “estimate,” “expect,” “intends,” “may,” “plan,” “possible,” “project,” “should,” “will,” “would” and similar expressions (including the negatives of these terms or variations of them) may identify forward-looking statements, but the absence of these words does not mean that a statement is not forward-looking. These forward-looking statements are based on current expectations and beliefs concerning future developments and their potential effects. There can be no assurance that future developments affecting GlycoMimetics, Crescent, the Proposed Transactions, or the reverse stock split will be those that have been anticipated. These forward-looking statements involve a number of risks, uncertainties (some of which are beyond the control of GlycoMimetics and Crescent) or other assumptions that may cause actual results, outcomes or performance to be materially different from those expressed or implied by these forward-looking statements. These risks and uncertainties include, but are not limited to, the risk that the conditions to the closing or consummation of the Proposed Transactions are not satisfied; the risk that the proposed pre-closing financing is not completed in a timely manner or at all; uncertainties as to the timing of the consummation of the Proposed Transactions and the ability of each of GlycoMimetics and Crescent to consummate the transactions contemplated by the Proposed Transactions; risks related to GlycoMimetics’ continued listing on Nasdaq until closing of the Proposed Transactions and the combined company’s ability to remain listed following the Proposed Transactions; risks related to GlycoMimetics’ and Crescent’s ability to correctly estimate their respective operating expenses and expenses associated with the Proposed Transactions, as applicable, as well as uncertainties regarding the impact any delay in the closing of any of the Proposed Transactions would have on the anticipated cash resources of the resulting combined company upon closing and other events and unanticipated spending and costs that could reduce the combined company’s cash resources; the failure or delay in obtaining required approvals from any governmental or quasi-governmental entity necessary to consummate the Proposed Transactions; the occurrence of any event, change or other circumstance or condition that could give rise to the termination of the business combination between GlycoMimetics and Crescent; costs related to the Merger; as a result of adjustments to the exchange ratio, Crescent stockholders and GlycoMimetics stockholders could own more or less of the combined company than is currently anticipated; the outcome of any legal proceedings that may be instituted against GlycoMimetics, Crescent or any of their respective directors or officers related to the merger agreement or the transactions contemplated thereby; unexpected costs, charges or expenses resulting from the Proposed Transactions; potential adverse reactions or changes to business relationships resulting from the announcement or completion of the Proposed Transactions; and those uncertainties and factors more fully described in filings with the Securities and Exchange Commission (the “SEC”), including reports filed on Form 10-K, 10-Q and 8-K, in other filings that GlycoMimetics makes and will make with the SEC in connection with the proposed Merger, including the proxy statement/prospectus, as well as discussions of potential risks, uncertainties, and other important factors included in other filings by GlycoMimetics from time to time, any risk factors related to GlycoMimetics or Crescent made available to you in connection with the Proposed Transactions, as well as risk factors associated with companies, such as Crescent, that operate in the biopharma industry. Should one or more of these risks or uncertainties materialize, or should any of GlycoMimetics’ or Crescent’s assumptions prove incorrect, actual results may vary in material respects from those projected in these forward-looking statements. Nothing in this press release should be regarded as a representation by any person that the forward-looking statements set forth herein will be achieved or that any of the contemplated results of such forward-looking statements will be achieved. You should not place undue reliance on forward-looking statements in this press release, which speak only as of the date they are made and are qualified in their entirety by reference to the cautionary statements herein. Neither GlycoMimetics nor Crescent undertakes or accepts any duty to release publicly any updates or revisions to any forward-looking statements. This press release does not purport to summarize all of the conditions, risks and other attributes of an investment in GlycoMimetics or Crescent.

No Offer or Solicitation

This press release and the information contained herein is not intended to and does not constitute (i) a solicitation of a proxy, consent or approval with respect to any securities or in respect of the Proposed Transactions or (ii) an offer to sell or the solicitation of an offer to subscribe for or buy or an invitation to purchase or subscribe for any securities pursuant to the Proposed Transactions or otherwise, nor shall there be any sale, issuance or transfer of securities in any jurisdiction in contravention of applicable law. No offer of securities shall be made except in accordance with the requirements of the Securities Act of 1933, as amended, or an exemption therefrom. Subject to certain exceptions to be approved by the relevant regulators or certain facts to be ascertained, no public offer will be made directly or indirectly, in or into any jurisdiction where to do so would constitute a violation of the laws of such jurisdiction, or by use of the mails or by any means or instrumentality (including without limitation, facsimile transmission, telephone and the internet) of interstate or foreign commerce, or any facility of a national securities exchange, of any such jurisdiction.

NEITHER THE SEC NOR ANY STATE SECURITIES COMMISSION HAS APPROVED OR DISAPPROVED OF THE SECURITIES OR DETERMINED IF THIS PRESS RELEASE IS TRUTHFUL OR COMPLETE.

Contacts

GlycoMimetics Investor Contact:
Argot Partners

212-600-1902

Glycomimetics@argotpartners.com

Crescent Biopharma Investor Contact:
Amy Reilly

Chief Communications Officer

amy.reilly@crescentbiopharma.com
617-465-0586

Massive Bio Recognized in Two Key Categories on CB Insights’ AI Drug Research & Development Market Map

Massive Bio Recognized in Two Key Categories on CB Insights’ AI Drug Research & Development Market Map




Massive Bio Recognized in Two Key Categories on CB Insights’ AI Drug Research & Development Market Map

CHICAGO–(BUSINESS WIRE)–Massive Bio, a leader in AI-powered oncology patient recruitment and clinical trial matching, has been named in two pivotal categories on CB Insights’ latest AI Drug Research & Development Market Map. This recognition underscores Massive Bio’s innovative contributions to revolutionizing cancer care through advanced artificial intelligence solutions.




CB Insights’ market map highlights companies at the forefront of leveraging AI to accelerate drug discovery and development. Massive Bio’s inclusion in both the “Clinical Trial Matching” and “Patient Recruitment” categories reflects its dual impact on streamlining clinical trial processes and enhancing patient access to cutting-edge therapies.

“Being recognized by CB Insights in two critical categories is a testament to our team’s dedication to transforming oncology care,” said Selin Kurnaz, PhD, CEO and Co-Founder of Massive Bio. “Our AI-driven platform is designed to bridge the gap between patients and clinical trials, ensuring that individuals receive the most appropriate and timely treatments available.”

Arturo Loaiza-Bonilla, MD, Co-Founder and Chief Medical Officer, added, “This acknowledgment validates our commitment to integrating advanced AI technologies into clinical workflows. By optimizing trial matching and patient recruitment, we’re not only improving operational efficiencies but also enhancing patient outcomes in oncology.”

This recognition from CB Insights follows a milestone presence at ASCO25, where Arturo Loaiza-Bonilla presented a poster session on AI-powered clinical trial matching and participated in the ASCO/ESMO Joint Session, emphasizing international collaboration in oncology innovation. In addition, Selin Kurnaz was named a PCC Wayfinder, honoring her leadership in advancing equitable access and data-driven transformation in cancer care.

Massive Bio’s platform utilizes sophisticated algorithms and real-time data analytics to match cancer patients with suitable clinical trials, considering factors such as genetic profiles, treatment histories, and geographic locations. This approach has significantly increased trial enrollment rates and reduced the time required to identify eligible participants.

The company’s dual recognition by CB Insights highlights its comprehensive approach to addressing challenges in clinical trial enrollment and patient engagement. As the demand for personalized cancer treatments grows, Massive Bio continues to lead in providing scalable, AI-driven solutions that connect patients with life-saving clinical trials.

About Massive Bio

Massive Bio, co-founded by Selin Kurnaz, Arturo Loaiza-Bonilla, and Çağatay Çulcuoğlu, transforms the pharmaceutical value chain with AI-driven solutions. As an AI-enabled real-world data company, it streamlines the patient journey, enhances access to advanced treatment options, and optimizes clinical trials. Massive Bio collaborates with pharmaceutical companies, research organizations, and healthcare institutions worldwide. A founding member of the CancerX public-private partnership and participant in the Cancer Moonshot White House initiative, the company has received recognition from the National Cancer Institute and operates across 17 countries with a global team of over 100 employees. For more information, visit www.massivebio.com.

Contacts

Massive Bio

Mert Turkkan

Marketing Director

+1 646 461 4946

pr@massivebio.com

AndHealth Dermatology Welcomes Dr. Drew Kurtzman to Its Practice in Kentucky and Ohio

AndHealth Dermatology Welcomes Dr. Drew Kurtzman to Its Practice in Kentucky and Ohio




AndHealth Dermatology Welcomes Dr. Drew Kurtzman to Its Practice in Kentucky and Ohio

COLUMBUS, Ohio–(BUSINESS WIRE)–AndHealth Dermatology has welcomed Dr. Drew Kurtzman to its practice starting in May 2025. Dr. Kurtzman is a renowned board-certified dermatologist from Kentucky who will now see patients in Kentucky and Ohio as a part of AndHealth Dermatology. Appointments can be scheduled by calling 614-398-0582, by emailing appointments@andhealth.com, or by visiting DrDrewKurtzmanDermatologist.com.




Dr. Kurtzman brings a deep commitment to providing compassionate, expert care for patients with complex skin conditions. He has advanced training in both dermatology and rheumatology, allowing him to offer highly specialized care for patients with autoimmune and inflammatory skin conditions. Dr. Kurtzman’s approach blends cutting-edge medical knowledge with a genuine focus on patient well-being, ensuring each individual receives personalized treatment tailored to their unique needs.

With over a decade of clinical experience, Dr. Kurtzman has served in both academic and private practice settings. Patients value his thoroughness, clear communication, and dedication to improving quality of life through effective dermatologic care. Whether managing chronic conditions or evaluating new concerns, Dr. Kurtzman strives to make every patient feel heard, informed, and supported throughout their journey to healthier skin.

By practicing at AndHealth, Dr. Kurtzman will now offer access to an integrated care model that provides everything patients need to be well. AndHealth combines convenient, affordable, and high-quality dermatology and rheumatology care with pharmacy services and comprehensive support for root causes, such as medically tailored meal delivery, sleep, movement, remote monitoring, and continuous access to providers and health coaching.

AndHealth upholds ambitious benchmarks for patients, including a 94 Net Promoter Score (NPS) for patient satisfaction. Patients will also no longer face long drives or delays, as patients can be seen virtually or in person and nine out of 10 patients have their first visit in under just two weeks.

Dr. Kurtzman is looking forward to continuing patient care at AndHealth and said, “AndHealth Dermatology epitomizes the real definition of healthcare: supporting a person’s ability to heal and be whole. AndHealth Dermatology does this by leveraging technology, behavioral change and cutting-edge medicines to empower our patients to own their health outcomes. These resources and core values are why I couldn’t imagine practicing medicine anywhere other than AndHealth Dermatology.”

About AndHealth Dermatology

AndHealth Dermatology provides comprehensive dermatology care alongside unique world-class services to meet the unique needs of patients with chronic autoimmune conditions, by directly integrating pharmacy support for complex specialty medications and personalized care plans that include continuous care delivery including health coaching, medically tailored meals, sleep and movement support, remote monitoring, and everything else patients need to be well.

Headquartered in Columbus, Ohio, AndHealth Dermatology treats patients in Ohio, Kentucky, Indiana, Boston, and soon Illinois (coming in mid-2025).

To learn more or schedule, visit DrDrewKurtzmanDermatologist.com.

Contacts

Julia Phillips

SVP, Marketing

AndHealth

press@andhealth.com

MeMed BV Surpasses 100,000 Patient Tests, Underscoring Adoption of Rapid Host-Response Diagnostics

MeMed BV Surpasses 100,000 Patient Tests, Underscoring Adoption of Rapid Host-Response Diagnostics




MeMed BV Surpasses 100,000 Patient Tests, Underscoring Adoption of Rapid Host-Response Diagnostics

— Milestone Achieved Through Growing Clinical Evidence Demonstrating Real-World Impact on Infection Management —

— MeMed and Physicians Premier Celebrated Milestone Event in Corpus Christi, Texas —

ANDOVER, Mass. & HAIFA, Israel–(BUSINESS WIRE)–#AMR–MeMed, a global leader in host-response diagnostics, today announced a major milestone: more than 100,000 patients have now been tested with MeMed BV®, the company’s flagship diagnostic that accurately distinguishes between bacterial and viral infections in just 15 minutes, based on the body’s immune response. This milestone highlights MeMed’s commitment to advancing precision medicine, empowering responsible antibiotic use by care providers, and transforming infection management across diverse care settings.




Advancing Antibiotic Stewardship and Clinical Decision-Making

The growing adoption of MeMed BV in emergency medicine, urgent care, and hospital settings indicates the industry’s move toward host-response and precision diagnostics. From hospital systems to decentralized care providers, MeMed BV has been integrated into real-world clinical workflows by clinicians committed to improving patient outcomes.

Among these trailblazing partners is Physicians Premier, an innovative network of freestanding emergency rooms that has embraced MeMed BV as part of its commitment to advanced, patient-centered care. The 100,000th patient test was performed at Physicians Premier’s Parkdale clinic in Corpus Christi, Texas, a symbolic moment that was marked with a joint celebration between MeMed and Physicians Premier leadership earlier today.

“At Physicians Premier, we are committed to delivering cutting edge, personalized care that prioritizes both patient well-being and best practices,” said Teri Cardenas, CEO of Physicians Premier. “MeMed BV has empowered our clinicians to make more informed decisions, reducing unnecessary antibiotic prescriptions while improving patient outcomes. We are proud to stand with MeMed at the forefront of diagnostic innovation.”

Scaling Global Impact through Strategic Partnerships

The 100,000-test milestone represents broader industry shifts toward rapid host-response diagnostics and underscores MeMed’s global growth strategy. The company remains focused on scaling through partnerships with decentralized and hospital-based providers, integrating high-throughput analyzers to serve acute care settings, and collaborating on distribution agreements across the U.S., Europe, and emerging markets.

“Crossing the 100,000-patient mark is more than a milestone—it’s a meaningful indicator of the clinical value we’re delivering,” said Eran Eden, Ph.D., Co-Founder and CEO of MeMed. “It reflects the trust of a growing network of forward-thinking healthcare partners like Physicians Premier, as we jointly transform the landscape of infectious disease management. With only a fraction of the potential market reached—and backed by strong clinical evidence and strategic partnerships—we anticipate accelerating momentum, bringing critical answers to clinicians and patients when they matter most.”

MeMed continues to engage healthcare providers and industry leaders to advance adoption of rapid, reliable diagnostics that improve patient care.

About MeMed

At MeMed, our mission is to translate the immune system’s complex signals into simple insights that transform the way diseases are diagnosed and treated, profoundly benefiting patients and society.

MeMed BV® is the first FDA-cleared host-immune response test for accurately distinguishing between bacterial and viral infections in 15 minutes.

MeMed Severity™ has received FDA Breakthrough Device Designation as a host-response test designed to aid early risk assessment in ED patients with suspected infection or sepsis. It predicts severe outcomes within 72 hours and mortality within 14 days. MeMed Severity is not yet cleared for sale in any territory.

Follow and connect with MeMed via LinkedIn, Twitter/X, and Facebook.

Contacts

MeMed Contact:
Tal Avziz

Vice President, Global Marketing

pr@me-med.com

Media Relations Contact:
Charya Wickremasinghe, Ph.D.

Brandwidth Solutions LLC

cwickremasinghe@brandwidthsolutions.com

Wedgewood Pharmacy Adds GS-441524 to Its FIP Treatment Portfolio

Wedgewood Pharmacy Adds GS-441524 to Its FIP Treatment Portfolio




Wedgewood Pharmacy Adds GS-441524 to Its FIP Treatment Portfolio

SWEDESBORO, N.J.–(BUSINESS WIRE)–#AnimalHealth–Wedgewood Pharmacy today announced the availability of a GS-441524 formula, a compounded oral antiviral formulation now part of its feline infectious peritonitis (FIP) treatment capabilities. With this addition, veterinarians can now prescribe both GS-441524 and Molnupiravir for their patients, two of the most requested compounded antivirals for FIP, through a single trusted source backed by pharmacist support and FDA-registered ingredient sourcing.


GS-441524 can be compounded as a 50mg/ml flavored oral oil suspension in multiple sizes, to improve compliance and ease of administration. The addition complements Wedgewood’s Molnupiravir formulations, giving veterinarians access to two antivirals with distinct mechanisms of action.

“FIP is one of the toughest diagnoses we face, not just clinically, but emotionally too,” said Dr. Rae Hutchins, Chief Veterinary Officer at Wedgewood. “For a long time, vets had to deal with inconsistent access and quality when it came to GS-441524. Now, by offering both GS-441524 and Molnupiravir from one trusted, pharmacist-supported source, we’re making it easier for veterinarians to focus on what matters most, giving their patients the best possible chance.”

“Having access to both GS-441524 and Molnupiravir compounded formulations through Wedgewood not only widens access to affordable FIP treatment across the US, but it also gives veterinarians the ability to easily choose and adapt treatment to best suit the needs of their patients and clients,” said Nicole Jacque, co-founder of FIP Global Cats. “Having pharmacists who understand the urgency and complexity of these cases partnering with veterinarians is key to ensuring the best treatment outcomes for cats with FIP.”

Until recently, many veterinarians relied on fragmented or unregulated sources for GS-441524, making it difficult to ensure consistency and continuity of care. The introduction of this option through Wedgewood reflects a direct response to those challenges, providing prescribers with a trusted, quality-assured formulation from a pharmacy they can count on.

The launch of GS-441524 builds on Wedgewood’s long-standing role in supporting veterinarians with customized treatment solutions for complex cases. As part of its commitment to responsible compounding, the pharmacy emphasizes that its GS-441524 formulation is not approved by the FDA, has not been studied in clinical trials, and Wedgewood makes no claims of efficacy or safety. Independent third-party studies related to GS-441524 are available for veterinary reference through Wedgewood’s FIP Resource Center.

To learn more about GS-441524 and access educational resources, visit www.Wedgewood.com/FIP.

About Wedgewood

Wedgewood is the nation’s largest and most trusted provider of compounded veterinary medications. Its next-generation home delivery platform, Blue Rabbit, streamlines patient care and marks a significant evolution in online pharmacy services. Together, Blue Rabbit and Wedgewood serve more than 70,000 veterinary professionals and more than one million animals annually. For more information visit www.Wedgewood.com.

About FIP Global Cats

FIP Global CATS® (Community, Advocacy, Treatment, Support) is a leading organization in the fight against feline infectious peritonitis (FIP). Uniting veterinarians, researchers, and pet owners, it provides crucial support to those facing an FIP diagnosis. The organization is committed to empowering pet parents, advocating for safe, effective and affordable legal treatments, and advancing FIP research. For more information, please visit https://www.fipglobalcats.com/.

Contacts

Jennifer Ravalli

jennifer.ravalli@wedgewood.com

Competitive Landscape in Healthcare Super Centers: Analysis of Key Players Leading Market Transformation, including CVS Health, Walmart Health, Emitac Healthcare Solutions and Mediclinic Middle East – ResearchAndMarkets.com

Competitive Landscape in Healthcare Super Centers: Analysis of Key Players Leading Market Transformation, including CVS Health, Walmart Health, Emitac Healthcare Solutions and Mediclinic Middle East – ResearchAndMarkets.com




Competitive Landscape in Healthcare Super Centers: Analysis of Key Players Leading Market Transformation, including CVS Health, Walmart Health, Emitac Healthcare Solutions and Mediclinic Middle East – ResearchAndMarkets.com

DUBLIN–(BUSINESS WIRE)–The “Healthcare Super Centers Market – Global Industry Size, Share, Trends, Opportunity, and Forecast, 2020-2030F” has been added to ResearchAndMarkets.com’s offering.


The Healthcare Super Centers Market was valued at USD 2.75 Billion in 2024, and is expected to reach USD 4.81 Billion by 2030, rising at a CAGR of 9.74%.

Healthcare Super Centers – also known as medical malls – are comprehensive health hubs designed to provide a wide array of medical services under one roof. These advanced facilities centralize access to general practitioners, specialists, diagnostic labs, pharmacies, and other health-related services, enabling patients to receive coordinated care in a single visit. By integrating services into one location, these centers streamline the patient journey, reduce wait times, and improve overall care efficiency.

The use of shared electronic health records (EHRs) ensures seamless information exchange among providers, enhancing treatment accuracy and patient outcomes. As patient expectations evolve toward convenience, transparency, and holistic care, Healthcare Super Centers are emerging as a pivotal model in transforming how medical services are delivered globally.

Key Market Drivers: Rising Demand of Comprehensive Care

The increasing preference for all-in-one healthcare solutions is driving the demand for Healthcare Super Centers. These facilities offer patients the convenience of accessing various services – including primary care, diagnostics, pharmacy, imaging, and specialty consultations – in a single location. This centralized approach eliminates the need for multiple appointments across different providers, saving time and simplifying the healthcare process.

By integrating services, super centers expedite diagnoses and treatment, particularly for urgent or chronic conditions, while fostering better communication among healthcare teams. They also promote preventive health through wellness programs, screenings, and lifestyle counseling. As the focus shifts toward patient-centric models and proactive health management, the appeal of super centers continues to grow. The combination of efficiency, comprehensiveness, and convenience positions them as a key solution for modern healthcare delivery.

Key Market Challenges: Regulatory and Licensing Hurdles

Launching and operating a Healthcare Super Center involves navigating a complex landscape of regulatory and licensure requirements, which differ significantly across regions. These centers often need multiple licenses covering diverse services, such as diagnostics, emergency care, and specialty consultations. The credentialing of healthcare providers within the facility adds further administrative complexity, requiring verification of qualifications, experience, and certifications.

In addition to meeting healthcare-specific laws, operators must comply with data privacy regulations, building codes, and safety standards. This multi-layered regulatory framework demands significant time, resources, and legal oversight. For new entrants, particularly those expanding into new jurisdictions, these compliance challenges can delay project timelines and inflate startup costs. Ensuring legal and operational alignment with local healthcare authorities is critical to maintaining high standards of care and patient safety.

Key Market Trends: Telehealth Integration

A prominent trend in the Healthcare Super Centers Market is the integration of telehealth services, enabling flexible and accessible care delivery. Telehealth bridges geographic gaps and enhances patient convenience, especially for those in remote or underserved areas. Through virtual consultations, patients can address minor illnesses, refill prescriptions, or manage chronic conditions without traveling to a facility. This hybrid care model – combining in-person and remote interactions – ensures consistent follow-up and care continuity.

Remote patient monitoring solutions also allow providers to track health metrics and intervene when necessary, improving outcomes for those recovering post-surgery or living with chronic diseases. As digital health tools gain traction, telehealth services are becoming a core offering in super centers, aligning with modern expectations for accessible, tech-enabled healthcare.

Key Market Players:

  • CVS Health Corporation
  • Walmart Health Centers
  • Taskar Group
  • Al Falah Healthcare Center
  • Emitac Healthcare Solutions
  • Mediclinic Middle East
  • Jackson Medical Mall Foundation

Key Attributes:

Report Attribute Details
No. of Pages 182
Forecast Period 2024 – 2030
Estimated Market Value (USD) in 2024 $2.75 Billion
Forecasted Market Value (USD) by 2030 $4.81 Billion
Compound Annual Growth Rate 9.7%
Regions Covered Global

Report Scope:

In this report, the Global Healthcare Super Centers Market has been segmented into the following categories, in addition to the industry trends which have also been detailed below:

Healthcare Super Centers Market, By Services:

  • Primary Medical Services
  • Dental Care
  • Diagnostic Services
  • Behavioural Health Services
  • Pharmacy Services
  • Telemedicine
  • Others

Healthcare Super Centers Market, By Product:

  • Medicines
  • Dietary-Nutrition & Supplements
  • Health & Wellness
  • Nursing Supplies
  • Health Gadgets
  • Rehabilitation Products & Aids
  • Baby Products
  • Others

Healthcare Super Centers Market, By Region:

  • North America

    • United States
    • Canada
    • Mexico
  • Europe

    • France
    • United Kingdom
    • Italy
    • Germany
    • Spain
  • Asia-Pacific

    • China
    • India
    • Japan
    • Australia
    • South Korea
  • South America

    • Brazil
    • Argentina
    • Colombia
  • Middle East & Africa

    • South Africa
    • Saudi Arabia
    • UAE

For more information about this report visit https://www.researchandmarkets.com/r/xwtom6

About ResearchAndMarkets.com

ResearchAndMarkets.com is the world’s leading source for international market research reports and market data. We provide you with the latest data on international and regional markets, key industries, the top companies, new products and the latest trends.

Contacts

ResearchAndMarkets.com

Laura Wood, Senior Press Manager

press@researchandmarkets.com

For E.S.T Office Hours Call 1-917-300-0470

For U.S./ CAN Toll Free Call 1-800-526-8630

For GMT Office Hours Call +353-1-416-8900

Oncolytic Virus Immunotherapy Strategic Research Business Report 2025-2030: Surge in Clinical Trials Combining Oncolytic Viruses With Checkpoint Inhibitors Expands Therapeutic Horizons – ResearchAndMarkets.com

Oncolytic Virus Immunotherapy Strategic Research Business Report 2025-2030: Surge in Clinical Trials Combining Oncolytic Viruses With Checkpoint Inhibitors Expands Therapeutic Horizons – ResearchAndMarkets.com




Oncolytic Virus Immunotherapy Strategic Research Business Report 2025-2030: Surge in Clinical Trials Combining Oncolytic Viruses With Checkpoint Inhibitors Expands Therapeutic Horizons – ResearchAndMarkets.com

DUBLIN–(BUSINESS WIRE)–The “Oncolytic Virus Immunotherapy – Global Strategic Business Report” has been added to ResearchAndMarkets.com’s offering.


The global market for Oncolytic Virus Immunotherapy was valued at US$156.8 Million in 2024 and is projected to reach US$429.1 Million by 2030, growing at a CAGR of 18.3% from 2024 to 2030. This comprehensive report provides an in-depth analysis of market trends, drivers, and forecasts, helping you make informed business decisions. The report includes the most recent global tariff developments and how they impact the Oncolytic Virus Immunotherapy market.

Oncolytic virus immunotherapy is gaining renewed momentum in oncology as a dual-action therapeutic strategy that combines direct tumor lysis with immune system priming. These genetically engineered or naturally occurring viruses selectively infect and replicate in tumor cells, causing their destruction while releasing tumor-associated antigens that stimulate anti-cancer immune responses. Unlike traditional chemotherapy or radiation, oncolytic viruses act locally at the tumor site and systemically through immune activation, positioning them as versatile agents in both solid and hematologic malignancies.

What Is Powering Long-Term Growth and Scientific Innovation in the Oncolytic Virus Immunotherapy Market?

The growth in the oncolytic virus immunotherapy market is powered by a paradigm shift toward immune-driven cancer control, rising incidence of refractory tumors, and growing regulatory openness to gene-modified biologicals. Oncolytic viruses offer a platform approach with customizable payloads and delivery options, making them highly adaptable to evolving immuno-oncology landscapes. Their ability to initiate cold-to-hot tumor conversion addresses one of the biggest challenges in cancer immunotherapy today.

Pharmaceutical companies are accelerating R&D through collaborations with academic virologists, biotech firms, and clinical oncology networks. AI-driven viral vector design, CRISPR-enabled transgene integration, and intratumoral microdosing techniques are improving specificity and safety profiles. Investment in scalable manufacturing, lyophilized formulations, and cold-chain logistics is supporting broader market readiness. As personalized cancer vaccines and immune cell therapies gain traction, oncolytic viruses are poised to serve as immune amplifiers that bridge innate and adaptive response layers. The future of cancer immunotherapy will be increasingly shaped by these programmable, self-amplifying, and immune-sensitizing viral agents.

How Are Genetic Engineering and Combination Protocols Expanding the Potential of Oncolytic Virotherapy?

Recent breakthroughs in synthetic biology and vector engineering are significantly enhancing the safety, selectivity, and immune-stimulatory capabilities of oncolytic viruses. New viral constructs – based on herpes simplex virus (HSV), adenovirus, vaccinia virus, and reovirus – are being armed with immune-boosting transgenes such as GM-CSF, interleukins, or checkpoint blockade peptides. These modifications allow the virus to not only destroy tumor cells but also convert the tumor microenvironment (TME) into an immunologically active site.

Combination therapies are a major focus, with oncolytic viruses increasingly paired with immune checkpoint inhibitors (e.g., anti-PD-1/PD-L1), CAR-T therapies, or radiotherapy to overcome resistance mechanisms and enhance systemic anti-tumor responses. Intratumoral delivery methods, dose escalation protocols, and multi-site administration strategies are improving virus biodistribution and reducing off-target effects. Liquid biopsy and imaging biomarkers are being developed to monitor viral persistence, immune infiltration, and treatment response in real time. These advancements are transitioning oncolytic virotherapy from a niche modality into an integral component of multi-modal cancer treatment frameworks.

Which Tumor Types and Geographies Are Shaping the Clinical and Commercial Landscape for Oncolytic Viruses?

Solid tumors with immunosuppressive microenvironments – such as melanoma, glioblastoma, pancreatic cancer, and hepatocellular carcinoma – are prime candidates for oncolytic virotherapy. These cancers typically respond poorly to conventional therapies and often lack T-cell infiltration, which oncolytic viruses can help overcome. Hematologic malignancies like lymphoma and multiple myeloma are also being targeted through engineered viruses capable of engaging both innate and adaptive immunity.

North America leads clinical development, with the U.S. hosting the majority of early-phase and pivotal trials. The presence of major virotherapy developers, robust funding ecosystems, and an innovation-friendly regulatory environment accelerates translational progress. Europe follows with strong academic-industry partnerships and regulatory support through the EMA’s Advanced Therapy Medicinal Product (ATMP) designation. Asia-Pacific is emerging as a competitive landscape, particularly in China, where biotech firms are investing heavily in oncolytic platforms and regulatory reforms are enabling faster trial initiation. Global oncology centers are increasingly integrating oncolytic viruses into compassionate use programs and combination trial protocols.

Report Scope

Report Features:

  • Comprehensive Market Data: Independent analysis of annual sales and market forecasts in US$ Million from 2024 to 2030.
  • In-Depth Regional Analysis: Detailed insights into key markets, including the U.S., China, Japan, Canada, Europe, Asia-Pacific, Latin America, Middle East, and Africa.
  • Company Profiles: Coverage of players such as Amgen Inc., CG Oncology, Creative Biolabs, Daiichi Sankyo Co., Ltd., Genelux Corporation and more.
  • Complimentary Updates: Receive free report updates for one year to keep you informed of the latest market developments.

Key Insights:

  • Market Growth: Understand the significant growth trajectory of the Herpes Simplex Virus segment, which is expected to reach US$189.7 Million by 2030 with a CAGR of a 18.6%. The Vaccinia Virus segment is also set to grow at 15.3% CAGR over the analysis period.
  • Regional Analysis: Gain insights into the U.S. market, valued at $42.7 Million in 2024, and China, forecasted to grow at an impressive 24.8% CAGR to reach $99.7 Million by 2030. Discover growth trends in other key regions, including Japan, Canada, Germany, and the Asia-Pacific.

Segments

  • Type (Herpes Simplex Virus, Vaccinia Virus, Adenovirus, Reovirus, Other Types)
  • Administration Route (Intratumoral Route, Intravenous Route)
  • Application (Melanoma Application, Non-small Cell Lung Cancer Application, Pancreatic Cancer Application, Breast Cancer Application, Other Applications)

Tariff Impact Analysis: Key Insights for 2025

What’s Included in This Edition:

  • Tariff-adjusted market forecasts by region and segment
  • Analysis of cost and supply chain implications by sourcing and trade exposure
  • Strategic insights into geographic shifts

Buyers receive a free July 2025 update with:

  • Finalized tariff impacts and new trade agreement effects
  • Updated projections reflecting global sourcing and cost shifts
  • Expanded country-specific coverage across the industry

Key Attributes:

Report Attribute Details
No. of Pages 383
Forecast Period 2024 – 2030
Estimated Market Value (USD) in 2024 $156.8 Million
Forecasted Market Value (USD) by 2030 $429.1 Million
Compound Annual Growth Rate 18.3%
Regions Covered Global 

Key Topics Covered:

MARKET OVERVIEW

  • Influencer Market Insights
  • World Market Trajectories
  • Impact of COVID-19 and a Looming Global Recession
  • Oncolytic Virus Immunotherapy – Global Key Competitors Percentage Market Share in 2025 (E)
  • Competitive Market Presence – Strong/Active/Niche/Trivial for Players Worldwide in 2025 (E)

MARKET TRENDS & DRIVERS

  • Rising Focus on Precision Oncology Spurs Development of Oncolytic Virus Platforms With Tumor Selectivity
  • Expansion of Immunotherapy Research Pipelines Strengthens Business Case for Oncolytic Virus Modalities
  • Increased Approval of Cancer Immunotherapies Throws the Spotlight on Next-Generation Viral Vectors
  • Breakthrough Designation Status and Fast Track Approvals Accelerate Regulatory Momentum
  • Advancements in Genetic Engineering of Viruses Drive Enhanced Tumor Targeting and Immune Activation
  • Surge in Clinical Trials Combining Oncolytic Viruses With Checkpoint Inhibitors Expands Therapeutic Horizons
  • Increased Use of Oncolytic Viruses as Neoadjuvant Therapies Supports Multimodal Cancer Management
  • Growing Investment From Biopharma and Venture Capital Enhances Innovation and Clinical Translation
  • Development of Tumor-Specific Viral Payloads Strengthens Oncolytic Virus Selectivity and Safety Profiles
  • Adoption of Intratumoral and Systemic Delivery Routes Expands Accessibility to Diverse Tumor Types
  • Improved Understanding of Tumor Microenvironment Enhances Viral Mechanism Optimization
  • Collaborative Efforts Between Academia and Industry Propel Translational Research in Viral Oncology
  • Expansion of Cold Chain Logistics Infrastructure Supports Global Supply of Virus-Based Therapies
  • Public and Philanthropic Funding for Rare Cancer Treatment Drives Orphan Application Development
  • Manufacturing Scale-Up of Viral Vectors Remains a Bottleneck for Commercialization Readiness
  • Development of Immune Response Biomarkers Facilitates Patient Selection and Treatment Monitoring
  • Increased Advocacy for Personalized Cancer Immunotherapy Supports Patient Enrollment in Viral Trials
  • Challenges in Viral Shedding and Immunogenicity Highlight Need for Improved Safety Profiling
  • Rising Global Cancer Incidence and Limited Success in Refractory Cancers Propel Need for Disruptive Modalities
  • Regulatory Alignment on Gene and Virus Therapies Enhances Global Clinical Trial Harmonization

FOCUS ON SELECT PLAYERS: Some of the 41 companies featured in this report

  • Amgen Inc.
  • CG Oncology
  • Creative Biolabs
  • Daiichi Sankyo Co., Ltd.
  • Genelux Corporation
  • ImmVirX
  • Imugene Limited
  • Lokon Pharma AB
  • Merck & Co., Inc.
  • Oncolys BioPharma Inc.
  • Oncolytics Biotech Inc.
  • Oncorus Inc.
  • Replimune Group Inc.
  • SillaJen, Inc.
  • Sorrento Therapeutics, Inc.
  • Syneos Health, Inc.
  • TILT Biotherapeutics Ltd.
  • Transgene S.A.
  • Viralytics Ltd.
  • ViraTherapeutics GmbH

For more information about this report visit https://www.researchandmarkets.com/r/uq4wts

About ResearchAndMarkets.com

ResearchAndMarkets.com is the world’s leading source for international market research reports and market data. We provide you with the latest data on international and regional markets, key industries, the top companies, new products and the latest trends.

Contacts

ResearchAndMarkets.com

Laura Wood, Senior Press Manager

press@researchandmarkets.com

For E.S.T Office Hours Call 1-917-300-0470

For U.S./ CAN Toll Free Call 1-800-526-8630

For GMT Office Hours Call +353-1-416-8900