Category Press Releases

Nominations Begin for the Second Annual Thomas J. Fogarty Prize Celebrating Transformative Medtech Innovations

Submissions Open for the Second Annual Thomas J. Fogarty Prize Recognizing Breakthrough Medtech Innovations Nominations are set to open on April 2, 2026, for the second annual Thomas J. Fogarty Innovation Prize, widely regarded as one of the most prestigious…

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Bayer Unveils U.S. Leadership Transition in Pharmaceuticals’ Worldwide Markets Division to Drive Future Growth

Bayer Implements U.S. Leadership Restructuring in Pharmaceuticals’ Worldwide Markets to Accelerate Growth Potential Bayer has announced a significant leadership transition within its Pharmaceuticals division, signaling a strategic move to accelerate growth and strengthen its position in the United States—one of…

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Tanner Pharma Group and Biodexa Introduce Global Early Access Initiative for Patients with FAP

Tanner Pharma Group and Biodexa Introduce Global Early Access Initiative for Patients with Familial Adenomatous Polyposis (FAP) Tanner Pharma Group, a globally recognized provider of specialty medicine access solutions, has entered into a strategic partnership with Biodexa Pharmaceuticals PLC, a…

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Merck

Merck’s Enlicitide Decanoate Shows Superior LDL-C Reduction at Eight Weeks vs. Oral Non-Statins

Merck Presents Phase 3 CORALreef AddOn Data for Enlicitide, Highlighting Strong LDL-C Reductions and Potential as First Oral PCSK9 Inhibitor Merck has unveiled compelling late-breaking results from its Phase 3 CORALreef AddOn study, demonstrating the potential of enlicitide decanoate, an…

Read MoreMerck’s Enlicitide Decanoate Shows Superior LDL-C Reduction at Eight Weeks vs. Oral Non-Statins

ACC.26 Data Highlight Benefits of Vutrisiran in ATTR-CM and Underscore Zilebesiran’s Potential in Hypertension Management

Alnylam Highlights New Cardiovascular Data at ACC.26, Reinforcing Potential of RNAi Therapies in ATTR-CM and Hypertension Alnylam Pharmaceuticals has unveiled a comprehensive set of new clinical and real-world findings from its cardiovascular portfolio at the American College of Cardiology Annual…

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Bristol Myers Squibb Reports Positive Phase 3 SCOUT-HCM Results for Camzyos in Adolescents with Symptomatic oHCM

Bristol Myers Squibb Reports Positive Phase 3 SCOUT-HCM Results for Camzyos in Adolescents with Symptomatic oHCM Bristol Myers Squibb has announced compelling results from its pivotal Phase 3 SCOUT-HCM clinical trial, highlighting the potential of Camzyos (mavacamten) as a transformative…

Read MoreBristol Myers Squibb Reports Positive Phase 3 SCOUT-HCM Results for Camzyos in Adolescents with Symptomatic oHCM

Bepirovirsen Gains European Medicines Agency Review as a Potential First-in-Class Therapy for Chronic Hepatitis B

Bepirovirsen advances to regulatory review by the European Medicines Agency as a promising first-in-class therapy for chronic hepatitis B GSK plc has announced a significant regulatory milestone as the European Medicines Agency (EMA) has formally accepted for review its marketing…

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Sensus Healthcare Files Breach of Contract Lawsuit Against SkinCure Oncology

Sensus Healthcare Files Breach of Contract Lawsuit Against SkinCure Oncology Sensus Healthcare, Inc., a developer of non-invasive and minimally invasive technologies for the treatment of both oncological and non-oncological skin conditions, has announced that it has initiated legal proceedings against…

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Ono Pharma Files Approval Application in Japan for Ripretinib in Advanced Gastrointestinal Stromal Tumor

Ono Pharma Files for Approval of Ripretinib (DCC-2618) to Treat Advanced Gastrointestinal Stromal Tumors in Japan Ono Pharmaceutical Co., Ltd. has announced the submission of a regulatory application in Japan seeking manufacturing and marketing approval for ripretinib (DCC-2618), an investigational…

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Novo Nordisk Secures U.S. Approval for Awiqli, the First Once-Weekly Basal Insulin for Adults with Type 2 Diabetes

Novo Nordisk Secures U.S. Approval for Awiqli, the First Once-Weekly Basal Insulin for Adults with Type 2 Diabetes Novo Nordisk today announced that the US Food and Drug Administration (FDA) has approved Awiqli® (insulin icodec-abae) injection 700 units/mL, the first and…

Read MoreNovo Nordisk Secures U.S. Approval for Awiqli, the First Once-Weekly Basal Insulin for Adults with Type 2 Diabetes