Category News

DiaMedica Therapeutics Announces Full-Year 2025 Financial Results and Key Business Highlights

DiaMedica Therapeutics Reports 2025 Financial Results and Advances Clinical Pipeline in Preeclampsia and Acute Ischemic Stroke DiaMedica Therapeutics Inc., a clinical-stage biopharmaceutical company dedicated to developing innovative therapies for serious and life-threatening conditions, has reported its financial results for the…

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Phase 2 CADENCE Trial Confirms Proof-of-Concept for WINREVAIR™ in CpcPH-HFpEF Patients

Phase 2 CADENCE Trial Shows Positive Results, Establishing WINREVAIR™ as a Proof-of-Concept Therapy in CpcPH and HFpEF Merck & Co.—known as MSD outside the United States and Canada—has unveiled comprehensive results from its Phase 2 CADENCE clinical trial, providing compelling…

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Lantern Pharma Reaffirms Panna Sharma as President and CEO, Addresses Misleading Third-Party Report

Lantern Pharma Reaffirms Panna Sharma’s Ongoing Role as President and CEO; Warns Investors of Misleading Third-Party Report Lantern Pharma Inc., an AI-driven oncology company focused on transforming cancer drug development through its proprietary RADR® platform, has issued a formal statement…

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Neurocrine Biosciences Unveils First Expert Consensus Guidelines for Tardive Dyskinesia in Long-Term Care Settings

Neurocrine Biosciences Unveils First Expert Consensus Guidelines for Managing Tardive Dyskinesia in Long-Term Care Settings Neurocrine Biosciences, Inc. today announced the presentation of the first expert consensus recommendations focused on screening, diagnosis and treatment of tardive dyskinesia among older adults in…

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Abcuro Reports Phase 2/3 MUSCLE Study Results of Ulviprubart in Inclusion Body Myositis at GCOM 2026

Abcuro Highlights Phase 2/3 MUSCLE Study Results of Ulviprubart in Inclusion Body Myositis at GCOM 2026 Abcuro, Inc. has announced new clinical data from its Phase 2/3 MUSCLE study evaluating ulviprubart (ABC008), an investigational monoclonal antibody therapy for inclusion body…

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Biocytogen Announces U.S. Food and Drug Administration IND Clearance for NEOK Bio’s NEOK002 Targeting Solid Tumors

Biocytogen Announces U.S. Food and Drug Administration IND Clearance for Partner NEOK Bio’s NEOK002 in Solid Tumor Indications Biocytogen Pharmaceuticals (Beijing) Co., Ltd. has announced a significant regulatory milestone achieved by its partner, NEOK Bio, Inc., highlighting continued progress in…

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Pet Partners and the Baxter Foundation Expand Therapy Animal Programs to Reach 100,000 Patients and Healthcare Workers in Two-Year Pilot

Pet Partners and Baxter Foundation Expand Therapy Animal Programs to Reach 100,000 Patients and Healthcare Workers in Two-Year Pilot Pet Partners and the Baxter Foundation, the charitable arm of Baxter International Inc., have announced a new partnership aimed at expanding…

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Ono Pharma Seeks Japanese Approval for Ripretinib (DCC-2618) in Advanced Gastrointestinal Stromal Tumor Patients

Ono Pharma Files Application in Japan for Ripretinib (DCC-2618) to Treat Advanced Gastrointestinal Stromal Tumors Ono Pharmaceutical, headquartered in Osaka, Japan, under the leadership of President Toichi Takino, has announced the submission of a regulatory application in Japan for the…

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