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FDA Reviews Weekly Subcutaneous Dosing Option for Eisai’s Alzheimer’s Drug

Jan 28, 2026
Eisai Co., Ltd. and Biogen Inc. have announced a key regulatory milestone for their Alzheimer’s disease therapy lecanemab-irmb, marketed in the United States as LEQEMBI®. The U.S. Food…
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WuXi Biologics and HanchorBio Partner on Next-Generation Fusion Therapies

Jan 27, 2026
WuXi Biologics and HanchorBio Inc. have announced a strategic collaboration aimed at accelerating the development and manufacturing of multiple next-generation bi- and multi-functional…
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Corxel Raises $287 Million to Advance Cardiometabolic Drug Pipeline

Jan 26, 2026
Corxel Pharmaceuticals Limited (CORXEL), a clinical-stage biopharmaceutical company focused on cardiometabolic diseases, has announced the successful completion of its Series D1…
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Janux and Bristol Myers Squibb Forge Global Oncology Collaboration

Jan 23, 2026
Janux Therapeutics, Inc., a clinical-stage biopharmaceutical company focused on next-generation immunotherapies, has entered into a collaboration and exclusive worldwide license…
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China Approves ENHERTU for Second-Line HER2-Positive Gastric Cancer

Jan 23, 2026
China’s National Medical Products Administration (NMPA) has approved ENHERTU® (trastuzumab deruxtecan) for the treatment of adult patients with locally advanced or metastatic…
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Insilico and Hygtia Partner to Advance AI-Discovered NLRP3 Inhibitor

Jan 22, 2026
Insilico Medicine and Hygtia Therapeutics have entered into an exclusive global license and co-development agreement to advance ISM8969, an investigational NLRP3 inhibitor designed for…
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Wugen’s Sofi-cel Secures FDA Breakthrough Status in T-ALL/LBL

Jan 22, 2026
Wugen has received a major regulatory endorsement from the U.S. Food and Drug Administration, which has granted Breakthrough Therapy Designation to its investigational CAR-T cell…
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Charles River and Gazi University Partner on Gene Therapy Development

Jan 22, 2026
Charles River Laboratories International and Gazi University Faculty of Medicine have entered into a strategic collaboration aimed at advancing gene therapy research for rare genetic…
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NEOK Bio Wins FDA IND Clearance for Bispecific ADC NEOK001

Jan 22, 2026
NEOK Bio has taken a key step toward clinical development after the U.S. Food and Drug Administration approved its Investigational New Drug application for NEOK001, clearing the way for…
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Opna Bio’s Zavabresib Wins FDA Orphan Status in Myelofibrosis

Jan 22, 2026
Opna Bio, a clinical-stage biopharmaceutical company focused on developing novel cancer therapies, has received a key regulatory boost for its myelofibrosis program. The U.S. Food and…
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