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Catalent Announces Collaboration with Galapagos to Further Expand Galapagos’ Decentralized CAR-T…

Jan 22, 2025
Catalent, Inc., a leader in enabling the development and supply of better treatments for patients worldwide, announced a strategic collaboration with Galapagos NV (Euronext &…
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Axcynsis Receives FDA Clearance for IND of AT03-65, CLDN6-Targeting ADC

Jan 16, 2025
Axcynsis Therapeutics Pte Ltd ("Axcynsis"), a privately held biopharmaceutical company specialized in delivering Antibody Drug Conjugates (ADCs) with breakthrough potential, proudly…
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FDA Approves Lilly’s Omvoh for Crohn’s Disease, Expanding IBD Treatment Options

Jan 16, 2025
Eli Lilly and Company announced that the U.S. Food and Drug Administration (FDA) has approved Omvoh (mirikizumab-mrkz) for the treatment of moderately to severely active Crohn's disease…
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AbbVie and Simcere Zaiming Partner to Develop Trispecific Antibody for Multiple Myeloma

Jan 16, 2025
AbbVie and Simcere Zaiming, a subsidiary of Simcere Pharmaceutical Group Ltd announced an option to license agreement to develop SIM0500, an investigational new drug candidate. SIM0500…
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Be Bio Announces Closing of $92M Series C Financing and Completes Transition to a Multi-Program,…

Jan 16, 2025
Be Biopharma, Inc. announced the closing of its $92M Series C financing. The round includes participation from new investor Nextech with existing investors including ARCH Venture…
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REGENXBIO and Nippon Shinyaku Form Exclusive Partnership to Develop RGX-121 and RGX-111 for MPS…

Jan 16, 2025
REGENXBIO Inc. and Nippon Shinyaku Co., Ltd. (Nippon Shinyaku) announced a strategic partnership for the development and commercialization of RGX-121 for the treatment of…
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Acadia Pharmaceuticals Submits EMA Application for Trofinetide in Rett Syndrome

Jan 16, 2025
Acadia Pharmaceuticals Inc. announced that the company has submitted a Marketing Authorization Application (MAA) to the European Medicines Agency (EMA) for trofinetide for the treatment…
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FDA Accepts LEQEMBI BLA for Subcutaneous Dosing in Early Alzheimer’s Treatment

Jan 15, 2025
Eisai Co., Ltd. and Biogen Inc. announced that the U.S. Food and Drug Administration (FDA) has accepted Eisai’s Biologics License Application (BLA) for lecanemab-irmb (U.S. brand name:…
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Daiichi Sankyo Acquires IP Rights for Anti-TA-MUC1 Antibody DS-3939 from Glycotope

Jan 15, 2025
Daiichi Sankyo Company, Ltd announced that it will pay Glycotope $132.5 million to acquire intellectual property rights of the anti-tumor-associated mucin-1 (TA-MUC1) antibody,…
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Umoja Biopharma Secures $100M in Oversubscribed Series C to Advance CAR T Pipeline

Jan 15, 2025
Umoja Biopharma, Inc. (Umoja), the clinical-stage leader of in vivo cell therapies that aim to realize the full reach and promise of CAR T cells, announced the closing of a $100 million…
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