News

Octapharma USA has received approval from the U.S. Food and Drug Administration for a new 2-gram presentation of Fibryga®, a human plasma-derived fibrinogen concentrate, expanding…
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GSK plc has reported positive results from two pivotal phase III clinical trials evaluating bepirovirsen, an investigational antisense oligonucleotide therapy for chronic hepatitis B…
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Takeda Pharmaceutical Company has entered into a global collaboration and license agreement with Halozyme Therapeutics to use Halozyme’s proprietary ENHANZE® drug delivery technology…
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Eli Lilly and Company has agreed to acquire Ventyx Biosciences in an all-cash transaction valued at approximately $1.2 billion, strengthening Lilly’s pipeline in inflammation-driven…
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Day One Biopharmaceuticals has completed its acquisition of Mersana Therapeutics, marking a significant expansion of its oncology pipeline and reinforcing its strategy to advance…
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Protara Therapeutics, Inc., a clinical-stage biotechnology company focused on cancer and rare diseases, has received multiple regulatory boosts from the U.S. Food and Drug…
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China’s drug regulator has expanded treatment options for patients with rare, genetically driven cancers by approving Zai Lab Limited’s AUGTYRO™ (repotrectinib) for adult patients with…
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Outlook Therapeutics has received a setback in its efforts to bring an FDA-approved bevacizumab treatment for retinal disease to the U.S. market. The company announced that the U.S.…
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Samsung Bioepis has started direct commercialization of BYOOVIZ, a biosimilar to Lucentis (ranibizumab), across Europe, marking a significant shift in the company’s regional strategy.…
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Eisai and Biogen have reached a new regulatory milestone in China with the acceptance of a Biologics License Application (BLA) for the subcutaneous formulation of LEQEMBI (lecanemab) by…
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Insilico Medicine, a global artificial intelligence (AI)–driven drug discovery company, has entered into a multi-year research and development collaboration with Servier, an independent…
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The US Food and Drug Administration (FDA) has accepted for priority review a supplemental biologic license application (sBLA) for Tzield (teplizumab-mzwv), a therapy designed to delay…
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Takeda and Protagonist Therapeutics have submitted a New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) seeking approval of rusfertide for the treatment of adults…
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Arrowhead Pharmaceuticals has received regulatory clearance from Health Canada for REDEMPLO (plozasiran), marking a significant advance for patients living with familial chylomicronemia…
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Harbour BioMed has entered into a multi-year, global strategic collaboration and license agreement with Bristol Myers Squibb aimed at advancing the discovery and development of…
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GSK has received U.S. Food and Drug Administration approval for Exdensur (depemokimab-ulaa), a new add-on maintenance treatment for patients aged 12 years and older with severe asthma…
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Alnylam Pharmaceuticals has announced plans to significantly expand its manufacturing footprint in Norton, Massachusetts, committing an investment of $250 million to build what it says…
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Astellas Pharma and Pfizer have reported positive topline results from an interim analysis of the Phase 3 EV-304 clinical trial, strengthening evidence that the combination of PADCEV™…
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Takeda Pharmaceutical Company has announced positive topline results from two pivotal Phase 3 clinical trials evaluating zasocitinib (TAK-279), a next-generation oral therapy for adults…
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Johnson & Johnson has secured U.S. Food and Drug Administration approval for RYBREVANT FASPRO™, marking a significant advance in the treatment of epidermal growth factor receptor…
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