News

Regeneron Pharmaceuticals, Inc. announced that the U.S. Food and Drug Administration (FDA) has granted accelerated approval for Lynozyfic (linvoseltamab-gcpt) to treat adult patients…
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The Japanese Ministry of Health, Labour and Welfare (MHLW) has granted orphan drug designation to riliprubart, an investigational monoclonal antibody developed by Sanofi, for the…
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Sobi announced that the U.S. Food and Drug Administration (FDA) approved Gamifant (emapalumab-lzsg) for the treatment of adult and pediatric (newborn and older) patients with…
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Bristol Myers Squibb announced that the U.S. Food and Drug Administration (FDA) has approved label updates for both of its CAR T cell therapies, Breyanzi (lisocabtagene maraleucel;…
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Vetter, a leading, globally operating Contract Development and Manufacturing Organization (CDMO), celebrated the start of construction for its new clinical manufacturing site in Des…
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Piramal Pharma Solutions, a leading global Contract Development and Manufacturing Organization (CDMO) and part of Piramal Pharma Ltd., recently announced a $90M investment plan to…
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AbbVie and Capstan Therapeutics, Inc. announced a definitive agreement under which AbbVie will acquire Capstan, including CPTX2309, a potential first-in-class in vivo tLNP anti-CD19…
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Takeda announced that the U.S. Food and Drug Administration (FDA) has approved GAMMAGARD LIQUID ERC, the first and only ready-to-use liquid immunoglobulin (IG) therapy with low…
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ProFound Therapeutics, a company pioneering the expanded human proteome to develop first-in-class medicines for multiple diseases, today announced a four-year collaboration with…
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Novartis has officially completed its acquisition of Regulus Therapeutics Inc., solidifying its strategic focus on advancing treatments for renal diseases. With the closing of the deal,…
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Porton Advanced Solutions, a global leader in cell and gene therapy contract development and manufacturing (CDMO), has signed a Memorandum of Understanding (MOU) with EVA Pharma, a…
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Bayer and Tsinghua University (THU) announced that they have extended their research collaboration of 16 years by an additional three years, to further accelerate the translation of…
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GE HealthCare announced that the U.S. Food and Drug Administration (FDA) has approved an updated label for its PET imaging agent Vizamyl™ (flutemetamol F 18 injection), used for…
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GSK plc has announced that the U.S. Food and Drug Administration (FDA) has approved a 200 mg/mL autoinjector form of Benlysta (belimumab) for subcutaneous injection in pediatric…
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Gilead Sciences, Inc. and Kymera Therapeutics, Inc. have announced an exclusive option and license agreement aimed at advancing a novel class of cancer treatments: molecular glue…
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Eli Lilly and Company announced that the U.S. FDA has approved a label update for Amyvid (florbetapir F 18 injection) for intravenous use. Amyvid is used for brain imaging to estimate…
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Vor Bio, Inc. has entered into an exclusive global licensing agreement with Chinese biopharmaceutical company RemeGen Co., Ltd., gaining rights to develop and commercialize the…
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Medera Inc., a clinical-stage biopharmaceutical company focused on cardiovascular disease therapies, and its pre-clinical subsidiary Novoheart, specializing in human cardiac tissue…
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Novo Nordisk announced that the European Medicines Agency’s (EMA) Committee for Medicinal Products for Human Use (CHMP) has given a positive opinion to update the label of Ozempic…
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The U.S. Food and Drug Administration (FDA) has granted accelerated approval for Datroway (datopotamab deruxtecan or Dato-DXd) for the treatment of adult patients with locally advanced…
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