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Sanofi to acquire Inhibrx, Inc., adding potential best-in-class rare disease asset for Alpha-1…

Jan 23, 2024
Sanofi and Inhibrx, Inc. (“Inhibrx”), a publicly traded clinical-stage biopharmaceutical company focused on developing a broad pipeline of novel biologic therapeutic candidates, have…
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Sandoz announces agreement to acquire CIMERLI business from Coherus, strengthening position in US…

Jan 22, 2024
Sandoz, the global leader in generic and biosimilar medicines, has signed an agreement to acquire the US biosimilar ranibizumab CIMERLI (ranibizumab-eqrn) from Coherus BioSciences, Inc.…
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FDA Grants Full Approval for BALVERSA to Treat Locally Advanced or Metastatic Bladder Cancer with…

Jan 22, 2024
Johnson & Johnson announced today that the U.S. Food and Drug Administration (FDA) approved a supplemental New Drug Application (sNDA) for BALVERSA (erdafitinib) for the treatment…
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Kyverna Therapeutics Granted FDA Fast Track Designation for KYV-101 in the Treatment of Patients…

Jan 22, 2024
Kyverna Therapeutics, Inc. (Kyverna), a patient-centered clinical-stage biopharmaceutical company focused on developing cell therapies for patients suffering from autoimmune diseases,…
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Verastem Oncology Granted Fast Track Designation for Combination of Avutometinib and Sotorasib for…

Jan 19, 2024
Verastem Oncology, a biopharmaceutical company committed to advancing new medicines for patients with cancer, announced the U.S. Food and Drug Administration (FDA) has granted Fast…
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bridgebio pharma secures up to $1.25 billion of capital from blue owl and cpp investments to…

Jan 19, 2024
BridgeBio Pharma, Inc. (BridgeBio or the Company), a commercial-stage biopharmaceutical company focused on genetic diseases and cancers, announced strategic financing from Blue Owl…
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Halozyme Announces argenx Received Approval in Japan for VYVDURA (efgartigimod alfa and…

Jan 18, 2024
Halozyme Therapeutics, Inc. announced that argenx received approval from Japan's Ministry of Health, Labour and Welfare (MHLW) for VYVDURA (efgartigimod alfa and hyaluronidase-qvfc)…
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European Commission approves Roche’s Tecentriq SC, the EU’s first PD-(L)1 cancer immunotherapy…

Jan 17, 2024
Roche announced that the European Commission has granted marketing authorisation for Tecentriq SC (atezolizumab), the European Union (EU)’s first PD-(L)1 cancer immunotherapy for…
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FDA Approves Takeda’s HYQVIA as Maintenance Therapy in Adults with Chronic Inflammatory…

Jan 17, 2024
Takeda announced that the U.S. Food and Drug Administration (FDA) has approved HYQVIA  for the treatment of chronic inflammatory demyelinating polyneuropathy (CIDP) as maintenance…
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Vertex Announces FDA Approval of CASGEVY (exagamglogene autotemcel) for the Treatment of…

Jan 17, 2024
Vertex Pharmaceuticals Incorporated announced that the U.S. Food and Drug Administration (FDA) has approved CASGEVY (exagamglogene autotemcel ), a CRISPR/Cas9 gene-edited cell therapy,…
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Industry Reports

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Press Releases

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