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Dupixent FDA approved as first and only treatment indicated for children aged 1 year and older with…

Jan 26, 2024
The U.S. Food and Drug Administration (FDA) has approved Dupixent (dupilumab) for the treatment of pediatric patients aged 1 to 11 years, weighing at least 15 kg, with eosinophilic…
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Repare Therapeutics Announces Achievement of $40 Million Roche Clinical Milestone Payment

Jan 25, 2024
Repare Therapeutics Inc. announced that, under its worldwide license and collaboration agreement with Roche for the development and commercialization of camonsertib, it has earned a $40…
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Evaxion to Develop Tailored Novel Cancer Vaccines Based upon a New Untapped Source of AI-Discovered…

Jan 24, 2024
Evaxion Biotech A/S, a clinical-stage TechBio company specializing in developing AI-Immunology powered vaccines, announces an expanded commitment to developing tailored cancer vaccines…
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The European Commission Grants Orphan Drug Designation to NS-229 for the Treatment of Eosinophilic…

Jan 23, 2024
NS Pharma, Inc. (NS Pharma), a subsidiary of Nippon Shinyaku Co., Ltd, announced today that the European Commission (EC) has granted orphan drug designation to NS-229, which is being…
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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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