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Pfizer’s BRAFTOVI Combo Boosts Survival in Phase 3 BREAKWATER Trial

Feb 4, 2025
Pfizer Inc. announced positive topline results from the progression-free survival (PFS) analysis of the Phase 3 BREAKWATER study of BRAFTOVI (encorafenib) in combination with cetuximab…
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Vertex Announces FDA Approval of First-in-Class Pain Treatment JOURNAVX for Adults

Feb 3, 2025
Vertex Pharmaceuticals Incorporated announced that the U.S. Food and Drug Administration (FDA) has approved JOURNAVX (suzetrigine), an oral, non-opioid, highly selective NaV1.8 pain…
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Sarclisa Approved in China as First Anti-CD38 Treatment for Newly Diagnosed Multiple Myeloma

Feb 3, 2025
The National Medical Products Administration (NMPA) in China has approved Sarclisa, in combination with a standard-of-care regimen, bortezomib, lenalidomide, and dexamethasone (VRd),…
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Kazia Therapeutics Launches Groundbreaking Trial of Paxalisib and Immunotherapy for Advanced Breast…

Feb 3, 2025
Kazia Therapeutics Limited an oncology-focused drug development company, is pleased to announce the regulatory approval and launch of a clinical trial evaluating the combination of…
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Orion and Invenra Partner to Develop Bispecific Antibody Cancer Therapies

Feb 3, 2025
Orion and Invenra announce discovery service and commercial license agreement to develop innovative bispecific antibody cancer therapeutics Orion Corporation (“Orion”) and Invenra…
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ImmunityBio Partners with BeiGene on Phase 3 Trial for ANKTIVA and PD-1 Combo in NSCLC

Feb 3, 2025
ImmunityBio, Inc. announced it has entered into a collaboration and supply agreement with BeiGene, Ltd. (to be changed to BeOne Medicines, Ltd.), a global oncology company, to conduct a…
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European Commission Approves ViiV’s Vocabria + Rekambys for HIV Treatment in Adolescents

Feb 2, 2025
ViiV Healthcare, the global specialist HIV company majority owned by GSK, with Pfizer and Shionogi as shareholders, announced that the European Commission has authorised…
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FDA Approves LEQEMBI IV Maintenance Dosing for Early Alzheimer’s Disease

Jan 28, 2025
Eisai Co., Ltd. and Biogen Inc. announced that the U.S. Food and Drug Administration (FDA) has approved the Supplemental Biologics License Application (sBLA) for once every four weeks…
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FDA Grants Priority Review to Merck’s WELIREG for Advanced Pheochromocytoma and Paraganglioma

Jan 28, 2025
Merck, known as MSD outside of the United States and Canada, announced the U.S. Food and Drug Administration (FDA) has accepted for priority review a supplemental new drug application…
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Pfizer’s BRAFTOVI Combination Regimen Demonstrates Improved Response in Patients with BRAF…

Jan 28, 2025
Pfizer Inc.announced positive results from the Phase 3 BREAKWATER trial evaluating BRAFTOVI (encorafenib) in combination with cetuximab (marketed as ERBITUX) and mFOLFOX6 (fluorouracil,…
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