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AbbVie Reaches Deal With Trump Administration on Drug Pricing

Jan 14, 2026
AbbVie has announced a voluntary agreement with the Trump administration aimed at expanding access and affordability of medicines for Americans while reinforcing the company’s long-term…
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AbbVie Licenses RemeGen’s RC148 in Major Oncology Partnership

Jan 14, 2026
AbbVie and RemeGen have entered into an exclusive global licensing agreement aimed at advancing RC148, a novel investigational bispecific antibody targeting both Programmed Cell Death-1…
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AbbVie to Acquire West’s Arizona Device Manufacturing Facility

Jan 14, 2026
AbbVie and West Pharmaceutical Services have announced a definitive agreement under which AbbVie will acquire a device manufacturing facility and associated intellectual property from…
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FDA Approves ZYCUBO as First Treatment for Rare Menkes Disease

Jan 14, 2026
Fortress Biotech, Inc. and its majority-owned subsidiary Cyprium Therapeutics have received a major regulatory milestone with the U.S. Food and Drug Administration’s approval of ZYCUBO®…
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BD Invests $110 Million to Expand U.S. Prefillable Syringe Manufacturing

Jan 14, 2026
BD (Becton, Dickinson and Company), a global leader in medical technology, has announced a $110 million investment to expand its production of prefillable syringes in the United States,…
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Solid Biosciences Advances Gene Therapy for Friedreich’s Ataxia

Jan 14, 2026
Solid Biosciences Inc., a life sciences company focused on developing precision genetic medicines for neuromuscular and cardiac diseases, has reached two important milestones in the…
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Synaffix and Sidewinder Partner to Develop Next-Generation Bispecific ADCs

Jan 9, 2026
Synaffix B.V., a Lonza company, and Sidewinder Therapeutics have entered into a multi-target licensing agreement aimed at developing first-in-class bispecific antibody-drug conjugate…
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FDA Grants Fast Track to Alessa’s Localized Prostate Cancer Therapy

Jan 9, 2026
Alessa Therapeutics has received Fast Track designation from the U.S. Food and Drug Administration for Enolen®, its lead investigational therapy for the treatment of low- to…
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FDA Grants Orphan Status to Cellenkos’ CK0804 in Myelofibrosis

Jan 9, 2026
Cellenkos Inc., a clinical-stage biotechnology company developing off-the-shelf regulatory T cell (Treg) therapies, has received Orphan Drug Designation from the U.S. Food and Drug…
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Santhera Licenses AGAMREE to Nxera in Key Asia-Pacific Markets

Jan 9, 2026
Santhera Pharmaceuticals has signed an exclusive licensing agreement with Nxera Pharma UK to develop, manufacture, and commercialize AGAMREE® (vamorolone) for the treatment of Duchenne…
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