Bayer Receives Breakthrough Therapy Designation in US and China for Sevabertinib in First-Line HER2-Mutant NSCLC on January 07, 2026 Bayer Breakthrough Therapy Designation CDE China First line treatment HER2-mutant Non-Small Cell Lung Carcinoma sevabertinib United States Food and Drug Administration +
Bayer Receives Breakthrough Therapy Designation in US and China for Sevabertinib in First-Line HER2-Mutant NSCLC on January 06, 2026 Bayer Breakthrough Therapy Designation CDE China First line treatment HER2-mutant Non-Small Cell Lung Carcinoma sevabertinib United States Food and Drug Administration +
Dyne Therapeutics Reports Positive Results for Duchenne Drug DYNE-251, Plans FDA Approval Submission on December 09, 2025 Biological Factors Breakthrough Therapy Designation Clinical Trials DELIVER (veterinary product) Dyne Therapeutics DYNE-251 Muscular Dystrophy, Duchenne United States Food and Drug Administration +
Merck to Acquire Cidara Therapeutics for $9.2 Billion on December 09, 2025 acquisition Antiviral Agents Breakthrough Therapy Designation CD388 Cidara Therapeutics Immunostimulating conjugate (antigen) influenza prevention Merck +