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Shandong Jincheng Pharma Subsidiary Jincheng Taier to Sell Proxyl Vaginal Capsule Tech & MAH Rights to Shanghai Hemony for RMB 50 M
CompanyDeals

Shandong Jincheng Pharma Subsidiary Jincheng Taier to Sell Proxyl Vaginal Capsule Tech & MAH Rights to Shanghai Hemony for RMB 50 M

Sinotau Receives FDA NDA Approval for MK‑6240 Tau PET Imaging Agent
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Sinotau Receives FDA NDA Approval for MK‑6240 Tau PET Imaging Agent

Baheal Pharma Locks CSL Behring Albumin Rights to Boost China’s Blood Product Supply
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Baheal Pharma Locks CSL Behring Albumin Rights to Boost China’s Blood Product Supply

Prelude Therapeutics Revamps Pipeline: Incyte Option on JAK2V617F, KAT6A Degrader Takes Center Stage, SMARCA2 Paused
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Prelude Therapeutics Revamps Pipeline: Incyte Option on JAK2V617F, KAT6A Degrader Takes Center Stage, SMARCA2 Paused

UCB Wins FDA Approval for KYGEVVI in Rare Mitochondrial Disease TK2d
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UCB Wins FDA Approval for KYGEVVI in Rare Mitochondrial Disease TK2d

Dizal Highlights Breakthrough Findings for golidocitinib and birelentinib at ASH 2025
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Dizal Highlights Breakthrough Findings for golidocitinib and birelentinib at ASH 2025

Jiangsu Vcare’s VC004 Joins NMPA’s SPARK Oncology Program
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Jiangsu Vcare’s VC004 Joins NMPA’s SPARK Oncology Program

Pfizer’s Q3 2025 Results: COVID‑19 Sales Slide While Eliquis Soars
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Pfizer’s Q3 2025 Results: COVID‑19 Sales Slide While Eliquis Soars

Jiangsu Hengrui Secures Priority Review for HRS‑5965 in China’s Rare‑Disease Portfolio
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Jiangsu Hengrui Secures Priority Review for HRS‑5965 in China’s Rare‑Disease Portfolio

Pluvicto Radioligand Therapy Receives Dual NMPA Approvals in China
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Pluvicto Radioligand Therapy Receives Dual NMPA Approvals in China

Sichuan Biokin Secures Breakthrough Therapy Designation for HER2‑Targeted ADC T‑Bren
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Sichuan Biokin Secures Breakthrough Therapy Designation for HER2‑Targeted ADC T‑Bren

Shenzhen Kangtai Biological Products Launches Phase I Trial for Infant Influenza Vaccine
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Shenzhen Kangtai Biological Products Launches Phase I Trial for Infant Influenza Vaccine