Protagonist Therapeutics and Takeda Pharmaceutical said on March 3 that rusfertide, an investigational therapy for the rare blood disorder polycythemia vera (PV), met the primary endpoint in a global PIII clinical study, VERIFY. The trial covered phlebotomy-dependent patients with PV,…
To read the full story
Related Article
- US FDA Accepts Takeda’s Rusfertide Filing, Grants Priority Review
March 3, 2026
- Takeda Files Polycythemia Vera Drug Rusfertide in US
January 7, 2026
- Takeda Bags Global Rights to Protagonist’s Rare Hematology Asset
February 2, 2024
BUSINESS
- Sumitomo Regains Growth Momentum, Eyes 350 Billion Yen from 2 Key Drugs in FY2028
March 3, 2026
- Middle East Turmoil Raises Fears over API Shipments as Key Airports Shut
March 3, 2026
- UCB, Daiichi Sankyo to Wind Up Japan Partnership for Vimpat
March 3, 2026
- Itochu Snaps Up CoreMed to Bolster Japan Entry Support
March 3, 2026
- Ono to Transfer Opalmon, Prostandin to Daito by November
March 3, 2026
I recently sat down with one of the leading medical directors in Japan to discuss the critical evolution of the medical science liaison (MSL) role.The MSL has transformed from a scientific resource into a strategic partner essential for successful product…





