Takeda Pharmaceutical said on November 9 that it has bagged US regulatory clearance for Adzynma as the first FDA-approved therapy for an ultra-rare blood clotting disorder called congenital thrombotic thrombocytopenic purpura (cTTP). Adzynma, a recombinant form of the ADAMTS13 protein,…
To read the full story
Related Article
- Takeda Files cTTP Therapy ADAMTS-13 in Japan
August 18, 2023
- Takeda’s cTTP Therapy Gets Priority Review in US
May 18, 2023
- Takeda’s TAK-755 Shows Promising PIII Interim Data for Ultra-Rare Blood Clotting Disorder
January 10, 2023
BUSINESS
- Sarclisa SC Can Meet Patient, Healthcare Worker Needs: Specialist
September 1, 2026
- Merck KGaA to Consolidate Japan Life Science Labs at Haneda Hub
September 1, 2026
- FDA Approves Takeda’s PV Drug Mimrylo
September 1, 2026
- Recordati Urges Rethink of Zero-Premium Rule on Cost Disclosure
August 31, 2026
- Sumitomo Pharma Goes Global with Adjuvants, Targets 100 Billion Yen
August 31, 2026
We had just gotten off a call with a client in Europe, and we’d received a bit of an earful. “Philip,” the client pressed, “what can this candidate bring to us? We know what he does, but what has he…





