Chugai Pharmaceutical said on September 6 that the US FDA has accepted for review a regulatory application for the company’s anti-C5 recycling monoclonal antibody crovalimab for the treatment of paroxysmal nocturnal hemoglobinuria (PNH). The filing is based on data from…
To read the full story
Related Article
- Chugai Files NDA for PNH Drug Crovalimab in Japan
June 15, 2023
BUSINESS
- SanBio to Move All Akuugo Manufacturing to Minaris’ Yokohama Site
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
- Sarclisa SC Can Meet Patient, Healthcare Worker Needs: Specialist
September 1, 2026
- Recordati Urges Rethink of Zero-Premium Rule on Cost Disclosure
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…





