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
- Japan Pharma Workforce Up Slightly; Generic Firms Drive Gains over 5 Years
April 10, 2026
- Zenyaku, Chugai to End Rituxan Co-Promotion in September
April 10, 2026
- Effexor’s GAD Nod Seen Boosting Diagnosis, Treatment in Japan: Expert
April 10, 2026
- MSD Japan Eyes Up to 8 Approvals, 8-Plus Filings under New Chief
April 10, 2026
- Pfizer Japan Files Tukysa Label Expansion in Breast, Biliary Tract Cancers
April 9, 2026
In the complex landscape of the Japanese pharmaceutical market, the “status quo” is often the safest harbor. But for leaders like Kennet Brysting, former president of Gilead Japan, the status quo is the most dangerous place to stay.Innovation in Japan…





