REGULATORY
Chugai’s PNH Med, Takeda’s cTTP Therapy Up for Advisory Panel Review on Feb. 29
A key health ministry advisory panel will discuss on February 29 whether to endorse approval for a batch of new medicines including Chugai Pharmaceutical’s anti-C5 recycling monoclonal antibody crovalimab for the treatment of paroxysmal nocturnal hemoglobinuria (PNH). Crovalimab is one…
To read the full story
Related Article
- Chugai’s PNH Med, Takeda’s cTTP Therapy Now in Line for Japan Approval
March 1, 2024
- Viatris Files Cystinosis Med in Japan
September 22, 2023
- Takeda Files cTTP Therapy ADAMTS-13 in Japan
August 18, 2023
- Meiji Seika Pharma Files GVHD Drug Belumosudil in Japan
June 28, 2023
- UCB Japan Seeks Lennox-Gastaut Syndrome Indication for Fintepla
June 28, 2023
- Chugai Files NDA for PNH Drug Crovalimab in Japan
June 15, 2023
REGULATORY
- MHLW Issues Q&A on Conditional Approval System
May 1, 2026
- Panel Backs Proposal to Allow Antibody Drugs Like Beyfortus in NIP
May 1, 2026
- METI Clarifies Naphtha Comments, Reaffirms Medical Priority
April 30, 2026
- Japan Minister Rules Out Full Self-Pay for OTC-Like Drugs
April 30, 2026
- Govt’s Bio-WG Wraps Up Biopharma Investment Roadmap Draft
April 30, 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…





