BUSINESS
Satralizumab Accepted for Review in Europe, US; Chugai Plans Japan Filing Before Year-End
Chugai Pharmaceutical said on October 30 that European and US regulators have accepted marketing applications for satralizumab (development code: SA237), an anti-IL-6 receptor humanized recycling antibody, for adult and adolescent patients with neuromyelitis optica spectrum disorder (NMOSD). The Medicines Agency…
To read the full story
Related Article
- Chugai’s Satralizumab Hits Primary Target in PIII Study
September 13, 2019
- Chugai’s Satralizumab Wins FDA Breakthrough Therapy Status
December 20, 2018
BUSINESS
- AGC Biologics Launches Bispecific Antibody CDMO Project in Japan
May 28, 2026
- Bayer Regulatory Chief Hails Japan’s Review System, Flexibility on PI Waivers
May 28, 2026
- Asahi Kasei Licenses ADC Technology from Noguchi Institute
May 28, 2026
- Kissei Files Rigel’s AML Drug Olutasidenib in Japan
May 28, 2026
- Japan OTC Market Falls 2.4% in April amid Weaker Inbound Demand: Intage
May 28, 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…





