Chugai Pharmaceutical said on December 7 that a key European advisory panel recommended approval of its humanized anti-human IL-6 receptor monoclonal antibody tocilizumab, known with the brand names of Actemra/RoActemra, for the treatment of severe COVID-19. The European Medicines Agency’s…
To read the full story
Related Article
- Chugai Files Actemra for COVID-19 Pneumonia in Japan
December 14, 2021
- Roche/Chugai’s Tocilizumab Approved for Severe COVID-19 in Europe
December 8, 2021
BUSINESS
- Chugai Files Enspryng for MOGAD Relapse Prevention in Japan
August 3, 2026
- Takeda CEO Says Orzeyful Could Redefine NT1 Standard of Care
July 31, 2026
- Pfizer Seeks Pediatric Expansion for Hympavzi in Japan
July 31, 2026
- Nippon Shinyaku Exercises Option for AB2 Bio’s Tadekinig Alfa in US
July 31, 2026
- Alfresa Takes Stake in Ember to Bolster Pharma Cold Chain in Japan
July 31, 2026
A few weeks ago, I had coffee with a very talented executive. Let’s call him Kenji. He has a great job, a big salary, and a solid team. But he was unhappy. He felt bored and wanted a new challenge.…





