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
- Viatris Recalls Sevoflurane Anesthetic over Manufacturing Deviation
August 3, 2026
- Belite Bio Japan Launches Stargardt Disease Awareness Initiative
August 3, 2026
- Otsuka Eyes 3.5 Trillion Yen Sales by 2035 on New Growth Drivers
August 3, 2026
- Daiichi Sankyo Cuts FY2027 Net Profit Outlook on Higher Tax Burden
August 3, 2026
- Kissei Slashes Tavneos Sales Forecast after Safety, Data Concerns
August 3, 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.…





