European regulators have granted approval for the label expansion of Roche’s 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 decision came just hours after the recommendation by…
To read the full story
Related Article
- Chugai Files Actemra for COVID-19 Pneumonia in Japan
December 14, 2021
- EU Panel Backs Tocilizumab for Severe COVID-19: Chugai
December 8, 2021
BUSINESS
- Eylea Biosimilar Shipment Restrictions to Be Lifted on June 5
May 27, 2026
- Bayer’s Low-Dose MRI Contrast Agent Ambelvist Debuts in Japan
May 27, 2026
- Eisai Eyes 1 Trillion yen in FY2028 Sales under 3-Year Plan
May 26, 2026
- Nippon Kayaku to Take Over AstraZeneca’s Zoladex in Japan
May 26, 2026
- Jardiance Triumphs in Six Promotion Channels in April: Intage
May 26, 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…





