REGULATORY
GSK’s Cost-Effectiveness Analysis for Trelegy Delayed, First Product under Full CEA Scheme
Last May, GlaxoSmithKline’s COPD therapy Trelegy (fluticasone furoate + umeclidinium + vilanterol) became the first drug selected for Japan’s full-scale cost-effectiveness assessment (CEA) scheme. A year later, regulators revealed that GSK’s CEA was delayed by two months, with the company…
To read the full story
Related Article
- MHLW Unveils Outline of Cost-Effective Assessment Scheme: Chuikyo
January 24, 2019
REGULATORY
- MHLW Lifts Part of Approval Conditions for Takeda’s Vyvanse
June 9, 2026
- Drug Makers Seek Govt Support for Immunoglobulin Plant Investments: LDP Hearing
June 9, 2026
- Japan Govt Likely to Slim Down Honebuto, but Details Remain Elusive
June 8, 2026
- Leqembi, Kisunla Labels Revised to Strengthen ARIA Monitoring
June 8, 2026
- Japan Tightens Oversight of Mounjaro Resales: Health Minister
June 8, 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…





