The US FDA has rejected Eisai’s and US Merck’s accelerated approval bid for their Lenvima (lenvatinib)-Keytruda (pembrolizumab) combination therapy in first-line liver cancer, apparently due to its nod given to Roche’s rival combo regimen in late May. The two partners…
To read the full story
Related Article
- Lenvima/Keytruda Combo Fails in PIII HCC Trial
August 4, 2022
BUSINESS
- PMP Returns Slam Drug Makers' Leading Products, Prazaxa Cut 45%: Jiho Poll
March 13, 2026
- Lilly to Invest Additional 20 Billion Yen in Japan's Seishin Plant
March 13, 2026
- Fujifilm Invests in Austria’s Valanx Biotech to Boost ADC Technology
March 13, 2026
- Merck, CDMO Cyto-Facto Join Hands on Cell and Gene Therapy
March 13, 2026
- Anti-PD-1 Agonist Antibody Enters PI in Australia for Autoimmune Diseases: Meiji
March 13, 2026
I recently sat down with one of the leading medical directors in Japan to discuss the critical evolution of the medical science liaison (MSL) role.The MSL has transformed from a scientific resource into a strategic partner essential for successful product…





