BUSINESS
Lenvima-Keytruda Combo Bags FDA’s Breakthrough Status for Endometrial Carcinoma
The US FDA has granted Breakthrough Therapy designation for a combination therapy pairing Eisai’s multi-kinase inhibitor Lenvima (lenvatinib) and US Merck’s PD-1 inhibitor Keytruda (pembrolizumab) for the treatment of a type of endometrial carcinoma, the two companies said on July…
To read the full story
Related Article
- Lenvima/Keytruda Gets FDA’s Breakthrough Status for HCC
July 24, 2019
- Lenvima-Keytruda Combo Earns FDA’s Breakthrough Designation for RCC
January 10, 2018
BUSINESS
- Pfizer, ASKA to Co-Promote RSV Vaccine Abrysvo in Japan
March 9, 2026
- Sumitomo to Launch Post-Marketing Study for iPSC Therapy by Year-End
March 9, 2026
- Drug Pricing Reform Draws Sharp Industry Backlash in Jiho Poll
March 9, 2026
- Nitrosamine Detected in Nichi-Iko’s Tryptanol, No Need to Halt Prescriptions
March 9, 2026
- Towa Broadens Label for Tacrolimus in Cell Transplantation
March 9, 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…





