Eisai and US Merck said that the US FDA has accepted supplemental new drug applications (sNDAs) for the combination of the tyrosine kinase inhibitor Lenvima (lenvatinib) and the hypoxia-inducible factor-2 alpha (HIF-2α) inhibitor Welireg (belzutifan).The filing seeks approval of the…
To read the full story
Related Article
- Lenvima-Keytruda Triplets Fail in First-Line RCC Trial
April 22, 2026
- Eisai, MSD File Lenvima-Welireg Combo in Japan for RCC
March 30, 2026
BUSINESS
- Keytruda Holds Top Spot for 35th Straight Month in August: Encise
September 7, 2026
- Fuji Curbs Shipments of Simponi, Ranmark Biosimilars Soon after Launch
September 4, 2026
- Leqembi Subcutaneous Autoinjector Approved in China
September 4, 2026
- Nxera Gets US$8.6 Million OX2R Milestone from Centessa
September 4, 2026
- Top Medipal Shareholder Seeks CEO Ouster, Special Dividend
September 4, 2026
We had just gotten off a call with a client in Europe, and we’d received a bit of an earful. “Philip,” the client pressed, “what can this candidate bring to us? We know what he does, but what has he…





