FDA approves Welireg for advanced renal cell carcinoma

15 December 2023

Two years after Welireg's (belzutifan) original approval in the rare von Hippel-Lindau (VHL) disease, the Food and Drug Administration has now approved the Merck & Co (NYSE: MRK) drug for a new indication.

The new FDA nod is for patients with advanced renal cell carcinoma (RCC) following a programmed death receptor-1 (PD-1) or programmed death-ligand 1 (PD-L1) inhibitor and a vascular endothelial growth factor tyrosine kinase inhibitor (VEGF-TKI).

Clinical backing

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