Merck and Eisai Report US FDA Approval of Welireg + Lenvima in Advanced Renal Cell Carcinoma

Shots: The US FDA has approved Welireg + Lenvima for the treatment of adults with advanced renal cell carcinoma with a clear cell component (ccRCC) following a PD-1 or PD-L1 inhibitor Approval was based on the P-III (LITESPARK-011) trial assessing Welireg (120mg, PO, QD) + Lenvima (20mg, PO, QD) vs cabozantinib in 747 pts with advanced ccRCC whose disease progressed on or after anti-PD-1/ PD-L1 therapy Trial met its 1EP of improved PFS by 26% (mPFS: 14.6 vs 10.6mos.), while the other 1EP of OS did not meet statistical significance. 2EPs showed ORR of 53% vs 40% plus DoR results were also reported  Ref: Businesswire   |   Image: Merck & Eisai   |  Press Release PharmaShots, your go-to media platform for customized news ranging across multiple indications. For more information, connect with us at connect@pharmashots.com The post Merck and Eisai Report US FDA Approval of Welireg + Lenvima in Advanced Renal Cell Carcinoma appeared first on PharmaShots.