BRIEF-Merck & Co Inc Says FDA Sets PDUFA Date Of June 19, 2026 For Welireg And Keytruda

Merck & Co., Inc.

Merck & Co., Inc.

MRK

0.00

- Merck & Co Inc MRK.N:

  • KEYTRUDA® (PEMBROLIZUMAB) PLUS WELIREG® (BELZUTIFAN) GIVEN AS ADJUVANT THERAPY REDUCED THE RISK OF DISEASE RECURRENCE OR DEATH BY 28% COMPARED TO KEYTRUDA MONOTHERAPY IN CERTAIN PATIENTS WITH EARLIER-STAGE RENAL CELL CARCINOMA (RCC)

  • MERCK & CO INC - KEYTRUDA PLUS WELIREG REDUCES RISK OF RECURRENCE OR DEATH BY 28%

  • MERCK & CO INC - FDA ACCEPTS PRIORITY REVIEW FOR WELIREG AND KEYTRUDA COMBINATION

  • MERCK & CO INC - FDA SETS PDUFA DATE OF JUNE 19, 2026 FOR WELIREG AND KEYTRUDA

Source text: ID:nBw7Rg3KLa

Further company coverage: MRK.N