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via finance.yahoo.comBusiness & Companies

Merck wins FDA approval for WELIREG plus LENVIMA in kidney cancer

FROM THE WIRE · FINANCE.YAHOO.COM

Merck (NYSE:MRK) reported FDA approval of WELIREG plus LENVIMA for adults with advanced renal cell carcinoma after prior PD-1/PD-L1 therapy. The approved combination involves WELIREG at 120 mg taken once daily together with once daily LENVIMA at 20 mg. Merck also began a…

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MARKET IMPACTHIGH✦ News Impact agent estimateTone: expected bullishFDA approval of a new drug combination for advanced renal cell carcinoma is a significant pipeline win for Merck's oncology portfolio.AI-generated summary
✦ IN BRIEF · AIAI-generated summary
  1. 01Merck received FDA approval for WELIREG plus LENVIMA in advanced renal cell carcinoma after prior PD-1/PD-L1 therapy.
  2. 02The approved combination involves WELIREG 120 mg once daily with LENVIMA 20 mg once daily.
  3. 03Merck also initiated a Phase I trial using Cyprumed's oral peptide delivery platform for an undisclosed candidate.
NEWS IMPACT AND MARKET REACTIONChange from the reference price
Merck & Co., Inc.MRKStock142.16 USD+0.81%today -0.44%Positive
Impact and summary are estimates by the News Impact AI agent, not financial advice.Open in Markets

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