New Efficacy Data for Non-Clear Cell Renal Cell Carcinoma From KEYNOTE-B61 Added to LENVIMA® (lenvatinib) US Label Supporting KEYTRUDA + LENVIMA Indication for the First-Line Treatment of ...
Merck & Company, Inc. (new) (MRK)
Last merck & company, inc. (new) earnings: 4/28 06:45 am
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Source: Yahoo! Finance
NUTLEY, N.J. June 27, 2024 /PRNewswire/ -- Eisai today announced a label update for LENVIMA, the orally available multiple receptor tyrosine kinase inhibitor discovered by Eisai, in the United States to include clinical efficacy data for the first-line treatment of advanced non-clear cell renal cell carcinoma (nccRCC). This update is based on data from KEYNOTE-B61, a Phase 2, single-arm trial evaluating KEYTRUDA ® (pembrolizumab), Merck's anti-PD-1 therapy, plus LENVIMA for the first-line treatment of adult patients with advanced nccRCC. While the label now includes efficacy data on the non-clear cell population, the approved indication for KEYTRUDA plus LENVIMA for the first-line treatment of adult patients with advanced RCC is unchanged. Merck, known as MSD outside of the United States and Canada , received an updated label for KEYTRUDA including this data as well. KEYTRUDA plus LENVIMA is the first and only immunotherapy and tyrosine kinase inhibitor (IO plus TKI) combination wi
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MRK
Earnings
- 4/25/24 - Beat
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Sec Filings
- 6/25/24 - Form 11-K
- 6/25/24 - Form 11-K
- 6/25/24 - Form 11-K
- MRK's page on the SEC website