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Merck & Co Newsroom
Merck Ends Development of Two Experimental Cancer Drugs
Merck (MRK.US) has terminated the development of anti-TIGIT and anti-LAG-3 antibodies.
On December 16, Merck (MRK.US) announced the termination of the development of the anti-TIGIT antibody Vibostolimab and the anti-LAG-3 antibody Favezelimab.
Merck's Respiratory Syncytial Virus Drug's Biologics License Application Accepted by FDA
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Merck Gets FDA Review of Clesrovimab RSV Vaccine Candidate
Express News | Merck & Co Inc - if Approved, Anticipates Clesrovimab Available for Ordering by July 2025
Express News | Merck Announces FDA Acceptance of Biologics License Application for Clesrovimab, an Investigational Long-Acting Monoclonal Antibody Designed to Protect Infants From Rsv Disease During Their First Rsv Season
Merck announced the termination of the development of two experimental anticancer drugs.
On December 17, Gelonghui reported that Merck announced on Monday that it has halted the development of the experimental cancer drugs vibostolimab and favezelimab after multiple trials failed when combined with the best-selling drug Keytruda to treat various cancers. Marjorie Green, head of Global Clinical Development Oncology at Merck Research, stated: "After careful analysis of the data, we have decided to stop the development of these candidate drugs to prioritize other ongoing projects."
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Merck Decides To End Favezelimab Clinical Development Program, And Stop Enrollment In Phase 3 KEYFORM-008 Trial
Express News | Merck & Co Inc - Patients in Keyform-008 Trial May Continue Therapy Until Study Completion
Express News | Merck & Co Inc - Discontinues Clinical Development Programs for Vibostolimab and Favezelimab
Merck Provides Update on KeyVibe and KEYFORM Clinical Development Programs Evaluating Investigational Vibostolimab and Favezelimab Fixed-Dose Combinations With Pembrolizumab
Express News | Merck Provides Update on Keyvibe and Keyform Clinical Development Programs Evaluating Investigational Vibostolimab and Favezelimab Fixed-Dose Combinations With Pembrolizumab
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CHMP Endorses Merck's Kidney Cancer Drug for Two Indications
Merck's KEYTRUDA Approved in Combination With Chemotherapy in China to Treat Lung Cancer
Express News | Merck’s Keytruda® (Pembrolizumab) Approved in China in Combination With Chemotherapy as Neoadjuvant Treatment, Then Continued as Monotherapy After Surgery as Adjuvant Treatment for Patients With Resectable Stage II, Iiia or Iiib Nsclc