Merck Ends Development of Immunotherapy Drugs Vibostolimab and Favezelimab Amid Late-Stage Failures

Merck has decided to halt the development of vibostolimab for non-small cell lung cancer (NSCLC) after the treatment, in combination with Keytruda, failed to demonstrate significant efficacy in late-stage trials. The decision follows the Phase III KeyVibe-003 and KeyVibe-007 trials, which did not meet the set objectives for overall survival, prompting an independent Data Monitoring Committee to recommend their termination[1][2]. Additionally, these studies reported a higher incidence of immune-related adverse events when vibostolimab was combined with Keytruda compared to Keytruda alone[1][2]. This discontinuation is part of Merck's strategic reevaluation of its oncology pipeline[2].
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What factors led Merck to prioritize other therapies over vibostolimab and favezelimab after the disappointing trial outcomes?
How does Merck plan to address the increased immune-related side effects observed with the combination of vibostolimab and Keytruda?
What promising cancer therapies is Merck focusing on now that they have halted the development of vibostolimab and favezelimab?
In what ways might Merck's strategic pipeline reevaluation impact their future clinical trials in oncology?
How will the discontinuation of favezelimab trials affect ongoing studies like the KEYFORM-008 trial for relapsed or refractory Hodgkin lymphoma?