First pivotal Phase 3 trial to show superiority of Keytruda plus a TROP2 antibody-drug conjugate, Trodelvy, versus standard of care in first-line metastatic TNBC
Manageable safety profile and encouraging antitumor activity observed for MK-1084 in KANDLELIT-001, both as a monotherapy and in studied combinations
WELIREG is the first and only oral hypoxia-inducible factor-2 alpha inhibitor approved in the European Union
Merck has also decided to end the favezelimab clinical development program
The INTerpath-009 clinical trial demonstrates continued expansion of the INTerpath clinical program
At 10 years, more than one-third (34.0%) of patients with advanced melanoma were alive after treatment with KEYTRUDA, compared to 23.6% of patients treated with ipilimumab
The companies have initiated Phase 3 studies in patients with high-risk melanoma and non-small cell lung cancer
Data showed that the primary endpoint of recurrence-free survival (RFS) met the pre-specified futility criteria
For the first-line treatment of certain patients with metastatic non-small cell lung cancer
Keynote -564 is the first Phase 3 trial to demonstrate superior overall survival (OS) with adjuvant therapy compared to placebo in patients with RCC
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