Merck and Moderna report positive Phase 3 melanoma trial results
The INTerpath-001 trial met endpoints for recurrence-free and distant metastasis-free survival with intismeran autogene plus KEYTRUDA.
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Research-intensive biopharmaceutical company
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In short: Merck outlined a $70 billion pipeline strategy to offset Keytruda's upcoming patent cliff while securing FDA approval for its first oral cholesterol pill.
The INTerpath-001 trial met endpoints for recurrence-free and distant metastasis-free survival with intismeran autogene plus KEYTRUDA.
The KANDLELIT-015 trial evaluates an oral KRAS G12C inhibitor in non-small cell lung cancer, marking the fifth Phase 3 study for this candidate.
EMA also accepted the application for the same population. If approved, children under two at increased risk could receive a second-season dose.
Sales grew 5% to $16.6B; FDA approved LIPFENDRA and KEYTRUDA combinations; completed $6.8B Terns acquisition.
https://www.merck.com/events/morgan-stanley-24th-annual-global-healthcare-conference...
As dueling data emerge between their drug ivonescimab and a rival Merck medication, Summit and Akeso...
The fact that Gilead Sciences' Trodelvy failed as a first-line treatm | Newly revealed global phase 3 data from Merck and Gilead's failed Trodelvy first-line...
Merck & Co., Inc. (NYSE:MRK) executives outlined a strategy centered on pipeline investment, new product launches and targeted business development as the company prepares for...
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