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VisitModerna and Merck Shares Rise on Positive KEYNOTE-942 Melanoma Therapy Results
Jun 3, 2024, 03:52 PM
Moderna and Merck have announced promising results from a Phase 2b clinical trial involving their investigational individualized neoantigen therapy, mRNA-4157 (V940), in combination with Merck's immunotherapy drug KEYTRUDA (pembrolizumab). The trial, known as KEYNOTE-942, included patients with high-risk stage III/IV melanoma following complete resection and demonstrated a sustained improvement in recurrence-free survival and distant metastasis-free survival compared to KEYTRUDA alone. Over a period of 34.9 months, the combination therapy reduced the risk of recurrence or death by 49% and the risk of distant metastasis by 62%, with a hazard ratio for recurrence-free survival of 0.51 and distant metastasis-free survival of 0.38. These findings were presented at the ASCO24 conference, and the companies have indicated that a Phase 3 trial is ongoing. The positive results have led to a rise in the shares of both Moderna and Merck.
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Phase III trial in the US • 25%
Approval in China • 25%
Approval in the EU • 25%
Partnership with another pharmaceutical company • 25%
FDA (USA) • 25%
EMA (Europe) • 25%
MHRA (UK) • 25%
TGA (Australia) • 25%
Yes • 50%
No • 50%
FDA approval • 33%
EMA approval • 33%
No major milestone • 33%
Additional Phase 3 trials • 33%
FDA Approval without additional trials • 33%
FDA Rejection • 33%
Merck • 33%
Moderna • 33%
Both equally • 34%