Merck and Moderna Report the INTerpath-001 Trial Data on Intismeran Autogene + Keytruda for Completely Resected Stage IIB-IV Melanoma
Shots:
- Merck & Moderna have reported the P-III (INTerpath-001) trial data assessing adj. intismeran autogene (1mg, Q3W for 9 doses) + Keytruda (400mg, Q6W up to 9 cycles) vs Keytruda alone in 1,137 pts with high-risk (stage IIB-IV) resected cutaneous melanoma
- Intismeran plus Keytruda as adj. therapy showed improvements in RFS (1EP) and DMFS (2EP) in pts without prior systemic therapy, while the study continues to assess key 2EPs, incl. OS. Data to be presented at an upcoming conference
- INTerpath program incl. 9 P-II & P-III trials across melanoma, NSCLC, bladder cancer & renal cell carcinoma, alongside P-IIb (KEYNOTE-942) trial in adj. melanoma & a P-I study in adj. PDAC, perioperative gastric carcinoma & perioperative NSCLC
Ref: Businesswire | Image: MSD & Moderna | Press Release
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