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Reading: US: Moderna-Merck Cancer Vaccine Meets Phase 3 Melanoma Goals
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Cancer vaccine research illustration with a scientist, cancer cells, and a human body.
PhotoNews Pakistan > Tech > US: Moderna-Merck Cancer Vaccine Meets Phase 3 Melanoma Goals
Tech

US: Moderna-Merck Cancer Vaccine Meets Phase 3 Melanoma Goals

Web Desk
By Web Desk Published August 29, 2026 2 Min Read
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Illustration of cancer vaccine research showing a scientist examining a sample alongside cancer cells and a human body.
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CAMBRIDGE, Mass., United States: The Moderna-Merck cancer vaccine met two key Phase 3 goals in melanoma patients. The companies tested the personalised vaccine with Merck’s Keytruda.

Moderna and Merck announced the results on August 19. The global INTerpath-001 trial enrolled 1,137 patients with stage IIB-IV melanoma after surgery.

The companies said the combination improved recurrence-free survival compared with Keytruda alone. It also improved distant metastasis-free survival. However, Moderna and Merck have not yet released the full Phase 3 results.

Success after a century of failures: Inside Moderna and Merck's cancer vaccine breakthrough https://t.co/rTyByQJKn3 https://t.co/rTyByQJKn3

— Reuters (@Reuters) August 28, 2026

Moderna developed intismeran autogene, also known as V940 or mRNA-4157, as a personalised cancer treatment. The vaccine uses genetic details from each patient’s tumour and can target up to 34 cancer-related mutations.

Meanwhile, Keytruda helps the immune system identify and attack cancer cells. Moderna and Merck have worked together on the treatment for about a decade.

Read: Australian Doctor Richard Scolyer Cancer-Free After Innovative Treatment

Earlier Phase 2b results also supported the approach. After five years, the treatment cut the risk of cancer returning or death by 49% compared with Keytruda alone. It also cut the risk of distant spread or death by 59%.

Read: Russia’s Enteromix Cancer Vaccine Shows Promise Preclinical Trials

The companies will next present the complete Phase 3 findings at an international medical meeting. They also plan to discuss regulatory filings with health authorities. However, they have not announced a date for a possible U.S. Food and Drug Administration approval.

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