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Merck and Moderna Report Positive Results for Personalized Cancer Vaccine Trial

Merck and Moderna reported that their personalized mRNA vaccine, used with Keytruda, significantly reduced melanoma recurrence risk in a Phase 3 trial. The study involved 1,137 patients and showed that 82.2% of those receiving the vaccine remained cancer-free after two years. Regulatory approval is being sought by Merck.

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Merck Moderna
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Dr. Marjorie Green Dr. Robert Vonderheide Dr. Shirin Bajaj

Merck and Moderna have announced promising results from a Phase 3 trial of a personalized mRNA cancer vaccine used in conjunction with Keytruda for melanoma treatment. The trial, involving 1,137 patients, showed a 42% reduction in the risk of melanoma recurrence or death. Two-year survival rates without recurrence were 82.2% for those receiving the vaccine, compared to 70% for those on Keytruda alone. Experts noted the need for further research and logistical planning for large-scale treatment implementation.

Key facts

  • Merck and Moderna conducted a Phase 3 trial with 1,137 melanoma patients.
  • The vaccine reduced melanoma recurrence risk by 42% compared to Keytruda alone.
  • 82.2% of patients receiving the vaccine were alive without recurrence after two years.
  • The combination therapy reduced the risk of cancer spreading or death by 38%.
  • Regulatory approval is being sought by Merck for the personalized vaccine.
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Original Headline

Personalized Cancer Vaccine Shows Promise In Major Trial

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Merck and Moderna Report Positive Results for Personalized Cancer Vaccine Trial