Moderna and Merck move toward approval of personalized melanoma vaccine
Moderna and Merck said their experimental melanoma vaccine showed strong results in a late-stage clinical trial, nearly halving patients' risk of cancer recurrence or death. The companies are now preparing to seek regulatory approval, with the treatment potentially reaching patients as early as 2027.
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A personalized cancer vaccine approval would mark a significant milestone for mRNA technology beyond infectious disease, showing it can be adapted to treat cancer by targeting mutations unique to each patient's tumor. If approved, it could open the door to similar personalized vaccines for other cancer types, though regulatory review and manufacturing at scale remain substantial hurdles.
- Late-stage trial results showed the vaccine nearly halved recurrence or death risk for melanoma patients
- Moderna and Merck plan to pursue regulatory approval based on these findings
- The vaccine could potentially become available to patients by 2027
Source: fastcompany.com, 2026-10-23
Published there as: “A personalized cancer vaccine could be available as soon as 2027. Here’s what we know”
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