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UNDERREPORTED

Biotech bets on tough cancer targets finally yield breakthrough therapies

Moderna reported strong late-stage results for a personalized melanoma vaccine and the FDA approved Revolution Medicines' new prostate-cancer pill, sparking major stock gains.

In late August, Moderna announced that its personalized melanoma vaccine achieved impressive late-stage trial results, driving its stock up dramatically. Shortly after, the FDA approved an oral prostate-cancer medication from Revolution Medicines that employs a molecular-glue mechanism to address mutations considered undruggable. Neither product is a cure, but both offer new options alongside standard treatments.

The breakthroughs trace back to high-risk investments by chemist Greg Verdine, who raised $125 million to target the RAS mutation, and former Moderna chief medical officer Tal Zaks, who backed the vaccine concept with a $450 million partnership with Merck. Their persistence has opened a new therapeutic landscape for cancers such as melanoma, prostate, and potentially others under ongoing trials.

Why it matters

These approvals validate risky biotech strategies and could expand treatment options for patients with hard-to-treat cancers.

In this story

personalized cancer vaccinemolecular glueRAS mutationprostate cancer pillbiotech investmentlate-stage trialFDA approvalhigh-risk drug development
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