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VERVE-102 · HEART-3

Lilly's Phase 2 plan is distinct from the positive Heart-2 Phase 1b data already disclosed. The registry supplies HEART-3's exact protocol; no result date is promised. VERVE-102 — phase 2 study in Atherosclerosis, Cardiovascular Disease, Hypercholesterolemia. NCT07839936 lists Percent Change from Baseline in LDL-C as a primary outcome (Baseline, Day 90). Registry status: not yet recruiting.

Verve Therapeutics, Inc.Drug catalystsClinical program monitorDate to watch

What matters

Track what the company has actually announced, the study or asset involved, and the evidence needed to confirm the milestone.

  • Specify the exact future analysis/cohort and verify that it remains unpublished before creating any tradeable question.
  • Registry design and recruitment status are not evidence of efficacy or regulatory approval.
  • Primary completion is not a guaranteed topline publication or regulatory decision date.
  • Registry primary completion: 2028-08 (estimated); verify independently before using it as a catalyst date.
  • An active study record does not establish that its primary outcome is still unannounced. Review sponsor disclosures before promotion to a future catalyst.

Primary evidence

Phase 2 monitor — result date unconfirmed

Potential outcome market

Will VERVE-102 meet the prespecified primary endpoint in NCT07839936 by a listing deadline still to be specified?

This event is research, not a listed market. A market needs a precise question, resolution rules and liquidity before trading opens.