Pipeline tracker

Intismeran autogene (V940 / mRNA-4157)

Phase 3Evidence reviewed by an editor
Intismeran autogene (V940 / mRNA-4157)Moderna and Merck · High-risk resected melanoma (with pembrolizumab)
Phase 3 · Individualized neoantigen mRNA cancer vaccineAs of Sep 25, 2026

Phase 3 INTerpath-001 (NCT05933577) met its primary recurrence-free survival endpoint, announced Aug. 19, 2026; the companies say they will engage regulators on filings (company release).

Phase 3 INTerpath-001 (NCT05933577) met its primary recurrence-free survival endpoint, announced Aug. 19, 2026; the companies say they will engage regulators on filings (company release).

What this stage means

Phase 3 trials test whether a treatment works better than, or as well as, existing care in larger groups of people — usually the last step before a regulator decides.

A development stage describes where the evidence stands for one specific use. It does not mean the product works for everyone, is available everywhere, or will succeed commercially.

Development stages, sourced

Elsewhere in the pipeline

Selected therapies and technologies at every stage, from preclinical research to approval. Each stage is dated and linked to a primary source.

Full tracker

Stages summarise the most advanced publicly documented status for the named use. “Approved” applies to specific indications and regions only. Nothing here is medical or investment advice.