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intismeran autogene

Generic: Intismeran Autogene

intismeran autogene: 8 clinical trials tracked.

intismeran autogene evidence translation

What we can confirm

8 tracked trials

No verified listed company relationship

What it means

AI will separate confirmed drug evidence from unknown company context.

What to watch

Watch trial status, endpoints, and the next source-backed update.
BioSniper AIPage evidence connected

Prepared research question

What is verified about intismeran autogene, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence4 indications · 0 study sponsors

Study sponsors

No additional listed-company sponsor is linked.

Clinical Trial Registry Records (8)

A Phase 2, Randomized, Double-Blind, Placebo-Controlled Study of V940 in Combination With Pembrolizumab and Chemotherapy as First-Line Treatment for Participants With Metastatic Squamous NSCLC (INTerpath-013)

NCT07221474Registry updated 2026-08-21·Phase 2
Recruiting

Primary endpoint: Progression Free Survival (PFS)

InterventionalRandomizedtriple180 targetStarted 2025-12Completion 2031-0550 sites · Argentina, Australia, Chile, France…Merck Sharp & Dohme LLC

A Phase 2, Randomized, Double-Blind, Placebo- and Active-Comparator-Controlled Clinical Study of V940 (mRNA-4157) Plus Pembrolizumab Versus Placebo Plus Pembrolizumab in Participants With First-Line Advanced Melanoma (INTerpath-012)

NCT06961006Registry updated 2026-07-02·Phase 2
Recruiting

Primary endpoint: Progression-free Survival (PFS)

InterventionalRandomizedtriple160 targetStarted 2025-05Completion 2031-0938 sites · Australia, Canada, France, Germany…Merck Sharp & Dohme LLC

A Phase 2 Open-label Randomized Study of V940 in Combination With BCG Versus BCG Monotherapy in Participants With High-risk Non-muscle Invasive Bladder Cancer (INTerpath-011)

NCT06833073Registry updated 2026-09-14·Phase 2
Recruiting

Primary endpoint: Cohort A: Event-free Survival (EFS)

InterventionalRandomizedopen308 targetStarted 2025-03Completion 2031-0950 sites · Argentina, Australia, Brazil, Canada…Merck Sharp & Dohme LLC

A Phase 3 Randomized Double-blind Study of Adjuvant Pembrolizumab With or Without V940 in Participants With Resectable Stage II to IIIB (N2) NSCLC Not Achieving pCR After Receiving Neoadjuvant Pembrolizumab With Platinum-based Doublet Chemotherapy (INTerpath-009)

NCT06623422Registry updated 2026-08-27·Phase 3
Recruiting

Primary endpoint: Disease-Free Survival (DFS)

InterventionalRandomizeddouble680 targetStarted 2024-10Completion 2038-0150 sites · United StatesMerck Sharp & Dohme LLC

A Phase 2, Randomized, Double-blind, Clinical Study of V940 (mRNA-4157) Plus Pembrolizumab (MK-3475) Versus Placebo Plus Pembrolizumab in the Adjuvant Treatment of Participants With Renal Cell Carcinoma (INTerpath-004).

NCT06307431Registry updated 2026-07-13·Phase 2
Active, not recruiting

Primary endpoint: Disease-Free Survival (DFS)

InterventionalRandomizedtriple272 targetStarted 2024-04Completion 2032-0650 sites · Argentina, Australia, Canada, Chile…Merck Sharp & Dohme LLC

A Phase 3, Randomized, Double-blind, Placebo- and Active-Comparator-Controlled Clinical Study of Adjuvant V940 (mRNA-4157) Plus Pembrolizumab Versus Adjuvant Placebo Plus Pembrolizumab in Participants With Resected Stage II, IIIA, IIIB (N2) Non-small Cell Lung Cancer (INTerpath-002)

NCT06077760Registry updated 2026-08-21·Phase 3
Recruiting

Primary endpoint: Disease- Free Survival (DFS)

InterventionalRandomizeddouble868 targetStarted 2023-12Completion 2035-1250 sites · United StatesMerck Sharp & Dohme LLC

A Phase 2 Randomized Study of Adjuvant Immunotherapy With the Personalized Cancer Vaccine mRNA-4157 and Pembrolizumab Versus Pembrolizumab Alone After Complete Resection of High-Risk Melanoma (KEYNOTE- 942)

NCT03897881Registry updated 2026-09-08·Phase 2
Active, not recruiting

Primary endpoint: Recurrence-Free Survival (RFS), Assessed Using Radiological Imaging

InterventionalRandomizedopen267 enrolledStarted 2019-07Completion 2032-1123 sites · Australia, United StatesModernaTX, Inc.

A Phase 1, Open-Label, Multicenter Study to Assess the Safety, Tolerability, and Immunogenicity of mRNA-4157 Alone and in Combination in Participants With Solid Tumors

NCT03313778Registry updated 2026-09-03·Phase 1
Active, not recruiting

Primary endpoint: Number of Participants with Adverse Events

Interventionalopen161 enrolledStarted 2017-08Completion 2027-1120 sites · Australia, Japan, United Kingdom, United StatesModernaTX, Inc.