Study of Avutometinib (VS-6766) + Adagrasib in KRAS G12C NSCLC Patients
← catalyst calendarSponsored by Verastem, Inc. (industry) · VSTM — their whole pipeline →. With Mirati Therapeutics Inc..
Phase
Phase 1/2
Status
Completed
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
12actual
Sites
8
Country
United States
Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →
Source: ClinicalTrials.gov, retrieved 2026-08-19
Dates
each axis at the precision it was filed, with the registry's own basis| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2022-08-01 | actual | When the study began enrolling |
| Primary completion | 2026-06-15 | actual | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2026-06-15 | actual | The whole study's end, after follow-up |
| First posted | 2022-05-17 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-07-02 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Conditions
- Non Small Cell Lung Cancer
- KRAS Activating Mutation
- Advanced Cancer
- Metastatic Cancer
- Malignant Neoplasm of Lung
- Malignant Neoplastic Disease
Intervention
- Drug: avutometinib (VS-6766) and adagrasib — also filed as KRAS G12C Inhibitor, adagrasib, KRAZATI®
Primary outcomes
what the primary-completion date above is the date OFPart A: To determine RP2D for avutometinib(VS-6766) in combination with adagrasib
measured From start of treatment to confirmation of RP2D; 28 days
To determine the efficacy of the optimal regimen identified from Part A
measured From start of treatment to confirmation of response; 16 weeks
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