A Phase 2 Study of VS-7375 in Patients With KRAS G12D-Mutated Colorectal Cancer
Condition(s) studied
Investigational drug(s) / intervention(s)
VS-7375: Taken by mouth
cetuximab: Intravenous infusion
panitumumab: Intravenous infusion
Cetuximab + mFOLFOX6: Intravenous infusion
Study summary
This study will assess the safety and efficacy of VS-7375 alone and in combination with cetuximab or panitumumab and cetuximab plus mFOLFOX in patients with metastatic KRAS G12D - mutated Colorectal Cancer
Eligibility
Primary outcome measure(s)
- Confirmed ORR by blinded independent central review (BICR) per RESIST v1.1 - 2L CRC only — 6 months
Overall Response Rate per RECIST version 1.1, per blinded independent central review (BICR) - To characterize the safety and tolerability of VS-7375 monotherapy or in combination with cetuximab or panitumumab, administered on a daily oral schedule in participants with KRAS G12D-mutated 2L+ CRC — 6 months
Proportion/number of participants with AEs, TEAEs, TRAEs, SAEs, and dose interruptions/reductions and discontinuations - To characterize the safety and tolerability of VS-7375 in combination with cetuximab + mFOLFOX, administered on a daily oral schedule in participants with KRAS G12D-mutated 1L CRC — 6 months
Proportion/number of participants with AEs, TEAEs, TRAEs, SAEs, and dose interruptions/reductions and discontinuations
Trial sites (23)
| Facility | City | Region | Status |
|---|---|---|---|
| START Los Angeles | Los Angeles | California | Recruiting |
| Valkyrie Clinical Trials (contact for more locations) | Los Angeles | California | Recruiting |
| BRCR - Tamarac | Tamarac | Florida | Recruiting |
| Moffitt Cancer Center | Tampa | Florida | Recruiting |
| Indiana University, Simon Comprehensive Cancer Center | Indianapolis | Indiana | Recruiting |
| START Midwest | Grand Rapids | Michigan | Recruiting |
| Washington University | St Louis | Missouri | Recruiting |
| START New Jersey | East Brunswick | New Jersey | Recruiting |
| Perlmutter Cancer Center at NYU Langone Health (contact for more locations) | New York | New York | Recruiting |
| University of North Carolina | Chapel Hill | North Carolina | Recruiting |
| Case Western, University Hospitals Cleveland Medical Center | Cleveland | Ohio | Recruiting |
| Sarah Cannon Research Institute Oncology Partners | Nashville | Tennessee | Recruiting |
| START Dallas Fort Worth | Fort Worth | Texas | Recruiting |
| The University of Texas MD Anderson Cancer Center | Houston | Texas | Recruiting |
| START Mountain Region | West Valley City | Utah | Recruiting |
| UVA Comprehensive Cancer Center | Charlottesville | Virginia | Recruiting |
| Virginia Cancer Specialists | Fairfax | Virginia | Recruiting |
| Virginia Mason Medical Center | Seattle | Washington | Recruiting |
| University of Wisconsin | Madison | Wisconsin | Recruiting |
| Macquarie University Hospital | Macquarie Park | New South Wales | Recruiting |
| Calvary Mater Newcastle | Waratah | New South Wales | Recruiting |
| Icon Cancer Centre South Brisbane | South Brisbane | Queensland | Recruiting |
| Icon Cancer Centre Adelaide | Kurralta Park | South Australia | Recruiting |
More Verastem, Inc. trials in Australia
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07659795 on ClinicalTrials.gov ↗ ← All trials in Australia