🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Writer Login
Latest
Clinical Trials in the USA / NCT07659795
Recruiting Phase 2

A Phase 2 Study of VS-7375 in Patients With KRAS G12D-Mutated Colorectal Cancer

NCT07659795 · tracked via the Priya Life Science USA tracker
Sponsor
Verastem, Inc.
Phase
Phase 2
Started
2026-07-28
Last updated
2026-09-16

Condition(s) studied

Colorectal Cancer

Investigational drug(s) / intervention(s)

VS-7375cetuximabpanitumumabCetuximab + mFOLFOX6

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

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: * Histopathology confirmed metastatic CRC * Measurable disease per RECIST 1.1 * Local testing confirmed KRAS G12D mutation (tissue required for confirmatory central testing) * ECOG PS=0 or 1 2L+ patients: * Must have received at least 1 standard chemotherapy for metastatic colorectal adenocarcinoma * Have documented disease progression during or following their most recent prior line of therapy * Have either stable disease, partial response (PR), or complete response (CR) by RECIST v1.1 as the best overall response (BOR) during at least 1 prior systemic therapy. 1L patients: * Treatment-naïve or received no more than 1 cycle of standard systemic therapy for metastatic disease. Exclusion Criteria: * Have any other documented co-existing common RAS mutation(s) * Prior anti-cancer Tx within 4 weeks or drug-specific timeline within first treatment dose, whichever shorter * Major surgery within 4 weeks of first treatment dose * Radiation therapy (RT) within 1 week of first treatment dose * Receipt of prior direct RAS inhibitor * Receipt of more than 1 investigational therapy * Untreated or symptomatic CNS metastasis * Receipt of strong CYP3A4 inhibitor/inducer or CYP3A4 sensitive substrates with narrow therapeutic index within 14 days or drug-specific timeline within first treatment dose, whichever is shorter * Receipt of PPI or H2 blocker within 5 days * Inability to swallow oral medication * Other protocol-defined inclusion/exclusion criteria may apply

Primary outcome measure(s)

Trial sites (16)

FacilityCityRegionStatus
START Los Angeles Los Angeles California Recruiting
Valkyrie Clinical Trials (contact for more locations) Los Angeles California 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
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 Mason Medical Center Seattle Washington Recruiting
Macquarie University Hospital Macquarie Park 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 the USA

Other trials for the same condition

Official registry record

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 the USA