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

RecruitingPhase 2

A Phase 2, Open-label Study of VS-7375, an Oral KRAS G12D (ON/OFF) Inhibitor, With and Without an Anti-EGFR Antibody, and With an Anti-EGFR Antibody and Chemotherapy, in Patients With Metastatic KRAS G12D-Mutated Colorectal Adenocarcinoma (TARGET-D 203)

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
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

About the study

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

What is being tested

Sponsor: Verastem, Inc. · Participants: 150 · Started: Jul 28, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07659795

Locations in the U.S.

CaliforniaSTART Los Angeles, Los Angeles
Valkyrie Clinical Trials (contact for more locations), Los Angeles
FloridaMoffitt Cancer Center, Tampa
IndianaIndiana University, Simon Comprehensive Cancer Center, Indianapolis
MichiganSTART Midwest, Grand Rapids
MissouriWashington University, St Louis
New JerseySTART New Jersey, East Brunswick
New YorkPerlmutter Cancer Center at NYU Langone Health (contact for more locations), New York
TennesseeSarah Cannon Research Institute Oncology Partners, Nashville
TexasSTART Dallas Fort Worth, Fort Worth
The University of Texas MD Anderson Cancer Center, Houston
UtahSTART Mountain Region, West Valley City
VirginiaUVA Comprehensive Cancer Center, Charlottesville
Virginia Cancer Specialists, Fairfax
WashingtonVirginia Mason Medical Center, Seattle

Conditions

From ClinicalTrials.gov, data retrieved Oct 2, 2026. Each study sets its own eligibility; the study team decides who can join.