A Phase 2 Study of VS-7375 in Patients With KRAS G12D-Mutated Colorectal Cancer
Sponsor: Verastem, Inc.
ClinicalTrials ID:NCT07659795
This Phase 2 trial evaluates the safety and efficacy of VS-7375, alone or with cetuximab, panitumumab, or cetuximab plus mFOLFOX, in metastatic KRAS G12D-mutated colorectal cancer. Eligible patients must have confirmed metastatic CRC, measurable disease, and specific prior treatment history. Interventions include oral VS-7375 and intravenous infusions of other drugs.
Patient Parameters
| Parameter | Options |
|---|
Program Overview
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 Criteria
Inclusion Criteria
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Histopathology confirmed metastatic CRC
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Measurable disease per RECIST 1.1
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Local testing confirmed KRAS G12D mutation (tissue required for confirmatory central testing)
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ECOG PS=0 or 1
2L+ patients:
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Must have received at least 1 standard chemotherapy for metastatic colorectal adenocarcinoma
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Have documented disease progression during or following their most recent prior line of therapy
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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:
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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
Locations
| FACILITY | ZIP | CITY | STATE |
|---|---|---|---|
| START Los Angeles | 90025 | Los Angeles | California |
| START Midwest | 49546 | Grand Rapids | Michigan |
| START New Jersey | 08816 | East Brunswick | New Jersey |
| START Dallas Fort Worth | 76104 | Fort Worth | Texas |
| START Mountain Region | 84119 | West Valley City | Utah |
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