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

Sponsor: Verastem, Inc.

Sponsor score: 0

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

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

  • 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

Locations

FACILITYZIPCITYSTATE
START Los Angeles90025Los AngelesCalifornia
START Midwest49546Grand RapidsMichigan
START New Jersey08816East BrunswickNew Jersey
START Dallas Fort Worth76104Fort WorthTexas
START Mountain Region84119West Valley CityUtah

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