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

RecruitingPhase 2

A Phase 2, Open-label Study of VS-7375, an Oral KRAS G12D (ON/OFF) Inhibitor, as Monotherapy and With Cetuximab, in Patients With Metastatic KRAS G12D-Mutated Pancreatic Cancer (TARGET-D 201)

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

* Histopathology confirmed PDAC
* Measurable disease per RECIST 1.1
* Local testing confirmed KRAS G12D mutation (tissue required for confirmatory central testing)
* ECOG PS=0 or 1

Adequate organ function

VS-7375 + cetuximab (2L PDAC) :

-Received only 1 prior Tx in the metastatic setting; prior adjuvant counts as a line if progressed within 6 months

VS-7375 + cetuximab (1L PDAC) :

-Treatment-naïve or received ≤ 1 cycle of SoC 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; RT to brain or lung within 2 weeks of first treatment dose
* History of drug-induced Interstitial Lung Disease
* Receipt of prior direct RAS inhibitor
* 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 in patients with metastatic KRAS G12D - mutated Pancreatic Cancer

What is being tested

Sponsor: Verastem, Inc. · Participants: 180 · Started: Jun 16, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07644559

Locations in the U.S.

CaliforniaCedars-Sinai Medical Center, Los Angeles
START- Los Angeles, Los Angeles
Valkyrie Clinical Trials, Los Angeles
FloridaMayo Clinical Florida, Jacksonville
Moffitt Cancer Center, Tampa
MarylandJohns Hopkins University, Baltimore
MassachusettsDana-Farber Cancer Institute, Boston
Massachusetts General Hospital, Boston
MichiganUniversity of Michigan, Ann Arbor
START Midwest, Grand Rapids
MinnesotaMayo Clinical Rochester, Rochester
MissouriWashington University, St Louis
New JerseySTART New Jersey, East Brunswick
New YorkNYU-Manhattan, New York
North CarolinaUniversity of North Carolina, Chapel Hill
TennesseeSarah Cannon Research Institute, Nashville
TexasSTART Dallas, Fort Worth
MD Anderson Cancer Center, Houston
START- San Antonio, San Antonio
UtahSTART- Mountain Region, West Valley City
VirginiaUVA Health, Charlottesville
Virginia Cancer Specialists, Fairfax
WashingtonVirginia Mason, Seattle
WisconsinUW Health, Madison

Conditions

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