Avutometinib and Defactinib for Diffuse Gastric Cancer

This study is testing a combination of two oral medications, avutometinib and defactinib, for people with diffuse-type stomach cancer that has spread or cannot be removed surgically. You may be eligible if your cancer has diffuse-type cells, mixed-type cells, or specific gene changes (like CDH1 or RHOA mutations), and has continued to grow after previous chemotherapy. Avutometinib works by blocking a pathway in cancer cells called the MAP kinase pathway, specifically targeting RAF and MEK proteins. Defactinib targets a protein called FAK, which can help stomach cancer grow. The main goal is to see if this combination treatment can extend the time you live without your cancer growing or spreading. The study aims to enroll 27 participants.

Study design
This is an interventional study, meaning participants will receive a specific treatment. It plans to enroll 27 participants.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
The study will measure how long participants live without their cancer growing or spreading at 6 months.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT06487221

Avutometinib and Defactinib in Diffuse Gastric Cancer

Recruiting
PHASE2Ages 18+InterventionalTreatment
Ryan H. Moy, MD, PhD
~27 participants
Updated 2025-11-04 on ClinicalTrials.gov
What's tested:AvutometinibDefactinib

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Progression-free survival (PFS) Rate
Measured over 6 months
Gastric Cancer
Stomach Cancer
1 sites across 1 states
New York1
  • Ryan Moy, MD, PhD · PRINCIPAL_INVESTIGATOR · Columbia University

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  • Progression-free survival (PFS) Rate6 months

    To determine the efficacy of combination defactinib and avutometinib in patients with metastatic diffuse gastric cancer (DGC) as measured by 6-month progression-free survival (PFS) rate. PFS is defined as the duration of time from start of treatment to time of progression or death, whichever occurs first.