Avutometinib and Defactinib in Diffuse Gastric Cancer
Part of paid clinical trials in New York, New York.
- Sponsor
- Ryan H. Moy, MD, PhD
- Study ID
- NCT06487221
- Phase
- PHASE2
- Status
- Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Avutometinib — DRUG3.2mg orally
- Defactinib — DRUG200 mg orally
Study Details
The purpose of this study is to determine if the combination study treatment with avutometinib and defactinib will prolong life in participants, is effective in decreasing the size of the tumor(s), and if it is safe in subjects with diffuse-type stomach cancer.
Key Dates
- Start date
- Oct 28, 2024
- Status verified
- Oct 2025
- Primary completion
- Nov 30, 2028
- Completion
- May 30, 2029
Study Design
- Enrollment
- 27 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Avutometinib & DefactinibAvutometinib: Study participants will receive Avutometinib 3.2mg orally two times per week for three weeks in a row followed by one week of rest Defactinib: Study participants will receive Defactinib 200mg twice daily for three weeks in a row followed by one week of rest
Primary Outcome Measure
Progression-free survival (PFS) Rate [ Time Frame: 6 months ]
Central Contacts
- Research Nurse Navigator212-342-5162
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Columbia University Irving Medical Center | New York | New York | 10032 | Ryan Moy, MD, PhD (PRINCIPAL_INVESTIGATOR) |
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