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RecruitingNCT05787561

A Study of Avutometinib (VS-6766) and Defactinib in People With Mesonephric Gynecologic Cancer

Single Arm Phase II Study of Avutometinib (VS-6766) and Defactinib in Advanced or Recurrent Mesonephric Gynecologic Cancer

Status
Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
40 (estimated)
Sponsor
Memorial Sloan Kettering Cancer Center · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study will test if Avutometinib (VS-6766) in combination with Defactinib is an effective treatment for advanced or recurrent mesonephric gynecologic cancer.

Conditions

Interventions

TypeNameDescription
DRUGAvutometinib (VS-6766)3.2 mg PO, twice weekly
DRUGDefactinib200 mg PO BID for 3 weeks, followed by a 1 week rest period, in each 4-week (28 day) cycle.

Timeline

Start date
2023-03-15
Primary completion
2027-03-01
Completion
2027-03-01
First posted
2023-03-28
Last updated
2026-03-12

Locations

7 sites across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT05787561. Inclusion in this directory is not an endorsement.

A Study of Avutometinib (VS-6766) and Defactinib in People With Mesonephric Gynecologic Cancer (NCT05787561) · Clinical Trials Directory