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RECRUITING Phase 3

A Study of Avutometinib (VS-6766) + Defactinib (VS-6063) in Recurrent Low-Grade Serous Ovarian Cancer

NCT06072781 · View on ClinicalTrials.gov ↗

Study Summary

This study will assess the safety and efficacy of avutometinib (VS-6766) in combination with defactinib versus Investigator's choice of treatments (ICT) in subjects with recurrent LGSOC who have progressed on a prior platinum-based therapy.

Interventions

  • DRUG Defactinib
  • DRUG Paclitaxel
  • DRUG Letrozole
  • DRUG Pegylated liposomal doxorubicin
  • DRUG avutometinib

Study Locations (20)

Florida

  • Florida Cancer Specialists - South — Fort Myers
  • Mount Sinai — Miami Beach
  • AdventHealth — Orlando
  • Moffitt Cancer Center — Tampa
  • Florida Cancer Specialists Research East — West Palm Beach

California

  • UCLA Health — Los Angeles
  • UC Davis — Sacramento
  • University of California, San Francisco — San Francisco

New York

  • Roswell Park Cancer Institute — Buffalo
  • Memorial Sloan Kettering Cancer Center — New York

Arizona

  • HonorHealth — Phoenix

Arkansas

  • University of Arkansas — Little Rock

Connecticut

  • Yale University — New Haven

Georgia

  • Winship Cancer Institute at Emory University — Atlanta

Illinois

  • NorthShore University HealthSystem — Evanston

Trial Details

FieldValue
Enrollment Target 270 participants
Start Date 2024-03-18
Est. Completion 2031-02-09
Phase Phase 3

Sponsor

Verastem

7 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06072781

The ClinicalTrials.gov registry entry for NCT06072781 describes a study currently listed as recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 270 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Verastem, which has 7 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Low Grade Serous Ovarian Cancer appearing as the primary indexed condition, and to 5 interventions — of which Defactinib is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06072781 reports 20 study locations spanning 13 distinct geographic areas — top geographies include Florida, California, New York. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06072781 about?

NCT06072781 is a clinical study titled "A Study of Avutometinib (VS-6766) + Defactinib (VS-6063) in Recurrent Low-Grade Serous Ovarian Cancer". This study will assess the safety and efficacy of avutometinib (VS-6766) in combination with defactinib versus Investigator's choice of treatments (ICT) in subjects with recurrent LGSOC who have progressed on a prior platinum-based therapy.

What is the current status of trial NCT06072781?

This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 270 participants. The study started on 2024-03-18. Estimated completion is 2031-02-09.

What conditions does trial NCT06072781 study?

This clinical trial studies the following conditions: Low Grade Serous Ovarian Cancer. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06072781?

The interventions under investigation include: Defactinib (DRUG), Paclitaxel (DRUG), Letrozole (DRUG), Pegylated liposomal doxorubicin (DRUG), avutometinib (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06072781?

This trial is sponsored by Verastem, which has 7 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06072781 being conducted?

This trial has 20 study locations across Arizona, Arkansas, California, Connecticut, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial