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Completed Phase 2 Interventional

Phase II Study of VS-6063 in Patients With KRAS Mutant Non-Small Cell Lung Cancer

ClinicalTrials.gov ID: NCT01951690

Public ClinicalTrials.gov record NCT01951690. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 5:17 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Phase II Study of VS-6063, A Focal Adhesion Kinase (FAK) Inhibitor, in Patients With KRAS Mutant Non-Small Cell Lung Cancer

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a Phase II, open-label, multicenter, multi cohort, study of VS-6063 (defactinib), a focal adhesion kinase inhibitor, in patients with KRAS mutant non-small cell lung cancer (NSCLC). NSCLC with a KRAS mutation is required for study entry and subjects will be enrolled into 1 of 4 cohorts based on the status of their INK4a/Arf and p53 mutations. The purpose of this study is to demonstrate if VS-6063 (defactinib) improves PFS within each cohort. The safety and tolerability of VS-6063, tumor response rate, progression free survival and overall survival will also be assessed. The pharmacodynamic effects of VS-6063 (defactinib) will be examined in a tumor biopsy and a blood sample.

Study identification

NCT ID
NCT01951690
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Verastem, Inc.
Industry
Enrollment
55 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 2013 (Type not available)
Primary completion
Jun 2016 (Actual)
Completion
Jun 2016 (Actual)
Last update posted
Apr 13, 2017

2013 – 2016

United States locations

U.S. sites
9
U.S. states
8
U.S. cities
9
Facility City State ZIP Site status
University of Colorado Cancer Center, Anschutz Medical Campus Denver Colorado 80045 —
Winship Cancer Institute of Emory University Atlanta Georgia 30322 —
Johns Hopkins Sidney Kimmel Comprehensive Cancer Center Baltimore Maryland 21287 —
Washington University School of Medicine St Louis Missouri 63110 —
Knight Cancer Institute, Oregon Health and Science University Portland Oregon 97239 —
University of Pittsburgh Medical Center Cancer Center Pittsburgh Pennsylvania 15232 —
Sarah Cannon Research Institute Nashville Tennessee 37203 —
University of Texas Southwestern Medical Center Dallas Texas 75390-8852 —
The University of Texas Health Science Center at San Antonio San Antonio Texas 78229-3900 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01951690, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 13, 2017 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01951690 live on ClinicalTrials.gov.

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