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Clinical Trials in the USA / NCT05669482
Active, not recruiting Phase 1/2

Study of Avutometinib (VS-6766) +Defactinib With Gemcitabine and Nab-paclitaxel in Patients With Pancreatic Cancer

NCT05669482 · tracked via the Priya Life Science USA tracker
Sponsor
Verastem, Inc.
Phase
Phase 1/2
Started
2023-03-22
Last updated
2025-09-02

Condition(s) studied

KRAS Activating MutationMetastatic CancerPancreas CancerNeoplasms PancreaticMalignant Neoplasm of Pancreas

Investigational drug(s) / intervention(s)

avutometinib (VS-6766) and defactinib in combination with gemcitabine and nab-paclitaxel

avutometinib (VS-6766) and defactinib in combination with gemcitabine and nab-paclitaxel: The RP2D of avutometinib (VS-6766) and defactinib in combination with gemcitabine and nab-paclitaxel determined in Part A will be used in Part B dose expansion.

Study summary

This study will assess the safety and efficacy of avutometinib (VS-6766) and defactinib in combination with gemcitabine and nab-paclitaxel in patients with Pancreatic Ductal Adenocarcinoma (PDAC) who have been previously untreated.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: * Male or female subjects ≥ 18 years of age * Histologic or cytologic evidence of metastatic pancreatic ductal adenocarcinoma. * An Eastern Cooperative Group (ECOG) performance status ≤ 1 * Measurable disease according to RECIST 1.1 * Adequate organ function * Adequate cardiac function * Agreement to use highly effective method of contraceptive Exclusion Criteria: * Patients with pancreatic neuroendocrine tumors * Prior or concomitant treatment for metastatic pancreatic ductal adenocarcinoma * Prior treatment with inhibitors of the RAS /MAPK pathway \[e.g. MEK inhibitors\] or inhibitors of FAK * History of prior malignancy, with the exception of curatively treated malignancies * Major surgery within 4 weeks (excluding placement of vascular access) * Concurrent heart disease or severe obstructive pulmonary disease * Concurrent ocular disorders * Active skin disorder that has required systemic therapy within the past 1 year * Patients with interstitial lung disease or pulmonary fibrosis or severe lung disease, pulmonary edema, and adult respiratory distress syndrome * Known SARS-Cov2 infection ≤28 days prior to first dose of study therapy

Primary outcome measure(s)

Trial sites (12)

FacilityCityRegionStatus
UCSF Helen Diller Family Comprehensive Cancer Center San Francisco California
University of Chicago Chicago Illinois
Dana Farber Cancer Institute Boston Massachusetts
University of Michigan Cancer Center Ann Arbor Michigan
Washington University School of Medicine St Louis Missouri
Laura & Isaac Perlmutter Cancer Center at NYU Langone Health New York New York
New York Presbyterian/Weill-Cornell Medical Center New York New York
Memorial Sloan Kettering Cancer Center New York New York
University of Pennsylvania Philadelphia Pennsylvania
University of Utah Huntsman Cancer Institute Salt Lake City Utah
Virginia Mason Medical Center Seattle Washington
Fred Hutchinson Cancer Center Seattle Washington
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05669482 on ClinicalTrials.gov ↗ ← All trials in the USA