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Spots Global Cancer Trial Database for A Study of Avelumab, Binimetinib and Talazoparib in Patients With Locally Advanced or Metastatic RAS-mutant Solid Tumors

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We do not endorse or review these studies in any way.

Trial Identification

Brief Title: A Study of Avelumab, Binimetinib and Talazoparib in Patients With Locally Advanced or Metastatic RAS-mutant Solid Tumors

Official Title: A PHASE 1B/2 STUDY TO EVALUATE SAFETY AND CLINICAL ACTIVITY OF COMBINATIONS OF AVELUMAB, BINIMETINIB AND TALAZOPARIB IN PATIENTS WITH LOCALLY ADVANCED OR METASTATIC RAS-MUTANT SOLID TUMORS

Study ID: NCT03637491

Study Description

Brief Summary: This Phase 1b/2 study will examine the effects of the study drugs, avelumab, binimetinib and talazoparib when given in a 2 (doublet) or 3 (triplet) drug combination, in patients with locally advanced or metastatic RAS-mutant solid tumors. The Phase 1b part of the study will assess if the different study drugs can be given together safely and which doses to use for further research. Phase 2 will test if the study treatments have an effect on tumor size and growth, and gather more information about potential side effects.

Detailed Description: This is a Phase 1b/2, open label, multi-center, safety, clinical activity, pharmacokinetic (PK), and pharmacodynamics (PD) study of combinations of avelumab, binimetinib and talazoparib in adult patients with metastatic pancreatic ductal adenocarcinoma and other locally advanced or metastatic KRAS- or NRAS-mutant solid tumors. The Phase 1b part of this study will initially assess doublet drug combinations to determine a recommended dose for further investigation. Following this, the recommended dose for the combination of avelumab, binimetinib and talazoparib (triplet) will be determined. The recommended doses for the doublet and triplet combinations will be used in the Phase 2 part of the study, which will assess the safety and preliminary anti-tumor activity of the study treatments.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Highlands Oncology Group, Fayetteville, Arkansas, United States

Highlands Oncology Group, Rogers, Arkansas, United States

Highlands Oncology Group, Springdale, Arkansas, United States

California Cancer Associates for Research and Excellence, Inc (cCARE), Encinitas, California, United States

University of Colorado Denver CTO (CTRC), Aurora, Colorado, United States

University of Colorado Hospital, Aurora, Colorado, United States

Horizon Oncology Research, LLC, Lafayette, Indiana, United States

UPMC Hillman Cancer Center, Pittsburgh, Pennsylvania, United States

The University of Texas MD Anderson Cancer Center, Houston, Texas, United States

University of Utah, Huntsman Cancer Hospital, Salt Lake City, Utah, United States

University of Utah, Huntsman Cancer Institute, Salt Lake City, Utah, United States

Institut Jules Bordet, Brussels, , Belgium

UZ Gent, Gent, , Belgium

Singapore National Eye Centre, Singapore, , Singapore

Singapore General Hospital, Singapore, , Singapore

SingHealth Investigational Medicine Unit, Singapore, , Singapore

National Heart Centre Singapore, Singapore, , Singapore

National Cancer Centre Singapore, Singapore, , Singapore

Contact Details

Name: Pfizer CT.gov Call Center

Affiliation: Pfizer

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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