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RECRUITING
NCT07050433

COMPASS Study for Metastatic Castration-resistant Prostate Cancer

Sponsor: Duke University

View on ClinicalTrials.gov

Summary

This study is a companion to the SYNERGY-201 clinical trial (NCT06228053), which investigates SX-682 and enzalutamide in individuals with prostate cancer. Individuals must be participating in SYNERGY-201 in order to participate in this study. The purpose of this companion study is to learn more about biomarkers, particularly a biomarker called CXCR2, and investigate if CXCR2 can predict who will receive benefit from the SYNERGY-201 drug combination. This study will also investigate how CXCR2 and other biomarkers change over time when participants receive the SYNERGY-201 drug combination. CXCR2 is of particular interest because the SYNERGY-201 drug, SX-682, inhibits CXCR2. After participants provide consent, blood samples will be collected for research purposes at three SYNERGY-201 visits (Baseline, Cycle 3 Day 1 and End of Study Drug). Up to 20 participants will also receive tumor biopsies at the Baseline and SYNERGY-201 Cycle 3 Day 1 visits. Clinical and study data collected as part of SYNERGY-201 will also be used for this study.

Official title: COMPASS: Correlative COMPAnion Study to Predict SYNERGY-201 Clinical Trial Responders

Key Details

Gender

MALE

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

48

Start Date

2025-08-07

Completion Date

2028-01-01

Last Updated

2026-05-04

Healthy Volunteers

No

Conditions

Interventions

DIAGNOSTIC_TEST

CXCR2 as a biomarker

CXCR2 biomarker expression will be measured in tumor and immune cell samples

Locations (3)

UCSF Helen Diller Family Comprehensive Cancer Center

San Francisco, California, United States

Rogel Cancer Center

Ann Arbor, Michigan, United States

Duke University

Durham, North Carolina, United States