RecruitingPhase 2NCT05502315

Study of Cabozantinib and Nivolumab in Metastatic Castration Resistant Prostate Cancer

A Phase 2 Study of Cabozantinib and Nivolumab in Metastatic Castration Resistant Prostate Cancer


Sponsor

Rana McKay, MD

Enrollment

47 participants

Start Date

Feb 2, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

This is a multicenter, single-arm, two-stage open-label phase 2 study of the combination of cabozantinib + nivolumab in subjects with advanced castration-resistant prostate cancer (CRPC).


Eligibility

Sex: MALEMin Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing the combination of two cancer drugs — cabozantinib (a targeted therapy) and nivolumab (an immunotherapy) — in men with metastatic castration-resistant prostate cancer (mCRPC), meaning prostate cancer that has spread and is no longer responding to hormone therapy. **You may be eligible if...** - You are a male 18 or older with prostate cancer confirmed by biopsy - Your cancer has spread (metastatic) and is progressing despite very low testosterone levels - Your overall health is acceptable (ECOG status 0–2) **You may NOT be eligible if...** - You have pure small cell (neuroendocrine) prostate cancer - You have uncontrolled heart disease or other serious medical conditions - Your organ function does not meet study requirements Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGCabozantinib

40 mg taken orally

DRUGNivolumab

480 mg by infusion


Locations(4)

University of California San Diego

La Jolla, California, United States

University of Chicago Medical Center

Chicago, Illinois, United States

University of Texas Southwestern Medical Center

Dallas, Texas, United States

University of Wisconsin

Madison, Wisconsin, United States

View Full Details on ClinicalTrials.gov

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NCT05502315


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