RecruitingPhase 1Phase 2NCT05663710

Phase 1b/2 Study of Combination 177Lu Girentuximab Plus Cabozantinib and Nivolumab in Treatment naïve Patients With Advanced Clear Cell RCC


Sponsor

M.D. Anderson Cancer Center

Enrollment

100 participants

Start Date

Jun 30, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

To learn if giving 177Lu girentuximab in combination with cabozantinib plus nivolumab can help to control advanced clear cell renal cell carcinoma (ccRCC).


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study tests a new combination of three cancer treatments — a targeted radioactive drug (177Lu girentuximab), a multi-kinase inhibitor (cabozantinib), and an immunotherapy drug (nivolumab) — in people who have advanced kidney cancer (clear cell renal cell carcinoma) that has not been treated before. **You may be eligible if...** - You are 18 or older - You have been diagnosed with advanced (metastatic or locally advanced) clear cell kidney cancer - You have not received any prior treatment for your kidney cancer - You have at least one measurable tumor on scans - You are in good health (ECOG 0–1) - Your kidney, liver, and blood counts meet the study requirements **You may NOT be eligible if...** - You have received prior treatment for kidney cancer - Your cancer is not clear cell subtype - You are pregnant or breastfeeding - Your organ function does not meet the study's requirements - You are unwilling to use effective contraception during and after the study 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

DRUG177Lu girentuximab

Given by IV (vein)

DRUGNivolumab

Given by IV (vein)

DRUGCabozantinib

Given by PO

DRUGArabinoFuranosylGuanine [18F]F-AraG

Given by IV (vein)


Locations(1)

MD Anderson Cancer Center

Houston, Texas, United States

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NCT05663710


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