← Eichor
Study identifier: NCT06432036 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Yttrium-90 (Y90) Radioembolization for the Treatment of Early Stage Renal Cell Carcinoma, The RENEGADE Trial

Condition: Stage I Renal Cell Cancer · Stage II Renal Cell Cancer  ·  Sponsor: Jonsson Comprehensive Cancer Center

PhasePhase 1/Phase 2
Planned participants25
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This phase I/II trial tests the safety, side effects and effectiveness of radioembolization with yttrium-90 (Y-90) in patients with early stage renal cell carcinoma. Y-90 is a radioactive chemical that is incorporated into millions of very tiny glass spheres. These spheres are injected into the artery that feeds the cancer. This process is called radioembolization. Y-90 radioembolization may be a safe and effective treatment for patients with early stage renal cell carcinoma.

This description comes directly from the study's public registry record.

Talk to the study team

Amelia Ferrer  ·  310-906-6028  ·  acferrer@mednet.ucla.edu

Saima Chaabane  ·  (310)794-8995  ·  schaabane@mednet.ucla.edu

Always discuss trial participation with your own doctor first.

Locations (2)

UCLA / Jonsson Comprehensive Cancer CenterLos Angeles, California, United StatesRecruiting
University of Colorado Anschutz Medical CampusAurora, Colorado, United StatesRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06432036