RecruitingPhase 2NCT06627244

Study of Tebentafusp and Radioembolization in the Treatment of Metastatic Uveal Melanoma

Phase 2, Single Arm Study of Tebentafusp and Radioembolization in the Treatment of Metastatic Uveal Melanoma


Sponsor

University of Miami

Enrollment

30 participants

Start Date

Feb 14, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to determine the effects (good and bad) that Tebentafusp in combination with Yttrium-90 (Y-90) radioembolization has on patients with metastatic uveal melanoma that has spread to the liver.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This trial tests combining tebentafusp-tebn (an immune-activating cancer drug) with radioembolization (a targeted liver radiation treatment using radioactive beads called Y-90) in patients with uveal melanoma — a rare eye cancer — that has spread to the liver. **You may be eligible if...** - You are 18 or older with metastatic uveal melanoma confirmed by pathology, mainly in the liver - Your liver function tests are within acceptable limits - A pre-study mapping procedure shows the liver treatment is safe and feasible - You carry a specific immune marker (HLA-A*02:01) - Your disease is measurable or evaluable on scans **You may NOT be eligible if...** - Any single tumor is larger than 8 cm - Your bilirubin or liver enzymes are significantly elevated - You have had prior treatment with tebentafusp-tebn Talk to your doctor to see if this trial is right for you.

This is a simplified summary. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interventions

DRUGTebentafusp

Tebentafusp will be administered intravenously to participants at or within 28 days of their first Y-90 TARE procedure. This 28-day period includes the 14- to 28-day Y-90 TARE Recovery Period. For administrative purposes, one cycle of tebentafusp treatment is 28 days in length. Tebentafusp will be administered on a dose escalation schedule for Cycle 1 starting at 20 mcg on Day 1, increasing to 30 mcg on Day 8, and a final dose of 68 mcg on Day 15, which will be administered once per week until unacceptable toxicity develops, disease progression, or withdrawal of consent, whichever occurs first.

RADIATIONTheraSphere™ Yttrium-90 Trans-Arterial Radioembolization

Participants will undergo radiographic and 99mTC-labeled macroaggregated albumin (99mTc-MAA) assessment for suitability prior to Y-90 absorbed glass microsphere treatment per institutional procedures. Y-90 trans-arterial radioembolization (TARE) is a standard of care treatment for intrahepatic metastases of uveal melanoma as indicated in the National Comprehensive Cancer Network (NCCN) consensus guidelines (NCCN Guidelines®, 2023). Y-90 absorbed glass microspheres will be administered at least one time prior to initiating Tebentafusp treatment. After the Y90-TARE procedure, participants will have a 14- to 28-day Y-90 TARE Recovery Period.


Locations(1)

University of Miami

Miami, Florida, United States

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06627244


Related Trials