Condition: Choroidal Melanoma · Indeterminate Lesions · Uveal Melanoma · Sponsor: Aura Biosciences
The primary objective is to determine the safety and efficacy of belzupacap sarotalocan (bel-sar) compared to sham control in patients with primary indeterminate lesions (IL) or small choroidal melanoma (CM).
This description comes directly from the study's public registry record.
Medical Monitor · 617-500-8864 · clinical@aurabiosciences.com
Always discuss trial participation with your own doctor first.
| Retina Consultants of Alabama | Birmingham, Alabama, United States | Withdrawn |
| UCSD Shiley Eye Institute, Jacobs Retina Center | La Jolla, California, United States | Recruiting |
| Doris Stein Eye Research Center | Los Angeles, California, United States | Recruiting |
| Stanford University School of Medicine | Palo Alto, California, United States | Recruiting |
| Retinal Consultants Medical Group, Inc. | Sacramento, California, United States | Recruiting |
| Bascom Palmer Eye Institute | Miami, Florida, United States | Withdrawn |
| Retina Associates of Florida, PA | Tampa, Florida, United States | Recruiting |
| Emory Eye Center | Atlanta, Georgia, United States | Recruiting |
| University of Illinois at Chicago | Chicago, Illinois, United States | Recruiting |
| Tufts Medical Center New England Eye Center | Boston, Massachusetts, United States | Recruiting |
| Massachusetts Eye and Ear | Boston, Massachusetts, United States | Recruiting |
| W.K. Kellogg Eye Center - University of Michigan | Ann Arbor, Michigan, United States | Recruiting |
+ 59 more locations — full list on the registry record.
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.
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/NCT06007690