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 is a randomized, sham-controlled, subject-, assessor-, and Sponsor- masked trial to establish the safety and efficacy of bel-sar treatment via suprachoroidal (SC) administration in subjects with primary IL/CM. Bel-sar treatment incorporates administration of bel-sar drug product using a suprachoroidal space (SCS) microinjector and activation of bel-sar by a laser photoactivation device.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
100
Bel-sar via suprachoroidal administration followed by laser application.
Suprachoroidal injection device
Laser application
Sham laser application
Sham injection device
Retina Consultants of Alabama
Birmingham, Alabama, United States
WITHDRAWNUCSD Shiley Eye Institute, Jacobs Retina Center
La Jolla, California, United States
RECRUITINGDoris Stein Eye Research Center
Los Angeles, California, United States
NOT_YET_RECRUITINGStanford University School of Medicine
Palo Alto, California, United States
Time to reach tumor progression
Tumor Progression
Time frame: 65 weeks
Time to composite endpoint
Tumor progression or visual acuity failure
Time frame: 65 weeks
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Retinal Consultants Medical Group, Inc.
Sacramento, California, United States
RECRUITINGBascom Palmer Eye Institute
Miami, Florida, United States
RECRUITINGRetina Associates of Florida, PA
Tampa, Florida, United States
RECRUITINGEmory Eye Center
Atlanta, Georgia, United States
RECRUITINGUniversity of Illinois at Chicago
Chicago, Illinois, United States
RECRUITINGTufts Medical Center New England Eye Center
Boston, Massachusetts, United States
RECRUITING...and 56 more locations