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Study identifier: NCT07158775 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

A Phase 1/2 Study to Evaluate the Safety and Efficacy of Intravitreal Administration of BS01 in Patients With Geographic Atrophy Secondary to Dry AMD

Condition: Geographic Atrophy (GA) Secondary to Dry Age-related Macular Degeneration (AMD)  ·  Sponsor: Bionic Sight LLC

PhasePhase 1/Phase 2
Planned participants40
Who can joinAll sexes, 50 Years to 85 Years
Healthy volunteersNo

About this study

This is a Phase 1/2 study, multi-center, dose-escalation interventional study of BS01 in subjects with GA secondary to dry AMD. Part 1 is an open label dose-escalation study; Part 2 is a dose-expansion study with dose(s) selected from Part 1 based on a benefit/risk assessment, and an untreated (sham injection) group to allow for a controlled comparison of efficacy and safety. This is a seamless Phase 1/2 study in up to 10 patients for Phase 1 and 30 patients Phase 2 in patients with GA secondary to dry AMD.

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

Talk to the study team

Sheila Nirenberg, PhD+  ·  1+9178425027  ·  snsheilan@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

NJ RetinaEdison, New Jersey, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07158775