drugset / Trial / NCT05893537

Study to Evaluate the Efficacy and Safety of Oral CT1812 in Participants With Geographic Atrophy (GA) Secondary to Dry Age-Related Macular Degeneration (AMD).

NCT05893537

Phase 2 Terminated 100 enrolled Cognition Therapeutics
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a Phase 2, prospective, multicenter, randomized, double-masked, placebo-controlled 104-week study to assess the efficacy, safety, and tolerability of orally delivered CT1812 compared to placebo in participants with GA associated with dry AMD.

Timeline

Start
2023-06-16
Primary completion
2025-03-04
Completion
2025-03-28

Drugs

EvaluationDrugModalityDoseRoute
Comparator CT1812 Small molecule 200 mg Oral