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Clinical Trial Summary

This is a dose finding study designed to evaluate the efficacy, safety, and pharmacokinetics of danicopan in participants with GA secondary to AMD. The study consists of a Screening Period of up to 6 weeks, a 104-week masked Treatment Period, followed by a 30-day Follow-up after the last dose. This study will have 4 treatments arms: 100 milligrams (mg) twice daily (bid), 200 mg bid, 400 mg once daily (qd), and matching placebo.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05019521
Study type Interventional
Source Alexion Pharmaceuticals, Inc.
Contact
Status Active, not recruiting
Phase Phase 2
Start date August 23, 2021
Completion date August 14, 2025

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