At a glance
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A Phase II, Multicenter, Randomized, Single-Masked, Sham Injection-Controlled Exposure-Response Study of Lampalizumab Intravitreal Injections Administered Every Two Weeks or Every Four Weeks to Patients With Geographic Atrophy
In Brief
A Phase 2 clinical trial evaluating Sham and Lampalizumab for Geographic Atrophy. Completed, enrolled 96 participants across 36 sites.
Detailed Summary
This multicenter, randomized, single-masked, sham injection-controlled study will investigate the exposure-response and safety of lampalizumab administered intravitreally every 2 weeks (Q2W) or every 4 weeks (Q4W) for 24 weeks in participants with geographic atrophy (GA) secondary to age-related macular degeneration (AMD). A safety run-in assessment will be conducted prior to initiating enrollment in the randomized study.
Study Details
Timeline
Interventions
Sham injection will be administered as a matching intravitreal injection of lampalizumab.
10 mg dose of lampalizumab administered intravitreally