drugset / Trial / NCT02247531

A Study Investigating the Safety and Efficacy of Lampalizumab Intravitreal Injections in Participants With Geographic Atrophy Secondary to Age-Related Macular Degeneration

NCT02247531 ↗

Phase 3 Terminated 975 enrolled Hoffmann-La Roche
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study is a Phase III, double-masked, multicenter, randomized, sham injection-controlled study evaluating the efficacy and safety of lampalizumab administered by intravitreal injections in participants with geographic atrophy (GA) secondary to age-related macular degeneration (AMD).

Timeline

Start
2014-10-06
Primary completion
2018-01-23
Completion
2018-01-23

Outcome

Missed primary endpoint

paper CONCLUSIONS AND RELEVANCE: In Chroma and Spectri, the largest studies of GA conducted to date, lampalizumab did not reduce GA enlargement vs sham during 48 weeks of treatment. PMID 29801123 ↗

release “The primary endpoint has not been met in Spectri, the first of two phase III studies evaluating the safety and efficacy of lampalizumab” gene.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Lampalizumab Monoclonal antibody 10 mg Intravitreal