drugset / Trial / NCT04058535

Clinical Study of ALT-L9 to Determine Safety, Efficacy and Pharmacokinetics in Neovascular AMD

NCT04058535

Phase 1 Completed 28 enrolled Alteogen, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

To evaluate the safety, efficacy and pharmacokinetics of repeated intravitreal administration of ALT-L9 2 mg/50uL compared with Eylea in patients with neovascular Age-related macular degeneration.

Timeline

Start
2020-02-05
Primary completion
2020-12-22
Completion
2020-12-22

Drugs

EvaluationDrugModalityDoseRoute
Subject ALT-L9 Unknown 2 mg Intravitreal
Comparator Aflibercept Protein / enzyme biologic 0.05 ml Intravitreal