drugset / Trial / NCT04857177

A Study To Evaluate CKD-701 and Lucentis® in Patients With Neovascular(Wet) Age Related Macular Degeneration

NCT04857177

Phase 3 Completed 312 enrolled Chong Kun Dang Pharmaceutical
RandomizedParallel-groupDouble-blindTreatment

Summary

This is a multicenter, randomized, double-blind, active-controlled, parallel group, Phase III Clinical Trial To Evaluate the Efficacy, Safety, Pharmacokinetics and Immunogenicity of CKD-701 and Lucentis® in Patients with Neovascular(wet) Age related Macular Degeneration

Timeline

Start
2018-10-19
Primary completion
2021-03-17
Completion
2021-03-17

Drugs

EvaluationDrugModalityDoseRoute
Subject CKD-701 Unknown 0.5 mg Intravitreal
Comparator Ranibizumab Monoclonal antibody 0.5 mg Intravitreal