drugset / Trial / NCT03223714

Conbercept Ophthalmic Injection for Patients of Central Retinal Vein Occlusion

NCT03223714

Phase 3 Completed 242 enrolled Chengdu Kanghong Biotech Co., Ltd.
RandomizedParallel-groupTriple-blindTreatment

Summary

This study evaluates the efficacy and safety of Conbercept ophthalmic injection. This is a multi-center, randomized, double-masked, placebo-controlled phase III clinical study. 237 patients with central retinal vein occlusion(CRVO) are expected to be enrolled in the study and randomly assigned into the Conbercept ophthalmic injection treatment group or the control group at a ratio of 2:1.

Timeline

Start
2016-05-24
Primary completion
2020-04-13
Completion
2020-09-28

Drugs

EvaluationDrugModalityDoseRoute
Subject Conbercept Protein / enzyme biologic 0.5 mg Intravitreal