drugset / Trial / NCT02098720

An Open, Single-center, Safety and Efficacy Study of Conbercept in Patients With Very Low Vision Secondary to Wet Age-related Macular Degeneration (wAMD)

NCT02098720

Phase 2 Unknown 30 enrolled Chengdu Kanghong Biotech Co., Ltd.
NaSingle-groupOpen-labelTreatment

Summary

This study is designed to evaluate the effect of Conbercept therapy on visual acuity and anatomic outcomes and safety observed in subjects with very low vision secondary to wet age-related macular degeneration.

Timeline

Start
2011-12
Primary completion
2014-03
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Conbercept Protein / enzyme biologic 0.5 mg Other