drugset / Trial / NCT04922151

601 Versus Ranibizumab in Patients With Pathological Myopic Choroidal Neovascularization (pmCNV)

NCT04922151

RandomizedParallel-groupTriple-blindTreatment

Summary

To evaluate the safety and efficacy of intravitreal recombinant humanized anti-VEGF monoclonal antibody in patients with visual impairment due to pmCNV

Timeline

Start
2021-06-04
Primary completion
2023-01-31
Completion
2023-07-31

Drugs

EvaluationDrugModalityDoseRoute
Subject 601 Unknown 1.25 mg Intravitreal
Comparator Ranibizumab Monoclonal antibody 0.5 mg Intravitreal