CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 80 target
Drug / intervention
conbercept +2 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02821520
NCT02821520Phase 4Completed

Efficacy and Safety of Initial Versus Delayed Verteporfin Photodynamic Therapy in Combination With Conbercept in Patients With Symptomatic Polypoidal Choroidal Vasculopathy

The Eye Hospital of Wenzhou Medical University·interventional·Posted Jul 1, 2016·Updated Jul 19, 2019

In Brief

A Phase 4 clinical trial evaluating conbercept, Initial PDT, and 1 other intervention for Polypoidal Choroidal Vasculopathy. Completed, enrolled 80 participants across 3 sites.

Detailed Summary

To compare the initial versus delayed verteporfin photodynamic therapy (PDT) in combination with conbercept in patients with symptomatic polypoidal choroidal vasculopathy (PCV).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesChina
Collaborators--

Timeline

Phase 4CompletedFinished
2017201820192020202120222023202420252026
First PostedJul 1, 2016
Enrollment StartJan 1, 2017
Primary CompletionJun 1, 2019
TodayJul 2, 2026
Enrollment to primary: 2.4 yearsPosted 10.0 years ago

Interventions

conberceptdrug

At baseline conbercept injection is administered.And thereafter is administered based on re-treatment criteria from month 1 to 11.The PRN conbercept re-injection should be monthly.

Initial PDTprocedure

At baseline PDT with verteporfin is administered initially.And thereafter PDT is administered based on re-treatment criteria from month 3 to 11.The PRN PDT retreatment intervals should be no less than 3 months.

Delayed PDTprocedure

PDT is administered based on re-treatment criteria from month 3 to 11.The PRN PDT retreatment intervals should be no less than 3 months.