At a glance
ClinicalIndex Comparison RecordPhase 1Completed· 4 enrolled
Drug / intervention
Ranibizumabdrug
Likely dose
Ranibizumab 0.5mgfrom 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.
Ranibizumab in Subjects With Dense Cataract and Rubeosis Due to Proliferative Diabetic Retinopathy (PDR)
In Brief
A Phase 1 clinical trial evaluating Ranibizumab for Rubeosis Iridis and Proliferative Diabetic Retinopathy. Completed, enrolled 4 participants across 1 site.
Detailed Summary
The purpose of this study was to determine the safety of ranibizumab: a) as a surgical adjunct during cataract surgery in subjects with proliferative diabetic retinopathy (PDR) induced rubeosis and, b) in treatment of proliferative diabetic retinopathy (PDR).
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
CollaboratorsGenentech, Inc.
Timeline
Phase 1CompletedFinished
200720082009201020112012201320142015201620172018201920202021202220232024202520262027
Enrollment StartJul 2007
First PostedFeb 2010
Primary CompletionDec 2011
Study CompletionJan 2012
TodayJul 2026
First PostedFeb 17, 2010
Enrollment StartJul 1, 2007
Primary CompletionDec 1, 2011
Study CompletionJan 1, 2012
TodayJul 2, 2026
Enrollment to primary: 4.4 yearsPosted 16.4 years ago
Interventions
Ranibizumabdrug
Intravitreally administered 0.5mg ranibizumab, 3 doses administered monthly.