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UnknownNCT01248117

Safety Study of High-Dose Ranibizumab for Polypoidal Choroidal Vasculopathy

Investigator Sponsored Trial of Polypoidal Choroidal Vasculopathy (PCV) Evaluation Assessing High-Dose Ranibizumab (2.0mg) Prospectively

Status
Unknown
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
20 (estimated)
Sponsor
Retina Consultants of Hawaii · Academic / Other
Sex
All
Age
25 Years
Healthy volunteers
Accepted

Summary

Monthly, continuous anti-vegf therapy for patients presenting with active polypoidal choroidal vasculopathy. Two arms, treatment naive and previously treated with an FDA approved anti-VEGF therapy, will be randomized and dosed with open label 2.0mg ranibizumab.

Detailed description

Patients will be followed with spectral oct, 4m BCVA, ICG, FA and monthly eye examinations for one year.

Conditions

Interventions

TypeNameDescription
DRUGranibizumab 2.0mgMonthly, intravitreal injection 0.05ml

Timeline

Start date
2010-11-01
Primary completion
2012-12-01
Completion
2013-02-01
First posted
2010-11-25
Last updated
2010-11-25

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT01248117. Inclusion in this directory is not an endorsement.

Safety Study of High-Dose Ranibizumab for Polypoidal Choroidal Vasculopathy (NCT01248117) · Clinical Trials Directory