Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT01256580

Intravitreal Bevacizumab vs.Combination Therapy for CNV Due to Other Than AMD

Pilot Study of Intravitreal Bevacizumab vs. Combination Therapy for Choroidal Neovascularization Secondary to Causes Other Than Age-related Macular Degeneration

Status
Withdrawn
Phase
N/A
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Massachusetts Eye and Ear Infirmary · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Anti-VEGF therapy has been proven efficacious for the wet (neovascular) form of macular degeneration and may be beneficial for the treatment of choroidal neovascularization (CNV) due to other causes. The limitation of this type of treatment is the necessity for frequent intraocular injections. The purpose of this study is to determine if using anti-VEGF therapy in combination with photodynamic therapy can reduce the number of treatments needed with monotherapy while achieving similar visual results. There are ongoing multicenter trials evaluating combination therapy in patients with wet AMD but no similar trial for patients with CNV due to non-AMD causes. Therefore, in this study the investigators will focus on patients with CNV not due to AMD.

Conditions

Interventions

TypeNameDescription
DRUGBevacizumab (Avastin; Genentech, Inc.)1.25 mg bevacizumab (Avastin; Genentech, Inc.) by intravitreal injection
DRUGBevacizumab, Dexamethasone, Verteporfin Photodynamic TherapyIntravitreal injection of 1.25 mg bevacizumab (Avastin; Genentech, Inc.) combined with reduced-fluence verteporfin PDT (Visudyne®; Novartis) and 200ug of intravitreal dexamethasone

Timeline

Start date
2010-08-01
Primary completion
2013-03-01
Completion
2013-09-01
First posted
2010-12-08
Last updated
2014-01-14

Source: ClinicalTrials.gov record NCT01256580. Inclusion in this directory is not an endorsement.