Clinical Trials Directory

Trials / Completed

CompletedNCT01769183

Squalamine for the Treatment in Proliferative Diabetic Retinopathy

Topical Squalamine in the Treatment of Retinal Neovascularization From Proliferative Diabetic Retinopathy

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
6 (actual)
Sponsor
Elman Retina Group · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to determine the efficacy in the use of topical Squalamine Lactate Ophthalmic Solution, 0.2% in the treatment of retinal neovascularization resulting from proliferative diabetic retinopathy.

Conditions

Interventions

TypeNameDescription
DRUGSqualamine Lactate ophthalmic solution 0.2%Patients will start with Squalamine one drop twice daily to the affected eye. If at one week the neovascularization shows no sign of regression, then the dose will be doubled to four times daily with a follow up at one day and one week following the increased dose frequency, then resuming the schedule at four weeks. If neovascularization returns within the study, the dose will be doubled to four times daily. In that case, a one day and one week visit will be added after increasing the dose. Squalamine treatment will discontinue after the week 20 visit.

Timeline

Start date
2013-02-01
Primary completion
2014-08-01
Completion
2014-08-01
First posted
2013-01-16
Last updated
2015-02-10

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01769183. Inclusion in this directory is not an endorsement.