Expired Study
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New Brunswick, New Jersey 08901


Purpose:

A randomized, controlled study of the safety and efficacy of Squalamine Lactate Eye Drops in combination with Ranibizumab intravitreal injections in patients with diabetic macular edema. The study duration is 52 weeks and patients will be randomized to one of four treatment arms.


Study summary:

A randomized, controlled study of the safety and efficacy of Squalamine Lactate eye drops in combination with Ranibizumab intravitreal injections in patients with diabetic macular edema. Subjects will be randomized to one of the following treatment arms: 1. Squalamine Lactate Ophthalmic Solution administered twice a day for 52 weeks in combination with monthly injections of ranibizumab from baseline through week 20 and ranibizumab as needed from week 24 through week 52. 2. Vehicle Ophthalmic Solution administered twice a day for 52 weeks in combination with monthly injection of ranibizumab from baseline through week 20 and ranibizumab as needed from week 24 through week 52. 3. Squalamine Lactate Ophthalmic Solution administered four times a day for 52 weeks in combination with monthly injections of ranibizumab from baseline through week 20 and ranibizumab as needed from week 24 through week 52. 4. Vehicle Ophthalmic Solution administered four times a day for 52 weeks in combination with monthly injection of ranibizumab from baseline through week 20 and ranibizumab as needed from week 24 through week 52.


Criteria:

Inclusion Criteria: - Subjects will have clinically significant diabetic macular edema of ≥ 300 microns with central involvement using the Heidelberg or Cirrus machine - Best corrected visual acuity of 20/32 to 20/320 inclusive in the study eye - Adults ≥ 18 years of age with type 1 or 2 diabetes mellitus with diabetic macular edema Exclusion Criteria: - History of vitreoretinal surgery in the study eye - Panretinal laser photocoagulation or macular laser photocoagulation in the study eye within 3 months of screening - Any prior laser in study eye - Previous use of intraocular or periocular corticosteroids in the study eye within 6 months of screening - Previous treatment with anti-angiogenic drugs in either eye within 3 months of screening - Uncontrolled diabetes mellitus with HbA1c levels greater than 12 - Ocular disorders in the study eye, other than diabetic macular edema, that my confound interpretation of study results


NCT ID:

NCT02349516


Primary Contact:

Principal Investigator
Daniel Roth, MD
NJ Retina


Backup Contact:

N/A


Location Contact:

New Brunswick, New Jersey 08901
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: November 23, 2017

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