Clinical Trials Directory

Trials / Terminated

TerminatedNCT02735369

A Study Assessing Efficacy and Safety of OC-10X in the Treatment of PDR

A Phase II, Randomized, Placebo-Controlled, Study Assessing Efficacy and Safety of OC-10X Ophthalmic Suspension in the Treatment of Proliferative Diabetic Retinopathy

Status
Terminated
Phase
Phase 2
Study type
Interventional
Enrollment
40 (estimated)
Sponsor
OcuCure Therapeutics, Inc. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The present study is intended to evaluate the efficacy and safety of topical OC-10X Ophthalmic Suspension in patients diagnosed with proliferative diabetic retinopathy (level 61, 65, 71, or 75). OcuCure Therapeutics, Inc. (Roanoke, VA) has developed a lead compound, known as OC-10X, which is a selective tubulin inhibitor under development for the treatment of Proliferative Diabetic Retinopathy (PDR) and Age-related Macular Degeneration (AMD). When administered as a topical eye drop, OC-10X has both anti-angiogenic (inhibition) and angiolytic (regression) properties in animal models of choroidal neovascularization (CNV). Unlike other therapies, OC-10X provides the efficacy of a vascular targeting agent without the traditional toxicity and works downstream independently of growth factors. As demonstrated by OcuCure's preclinical data, tubulin inhibition, using OC-10X, may be a promising new approach to the treatment of PDR and AMD. Like AMD, PDR is a major cause of blindness in adults and is also caused by the growth of abnormal blood vessels. Importantly, the Phase I Study found that OC-10X can be safely applied topically in human eyes without adverse ocular or systemic effects. Currently, there are few options for the treatment of PDR. Clinical options, such as laser photocoagulation or vitrectomy, require surgery and can permanently impair patients' vision. With few treatment options available, administration of OC-10X as a topical therapy, along with its novel mechanism, has the potential to provide benefits to patients with ocular diseases associated with angiogenesis.

Conditions

Interventions

TypeNameDescription
DRUG2% OC-10X2% OC-10X
DRUGPlacebo ComparatorPlacebo

Timeline

Start date
2014-12-01
Primary completion
2016-10-01
Completion
2016-10-01
First posted
2016-04-12
Last updated
2017-04-05

Locations

1 site across 1 country: Bangladesh

Source: ClinicalTrials.gov record NCT02735369. Inclusion in this directory is not an endorsement.