RP Cure Tracker

Trials / NCT00447993

A Study of Encapsulated Cell Technology (ECT) Implant for Patients With Late Stage Retinitis Pigmentosa

Completed Phase 2 Drug / neuroprotection

Sponsor
Neurotech Pharmaceuticals
Treatment
Low Dose NT-501; High Dose NT-501
Gene
Not stated
Conditions
Retinitis Pigmentosa
Ages
18 Years to 68 Years
Enrollment
67 participants
Started
2007-01-08
Main results expected
2009-05-26
Results posted
Yes
Record last updated
2024-08-13

What the study is testing

The purpose of this study is to look at the safety and effectiveness of CNTF implants on vision in persons with retinitis pigmentosa, Usher type II \& III, and Choroideremia. This research is being done because there are no effective therapies for people with these retinal degenerations. They are genetic disorders that affect our ability to see at night, and later cause tunnel vision and loss of central vision. Retinal degenerations affect the retina, a light sensitive layer of cells in the back of the eye. Slowly over time, these cells die and cause permanent loss of vision.

The implant is a small capsule that contains human retinal pigment epithelium cells. These cells have been given the ability to make CNTF and release it through the capsule membrane into the surrounding fluid. This study will look at the effect of the implant on vision loss by retinitis pigmentosa, Usher type II \& III, and Choroideremia. In this study, two different CNTF dose levels will be used: a high dose and a low dose in one eye, as well as a sham (or placebo) surgery in the other eye.

Where it runs

United States (11)

Open on ClinicalTrials.gov for contacts and eligibility