CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 53 enrolled
Drug / intervention
High Dose NT-501 implant +2 morecombination
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00447954
NCT00447954Phase 2Completed

A Phase II Study of Implants of Encapsulated Human NTC-201 Cells Releasing Ciliary Neurotrophic Factor (CNTF), in Participants With Visual Acuity Impairment Associated With Atrophic Macular Degeneration

Neurotech Pharmaceuticals·interventional·Posted Mar 15, 2007·Updated Mar 28, 2025

In Brief

A Phase 2 clinical trial evaluating High Dose NT-501 implant, Low Dose NT-501 implant, and 1 other intervention for Nonexudative Age-Related Macular Degeneration, Unspecified Eye, Intermediate Dry Stage. Completed, enrolled 53 participants across 8 sites.

Detailed Summary

The purpose of this study is to look at the safety and effectiveness of CNTF implants on vision in participants with atrophic macular degeneration. This research is being done because there are no effective therapies for people with atrophic macular degeneration. Age-related macular degeneration (AMD) is a condition that affects the macula, the central part of the retina that we use for seeing details. There are two types of AMD, one is the wet type in which new blood vessels grow, also known as choroidal neovascularization (CNV), but the other is the dry type in which the healthy cells die, and that is the target of this study. This is called atrophic macular degeneration. 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. In this study, two different CNTF dose levels will be used: a high dose and a low dose, as well as a sham surgery (or placebo) group.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedMar 15, 2007
Enrollment StartJan 5, 2007
Primary CompletionMay 11, 2009
TodayJul 2, 2026
Enrollment to primary: 2.4 yearsPosted 19.3 years ago

Interventions

High Dose NT-501 implantcombination

High Dose NT-501

Low Dose NT-501 implantcombination

Low Dose NT-501

Shamother

Sham Procedure