Clinical Trial: Oral N-acetylcysteine for Retinitis Pigmentosa

Study Status: RECRUITING
Recruit Status: RECRUITING
Study Type: INTERVENTIONAL




Official Title: NAC Attack, A Phase III, Multicenter, Randomized, Parallel, Double Masked, Placebo-Controlled Study Evaluating the Efficacy and Safety of Oral N-Acetylcysteine in Patients With Retinitis Pigmentosa

Brief Summary: Retinitis pigmentosa (RP) is an inherited retinal degeneration caused by one of several mistakes in the genetic code.
Such mistakes are called mutations.
The mutations cause degeneration of rod photoreceptors which are responsible for vision in dim illumination resulting in night blindness.
After rod photoreceptors are eliminated, gradual degeneration of cone photoreceptors occurs resulting in gradual constriction of side vision that eventually causes tunnel vision.
Oxidative stress contributes to cone degeneration.
N-acetylcysteine (NAC) reduces oxidative stress and in animal models of RP it slowed cone degeneration.
In a phase I clinical trial in patients with RP, NAC taken by month for 6 months caused some small improvements in two different vision tests suggesting that long-term administration of NAC might slow cone degeneration in RP.
NAC Attack is a clinical trial being conducted at many institutions in the US, Canada, Mexico, and Europe designed to determine if taking NAC for several years provides benefit in patients with RP.