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Retinitis Pigmentosa (RP) is a disease in which one of several different mutations
differentially causes degeneration of rod photoreceptors while sparing cone
photoreceptors. The loss of rod photoreceptors results in poor vision in dim illumination
(night blindness), but does not affect most activities of daily life including reading or
driving. However, after most rod photoreceptors are eliminated, cone photoreceptors begin
to die, resulting in gradual constriction of visual fields which over time causes visual
disability.
Rods outnumber cones by a ratio of 95:5 and therefore after mutation-induced degeneration
of rods, the majority of cells in the outer retina have been eliminated, markedly
reducing oxygen utilization. However, oxygen supply is unchanged resulting in a large
excess of tissue oxygen surrounding cones. This results in progressive oxidative damage
that contributes to slowly progressive degeneration of cone photoreceptors.
N-acetylcysteine (NAC) is a strong antioxidant that is approved for acetaminophen
overdose. Orally administered NAC in a mouse model of RP reduced oxidative damage to
cones and promoted maintenance of function and survival of cones. In a phase I clinical
trial in patients with RP, oral administration of NAC for 6 months was well-tolerated and
resulted in a small but statistically significant improvement in visual acuity and light
sensitivity in the retina. This suggests that long-term administration of NAC may promote
survival and maintenance of function of cones. NAC Attack is a phase III, multicenter,
randomized, placebo controlled trial that will determine if oral NAC provides benefit and
is safe in patients with RP.
1Research sites
438Patients around the world