Oxidative damage has been linked to the etiology of a wide range of diseases including age related cardiovascular, eye and neurodegenerative diseases. It also plays a role in cancer and many genetic diseases. The initial targets for these small molecule drugs that induce cellular protection against oxidative damage are:
1) Retinitis pigmentosa, a genetic eye disease and age-related eye diseases such as macular degeneration and glaucoma.
2) Cardiovascular diseases with the goal of protecting the heart and other organs against ischemia/reperfusion damage, as occurs in heart attacks and stroke.
3) A gene therapy approach to increase the level of MSR enzymes in tissues is being developed, since recent findings have shown that specific methionine oxidation in proteins may play a role in disease pathogenesis.
Lead compound and initial focus
Prolindox has promising results using 3 drugs that protect cells against oxidative damage. One of the drugs is effective in slowing blindness in an animal model of the genetic disease, retinitis pigmentosa.
Prolindox has obtained Orphan Drug Designation from the FDA for this lead compound to treat retinitis pigmentosa
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