drugset / Trial / NCT01233609

Trial of Oral Valproic Acid for Retinitis Pigmentosa

NCT01233609

RandomizedParallel-groupQuadruple-blindTreatment

Summary

The objectives of this study are to evaluate the efficacy of Valproic Acid (VPA) to both slow the progression of visual function loss and/or to restore visual function in patients with Autosomal Dominant Retinitis Pigmentosa (RP) and to collect safety and tolerability information.

Timeline

Start
2010-11
Primary completion
2015-12
Completion
2015-12

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Valproic Acid Small molecule 500 mg Oral
Comparator Valproic Acid Small molecule 1000 mg Oral

Indications