drugset / Trial / NCT07226141

Valproate for the Treatment of Residual Amblyopia

NCT07226141

Phase 1/2 Not yet recruiting 28 enrolled Boston Children's Hospital
RandomizedCrossoverDouble-blindTreatment

Summary

The goal of this clinical trial is to determine the efficacy of valproate as an adjunct therapy to treat amblyopia beyond the critical period in children aged 8-17 years who have amblyopia of ≥3 lines of interocular best-corrected (with glasses) visual acuity difference. The main questions it aims to answer are: * Does valproate enable clinically meaningful and durable visual recovery from amblyopia? * Do valproate-treated patients show a change in amblyopic eye visual acuity (lines)? Participants will undergo daily patching for 2 hours (standard of care) plus the addition of valproate or placebo for a total of 16 weeks.

Timeline

Start
2026-01-01
Primary completion
2027-09-30
Completion
2027-09-30

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Valproate Small molecule 15 mg/kg Oral
Subject Valproate Small molecule 30 mg/kg Oral