drugset / Trial / NCT01592747

Withdrawal Study of Memantine in Pediatric Patients With Autism, Asperger's Disorder, or Pervasive Developmental Disorder Not Otherwise Specified Previously Treated With Memantine

NCT01592747

Phase 2 Completed 479 enrolled Forest Laboratories
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this randomized withdrawal study is to evaluate the safety, tolerability, and efficacy of memantine compared with placebo in pediatric patients with autism, Asperger's Disorder, or Pervasive Developmental Disorder Not Otherwise Specified (PDD-NOS).

Timeline

Start
2012-09
Primary completion
2013-09
Completion
2013-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Memantine Unknown 3 mg Oral
Subject Memantine Unknown 6 mg Oral
Subject Memantine Unknown 15 mg Oral

Indications