drugset / Trial / NCT01592773

Safety Study of Memantine in Pediatric Patients With Autism, Asperger's Disorder or Pervasive Developmental Disorder Not Otherwise Specified (PDD-NOS)

NCT01592773

Phase 2 Terminated 747 enrolled Forest Laboratories
NaSingle-groupOpen-labelTreatment

Summary

The objective of this study is to evaluate the long-term safety and tolerability of memantine in the treatment of pediatric patients with autism, Asperger's Disorder or Pervasive Developmental Disorder Not Otherwise Specified (PDD-NOS).

Timeline

Start
2012-10
Primary completion
2014-01
Completion
2014-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Memantine Unknown 3 mg Oral
Subject Memantine Unknown 6 mg Oral
Subject Memantine Unknown 9 mg Oral
Subject Memantine Unknown 15 mg Oral