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Completed Phase 2 Interventional Results available

Open-label Study of Safety and Tolerability of Memantine in Children With Autism

ClinicalTrials.gov ID: NCT01999894

Public ClinicalTrials.gov record NCT01999894. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 1, 2026, 9:33 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

An Open-label Extension Study of the Safety and Tolerability of Memantine in Pediatric Patients With Autism

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to evaluate the long-term safety and tolerability of memantine in the treatment of autism in pediatric patients.

Study identification

NCT ID
NCT01999894
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Forest Laboratories
Industry
Enrollment
102 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
6 Years to 18 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 31, 2009
Primary completion
Jan 31, 2013
Completion
Jan 31, 2013
Last update posted
Mar 17, 2014

2009 – 2013

United States locations

U.S. sites
19
U.S. states
10
U.S. cities
17
Facility City State ZIP Site status
Forest Investigative Site 005 Phoenix Arizona 85006
Forest Investigative Site 003 Sacramento California 95817
Forest Investigative Site 021 San Francisco California 94143
Forest Investigative Site 026 Santa Ana California 92701
Forest Investigative Site 020 Santa Ana California 92705
Forest Investigative Site 002 Stanford California 94305
Forest Investigative Site 024 Jacksonville Beach Florida 32250
Forest Investigative Site 007 St. Petersburg Florida 33701
Forest Investigative Site 014 Hoffman Estates Illinois 60169
Forest Investigative Site 023 Naperville Illinois 60563
Forest Investigative Site 010 Indianapolis Indiana 46202
Forest Investigative Site 025 Cambridge Massachusetts 02138
Forest Investigative Site 011 Toms River New Jersey 08755
Forest Investigative Site 006 Voorhees Township New Jersey 08043
Forest Investigative Site 017 Manhasset New York 10030
Forest Investigative Site 013 Cleveland Ohio 44106
Forest Investigative Site 015 Cleveland Ohio 44106
Forest Investigative Site 001 Columbus Ohio 43210
Forest Investigative Site 019 Oklahoma City Oklahoma 73116

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01999894, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 17, 2014 · Synced Sep 1, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01999894 live on ClinicalTrials.gov.

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