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Completed Phase 2 Interventional

Open-Label, Extension Study to 810P202

ClinicalTrials.gov ID: NCT01416064

Public ClinicalTrials.gov record NCT01416064. 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 Jul 22, 2026, 10:46 AM EDT

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

Official title

Open-Label Extension Study to Evaluate the Safety of Molindone Hydrochloride Extended-Release Tablets as Adjunctive Therapy in Children With Impulsive Aggression Comorbid With Attention-Deficit/Hyperactivity Disorder (ADHD)

Study identification

NCT ID
NCT01416064
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Supernus Pharmaceuticals, Inc.
Industry
Enrollment
78 participants

Conditions and interventions

Interventions

  • Molindone Drug

Drug

Eligibility (public fields only)

Age range
6 Years to 12 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
Aug 31, 2011
Primary completion
Dec 31, 2012
Completion
Jan 31, 2013
Last update posted
May 1, 2017

2011 – 2013

United States locations

U.S. sites
28
U.S. states
15
U.S. cities
28
Facility City State ZIP Site status
Not listed Dothan Alabama
Not listed Los Angeles California
Not listed Santa Ana California
Not listed Wildomar California
Not listed Washington D.C. District of Columbia
Not listed Bradenton Florida
Not listed Gainesville Florida
Not listed Hialeah Florida
Not listed Jacksonville Florida
Not listed Maitland Florida
Not listed North Miami Florida
Not listed Orlando Florida
Not listed Tampa Florida
Not listed Atlanta Georgia
Not listed Libertyville Illinois
Not listed Indianapolis Indiana
Not listed Terre Haute Indiana
Not listed Owensboro Kentucky
Not listed Toms River New Jersey
Not listed Stony Brook New York
Not listed Cleveland Ohio
Not listed Columbus Ohio
Not listed Philadelphia Pennsylvania
Not listed Pittsburgh Pennsylvania
Not listed Charleston South Carolina
Not listed Memphis Tennessee
Not listed Bellevue Washington
Not listed Bothell Washington

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 NCT01416064, 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 May 1, 2017 · Synced Jul 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01416064 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →