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Completed Phase 4 Interventional Results available

Open-Label Study of SPN-812 Administered With Psychostimulants in Children and Adolescents With ADHD

ClinicalTrials.gov ID: NCT04786990

Public ClinicalTrials.gov record NCT04786990. 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 Oct 17, 2026, 6:12 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

A Phase IV, Open-Label, Flexible-Dose Safety Trial Evaluating SPN-812 Administered With Psychostimulants in Children and Adolescents (6 to 17 Years of Age) With Attention-Deficit/Hyperactivity Disorder (ADHD)

Brief summary

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

This open label, flexible-dose study evaluating the safety and efficacy of SPN-812 administered with psychostimulants in children and adolescents (6 to 17 years of age) with Attention-Deficit/Hyperactivity Disorder (ADHD).

Study identification

NCT ID
NCT04786990
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Supernus Pharmaceuticals, Inc.
Industry
Enrollment
96 participants

Conditions and interventions

Eligibility (public fields only)

Age range
6 Years to 17 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
Jul 27, 2021 (Actual)
Primary completion
May 23, 2023 (Actual)
Completion
Jul 26, 2023 (Actual)
Last update posted
May 1, 2024

2021 – 2023

United States locations

U.S. sites
16
U.S. states
13
U.S. cities
16
Facility City State ZIP Site status
Preferred Research Partners, Inc. Little Rock Arkansas 72211 —
NRC Research Institute Orange California 92868 —
Miami Clinical Research Miami Florida 33155 —
APG Research, LLC Orlando Florida 32803 —
Elite Clinical Trials Blackfoot Idaho 83221 —
Elite Clinical Trials Rexburg Idaho 83440 —
Qualmedica Research, LLC Evansville Indiana 47715 —
Psychiatric Associates Purehealth Medical Center Overland Park Kansas 66221 —
Midwest Research Group Saint Charles Missouri 63304 —
Alivation Research, LLC Lincoln Nebraska 68526 —
Center for Psychiatry and Behavioral Medicine Las Vegas Nevada 89128 —
SP Research, PLLC Oklahoma City Oklahoma 73112 —
Coastal Carolina Research Center North Charleston South Carolina 29405 —
Gadolin Research, LLC Beaumont Texas 77702 —
Family Psychiatry of The Woodlands The Woodlands Texas 77381 —
Northwest Clinical Research Center Bellevue Washington 98007 —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04786990, 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, 2024 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04786990 live on ClinicalTrials.gov.

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