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ACTIVE NOT RECRUITING Phase 3

Open-label Study to Evaluate Long-term Safety and Efficacy of SPN-812 (Viloxazine Extended-release Capsule)

NCT02736656 · View on ClinicalTrials.gov ↗

Study Summary

Open label extension, long-term multicenter study of safety and efficacy of SPN-812 in pediatric ADHD patients

Interventions

  • DRUG SPN-812

Study Locations (16)

Florida

  • Meridien Research at Florida Clinical Research Center — Bradenton
  • Sarkis Clinical Trials — Gainesville
  • Indago Research & Health Center, Inc. — Hialeah
  • Florida Clinical Research Center, LLC. — Maitland
  • Florida Clinical Research Center, LLC — Maitland

Oklahoma

  • IPS Research — Oklahoma City
  • Paradigm Research Professionals — Oklahoma City

Tennessee

  • Clinical Neuroscience Solutions, Inc. — Memphis
  • CNS Healthcare — Memphis

Texas

  • Bayou City Research Corporation — Houston
  • Road Runner Research — San Antonio

Arkansas

  • Woodland International Research Group — Little Rock

California

  • Alliance for Wellness dba Alliance for Research — Long Beach

Colorado

  • MCB Clinical Research Centers, LLC — Colorado Springs

Utah

  • Ericksen Research & Development — Clinton

Trial Details

FieldValue
Enrollment Target 1,400 participants
Start Date 2016-02-02
Est. Completion 2026-09
Phase Phase 3

Sponsor

Supernus Pharmaceuticals

43 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02736656

The ClinicalTrials.gov registry entry for NCT02736656 describes a study currently listed as active not recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 1,400 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Supernus Pharmaceuticals, which has 43 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Attention-Deficit/Hyperactivity Disorder appearing as the primary indexed condition, and to 1 intervention — of which SPN-812 is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT02736656 reports 16 study locations spanning 9 distinct geographic areas — top geographies include Florida, Oklahoma, Tennessee. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT02736656 about?

NCT02736656 is a clinical study titled "Open-label Study to Evaluate Long-term Safety and Efficacy of SPN-812 (Viloxazine Extended-release Capsule)". Open label extension, long-term multicenter study of safety and efficacy of SPN-812 in pediatric ADHD patients

What is the current status of trial NCT02736656?

This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 1,400 participants. The study started on 2016-02-02. Estimated completion is 2026-09.

What conditions does trial NCT02736656 study?

This clinical trial studies the following conditions: Attention-Deficit/Hyperactivity Disorder. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02736656?

The interventions under investigation include: SPN-812 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02736656?

This trial is sponsored by Supernus Pharmaceuticals, which has 43 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02736656 being conducted?

This trial has 16 study locations across Arkansas, California, Colorado, Florida, Oklahoma. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial