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Supernus Pharmaceuticals clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine and the EU Clinical Trials Information System (CTIS) — current trials in our USA and EU (CTIS) registers with Supernus Pharmaceuticals as lead sponsor. Synced 26 Sep 2026
8Current trials
6Recruiting now
3Drugs in these trials
2Trial registers
Maintained by Sreepriya Prasannan
MSc Digital Transformation of Life Sciences (Innopharma Education / Griffith College); MSc & BSc Botany HSE Spark Ignite 2026 — Top 14 finalist
Compiled from ClinicalTrials.gov and CTIS registry records · Last verified · Editorial standards
At a glance

Supernus Pharmaceuticals is the lead sponsor of 8 current clinical trials in our USA and EU (CTIS) registers. 6 are recruiting patients now. The most common phase is Phase 2. The drugs named most often in its trials are SPN-812, SPN-817 and Huperzine A. The most-studied condition is Attention-Deficit/Hyperactivity Disorder.

ClinicalTrials.gov trials by status

  • Recruiting686%
  • Active, closed114%

Trials by phase

  • Phase 2457%
  • Observational114%
  • Phase 3114%
  • Phase 4114%
01

Clinical trials sponsored by Supernus Pharmaceuticals

7 on ClinicalTrials.gov
StudyPhaseStatusStartRegisters
Safety and Tolerability Study of SPN-817 in Adult Patients With Treatment Resistant Epilepsy
NCT05518578 · Epilepsy, Seizures, Epileptic
Drug: SPN-817
Phase 2 Recruiting 2023-02 USA
Real-World Patient Experiences Using Continuous Subcutaneous Apomorphine Infusion (ONAPGOTM) in the United States:
NCT07219927 · ClinicalTrials.gov ↗ · Parkinson Disease
Observational Recruiting 2025-03 USA
Double-blind, Placebo-controlled Study in Adults With Major Depressive Disorder
NCT07226661 · ClinicalTrials.gov ↗ · Major Depressive Disorder (MDD)
Phase 2 Recruiting 2026-01 USA
Evaluation of SPN-812 (Viloxazine Extended-release Capsule) in Preschool-age Children With ADHD
NCT04781140 · ClinicalTrials.gov ↗ · Attention-Deficit/Hyperactivity Disorder
Drug: SPN-812
Phase 4 Recruiting 2024-03 USA
RENAISSANCE 2: SPN-817 Phase 2, Double-Blind, Placebo-Controlled Study in Adults With Focal Onset Seizures
NCT06798896 · ClinicalTrials.gov ↗ · Focal Onset Seizures
Drug: SPN-817
Phase 2 Recruiting 2024-12 USA
SPN-817 Open-Label Extension Study in Adults With Focal Onset Seizures
NCT07141329 · ClinicalTrials.gov ↗ · Focal Onset Seizures
Phase 2 Recruiting 2025-07 USA
Open-label Study to Evaluate Long-term Safety and Efficacy of SPN-812 (Viloxazine Extended-release Capsule)
NCT02736656 · ClinicalTrials.gov ↗ · Attention-Deficit/Hyperactivity Disorder
Drug: SPN-812
Phase 3 Active, closed 2016-02 USA

Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Titles and statuses are copied from the registry as published.

02

Supernus Pharmaceuticals in the EU trials register (CTIS)

1 trial

Authorised or ongoing trials in the EU Clinical Trials Information System with Supernus Pharmaceuticals as sponsor. Some are the same study as a ClinicalTrials.gov record above; the two registries share no common ID. Trials with a site in Ireland are listed first.

StudyPhaseStatusCountries
RENAISSANCE 2: A Double-Blind, Randomized, Placebo-Controlled, Multicenter, Parallel-Group Study to Evaluate the Efficacy, Safety, and Tolerability of SPN-817 in Adults with Focal Onset Seizures
2025-520587-18-00 · CTIS ↗ · Nervous System Diseases
Phase 2 Ongoing Poland, Hungary, Bulgaria
03

Drugs in Supernus Pharmaceuticals trials

3 compounds

Drugs and biologicals named as interventions in these trials, with the number of this sponsor's trials that name each one. Placebos and generic comparators are excluded.

04

Conditions in Supernus Pharmaceuticals trials

6 conditions
Attention-Deficit/Hyperactivity Disorder2Focal Onset Seizures2Epilepsy1Seizures, Epileptic1Parkinson Disease1Major Depressive Disorder (MDD)1
05

By trial register

RegisterTrialsRecruiting
Clinical trials in USA76
EU register (CTIS)1—

A trial with sites in more than one country appears in each of those registers.

06

Questions about Supernus Pharmaceuticals trials

How many clinical trials does Supernus Pharmaceuticals sponsor?

Supernus Pharmaceuticals is the lead sponsor of 7 current trials on ClinicalTrials.gov in our USA register, and 1 authorised or ongoing trial in the EU register (CTIS), as of the registry sync on 26 September 2026. Completed and withdrawn studies are not counted.

Are Supernus Pharmaceuticals trials recruiting?

Yes. 6 of its 7 ClinicalTrials.gov trials are recruiting. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Which drugs is Supernus Pharmaceuticals testing?

Its current trials name 3 drugs and biologicals as interventions. The most frequent are SPN-812 (2), SPN-817 (2) and Huperzine A (1). The number in brackets is how many of its trials name each drug.

Where does this information come from?

Every trial, status, phase and condition on this page is copied from public ClinicalTrials.gov and EU CTIS records by a daily sync, grouped by the sponsor name each registry records. It says nothing about the organisation beyond its registered trials, and it is not medical advice.

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How this page is built

Everything on this page is copied from public registry records — it is not written from memory, and nothing here describes the organisation beyond its registered trials. Each trial links to its own record so you can check it yourself.

This page is built automatically: a daily sync job reads the registry records behind our trial registers and groups every current trial by its lead sponsor name, ignoring legal-form suffixes such as Inc. or Ltd. A small, hand-checked list joins the same organisation's different registry names (for example its EU legal entity). There is no AI drafting and no per-sponsor editorial pass. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The the registries data on this page was last retrieved on 26 Sep 2026.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician — our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us — we correct promptly and log it.