Clinical Trials Directory

Trials / Sponsors / Supernus Pharmaceuticals, Inc.

Supernus Pharmaceuticals, Inc.

Industry · 68 registered clinical trials5 currently recruiting.

StatusTrialPhaseStarted
RecruitingDouble-blind, Placebo-controlled Study in Adults With Major Depressive Disorder
Major Depressive Disorder (MDD)
Phase 22026-01-19
RecruitingSPN-817 Open-Label Extension Study in Adults With Focal Onset Seizures
Focal Onset Seizures
Phase 22025-07-30
RecruitingReal-World Patient Experiences Using Continuous Subcutaneous Apomorphine Infusion (ONAPGOTM) in the United Sta
Parkinson Disease
2025-03-31
RecruitingRENAISSANCE 2: SPN-817 Phase 2, Double-Blind, Placebo-Controlled Study in Adults with Focal Onset Seizures
Focal Onset Seizures
Phase 22024-12-30
CompletedOpen-label Safety and Efficacy of SPN-812 (Viloxazine Extended-release Capsule) in Adults With ADHD and Mood S
Attention-Deficit/Hyperactivity Disorder
Phase 42024-03-25
RecruitingEvaluation of SPN-812 (Viloxazine Extended-release Capsule) in Preschool-age Children With ADHD
Attention-Deficit/Hyperactivity Disorder
Phase 42024-03-19
CompletedEvaluation of Viloxazine and Its Metabolite 5-Hydroxy-viloxazine Glucuronide Into Breast Milk in Healthy Lacta
Healthy Lactating Women
Phase 42023-05-23
CompletedAn Open-Label Study Evaluating Brexanolone in Adults With Tinnitus
Tinnitus
Phase 22023-05-10
UnknownSafety and Tolerability Study of SPN-817 in Adult Patients With Treatment Resistant Epilepsy
Epilepsy, Seizures, Epileptic
Phase 22023-02-07
TerminatedA Study to Evaluate the Safety and Tolerability of SAGE-718 in Participants With Huntington's Disease
Huntington's Disease
Phase 32022-12-14
CompletedA Study to Evaluate the Effects of SAGE-718 in Participants With Mild Cognitive Impairment or Mild Dementia Du
Mild Cognitive Impairment, Mild Dementia, Alzheimer's Disease
Phase 22022-11-29
CompletedA Study to Evaluate the Effects of SAGE-718 in Participants With Parkinson's Disease Cognitive Impairment
Parkinson Disease, Cognitive Dysfunction
Phase 22022-06-06
Completed28-Day Study of SAGE-718 on Functioning Capacity in Participants With Huntington's Disease
Huntington Disease
Phase 22022-05-26
CompletedA Study to Evaluate the Effect of SAGE-718 on Cognitive Function in Participants With Huntington's Disease (HD
Huntington's Disease
Phase 22022-01-26
UnknownEfficacy and Safety Study of MYOBLOC® in the Treatment of Adult Upper Limb Spasticity
Spasticity, Cerebrovascular Accident, Multiple Sclerosis
Phase 2 / Phase 32021-11-16
CompletedMass Balance Study of NV-5138 in Healthy Male Subjects
Healthy Volunteers
Phase 12021-11-11
CompletedEvaluating the Safety and Relative Bioavailability of Three SPN-817 Treatments (A, B and C) in Healthy Adult S
Healthy Volunteer
EARLY_Phase 12021-10-19
CompletedA Study To Assess The Safe-Use Conditions For Administration of ZULRESSO® in a Home Setting
Postpartum Depression
Phase 42021-10-08
CompletedStudy of SAGE-904 Using a Ketamine Challenge to Evaluate Electrophysiology, Safety, Tolerability, and Pharmaco
Healthy Volunteer
Phase 12021-09-21
CompletedOpen-Label Study of SPN-812 Administered With Psychostimulants in Children and Adolescents With ADHD
Attention-Deficit/Hyperactivity Disorder (ADHD)
Phase 42021-07-27
CompletedA Study to Evaluate the Safety and Tolerability of SAGE-718 in Participants With Mild Cognitive Impairment or
Alzheimer Disease, Cognitive Dysfunction, Mild Dementia
Phase 22020-12-07
CompletedA Study to Evaluate the Safety and Tolerability of SAGE-718 in Participants With Parkinson's Disease Mild Cogn
Parkinson Disease, Cognitive Dysfunction
Phase 22020-07-31
TerminatedTherapy for Migraine Prevention in Children 6-11 Years of Age
Migraine Disorders, Headache Disorders
Phase 42020-07-14
CompletedOpen-label Long-Term Safety and Efficacy of SPN-812 (Viloxazine Extended-release Capsule) in Adults With ADHD
Attention-Deficit/Hyperactivity Disorder
Phase 32020-01-23
UnknownEfficacy and Safety Study of MYOBLOC® in the Treatment of Adult Lower Limb Spasticity
Spasticity
Phase 2 / Phase 32019-12-17
CompletedEvaluation of SPN-812 (Viloxazine Extended-release Capsule) in Adults With ADHD
Attention-Deficit/Hyperactivity Disorder (ADHD)
Phase 32019-11-20
WithdrawnClassroom Study of SPN-812 in Children With ADHD
ADHD
Phase 32019-08-01
TerminatedExploratory fMRI Study on the Treatment for Impulsive Aggression in Children With ADHD
Attention Deficit Hyperactivity Disorder (ADHD), Impulsive Aggression
Phase 22019-05-30
CompletedA Study to Evaluate Safety, Tolerability, and Pharmacokinetics of SAGE-718 Oral Solution in Patients With Hunt
Huntington Disease
Phase 12019-02-28
CompletedA Study to Assess Electrophysiology, Safety, Tolerability, and Pharmacokinetics of Multiple Doses of SAGE-718
Healthy Volunteer
Phase 12018-12-27
CompletedA Study to Assess the Electrophysiology, Safety, Tolerability, Pharmacokinetics and Pharmacodynamics Response
Healthy Volunteer
Phase 12018-11-12
CompletedA Study to Assess the Electrophysiology, Safety, Tolerability, and Pharmacokinetics of SAGE-718 Using a Ketami
Healthy Volunteer
Phase 12018-09-24
CompletedA Study to Assess the Safety of Brexanolone in the Treatment of Adolescent Female Participants With Postpartum
Post Partum Depression
Phase 32018-09-07
CompletedFunctional MRI Study in Healthy Children Engaged in Aggressive Behaviors
Impulsive Aggression
2018-08-10
TerminatedTreatment of Impulsive Aggression (IA) in Adolescent With ADHD in Conjunction With Standard ADHD Treatment
Attention Deficit Hyperactivity Disorder
Phase 32018-07-31
Active Not RecruitingBIS-001-ER for the Treatment of Adult Focal Impaired Awareness Seizures
Focal Impaired Awareness Seizures
Phase 1 / Phase 22018-04-10
CompletedClinical Outcome Assessment of Parkinson's Disease Patients Treated With XADAGO (Safinamide)
Idiopathic Parkinson Disease
2017-11-30
CompletedEvaluation of SPN-812 (Viloxazine Extended-release Capsule) High Dose in Adolescents With ADHD
ADHD
Phase 32017-11-20
CompletedEvaluation of SPN-812 (Viloxazine Extended-release Capsule) Low Dose in Adolescents With ADHD
ADHD
Phase 32017-11-02
CompletedEvaluation of SPN-812 (Viloxazine Extended-release Capsule) High Dose in Children With ADHD
ADHD
Phase 32017-10-31
CompletedEvaluation of SPN-812 (Viloxazine Extended-release Capsule) Low Dose in Children With ADHD
ADHD
Phase 32017-10-20
CompletedBioavailability, Safety, and Tolerability of BIS-001 ER
Epilepsy, Complex Partial
Phase 12017-05-22
CompletedA Study to Evaluate Efficacy and Safety of SAGE-547 in Participants With Severe Postpartum Depression (547-PPD
Postpartum Depression
Phase 32016-08-01
CompletedA Study to Evaluate Safety and Efficacy of SAGE-547 in Participants With Moderate Postpartum Depression (547-P
Postpartum Depression
Phase 32016-07-01
TerminatedTreatment of Impulsive Aggression in Subjects With ADHD in Conjunction With Standard ADHD Treatment (CHIME 4)
Attention Deficit Hyperactivity Disorder (ADHD)
Phase 32016-04-01
CompletedTreatment of Impulsive Aggression in Subjects With ADHD in Conjunction With Standard ADHD Treatment (CHIME 2)
Attention Deficit Hyperactivity Disorder (ADHD)
Phase 32016-02-16
Active Not RecruitingOpen-label Study to Evaluate Long-term Safety and Efficacy of SPN-812 (Viloxazine Extended-release Capsule)
Attention-Deficit/Hyperactivity Disorder
Phase 32016-02-02
CompletedEfficacy and Safety of SPN-812 (Viloxazine Extended-release Capsule) in Children With ADHD
Attention-Deficit/Hyperactivity Disorder (ADHD)
Phase 22016-02-01
CompletedTreatment of Impulsive Aggression in Subjects With ADHD in Conjunction With Standard ADHD Treatment (CHIME 1)
Attention Deficit Hyperactivity Disorder (ADHD)
Phase 32016-01-25
CompletedA Study to Evaluate SAGE-547 in Participants With Severe Postpartum Depression
Severe Postpartum Depression
Phase 22015-12-15
CompletedOpen-Label and Single-Arm Study of MYOBLOC® in the Treatment of Troublesome Sialorrhea in Adults
Sialorrhea
Phase 32015-10-01
CompletedA Study With SAGE-547 for Super-Refractory Status Epilepticus
Super-Refractory Status Epilepticus
Phase 32015-06-01
CompletedEvaluate SAGE-547 in Female Participants With Severe Postpartum Depression
Postpartum Depression
Phase 22015-01-07
CompletedStudy to Evaluate SAGE-547 Injection as Adjunctive Therapy for the Treatment of Super-Refractory Status Epilep
Super-refractory Status Epilepticus
Phase 1 / Phase 22014-03-21
CompletedEfficacy and Safety Study of MYOBLOC® Followed by Open-Label Multiple-Treatment With MYOBLOC® in the Treatment
Sialorrhea
Phase 32013-11-01
CompletedPhase I Study to Assess the Absorption, Metabolism, and Excretion of [14C] Labeled SPN-810M
Impulsive Aggression Comorbid With ADHD
Phase 12013-11-01
CompletedOpen-Label, Extension Study to 810P202
Impulsive Aggression Comorbid With ADHD in Children
Phase 22011-09-01
CompletedA Study to Evaluate the Efficacy and Safety of SPN-810 as Adjunctive Therapy in Children With Impulsive Aggres
Impulsive Aggression Comorbid With ADHD
Phase 22011-06-01
CompletedEvaluation of the Pharmacokinetics, Safety, and Tolerability of TPM XR as Adjunctive Therapy in Pediatric Subj
Epilepsy
Phase 1 / Phase 22011-01-01
CompletedEvaluation of Immediate-Release Viloxazine in Adults With ADHD
Attention-Deficit/Hyperactivity Disorder (ADHD)
Phase 1 / Phase 22010-06-01
CompletedA Conversion Study of Immediate Release (IR) and Modified Release (MR) Forms of Topiramate (TPM)
Epilepsy
Phase 12010-06-01
CompletedSafety and Tolerability of OXC XR as Adjunctive Therapy in Subjects With Refractory Partial Epilepsy
Partial Epilepsy
Phase 32009-06-01
Approved For MarketingLong Term Study of the Safety of OXC XR as in Pediatric Epilepsy Subjects
Epilepsy
2009-06-01
CompletedStudy of PK and Safety of OXC (Oxcarbazepine) XR (Extended Release) as Adjunctive Therapy in Pediatric Epileps
Epilepsies, Partial
Phase 12009-06-01
CompletedEvaluation of Efficacy and Safety of OXC XR as Adjunctive Therapy for Partial Seizures
Epilepsies, Partial
Phase 32008-11-01
CompletedPhase 2a Study of Safety and Tolerability of SPN-810 in Children With ADHD and Persistent Serious Conduct Prob
Attention Deficit Disorder With Hyperactivity, Conduct Disorder
Phase 22008-10-21
Approved For MarketingExpanded Access Protocol of ZULRESSO™ (Brexanolone) Injection for Adult Patients With Postpartum Depression
Postpartum Depression
No Longer AvailableAn Open Label, Expanded Access Protocol With SAGE-547 for Super-Refractory Status Epilepticus
Super-Refractory Status Epilepticus