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Last Updated: November 4, 2024

CLINICAL TRIALS PROFILE FOR VILOXAZINE HYDROCHLORIDE


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All Clinical Trials for VILOXAZINE HYDROCHLORIDE

Trial ID Title Status Sponsor Phase Start Date Summary
NCT01107496 ↗ A Phase I/IIa, Randomized, Double-Blind Study of the Safety and Efficacy of SPN-812 in Adults With ADHD Completed Supernus Pharmaceuticals, Inc. Phase 1/Phase 2 2010-06-01 This will be a randomized, double-blind, placebo-controlled, parallel group, safety and tolerability study in adults with ADHD. The target subjects are healthy male or female adults aged 18 to 64 years, inclusive, with a diagnosis of ADHD. A total of fifty subjects will be enrolled at approximately 5 sites in the US. Subjects will be randomized (1:1) to one of two treatment groups, SPN-812V or placebo.
NCT02633527 ↗ Efficacy and Safety of SPN-812 (Viloxazine Extended-release Capsule) in Children With ADHD Completed Supernus Pharmaceuticals, Inc. Phase 2 2016-02-01 This was a randomized, double-blind, placebo-controlled, multicenter, 5-arm, parallel-group, dose-ranging study to assess the efficacy and safety of SPN-812 (Viloxazine Extended-release Capsule) in children 6-12 years of age with ADHD.
NCT03247517 ↗ Evaluation of SPN-812 (Viloxazine Extended-release Capsule) Low Dose in Adolescents With ADHD Completed Supernus Pharmaceuticals, Inc. Phase 3 2017-11-02 This study will evaluate the efficacy and safety of low doses of SPN-812 in adolescents 12-17 years of age.
NCT03247530 ↗ Evaluation of SPN-812 (Viloxazine Extended-release Capsule) Low Dose in Children With ADHD Completed Supernus Pharmaceuticals, Inc. Phase 3 2017-10-20 This study will evaluate the efficacy and safety of low doses of SPN-812 in children 6-11 years of age diagnosed with ADHD.
NCT03247543 ↗ Evaluation of SPN-812 (Viloxazine Extended-release Capsule) High Dose in Children With ADHD Completed Supernus Pharmaceuticals, Inc. Phase 3 2017-10-31 This study will evaluate the efficacy and safety of high doses of SPN 812 in children with ADHD
NCT03247556 ↗ Evaluation of SPN-812 (Viloxazine Extended-release Capsule) High Dose in Adolescents With ADHD Completed Supernus Pharmaceuticals, Inc. Phase 3 2017-11-20 This study will evaluate the efficacy and safety of high doses of SPN-812 in adolescents (12-17 years old) with ADHD
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for VILOXAZINE HYDROCHLORIDE

Condition Name

Condition Name for VILOXAZINE HYDROCHLORIDE
Intervention Trials
ADHD 8
Attention-Deficit/Hyperactivity Disorder 3
Attention-Deficit/Hyperactivity Disorder (ADHD) 1
Obstructive Sleep Apnea 1
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Condition MeSH

Condition MeSH for VILOXAZINE HYDROCHLORIDE
Intervention Trials
Attention Deficit Disorder with Hyperactivity 7
Hyperkinesis 3
Sleep Apnea, Obstructive 1
Sleep Apnea Syndromes 1
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Clinical Trial Locations for VILOXAZINE HYDROCHLORIDE

Trials by Country

Trials by Country for VILOXAZINE HYDROCHLORIDE
Location Trials
United States 64
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Trials by US State

Trials by US State for VILOXAZINE HYDROCHLORIDE
Location Trials
Florida 8
California 6
Texas 6
New York 5
Oklahoma 4
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Clinical Trial Progress for VILOXAZINE HYDROCHLORIDE

Clinical Trial Phase

Clinical Trial Phase for VILOXAZINE HYDROCHLORIDE
Clinical Trial Phase Trials
Phase 4 2
Phase 3 7
Phase 2 2
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Clinical Trial Status

Clinical Trial Status for VILOXAZINE HYDROCHLORIDE
Clinical Trial Phase Trials
Completed 7
Not yet recruiting 2
Recruiting 1
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Clinical Trial Sponsors for VILOXAZINE HYDROCHLORIDE

Sponsor Name

Sponsor Name for VILOXAZINE HYDROCHLORIDE
Sponsor Trials
Supernus Pharmaceuticals, Inc. 11
Apnimed 1
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Sponsor Type

Sponsor Type for VILOXAZINE HYDROCHLORIDE
Sponsor Trials
Industry 12
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