HopeStage
Back to all studies
CompletedNCT03247556

Evaluation of SPN-812 (Viloxazine Extended-release Capsule) High Dose in Adolescents With ADHD

Researchers compared 400mg SPN-812, 600mg SPN-812 and placebo to find out how the approaches affected ADHD symptoms in young people with ADHD.

Medication studyAges 12–17United States
The study in practice

Understand this study

What did researchers investigate?

Researchers compared 400mg SPN-812, 600mg SPN-812 and placebo to find out how the approaches affected ADHD symptoms in young people with ADHD.

Who was this study for?

This study was for people with ADHD. Listed age limits: 12 years to 17 years. Other eligibility criteria applied.

Listed locations
Long Beach and 13 more locationsSee all locations and recruitment
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
Study clarity

Study information

Study start dateStarted: November 20, 2017
Recruitment status
Completed
Enrollment listed in the registry
297
Sponsor
Supernus Pharmaceuticals, Inc.
Sponsor type
Pharmaceutical company
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
Locations
United States
Age range
From 12 Years to 17 Years
Official registry ID
NCT03247556
Official title
Show the full official title

Evaluation of SPN-812 (Viloxazine Extended-release Capsule) 400 and 600 mg Efficacy and Safety in Adolescents With ADHD - A Double-Blind, Placebo-Controlled, Pivotal Trial

Looking for a study you can join?

Explore recruiting studies

Recruitment & locations

Completed

Long Beach · Colorado Springs · Bradenton

9 more locations
  • Lauderhill
  • Miami
  • Orlando
  • Decatur
  • Oklahoma City
  • Charleston
  • Beaumont
  • Houston
  • Clinton
FAQ

Questions about this study

What did researchers investigate?

Researchers compared 400mg SPN-812, 600mg SPN-812 and placebo to find out how the approaches affected ADHD symptoms in young people with ADHD.

Who is behind this study?

The study sponsor is Supernus Pharmaceuticals, Inc., a pharmaceutical company.

Did this study involve medication?

Yes. The study involved medication, including Placebo, 400mg SPN-812 and 600mg SPN-812.

Who was this study for?

This study was for people with ADHD. Listed age limits: 12 years to 17 years. Other eligibility criteria applied.

Explore other studies

Want to find a study that may fit you better?

Answer a few simple questions to explore HopeStage studies by condition, country, and situation.

Find a study that may fit me