drugset / Trial / NCT03088267

Dyanavel® XR Extended-Release Oral Suspension in the Treatment of Children With ADHD: A Laboratory School Study

NCT03088267

Phase 3 Completed 18 enrolled Tris Pharma, Inc.
RandomizedCrossoverDouble-blindTreatment

Summary

This study was conducted to assess the efficacy and safety of DYANAVEL XR (amphetamine extended-release oral suspension, CII) for the treatment of symptoms of attention-deficit/hyperactivity disorder (ADHD) in children aged 6-12 years.

Timeline

Start
2017-02-11
Primary completion
2017-02-25
Completion
2017-10-30

Drugs

EvaluationDrugModalityDoseRoute
Comparator Amphetamine Unknown 5 mg Oral
Comparator Amphetamine Unknown 17.5 mg Oral
Comparator Amphetamine Unknown 20 mg Oral