drugset / Trial / NCT02493777

A Pivotal Efficacy Trial to Evaluate HLD200 in Children With ADHD in a Classroom Setting

NCT02493777

Phase 3 Completed 125 enrolled Ironshore Pharmaceuticals and Development, Inc
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This Phase 3 pivotal efficacy trial will examine the effects of HLD200 (methylphenidate) in patients aged 6-12 years with ADHD in a laboratory classroom setting. This study has a 6-week open-label treatment optimization period followed by a one week randomized, double-blind, placebo-controlled test phase.

Timeline

Start
2015-07
Primary completion
2016-02
Completion
2016-03

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Methylphenidate Small molecule 20 mg
Subject Methylphenidate Small molecule 40 mg
Subject Methylphenidate Small molecule 60 mg
Subject Methylphenidate Small molecule 80 mg
Subject Methylphenidate Small molecule 100 mg