Overview

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

Status:
Completed
Trial end date:
2016-03-01
Target enrollment:
Participant gender:
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.
Phase:
Phase 3
Details
Lead Sponsor:
Ironshore Pharmaceuticals and Development, Inc
Treatments:
Methylphenidate