A Phase II, Adaptive Trial Design Examining the Pharmacokinetic and Pharmacodynamic Effects of Modified Release Amphetamine (HLD100, Formulations B, C and E)) in Adolescents and Children With Attention-Deficit Hyperactivity Disorder (ADHD)

Last updated:
2026-07-11
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View trial details

Overview

Official protocol title:

A PHASE II, TWO-STAGE, OPEN-LABEL, SINGLE-TREATMENT, ADAPTIVE TRIAL DESIGN EXAMINING THE PHARMACOKINETIC AND PHARMACODYNAMIC EFFECTS OF UP TO THREE SEPARATE HLD100 MODIFIED RELEASE FORMULATIONS OF DEXTROAMPHETAMINE SULFATE IN ADOLESCENT (STAGE 1) AND PEDIATRIC (STAGE 2) PATIENTS WITH ATTENTION-DEFICIT HYPERACTIVITY DISORDER.

Intervention/treatment:
DEXTROAMPHETAMINE (HLD100)
Medical condition:
ATTENTION DEFICIT HYPERACTIVITY DISORDER (ADHD)
Protocol code:
HDL100-102
Control number:
163513
Status:
Closed
Approved:
May 03, 2013
Trial phase:
Phase 1, Phase 2
For more information:
ClinicalTrials.gov - NCT01886469
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
6 Years to 17 Years
Accepts healthy volunteers: No

Contacts and locations

Contact
Sponsor
IRONSHORE PHARMACEUTICALS & DEVELOPMENT INC

Locations

Saskatchewan

Saskatoon Centre for Patient-Oriented Research, Royal University Hospital, Room 5681, C Wing
Saskatoon, Saskatchewan, S7N 0W8
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