Evaluate Long-term Safety and Efficacy of ORADUR®-Methylphenidate in Children and Adolescents With ADHD

PHASE3CompletedINTERVENTIONAL
Enrollment

64

Participants

Timeline

Start Date

January 31, 2016

Primary Completion Date

August 31, 2019

Study Completion Date

August 31, 2019

Conditions
Attention Deficit Hyperactivity Disorder
Interventions
DRUG

ORADUR®-Methylphenidate

ORADUR®-Methylphenidate is available in three dosage forms, 22 mg, 33 mg or 44 mg. Subjects will continue to receive ORADUR®-Methylphenidate at the previously determined optimal dose for 24 months.

Trial Locations (3)

100

National Taiwan University Hospital, Taipei

Unknown

Chang Gung Medical Foundation- Chiayi Branch, Chiayi City

Chang Gung Medical Foundation- Linkuo Branch, Taoyuan District

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Durect

INDUSTRY

lead

Orient Pharma Co., Ltd.

INDUSTRY