Viewing Study NCT04113551


Ignite Creation Date: 2025-12-24 @ 11:40 PM
Ignite Modification Date: 2026-02-20 @ 6:42 PM
Study NCT ID: NCT04113551
Status: COMPLETED
Last Update Posted: 2025-04-27
First Post: 2019-10-01
Is Gene Therapy: True
Has Adverse Events: False

Brief Title: A Study of Label Compliance for Attention Deficit/Hyperactivity Disorder (ADHD) Medications in Japan
Sponsor: Janssen Research & Development, LLC
Organization:

Study Overview

Official Title: Attention Deficit/Hyperactivity Disorder (ADHD) Medications in Japan: A Retrospective Cohort Study of Label Compliance
Status: COMPLETED
Status Verified Date: 2025-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is to document the extent of on-label and off-label use of Methylphenidate (MPH) (Concerta), MPH (Ritalin), Atomoxetine (ATO), and Guanfacine (GFC) in Japan.
Detailed Description: None

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: True
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?:

Secondary ID Infos

Secondary ID Type Domain Link View
PCSESP001604 OTHER Janssen Research and Development, LLC View