Viewing Study NCT00228553



Ignite Creation Date: 2024-05-05 @ 12:02 PM
Last Modification Date: 2024-10-26 @ 9:19 AM
Study NCT ID: NCT00228553
Status: COMPLETED
Last Update Posted: 2013-07-19
First Post: 2005-09-27

Brief Title: Extension Study of the Safety and Efficacy of Armodafinil in the Treatment of Patients With Excessive Sleepiness
Sponsor: Cephalon
Organization: Teva Branded Pharmaceutical Products RD Inc

Study Overview

Official Title: A 12-Month Open-Label Flexible-Dosage 100 to 250 mgDay Extension Study of the Safety and Efficacy of Armodafinil CEP-10953 in the Treatment of Patients With Excessive Sleepiness Associated With Narcolepsy Obstructive Sleep ApneaHypopnea Syndrome or Chronic Shift Work Sleep Disorder With an Open-Ended Extension Period
Status: COMPLETED
Status Verified Date: 2013-07
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: A 12 Month Open-Label Flexible Dosage Extension Study of the Safety and Efficacy of Armodafinil CEP-10953 in the Treatment of Patients with Excessive Sleepiness Associated with Narcolepsy Obstructive Sleep ApneaHypopnea Syndrome or Chronic Shift Work Sleep Disorder
Detailed Description: None

Study Oversight

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