Viewing Study NCT00044057



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Last Modification Date: 2024-10-26 @ 9:07 AM
Study NCT ID: NCT00044057
Status: COMPLETED
Last Update Posted: 2006-04-03
First Post: 2002-08-16

Brief Title: A Study to Evaluate the Effects of YM872 on Brain Function and Disability When Administered in Combination With Alteplase Tissue Plasminogen Activator
Sponsor: Astellas Pharma Inc
Organization: Astellas Pharma Inc

Study Overview

Official Title: A Multicenter Stratified Randomized Double-Blind Placebo-Controlled Study to Evaluate Neurologic Function and Disability in Patients With Acute Ischemic Stroke Given Tissue Plasminogen Activator Plus YM872 or Tissue Plasminogen Activator Plus Placebo
Status: COMPLETED
Status Verified Date: 2006-03
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: The purpose of this study is to determine if YM872 in combination with t-PA can reduce disability and brain damage from stroke YM872 or placebo will be given as a continuous intravenous iv infusion for 24 hours It is important that the study medication YM872 or placebo is administered prior to the completion of the t-PA administration The clinical effects of YM872 in addition to t-PA will be determined by assessing neurological function and disability scores at follow up visits through Day 90 of the study
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