Ignite Creation Date:
2024-05-05 @ 6:33 PM
Last Modification Date:
2024-10-26 @ 9:35 AM
Study NCT ID:
NCT00509756
Status:
TERMINATED
Last Update Posted:
2010-10-22
First Post:
2007-07-30
Brief Title:
Study Evaluating FXR-450 in Healthy Japanese Men
Sponsor:
Wyeth is now a wholly owned subsidiary of Pfizer
Organization:
Wyeth is now a wholly owned subsidiary of Pfizer
Study Overview
Official Title:
Single Ascending Dose Study of the Safety Tolerability and Pharmacokinetics of FXR-450 Administered Orally to Healthy Japanese Male Subjects
Status:
TERMINATED
Status Verified Date:
2010-10
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Please see termination statement in the detailed description
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The primary purpose of this study is to evaluate the safety tolerability and pharmacokinetics of a single dose of FXR-450 in healthy Japanese men
Detailed Description:
This study was terminated on May 2008 The reason for termination was due to pharmacokinetics issues The decision to terminate was not due to safety and tolerability
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