Viewing Study NCT00079976



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Last Modification Date: 2024-10-26 @ 9:10 AM
Study NCT ID: NCT00079976
Status: COMPLETED
Last Update Posted: 2013-02-08
First Post: 2004-03-19

Brief Title: Study Evaluating Tigecycline in Selected Serious Infections Caused by Vancomycin-Resistant Enterococcus VRE or Methicillin-Resistant Staphylococcus Aureus MRSA
Sponsor: Wyeth is now a wholly owned subsidiary of Pfizer
Organization: Wyeth is now a wholly owned subsidiary of Pfizer

Study Overview

Official Title: A Clinical Research Study to Evaluate the Safety and Efficacy of Tigecycline in the Treatment of Selected Serious Infections Caused by Vancomycin-Resistant Enterococcus VRE or Methicillin-Resistant Staphylococcus Aureus MRSA
Status: COMPLETED
Status Verified Date: 2013-02
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: To evaluate the safety and efficacy of tigecycline in the treatment of selected serious infections caused by VRE The primary efficacy endpoint will be the clinical response for all subjects
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