Viewing Study NCT01198626



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Last Modification Date: 2024-10-26 @ 10:24 AM
Study NCT ID: NCT01198626
Status: TERMINATED
Last Update Posted: 2011-12-08
First Post: 2010-09-07

Brief Title: Efficacy and Safety Study of JNJ-32729463 Compared With Moxifloxacin for the Treatment of Subjects Requiring Hospitalization for Community-Acquired Bacterial Pneumonia
Sponsor: Furiex Pharmaceuticals Inc
Organization: Furiex Pharmaceuticals Inc

Study Overview

Official Title: A Randomized Controlled Double Blind Multicenter Phase 2 Study of the SafetyTolerability and Efficacy of JNJ-32729463 Compared With Moxifloxacin for the Treatment of Subjects Requiring Hospitalization for Community-Acquired Bacterial Pneumonia CABP With a PORT Score of II or Greater
Status: TERMINATED
Status Verified Date: 2011-12
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Enrollment would not have been met prior to the end of the pneumonia season Termination is based on slow enrollment and not related to safety or efficacy
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 determine the efficacy safety and tolerability of JNJ-32729463 compared to moxifloxacin for the treatment of subjects requiring hospitalization for Community-Acquired Bacterial Pneumonia CABP
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