Viewing Study NCT00225199



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Last Modification Date: 2024-10-26 @ 9:19 AM
Study NCT ID: NCT00225199
Status: COMPLETED
Last Update Posted: 2010-04-23
First Post: 2005-09-22

Brief Title: Efficacy and Safety of SH T00660AA in Treatment of Endometriosis
Sponsor: Bayer
Organization: Bayer

Study Overview

Official Title: A Multicenter Double-blind Randomized Placebo-controlled Parallel-group Study to Investigate the Efficacy and Safety of Daily Oral Administration of SH T00660AA for the Treatment of Endometriosis Over 12 Weeks
Status: COMPLETED
Status Verified Date: 2010-04
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: The purpose of this study is to demonstrate safety and efficacy of SH T00660AA compared to placebo in the treatment of endometriosis
Detailed Description: The study has previously been posted by Schering AG Germany Schering AG Germany has been renamed to Bayer Schering Pharma AG Germany

Bayer Schering Pharma AG Germany is the sponsor of the trial

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
Secondary IDs
Secondary ID Type Domain Link
307041 None None None