Viewing Study NCT00399542



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Last Modification Date: 2024-10-26 @ 9:28 AM
Study NCT ID: NCT00399542
Status: COMPLETED
Last Update Posted: 2019-12-17
First Post: 2006-11-13

Brief Title: Efficacy and Safety of Lubiprostone in Patients With Irritable Bowel Syndrome With Constipation
Sponsor: Sucampo Pharma Americas LLC
Organization: Mallinckrodt

Study Overview

Official Title: Phase 3 12-Week Multicenter Double-Blind Randomized Efficacy and Safety Study of Lubiprostone for the Treatment of Irritable Bowel Syndrome With Constipation
Status: COMPLETED
Status Verified Date: 2013-09
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 primary purpose of this study is to evaluate the efficacy and safety of administration of lubiprostone in patients with irritable bowel syndrome with constipation
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