Viewing Study NCT00384930



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Last Modification Date: 2024-10-26 @ 9:28 AM
Study NCT ID: NCT00384930
Status: COMPLETED
Last Update Posted: 2009-09-02
First Post: 2006-10-03

Brief Title: Study of Tadalafil Once-a Day for 12 Weeks in Men With Signs and Symptoms of Benign Prostatic Hyperplasia
Sponsor: Eli Lilly and Company
Organization: Eli Lilly and Company

Study Overview

Official Title: A Randomized Double-Blind Placebo-Controlled Parallel-Design 5-Group Multinational Study to Evaluate the Efficacy Dose Response and Safety of Tadalafil Once-a-Day Dosing for 12 Weeks in Men With Signs and Symptoms of Benign Prostatic Hyperplasia
Status: COMPLETED
Status Verified Date: 2009-08
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: This is a randomized double-blind placebo-controlled parallel-design multinational 12-week study to compare the efficacy dose response and safety of tadalafil once a day versus placebo in men with signs and symptoms of benign prostatic hyperplasia including lower urinary tract symptoms
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
Secondary IDs
Secondary ID Type Domain Link
H6D-MC-LVHG None None None