Viewing Study NCT00042575



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Last Modification Date: 2024-10-26 @ 9:07 AM
Study NCT ID: NCT00042575
Status: COMPLETED
Last Update Posted: 2006-07-19
First Post: 2002-07-31

Brief Title: Dose Escalation Double-Blind Treatment With Duloxetine Hydrochloride Once Daily Dosing for Evaluation of Safety in Major Depression
Sponsor: Eli Lilly and Company
Organization: Eli Lilly and Company

Study Overview

Official Title: Protocol F1J-US-HMBY Dose Escalation Double-Blind Treatment With Duloxetine Hydrochloride Once Daily Dosing for Evaluation of Safety in Major Depression
Status: COMPLETED
Status Verified Date: 2006-07
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The Purposes of this Study are to determine

The safety of duloxetine and any side effects that might be associated with it

Whether duloxetine can help patients with major depression

It is possible that information collected during this study will be analyzed by the sponsor in the future to evaluate duloxetine for other possible uses or for other medical or scientific purposes other than those currently proposed

Duloxetine might not have any good effects for you
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
F1J-US-HMBY None None None