Viewing Study NCT01687478



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Last Modification Date: 2024-10-26 @ 10:56 AM
Study NCT ID: NCT01687478
Status: TERMINATED
Last Update Posted: 2019-10-09
First Post: 2012-09-07

Brief Title: A Study of Olanzapine and Fluoxetine for Treatment-resistant Depression
Sponsor: Eli Lilly and Company
Organization: Eli Lilly and Company

Study Overview

Official Title: A Study to Assess the Short-Term Efficacy and Safety of Olanzapine and Fluoxetine Compared to Placebo and Fluoxetine for Nonpsychotic Treatment-Resistant Depression
Status: TERMINATED
Status Verified Date: 2019-09
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Interim assessment Lack of 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 assess the efficacy and safety of olanzapine and fluoxetine compared to placebo and fluoxetine as treatment for treatment-resistant depression TRD in Chinese participants
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
F1D-CR-HGNB OTHER Eli Lilly and Company None