Viewing Study NCT00044044



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Last Modification Date: 2024-10-26 @ 9:07 AM
Study NCT ID: NCT00044044
Status: COMPLETED
Last Update Posted: 2014-04-17
First Post: 2002-08-16

Brief Title: A Comparison of Study Drug With Placebo and Haloperidol in Patients With Schizophrenia
Sponsor: Sumitomo Pharma America Inc
Organization: Sumitomo Pharma America Inc

Study Overview

Official Title: A 6-Week Double-Blind Randomized Fixed-Dose Parallel-Group Study of the Efficacy and Safety of Three Dose Levels of SM-13496 Compared to Placebo and Haloperidol in Patients With Schizophrenia Who Are Experiencing an Acute Exacerbation of Symptoms
Status: COMPLETED
Status Verified Date: 2014-03
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 evaluate the efficacy of the drug SM-13496 compared to a placebo and to haloperidol in patients with schizophrenia
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