Study Of 323U66 SR In Major Depressive Disorder

NCT00135512 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 234

Last updated 2019-02-01

Study results available
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Summary

This study was designed to evaluate the efficacy and safety in major depressive disorder patients.

Conditions

  • Depressive Disorder

Interventions

DRUG

bupropion hydrochloride

Study drug

Sponsors & Collaborators

Principal Investigators

  • GSK Clinical Trials · GlaxoSmithKline

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
64 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2004-12-01
Primary Completion
2007-05-28
Completion
2007-05-28

Countries

  • Japan

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00135512 on ClinicalTrials.gov