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Safety and Efficacy of Vilazodone in Major Depressive Disorder

NCT01473381 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 1162

Last updated 2014-08-08

Study results available
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Summary

The purpose of this study was to evaluate the efficacy, safety, and tolerability of 2 fixed dose levels of vilazodone compared to placebo in patients with major depressive disorder.

Conditions

Interventions

DRUG

Vilazodone

Vilazodone was supplied as film-coated tablets.

DRUG

Placebo to citalopram

Placebo to citalopram was supplied as a capsule.

DRUG

Placebo to vilazodone

Placebo to vilazodone was supplied as film-coated tablets.

DRUG

Citalopram

Citalopram was supplied as encapsulated tablets.

Sponsors & Collaborators

  • Forest Laboratories

    lead INDUSTRY

Principal Investigators

  • Carl Gommoll, MS · Forest Laboratories

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2011-12-31
Primary Completion
2013-06-30
Completion
2013-06-30

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

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 NCT01473381 on ClinicalTrials.gov