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The Antidepressant Effects Of The NMDA Antagonist, CP-101,606, In Patients With MDD
This study has been completed.
Sponsored by: Pfizer
Information provided by: Pfizer
ClinicalTrials.gov Identifier: NCT00163059
  Purpose

To determine if the NMDA antagonist, CP-101,606, is effective for depression


Condition Intervention Phase
Depressive Disorder, Major
Drug: NMDA Antagonist, CP-101,606 (traxoprodil)
Phase II

MedlinePlus related topics: Antidepressants Depression
Drug Information available for: Traxoprodil
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Single Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study
Official Title: A Randomized, Double-Blinded, Placebo-Controlled Trial To Assess The Antidepressant Effects Of The NMDA Antagonist, CP-101,606, In Patients With Treatment Refractory Major Depressive Disorder

Further study details as provided by Pfizer:

Primary Outcome Measures:
  • MADRS

Secondary Outcome Measures:
  • HAM-D

Estimated Enrollment: 30
Study Start Date: May 2004
Estimated Study Completion Date: December 2005
  Eligibility

Ages Eligible for Study:   18 Years to 55 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Primary DSM-IV diagnosis of MDD

Exclusion Criteria:

  • Subjects with evidence or history of clinically significant hematological, renal, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric, neurologic, or allergic disease (including drug allergies, but excluding untreated, asymptomatic, seasonal allergies at time of dosing).
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00163059

Locations
United States, Kansas
Pfizer Investigational Site
Wichita, Kansas, United States, 67214-2878
Sponsors and Collaborators
Pfizer
Investigators
Study Director: Pfizer CT.gov Call Center Pfizer
  More Information

To obtain contact information for a study center near you, click here.  This link exits the ClinicalTrials.gov site

Study ID Numbers: A1611006
Study First Received: September 9, 2005
Last Updated: September 21, 2006
ClinicalTrials.gov Identifier: NCT00163059  
Health Authority: United States: Food and Drug Administration

Study placed in the following topic categories:
Depression
Mental Disorders
Mood Disorders
Depressive Disorder, Major
Depressive Disorder
Behavioral Symptoms

Additional relevant MeSH terms:
Pathologic Processes
Disease

ClinicalTrials.gov processed this record on January 15, 2009