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Sponsored by: |
Pfizer |
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Information provided by: | Pfizer |
ClinicalTrials.gov Identifier: | NCT00163059 |
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 |
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 |
Ages Eligible for Study: | 18 Years to 55 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
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 |
Depression Mental Disorders Mood Disorders |
Depressive Disorder, Major Depressive Disorder Behavioral Symptoms |
Pathologic Processes Disease |