Clinical Trial of Memantine for Major Depression

Completed · Phase 3

Conditions studied: Depression

In brief

The purpose of this study is to determine the safety and effectiveness of the drug memantine for treating major depression. Major depression is a serious public health concern that contributes to significant morbidity and mortality. Despite the availability of a wide range of antidepressant drugs, a proportion of patients with major depression fail to respond to first-line antidepressant treatment, despite adequate dosage, duration, and compliance. Recent studies suggest that the glutamatergic system may play a role in the pathophysiology and treatment of depression. Memantine and other agents which reduce glutamatergic neurotransmission may represent a novel class of antidepressants. The study consists of three phases. In Phase 1, participants will be tapered off all psychiatric medications over a 2-week washout period. In Phase 2, participants will be randomly assigned to receive either memantine or placebo (an inactive pill) three times a day for 8 weeks. Participants who do not respond to the treatment after 8 weeks will be taken off the study and offered standard treatment. Weekly psychiatric evaluations will evaluate treatment response. During Phase 2, participants who respond well to treatment will enter Phase 3, a 16-week continuation phase of either memantine or placebo. Interviews will be conducted every other week in the first month , then monthly thereafter. Participants will have a physical examination, neuropsychological tests, and eye blink tests at baseline and at the end of the study. Pulse, blood pressure, and blood samples will be taken throughout the study. Participants will undergo an electrocardiogram as well as positron emission tomography (PET) and magnetic resonance imaging (MRI) scans of the brain.

Key facts

Study ID

NCT00040261

Run by

National Institute of Mental Health (NIMH)

People needed

112

Starts

2002-06-01

Expected to finish

2005-03-01

Last updated by the study team

2008-03-04

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subjects may be included in the study only if they meet all of the following criteria:
• Male or female subjects, 18 to 80 years of age.
• Female subjects of childbearing potential must be using a medically accepted means of contraception.
• Each subject must have a level of understanding sufficient to agree to all tests and examinations required by the protocol.
• Subjects must be considered reliable.
• Each subject must understand the nature of the study and must sign an informed consent document.
• Subjects must fulfill the criteria for major depression, recurrent without psychotic features as defined in DSM-IV based on clinical assessment and confirmed by structured diagnostic interview SCID-P.
• Subjects must have an initial score at Visit 1 and Visit 2 of at least 22 on the MADRS.
• Subjects must not have a decrease in the total score of MADRS of greater than 20 % during washout (between Visits 1 and 2).
• Current major depressive episode of at least 4 weeks duration.

You may not qualify if…

• Subjects will be excluded from the study for any of the following reasons:
• Lack of response to more than 2 antidepressants (adequate dose and duration).
• Participation in a clinical trial of another investigational drug within 1 month (30 days) prior to study entry (Visit 1).
• Female subjects who are either pregnant or nursing.
• Serious, unstable illnesses including hepatic, renal, gastroenterologic, respiratory, cardiovascular (including ischemic heart disease), endocrinologic, neurologic, immunologic, or hematologic disease.
• Subjects with uncorrected hypothyroidism or hyperthyroidism.
• Subjects with one or more seizures without a clear and resolved etiology.
• Documented history of hypersensitivity or intolerance to amantadine or prior treatment with memantine.
• DSM-IV substance abuse or dependence (except nicotine and caffeine) within the past 90 days.
• Treatment with an injectable depot neuroleptic within less than one dosing interval between depot neuroleptic injections prior to Visit 2.
• Treatment with a reversible monoamine oxidase inhibitor, guanethidine, or guanadrel within 1 week prior to Visit 2.
• Treatment with fluoxetine within 6 weeks prior to Visit 2.
• Treatment with any other concomitant medication with primarily CNS activity.
• Treatment with clozapine within 4 weeks prior to Visit 2.
• Treatment with amitriptyline (elavil) within 4 weeks prior to Visit 2 since amitriptyline and similar TCAs may manifest a mild NMDA receptor antagonism, as demonstrated in electrophysiological studies.
• Treatment with the anticonvulsants carbamazepine (tegretol, carbatrol, tegretol XR and similar derivatives), gabapentin (neurontin) or felbamate (felbatol) within 4 weeks prior to Visit 2 because these drugs may interfere with NMDA receptor function.
• Treatment with electroconvulsive therapy (ECT) within 3 months (90 days) prior to Visit 2.
• Current diagnosis of schizophrenia or other psychotic or bipolar disorder as defined in the DSM-IV.
• Judged clinically to be at serious suicidal risk.

Where it is running

• National Institute of Mental Health (NIMH) — Bethesda, Maryland, United States

Full record on ClinicalTrials.gov

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