Major Depressive Disorder Clinical Trial
Official title:
Developing a Biomarker to Predict Response in Treatment Resistant Depression
The primary objectives of the study are to test whether brain Mono Amine Oxidase-A (MAO-A) levels are elevated in patients with treatment-resistant major depression, and to explore whether MAO-A brain levels predict treatment outcome with Mono Amine Oxidase Inhibitor (MAOI) medication in this population.
While Major Depressive Disorder (MDD) is prevalent and disabling, compelling recent data
from the Sequenced Treatment Alternatives to Relieve Depression (STAR*D) study indicate that
only about half of patients attain remission from MDD, even after multiple antidepressant
medication trials. Further, no biomarker has been validated which can select an effective
treatment for such patients, presenting critical unmet intellectual and clinical challenges.
The recent landmark finding of an markedly elevated level of monoamine oxidase A (MAO-A) in
the brains of depressed patients with MDD compared to controls, using positron emission
tomography (PET) with a positron-emitting carbon isotope, (carbon 11 [11C]) labeled
monoamine oxidase inhibitor (MAOI), has provided an unparalleled opportunity to address
these challenges. It has long been known that MAOIs are effective for some patients with
treatment-resistant MDD, although their side effect profile makes them highly unacceptable
both to patients and physicians, severely curtailing their utility.
This study seeks to: 1) replicate this study using PET scans in 20 subjects with MDD but
extending it to patients with treatment-resistant depression (TRD). (Results from these
participants with be compared to those from 10 non-depressed controls; 2) explore the
correlation of the brain MAO-A level biomarker to treatment outcome by treating the 20
PET-imaged TRD patients with an MAOI, hypothesizing that their MAOI response will be related
to their level of MAO-A. Brain MAO-A is an ideal candidate biomarker for this study since it
appears to be significantly abnormally elevated in MDD, yet it has a broad range of values
even among depressed patients. Most importantly, the MAO-A biomarker is known to be the
single pharmacologic target of the treatment, making it appear likely that outcome with MAOI
treatment will be related to MAO-A.
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Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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