Major Depressive Disorder Clinical Trial
Official title:
Treatment-Resistant Depression Augmentation Therapy With An Analog of the Neuroactive Steroid Allopregnanolone: A Pilot Study
Major depressive disorder (MDD) is highly prevalent and nearly 70% of individuals with MDD do not respond to standard antidepressant therapies despite adequate dosing. An effective and well-tolerated antidepressant augmentation therapy would have important clinical and public health implications. Neuroactive steroid hormones are known to directly activate neurotransmitter receptors in the brain, and thus are potential candidates for augmentation therapies to enhance the effect of traditional antidepressants. Investigators hypothesize that administration of an allopregnanolone analog in women with treatment-resistant depression will improve depressive symptoms.
Major depressive disorder (MDD) is highly prevalent and can have profoundly negative
consequences on one's health, well-being and productivity. Women are twice as likely as men
to experience depression during their lifetimes. In fact, it is reported that twelve million
women in the U.S. each year will experience depression, and that one in eight women will
experience a clinical depressive episode during their lifetimes. Additionally, nearly 70% of
individuals with MDD do not respond to standard antidepressant therapies despite adequate
dosing. Therefore, the identification of an effective and well-tolerated antidepressant
augmentation therapy would have important clinical and public health implications.
Neuroactive steroid hormones are known to directly activate neurotransmitter receptors in
the brain, and thus are potential candidates for augmentation therapies to enhance the
effect of traditional antidepressants. Specifically, allopregnanolone, a steroid hormone
derived from progesterone, is a potent positive modulator of GABA action at GABA-A
receptors, which are known to have positive effects on mood symptoms. Data suggest that
depression, chronic stress and posttraumatic stress disorder may be associated with low
central nervous system allopregnanolone levels.
Investigators propose to administer an oral allopregnanolone analog to 10 postmenopausal
women with treatment-resistant depression as an add-on therapy to their current treatment
for a period of two months. Investigators hypothesize that administration of the oral
allopregnanolone analog in women with treatment-resistant depression will improve depressive
symptoms.
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Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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