Depression Clinical Trial
Official title:
The Effects of ARA290 on the Cognitive and Neural Processing of Emotions in Healthy Volunteers
Studies on the hormone Erythropoietin (EPO) have indicated that EPO may have antidepressant properties. However, EPO may cause serious side-effects with repeated administration (thrombosis), which limits its usefulness as an antidepressant. ARA290 is a peptide that does not have the effects of EPO on blood cells but may still have its effect on brain function. In an attempt to replicate previous findings with (a single dose of) EPO in healthy volunteers, we study the effects of ARA290 on the cognitive and neural processing of emotions in healthy volunteers. We hypothesize that a single dose of ARA290 will lead to a positive shift in information processing compared to placebo, 7 days post-administration.
SUMMARY Rationale: Studies on the cognitive and neuronal effects of a single administration
of Erythropoietin (EPO) in healthy volunteers and in depressed patients have suggested that
EPO may have antidepressant effects. Due to its haematopoietic effects, EPO may cause
serious side-effects with repeated administration, which limits its usefulness as an
antidepressant. ARA290 is a peptide that does not have the haematopoietic effects of EPO but
may still have its neurotrophic effects.
Objective: To study the effects of ARA290 on the cognitive and neural processing of emotions
in healthy volunteers 7 days post-administration.
Study design: Randomized double-blind placebo-controlled experiment. Study population: Male
and female healthy volunteers, n= 36; 18-35 yr old. Intervention: One group receives a
single dose of 2 mg ARA290, the other group receives placebo.
Main study parameters/endpoints:
1. Behavioral study: Performance on an Emotional Test battery (ETB) which has been shown
sensitive to antidepressant administration in healthy volunteers. The ETB includes a
measure of facial expression recognition, emotional memory and attentional vigilance.
2. Neuroimaging study: Neural processing of emotions, in particular amygdala, hippocampal
and VMPFC response to viewing facial stimuli expressing negative versus positive
emotions.
Nature and extent of the burden and risks and benefits associated with participation:
Risks: No adverse events have been associated with the administration of a single dose of 70
-2000 μg ARA290 among 36 individuals, with the exception of one individual (with an
undisclosed significant prior history of fainting) who fainted shortly after the intravenous
dose administration of 700 μg ARA290 and recovered without medical intervention. Fourteen
individuals have participated in a multiple dosing study with no serious adverse effects.
Single doses of ARA290 in patients with renal impairment did not raise a safety signal.
Burden: Minimal. Emotional information processing test battery, burden comparable with
playing computer games. fMRI measurement.
Benefits: Probably none. Possibly transient and small improvement of mood state. Financial
compensation for participating.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Basic Science
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