The Relationship Among Changes in Brain Network Activation in Adult Outpatients With Major Depressive Disorder

• Register: ClinicalTrials.gov
• Last refreshed on: 6 October 2015
• Main ID: NCT02559947
• Date of registration: 23/09/2015
• Prospective Registration: Yes
• Primary sponsor: Psychiatric Medicine Associates, L.L.C.
• Public title: The Relationship Among Changes in Brain Network Activation in Adult Outpatients With Major Depressive Disorder
• Scientific title: Relationship Among Changes in Brain Network Activation, Changes in Core Depressive and Cognitive Symptoms and Safety and Tolerability in Adults With Major Depressive Disorder Treated With Open-label, Flexible-dose Vortioxetine
• Date of first enrolment: October 2015
• Target sample size: 50
• Recruitment status: Not yet recruiting
• URL: https://clinicaltrials.gov/show/NCT02559947
• Study type: Interventional
• Study design: Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic
• Phase: Phase 4

Countries of recruitment

United States

Contacts

• Name: Michael E Topel, PsyD
• Affiliation: Partner

• Name: Michael E Topel, PsyD

• Name: John M Zajecka, MD
• Affiliation: Partner

• Name: Erick J Rios

Key inclusion & exclusion criteria

Inclusion Criteria:

- The subject has single episode or recurrent MDD (acute onset of recurrence of
recurrent MDD with poor inter-episode recovery) (inter-episode periods cannot meet
full MDD criteria) as the primary diagnosis according to DSM-IV-TR criteria. The
current MDE will be confirmed using the Mini International Neuropsychiatric Interview
(MINI V6.0.0).

- The subject has a MADRS total score =26.

- Subject reports subjective cognitive dysfunction (such as difficulty concentrating,
slow thinking, and difficulty in learning new things or remembering things).

- The reported duration of the current MDE is at least 3 months and no longer than 24
months.

- The subject is a man or woman between 18 and 65 years old, inclusive.

- Right-handed, normal (corrected) vision, and normal hearing.

Exclusion Criteria:

- The subject has a score of =70 on the DSST at the Baseline Visit.

- Failure to respond to or inability to tolerate an adequate trial of vortioxetine in
the past.

- Exposure to an investigational compound 30 days prior to enrollment

- Exposure to any psychoactive or otherwise excluded medication within five half-lives
of the baseline visit or during the study. Excluded medications include:
antidepressants, anxiolytics, anticonvulsants, barbiturates, chloral hydrate,
lithium, antipsychotics, benzodiazepines, hypnotics, MAO-Inhibitors, muscle relaxers,
Triptans, centrally-acting antihistamines, central alpha-2 agonists, decongestants,
psychostimulants, dopamine agonists, opioid pain medications, oral corticosteroids,
L-methylfolate, SAMe, 5-HTP, St. John's Wort,

- The subject has 1 or more of the following:

- Primary psychiatric disorder other than MDD as defined in the DSM-IV-TR (as
assessed by the MINI, Version 6.0.0).

- Current or history of attention deficit hyperactivity disorder (ADHD), pervasive
developmental disorder, manic or hypomanic episode, schizophrenia, or any other
psychotic disorder, including major depression with psychotic features, mental
retardation, organic mental disorders, or mental disorders due to a general
medical condition as defined in the DSM-IV-TR.

- Current diagnosis of alcohol or other substance abuse or dependence (excluding
nicotine or caffeine) as defined in the DSM-TV-TR that has not been in sustained
full remission for at least 6 months (for abuse) and 12 months (for dependence)
prior to Screening.

- Positive urine drug screen prior to Baseline.

- Presence or history of a clinically significant neurological disorder (including
epilepsy).

- Neurodegenerative disorder (Alzheimer Disease, Parkinson Disease, multiple
sclerosis, Huntington Disease, etc).

- Any unstable medical condition as determined by the principal investigator (PI).

- Any DSM-IV Axis II disorder that might compromise the study as determined by the
PI.

- The subject has any other disorder for which the treatment takes priority over
treatment of MDD or is likely to interfere with study treatment or impair treatment
compliance.

- The subject has physical, cognitive, or language impairment of such severity as to
adversely affect the validity of the data derived from the neuropsychological tests.

- The subject has a significant risk of suicide according to the PI's clinical
judgment.

- The subject, in the opinion of the PI, poses a risk of harm to others.

- The subject has initiated formal cognitive or behavioral therapy, systemic
psychotherapy within less than 6 months of study screening, or has plans to initiate
such therapy during the study.

- The subject has received electroconvulsive therapy, vagus nerve stimulation, or
repetitive transcranial magnetic stimulation within 12 months prior to Screening.

- The current MDE is considered by the PI to have been resistant to 2 adequate
antidepressant treatments of at least 6 weeks duration each at the recommended dose.

- The subject is pregnant or breastfeeding, or is intending to become pregnant before,
during, or within 30 days after participating in this study.



Age minimum: 18 Years
Age maximum: 65 Years
Gender: Both

Health Condition(s) or Problem(s) studied

Major Depressive Disorder

Intervention(s)

Drug: Vortioxetine

Primary Outcome(s)

Montgomery and Asberg Depression Scale (MADRS) [Time Frame: 7 days]

Secondary ID(s)

IISR-2014-100702

Source(s) of Monetary Support

Please refer to primary and secondary sponsors

Secondary Sponsor(s)

Takeda Pharmaceuticals North America, Inc.

ElMindA Ltd