The Effects of JNJ-39393406 on Psychometric Performance and Residual Depressive (JNJ-DEP)

Tangent Data

Status and phase

Completed

Phase 2

Conditions

Depression

Treatments

Drug: JNJ-39393406

Drug: Placebo

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT02677207

JNJ-DEP

Details and patient eligibility

About

To evaluate the effects of the nicotinic allosteric modulator JNJ-39393406 on psychometric performance and residual depressive symptoms in patients who have been diagnosed with unipolar and bipolar depression but currently DO NOT meet criteria for an episode of Major Depression or Manic Episode.

Full description

Hypothesis: Allosteric modulation of the a7nAChR with JNJ-39393406 improves psychometric performance and residual depressive symptoms in patients with unipolar major depression disorder (MDD) or bipolar depression (BPD).

Outcome measurements:

BACS
MADRS
BNSS
CGI-S- BP,
Questionnaire on smoking urges (QSU) and time to the first cigarette after waking up in the morning,
Readiness for discharge scale.

Enrollment

80 patients

Sex

All

Ages

18 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Meet DSM V criteria for history of MDD or BPD by MINI.
Between 18-50 years of age, male or female subjects of any race, smokers and non-smokers.
Able to provide informed consent. All participant patients must have signed an informed consent document indicating they understand the purpose of the study and the procedures required for the study and are willing to participate by complying with the study procedures and restrictions.
Have a MADRS ≥ 10 and ≤ 34 and an YMRS < 7.
In the opinion of the investigator, basic education and severity of symptoms (psychotic, negative, manic, agitation, depression) do not prevent the patient from attending to the cognitive tasks.
In the opinion of the investigator the patient can be safely treated with no more than 2 psychotropic medications as background therapy (SOS for agitation and sleeping medication are allowed in addition to the 2 psychotropics).
The background psychotropic(s) that will be continued through-out the 2 week trial must have been started at least 2 weeks prior to the baseline day at doses allowed by the local regulations and no changes in dose have been made during this pre-baseline 2 week period.
Inpatients or out-patients at the discretion of the investigator (If outpatients the Readiness for Discharge Scale has to be administered at baseline and at each visit.)

Exclusion criteria

Women of child bearing potential who do not practice contraception.
Psychosis, florid manic or major depressive episode during the 4 weeks preceding baseline day or current psychosis.
Patients on more than 2 psychotropic (hypnotics for sleep and occasional SOS for agitation do not count).
Smokes more than 40 cigarettes per day.
Unstable medical disease (malignancy, poorly controlled diabetes, or cardiomyopathy, serious pulmonary disease, kidney disease, impaired liver functioning. Particular attention should be given to exclude patients with ischemic heart disease).
Has a clinically significant abnormal 12-lead electrocardiogram (ECG) at Screening Visit 1 as determined by the Investigator.
At significant risk of committing suicide, or in the opinion of the Investigator, currently is at imminent risk of suicide or harming others.
Patients with a current DSM-V substance or alcohol dependence.
Concurrent delirium, mental retardation, drug-induced psychosis, or history of stroke, brain degenerative disorders and brain trauma.