To evaluate the effects on psychometric performance and residual depressive symptoms in patients who have been diagnosed with unipolar and bipolar depressio

Phase 1

• Conditions: nipolar and bipolar depression; MedDRA version: 19.0Level: LLTClassification code 10004936Term: Bipolar depressionSystem Organ Class: 100000004873; MedDRA version: 19.0Level: LLTClassification code 10045543Term: Unipolar depressionSystem Organ Class: 100000004873; Therapeutic area: Psychiatry and Psychology [F] - Mental Disorders [F03]

• Registration Number: EUCTR2015-002106-36-RO
• Lead Sponsor: Clinirx Tangent Research

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2015-10-26
• Last Update Posted: 20 June 2016

Recruitment & Eligibility

• Status: ot Recruiting
• Sex: All
• Target Recruitment: 80

Inclusion Criteria

1.Meet DSM V criteria for history of MDD or BPD by MINI.
2.Between 18-50 years of age, male or female subjects of any race, smokers and non-smokers.
3.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.
4.Have a MADRS = 10 and = 34 and an YMRS < 7.
5.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.
6.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).
7.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.
8. 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.)

Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 80
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

1.Women of child bearing potential who do not practice contraception.
2.Psychosis, florid manic or major depressive episode during the 4 weeks preceding baseline day or current psychosis.
3.Patients on more than 2 psychotropic (hypnotics for sleep and occasional SOS for agitation do not count).
4.Smokes more than 40 cigarettes per day.
5.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).
6.Has a clinically significant abnormal 12-lead electrocardiogram (ECG) at Screening Visit 1 as determined by the Investigator.
7.At significant risk of committing suicide, or in the opinion of the Investigator, currently is at imminent risk of suicide or harming others.
8.Patients with a current DSM-IV substance or alcohol dependence.
9.Concurrent delirium, mental retardation, drug-induced psychosis, or history of stroke, brain degenerative disorders and brain trauma.

Study & Design

• Study Type: Interventional clinical trial of medicinal product
• Study Design: Not specified