Investigate Efficacy & Safety of RO4995819 vs. Placebo as Adjunct Tx in Patients w/Major Depressive Disorder

Stanford University

Status and phase: Withdrawn; Phase 2

Conditions: Major Depressive Disorder; Depression

Treatments: Biological: RO4995819

Study type: Interventional

Funder types: Other

Identifiers

NCT01733654

23708

Details and patient eligibility

About

The purpose of the study is to explore the efficacy of 6 weeks treatment of an investigational medication, RO4995819, versus placebo as adjunctive therapy in patients with major depression.

Full description

The investigators hope to learn the efficacy of 6 weeks treatment of RO4995819 versus placebo as adjunctive therapy in patients with MDD having inadequate response to ongoing antidepressant treatment based on mean change in Montgomery Asberg Depression Rating Scale (MADRS) scores from baseline to end of treatment.

This knowledge is valuable because it is a new medication, which may have utility in the population of patients with major depressive disorder.

Sex: All

Ages: 18 to 65 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

Patients are eligible for enrollment in this study if they meet all of the following criteria:

1. An outpatient w/a primary diagnosis of major depressive disorder w/out psychotic features

2. Inadequate response to current, ongoing antidepressant tx of SSRI/SNRI.

3. Having at least 1 but no more than 2 antidepressant treatment failures w/in the index depressive episode

4. Dose/duration of antidepressant treatment in index episode can be verified by documentation from one of following:

   1. Med records;
   2. Pharmacy records;
   3. Treating and/or referring physician (indicating medication, dose, dates of treatment).

5. Documentation of clinical/treatment history must be available.

6. Index depressive episode started w/in 1 year of screening.

7. Confirmed compliance w/current SSRI/SNRI treatment based on blood screen.

8. Existing med regimens should be stable for 6 wks prior to screening

9. 18-65 y.o. at time of consent

10. BMI 18.0 to 35.0 kg/m2 inc.

11. Patients w/reproductive potential must agree to use specified contraceptive protection during tx period and for at least 90 days after last dose of study drug:

    • Males w/partners of childbearing potential or partners must use a barrier method of contraception or remain sexually abstinent.
    • Females who are not either surgically sterile (tubal ligation, removal of ovaries or uterus) or post-menopausal (no spontaneous menstrual periods for at least 1 yr confirmed by a hormone panel [FSH and 17βestradiol])must agree to use 2 adequate methods of contraception, including at least one method w/ failure rate of < 1% per yr (e.g., hormonal implants, combined oral contraceptives, vasectomized partner, abstinence).

12. Able to participate and willing to give written informed consent.

Exclusion criteria

Patients are excluded from this study if the answer is 'yes' to any of the following:

Current and past treatment history:

1. Currently receiving tx w/3 or more antidepressants.
2. Currently receiving tx w/prohibited meds.
3. Significant ongoing use of high doses of barbiturates, benzodiazepines or other anxiolytic drugs.
4. Previously received RO4995819.
5. Participated in investigational drug or device study w/in 6 mos of screening or in index depressive episode.
6. History of non-response to Electroconvulsive Therapy (ECT), Vagus Nerve Stimulation (VNS),or Repetitive Transcranial Magnetic Stimulation (RTMS).
7. Planning to begin/change current regimen of individual psychotherapy including cognitive behavioral therapy during the 6 week treatment period of the study and the first 2 weeks of follow-up.
8. Present DSM-IV-TR axis I diagnosis except for anxiety comorbidity
9. Past or present psychotic symptoms.
10. Mood disorder due to medical condition or substance use/abuse/dependence.
11. Established personality disorder
12. Alcohol and/or substance abuse/dependence during the last 6 months.
13. A significant risk for suicidal behavior
14. Past or present neurological disorder.
15. Present eating disorder
16. Abnormal thyroid function.
17. Active upper gastrointestinal tract disease
18. Unstable medical condition that could pose unacceptable risk to the patient in this study.
19. Positive result on hepatitis B (HBV), hepatitis C (HCV), or HIV 1 and 2.
20. Positive test for drugs of abuse.
21. Abnormality on 12-lead electrocardiogram (ECG), including a QTcF of ≥450 milliseconds.
22. Lab abnormality
23. Positive pregnancy test, breast feeding,or intention to become pregnant during the course of the trial.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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0 participants in 4 patient groups, including a placebo group

RO4995819 5mg

Active Comparator group

Description:

RO4995819 5mgX6wks

Treatment:

Biological: RO4995819

RO4995819 15mg

Active Comparator group

Description:

RO4995819 15mg X 6 weeks

Treatment:

Biological: RO4995819

RO4995819 30mg

Active Comparator group

Description:

RO4995819 30mg X 6 weeks

Treatment:

Biological: RO4995819

Placebo

Placebo Comparator group

Description:

Placebo X 6 weeks

Treatment:

Biological: RO4995819