Phase 2
Completed N=142
Efficacy and Safety Study of a Combination Product [Drug:BCI-024 (Buspirone) and Drug:BCI-049 (Melatonin)] to Treat Major Depressive Disorder (MDD)
Source: ClinicalTrials.gov NCT00705003 ↗Enrolled (actual)
142
Serious AEs
0.0%
Results posted
Jun 2014
Primary outcomePrimary: The Score on the Clinical Global Impression-Improvement (CGI-I) at Week 6 — 2.37; 2.82; 2.86 units on a scale
Summary
The primary objective of this study are to evaluate the synergistic effect of a combination product, consisting of drug BCI-024 (buspirone) and drug BCI-049 (melatonin), in reducing symptoms of depression in patients with Major Depressive Disorder.
The safety and tolerability of the combination product will also be evaluated as measured by adverse events and vital signs.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY The Score on the Clinical Global Impression-Improvement (CGI-I) at Week 6 |
2.37; 2.82; 2.86 | — |
| SECONDARY The Change From Baseline in the CGI-S at Week 6 |
1.43; .93; 0.97 | — |
| SECONDARY The Change From Baseline in the IDS-C30 at Week 6 |
19.24; 16.35; 14.42 | — |
| SECONDARY The Change From Baseline in the Quick Inventory of Depressive Symptomatology - 16 Item Self-Report (QIDS-SR16) at Week 6 |
8.57; 6.65; 7.31 | — |
| SECONDARY The Change From Baseline on the HAM-A at Week 6 |
9.04; 6.69; 6.51 | — |
Eligibility Criteria
Inclusion Criteria
- Subjects will be male and female subjects between the ages of 18 to 65 meeting the Diagnostic and Statistical Manual of Mental Disorders-IV-Text Revision (DSM-IV-TR) criteria for Major Depressive Disorder with a Quick Inventory of Depressive Symptomatology-16 Item Self Report (QIDS-SR16) score of >14 at the Screening and Baseline Visits.
- Female subjects must be on a stable and medically reliable form of birth control, must agree to continue use of this birth control during the study, and must have negative urine pregnancy tests at the Screening Visit.
Exclusion Criteria
- Subjects with any other psychiatric Axis-I disorder as a principal diagnosis within 6 months of screening or subjects with a history of obsessive compulsive disorder, psychotic disorder, bipolar disorder, or mental retardation at any time are not eligible for the study.
- Subjects who pose a suicidal risk or who have a history of eating disorder or substance dependence within 6 months of screening, or a history of substance abuse within 3 months of screening are also ineligible.
- Subjects with clinically significant abnormalities on any Screening or Baseline assessments, including laboratory tests, are excluded.
- Subjects with a known intolerance to either buspirone or melatonin are excluded, as are subjects with clinically significant medical or psychiatric conditions that might be detrimental to the subject should they participate in the study.
- Subjects who have used selective serotonin reuptake inhibitors (SSRIs) within 2 weeks of Screening (within 4 weeks for fluoxetine) are excluded as are subjects requiring concomitant use of antipsychotic and anxiolytic medications and any drugs with known psychotropic properties. Concomitant medications that are not excluded by the protocol and that are taken chronically must be at a stable dosage for at least 4 weeks prior to screening.
Data sourced from ClinicalTrials.gov (NCT00705003). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.