Bipolar Disorder
Conditions
Brief summary
To compare combination treatment of aripiprazole plus valproate versus valproate alone in the prevention of relapse in bipolar I disorder patients with symptomatic remission after 5-6 weeks open-label acute treatment with aripiprazole plus valproate for manic or mixed episode, with or without psychotic features.
Detailed description
Further study details as provided by Korea OIAA
Interventions
DRUGaripiprazole
15-30 mg/day aripiprazole, 22 weeks
DRUGvalproate
sufficient dose as determined by investigator to maintain the therapeutic level.
DRUGplacebo
placebo to aripiprazole, 22 weeks
Sponsors
Korea Otsuka International Asia Arab
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No
Inclusion criteria
1. Subjects able to give informed consent, and/or consent obtained from a legally acceptable representative (as required by IRB/IEC) prior to the initiation of any protocol required procedures; 2. Subjects with Bipolar I Disorder, manic or mixed episode, with or without psychotic features, as defined by DSM-IV-TR and confirmed by the M.I.N.I.; 3. Subjects who are able to understand the nature of the study and follow protocol requirements including the prescribed dosage regimens, capsule/tablet ingestion, discontinuation of prohibited concomitant medications, and who can be reliably rated on assessment scales; 4. Subjects willing to discontinue all medication starting from the signing of the informed consent and during the study phases (allowed exceptions noted in Section 6.4.2); 5. Men or women aged ≥ 18 and ≤ 65 years; 6. Subjects with YMRS total score ≥ 20 (to be assessed prior entry into open-label acute treatment phase); 7. YMRS total score ≤ 12 for 2 consecutive visits (to be assessed at Week 5 and/or Week6 prior entry into double-blind treatment phase).
Exclusion criteria
1. WOCBP who are unwilling or unable to use an acceptable method to avoid pregnancy for the entire study period and for up to four weeks after completion of the study. Acceptable methods include oral, injectable or implanted contraceptives, intrauterine devices or barrier methods such as condoms, diaphragm, and spermicides; 2. Women who are pregnant or breast-feeding; 3. Subjects presenting clinically with a current DSM-IV-TR diagnosis of delirium, dementia, amnestic or other cognitive disorders, or a psychotic disorder (e.g., schizophrenia or schizoaffective disorder). Also, subjects with borderline, paranoid, histrionic, schizotypal, schizoid, or antisocial personality disorder; 4. Subjects with a current Axis I (DSM-IV-TR) diagnosis of Bipolar II Disorder, rapid cyclers (experiencing four or more manic or depressive episodes per year), Bipolar Disorder NOS, or any other primary psychiatric disorder other than Bipolar I Disorder; 5. Subjects with documented evidence of first manic episode; 6. Subjects considered treatment refractory for manic symptoms; (Note: if a subject has failed ≥ 2 antimanic treatments, e.g., antipsychotic, lithium, valproate or carbamazepine at therapeutic dose and duration, exclusive of the current episode, obtain permission from the Otsuka medical monitor to include the subject) 7. Subjects previously nonresponsive to aripiprazole for manic symptoms; 8. Subjects with a significant risk of committing suicide based on history, mental status exam, or investigator's judgment; 9. Subjects who have met DSM-IV-TR criteria for substance abuse within the past three months, or substance dependence\* within the past 6 months, including benzodiazepines; (\* exceptional for subjects with substance dependence on nicotine or caffeine); 10. Subjects with thyroid pathology (e.g., hypothyroidism or hyperthyroidism) unless condition has been stabilized with medications for at least the past three months; (Note: Subjects with an abnormal thyroid function test may be retested prior to the start of study medication. Subjects with an abnormal thyroid function test at screening will not be eligible for the study, unless permission is obtained from Otsuka); 11. Subjects who have a history or evidence of a medical condition that would expose them to an undue risk of a significant adverse event or interfere with assessments of safety or efficacy during the course of the trial, including but not limited to hepatic, renal, respiratory, cardiovascular, endocrine (e.g., Addison's Disease), immune, neurologic, or hematologic disease as determined by the clinical judgment of the investigator; 12. Subjects with a significant history of seizure disorder (e.g., epilepsy); 13. The following laboratory tests results, vital signs, and ECG findings are exclusionary: * Platelets ≤ 75000/mm3 * Hemoglobin ≤ 9g/dL * Neutrophils, absolute ≤ 1000/ mm3 * SGOT (AST) \> 3x Upper Limit of Normal * SGPT (ALT) \> 3x Upper Limit of Normal * Creatinine ≥ 2 mg/dL * QTc \> 475 msec 14. Subjects with a recent antipsychotic use who have a CPK ≥ 550 IU (Otsuka should be contacted to discuss any elevated CPK levels); 15. Subjects who are known to be allergic, intolerant, or unresponsive to valproate or to aripiprazole; 16. Subjects with a history of neuroleptic malignant syndrome from antipsychotic agents; 17. Subjects likely to require prohibited concomitant therapy during the study as indicated in Section 6.4 of the protocol; 18. Recent treatment of their most recent manic or mixed acute episode with a long acting antipsychotic in which the last dose was less than one full cycle plus one week prior to entering Phase 2 (haloperidol decanoate treatment within the past five weeks, fluphenazine decanoate treatment within the past three weeks or Risperdal ConstaTM treatment within the past three weeks); 19. Subjects likely to require the initiation of intensive individual psychotherapy during the course of the study (Note: Group and supportive therapy is allowed, if part of the subject's ongoing treatment. Individual psychotherapy is allowed if the subject has consistently received psychotherapy for at least 3 months prior to the study and will continue during the study); 20. ECT treatment within the current episode or within two months prior to the study; 21. Prisoners or subjects who are compulsorily detained (involuntarily incarcerated) for treatment of either a psychiatric or physical (e.g., infectious disease) illness must not be enrolled into this study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Time to relapse in double-blind treatment phase | throughout the study |
Secondary
| Measure | Time frame |
|---|---|
| Mean change from baseline to all time point in YMRS total score; | throughout the study |
| Mean change from baseline to all time points in MADRS total score | throughout the study |
| Response rate (≥ 50% improvement in YMRS total score) at all time points | throughout the study |
Countries
Hong Kong, Philippines, Taiwan, Thailand
Outcome results
None listed