Expired Study
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Stanford, California 94305


Purpose:

We will assess the effect of olanzapine compared to placebo added to prior treatment on CGI-S in a one-week randomized double-blind study. We will also assess the effect of olanzapine added to prior treatment on CGI-S in an eight-week open treatment study. In addition, we will assess the effect of olanzapine on Young Mania Rating Scale (YMRS), Hamilton and Montgomery-Asberg Depression Rating Scales (HDRS, and MADRS), and Hamilton Anxiety Rating Scales (HARS) in the above paradigms. We will also assess the influence of presentation severity (CGI-S) and polarity (mood elevation versus depression) on olanzapine response. Finally, we will assess safety and tolerability of olanzapine in the above paradigms. We hypothesize that in diverse mild syndromal and subsyndromal exacerbations of BD in outpatients, randomized double-blind flexibly dosed olanzapine added to prior treatment (including no treatment) will yield greater CGI-S improvement than placebo by the end of one week, and that such improvement will persist over one week of open continuation treatment.


Study summary:

Development and marketing of new therapies for bipolar disorders (BD) has typically entailed performing double-blind placebo-controlled trials in acute mania 1, 2, maintenance studies 3, 4, and more recently acute depression studies 5. Such an approach addresses BD primarily in terms of episodes and has the strength of studying levels of pathology sufficiently high to permit detection of treatment effects, and guiding clinicians when they encounter syndromal mood episodes. However, this approach has the important limitation of not addressing an important unmet clinical need, namely the management of subsyndromal symptoms. Indeed, emerging data suggest that in BD subsyndromal symptoms compared to syndromal episodes are far more pervasive 6, 7. Also such an approach runs the risk of not paying sufficient attention to the disorder construct, in a sense permitting preoccupation with syndromal episodes to carry more importance than the disorder. Our group has published a novel open study of olanzapine in diverse exacerbations of BD 8. Twenty-five bipolar disorder [14 bipolar I (BPI), 10 bipolar II (BPII) and one bipolar disorder not otherwise specified (BP NOS)] outpatients received open olanzapine (15 adjunctive, 10 monotherapy). Thirteen had elevated (11 syndromal, two subsyndromal) and 12 depressed (four syndromal, eight subsyndromal) mood symptoms of at least mild severity, with Clinical Global Impression-Severity (CGI-S) scores of at least 3. Only one had psychotic symptoms. With open olanzapine (15 adjunctive, 10 monotherapy), overall symptom severity (CGI-S) as well as mood elevation (Young Mania Rating Scale), depression (Hamilton and Montgomery-Asberg Depression Rating Scales), and anxiety (Hamilton Anxiety Rating Scale), rapidly decreased (significantly by days 2-3). Patients with the greatest baseline severity (CGI-S) had the greatest improvement. Fifteen of 25 (60%) patients responded. Time to consistent response was bimodal, with five early (by 0.5 +/- 0.3 weeks) and 10 late (by 7.0 +/- 1.9 weeks) responders. Early compared with late responders had 51% lower final olanzapine doses. Olanzapine was generally well tolerated, with sedation and weight gain the most common adverse effects. Thus, olanzapine appeared effective in diverse exacerbations of BD in outpatients. Controlled studies are warranted to further explore these preliminary observations.


Criteria:

Inclusion Criteria:Patients must meet the following criteria to be eligible to participate in the study: - Male or female outpatients, 18 to 70 years of age - Female patients of childbearing potential must be using a medically accepted means of contraception - Able to communicate intelligently with the investigator, and study coordinator - Able to give informed consent - DSM-IV diagnosis of bipolar I, bipolar II, cyclothymic disorder or bipolar disorder not otherwise specified, experiencing an acute exacerbation of their illness at Visit 1 (hypomania, subsyndromal depression, hypomania and subsyndromal depression, depression and hypomania, or depression if diagnosed with bipolar II) as verified by SCID-I/P - CGI-BP Overall Severity score greater than or equal to mildly ill at Visit 1 - Must have been on prior medications for at least 2 weeks (6 weeks for fluoxetine) immediately prior to study entry Exclusion Criteria:Patients may not participate in the study if they have any of the following conditions: - Pregnant, nursing, or intending to become pregnant during the study - Serious, unstable illnesses including hepatic, renal, gastroenterologic, respiratory, cardiovascular (including ischemic heart disease), endocrinologic, neurologic, immunologic, or hematologic disease such that hospitalization for the disease is anticipated within 3 months or death is anticipated within 3 years. - A history of seizure disorder - History of leukopenia without a clear and resolved etiology. - DSM-IV substance (except nicotine or caffeine) dependence within the past month - Judged clinically to be at serious suicidal risk - Participation in clinical trial of another investigational drug within 1 month (30 days) prior to study entry. - Treatment with an injectable depot neuroleptic within less than one dosing interval between depot neuroleptic injections prior to study entry - Treatment resistance, non-response, or intolerability with olanzapine by the investigator's judgment - Treatment with clozapine within 3 months prior to study entry - Treatment with remoxipride within 6 months (180 days) prior to study entry - Treatment with an oral antipsychotic within 2 days prior to study entry - A course of ECT (electroconvulsive therapy) in the preceding 4 weeks - Excluded mood symptoms noted in Table 1 [of protocol] - Unstable thyroid pathology and treatment-initiated or altered within the past 3 months - Meet criteria for antisocial personality disorder


Study is Available At:


Original ID:

79897


NCT ID:

NCT00186017


Secondary ID:

F1D-US-X279


Study Acronym:


Brief Title:

Short Term Rescue Study of Olanzapine


Official Title:

Double-Blind Placebo-Controlled Olanzapine Add-on Therapy in the Treatment of Acute Syndromal and Subsyndromal Exacerbations in Bipolar Disorders


Overall Status:

Completed


Study Phase:

Phase 4


Genders:

Both


Minimum Age:

18 Years


Maximum Age:

70 Years


Quick Facts

Healthy Volunteers
Oversight Has DMC
Study Is FDA Regulated
Study Is Section 801
Has Expanded Access

Study Source:

Stanford University


Oversight Authority:

United States: Food and Drug Administration


Reasons Why Stopped:


Study Type:

Interventional


Study Design:

Allocation: Randomized, Endpoint Classification:


Number of Arms:

2


Number of Groups:

0


Total Enrollment:

50


Enrollment Type:

Actual


Overall Contact Information

Official Name:Terence Arthur Ketter
Principal Investigator
Stanford University

Study Dates

Start Date:July 2005
Completion Date:June 2010
Completion Type:Actual
Primary Completion Date:June 2010
Primary Completion Type:Actual
Verification Date:December 2012
Last Changed Date:December 11, 2012
First Received Date:September 12, 2005

Study Outcomes

Outcome Type:Primary Outcome
Measure:CGI-S
Time Frame:prior week
Safety Issues:False
Outcome Type:Secondary Outcome
Measure:YMRS
Time Frame:prior week
Safety Issues:True
Outcome Type:Secondary Outcome
Measure:Hamilton and Montgomery-Asberg Depression Rating Scales (HDRS, and MADRS)
Time Frame:Prior week
Safety Issues:False
Outcome Type:Secondary Outcome
Measure:Hamilton Anxiety Rating Scales (HARS)
Time Frame:Prior week
Safety Issues:False

Study Interventions

Intervention Type:Drug
Name:Olanzapine/Zyprexa
Arm Name:Olanzapine/Zyprexa

Study Arms

Study Arm Type:Experimental
Arm Name:Olanzapine/Zyprexa
Description:Olanzapine/Zyprexa 2.5 mg up to 8 per day for 1 week
Study Arm Type:Placebo Comparator
Arm Name:Placebo
Description:Placebo

Study Agencies

Agency Class:Other
Agency Type:Lead Sponsor
Agency Name:Stanford University
Agency Class:Industry
Agency Type:Collaborator
Agency Name:Eli Lilly and Company

Sample and Retention Information

There are no available Sample and Retention Information

Study References

There are no available Study References

Data Source: ClinicalTrials.gov

Date Processed: November 18, 2019

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