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Olanzapine vs. Comparator and Placebo in the Treatment of Patients With Bipolar I Disorder

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT00094549
Recruitment Status : Completed
First Posted : October 21, 2004
Last Update Posted : January 26, 2007
Sponsor:
Information provided by:
Eli Lilly and Company

Brief Summary:

The goals of this study are:

A. To determine whether olanzapine can help patients with bipolar disorder who currently have mild to moderate mania.

B. To assess the safety of olanzapine and any side effects that might be associated with it, as well as the quality of life and functioning of patients treated with olanzapine.

C. To assess how olanzapine compares to divalproex.


Condition or disease Intervention/treatment Phase
Bipolar Disorder Drug: olanzapine Drug: divalproex sodium Drug: placebo Phase 4

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Study Type : Interventional  (Clinical Trial)
Enrollment : 500 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double
Primary Purpose: Treatment
Official Title: Olanzapine Versus Divalproex and Placebo in the Treatment of Mild to Moderate Mania Associated With Bipolar I Disorder
Study Start Date : October 2004
Study Completion Date : December 2006

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Bipolar Disorder




Primary Outcome Measures :
  1. To test the superiority of olanzapine compared with divalproex in improving overall manic symptomatology in patients with mild to moderate
  2. mania associated with bipolar I disorder, as measured by reductions on the Young Mania Rating Scale (YMRS) total score from baseline to the endpoint of Study Period II (3-week acute therapy phase).

Secondary Outcome Measures :
  1. Treatment comparison for the reductions of the YMRS total score from baseline to the endpoint of Study Period II: Assess the superiority of olanzapine compared to placebo;
  2. Assess the superiority of divalproex compared to placebo;
  3. In the event that olanzapine vs. divalproex comparison is not significant, and that divalproex is superior to placebo, an assessment of non-inferiority of olanzapine compared with divalproex will be performed
  4. Assess the acute efficacy of olanzapine compared with divalproex and placebo in improving clinical symptomatology during Study Period II, using several measures: Rate of response, with response defined as reduction of
  5. 50% or more in the YMRS total score at the endpoint of Study Period II; Time to response, with time to response defined as the time in days from first dose at which a reduction of 50% or more in the YMRS total score is first
  6. observed
  7. given that a response is achieved at the endpoint of Study Period II;
  8. Rate of remission of mania, with remission defined as a YMRS total score of less than or equal to 12 at endpoint of Study Period II; Time to remission of mania, with time to remission defined as the time in days from first
  9. dose at which a YMRS total score of less than or equal to 12 is first observed given that remission is achieved at the endpoint of Study Period II; Reductions from baseline to endpoint of Study Period II on the
  10. Montgomery-Asberg Depression Rating Scale (MADRS) total score and the Clinical Global Impressions-Bipolar Version Severity of Illness (CGI-BP Severity) score
  11. Assess the longer-term efficacy of olanzapine compared with divalproex during Study Period III, using several measures: Reductions in the YMRS, MADRS, and CGI-BP scores from the endpoint of Study Period II to the
  12. endpoint of Study Period III; Rate of failure to maintain response during Study Period III, as measured by a return to a YMRS total score greater than or equal to 20 AND/OR hospitalization due to deterioration in clinical
  13. symptoms of mania at any Study Period III visit, among patients who had achieved response by the endpoint of Study Period II; Time to failure to maintain response during Study Period III, as measured by the time
  14. in days from the endpoint of Study Period II to a return to a YMRS total score greater than or equal to 20 AND/OR hospitalization due to deterioration in clinical symptoms of mania, among patients who had achieved
  15. response by the endpoint of Study Period II; Rate of relapse of mania, where relapse is defined as achieving a YMRS total score greater than or equal to 15 AND/OR hospitalization due to deterioration in clinical symptoms
  16. of mania, at any Study Period III visit, among patients who had achieved remission at the endpoint of Study Period II; Time to relapse of mania, as measured by the time in days from the endpoint of Study Period II to a
  17. return to a YMRS total score greater than or equal to 15 AND/OR hospitalization due to deterioration in clinical symptoms of mania, among patients who had achieved remission at the endpoint of Study Period II
  18. Assess the Treatment by Subgroup interaction of Manic vs. Mixed, as defined by DSM-IV (as assessed by the Clinician's Version of the Structured Clinical Interview for DSM-IV [SCID-CV]), during both Study Period II and
  19. Study Period III for efficacy variables of YMRS and CGI-BP
  20. Assess the rate of switch to a depressive episode in patients not depressed at baseline (MADRS score less than or equal to 12, with a depressive episode defined as a MADRS score greater than or equal to 16 OR
  21. hospitalization due to deterioration in clinical symptoms of depression
  22. Assess the safety of olanzapine compared with divalproex and placebo during Study Period II, and to assess the safety of olanzapine compared with divalproex during Study Period III; Safety evaluations will include
  23. assessment of treatment-emergent adverse events, vital signs and weight, laboratory evaluations, electrocardiograms (ECGs), and extrapyramidal symptoms as assessed using the Barnes Akathisia Scale (Barnes),
  24. Abnormal Involuntary Movement Scale (AIMS), and Simpson-Angus Scale
  25. Evaluate functional status and health-related quality of life associated with olanzapine compared with divalproex as measured by change from baseline to endpoints of Study Period II and Study Period III in
  26. the Medical Outcomes Study 36-Item Short Form Health Survey (SF-36)total score and subscale total scores
  27. Evaluate the level of health resource utilization and resource utilization costs associated with olanzapine compared with divalproex during Study Periods II and III (up to 12 weeks of therapy) using the
  28. Resource Utilization
  29. Assess the rate of hospitalization of patients on olanzapine compared with patients on divalproex during Study Periods II and III (up to 12 weeks of therapy) using the Hospitalization Inventory
  30. Evaluate psychosocial outcomes associated with olanzapine compared with divalproex as measured by change from baseline to endpoints of Study Period II and Study Period III on the Streamlined Longitudinal
  31. Interview Clinical Evaluation from the Longitudinal Interval Follow-up Evaluation (SLICE/LIFE)


Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 65 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • You must be 18 to 65 years old.
  • You must have a diagnosis of bipolar I disorder and must be experiencing a manic or mixed (symptoms of mania and depression occurring together) episode.
  • You must be able to visit the doctor's office as scheduled for 15 weeks.
  • All female patients must test negative for pregnancy and, if of childbearing potential, must be using a medically accepted means of contraception.

Exclusion Criteria:

  • You have rapid cycling bipolar disorder, or are having hallucinations or delusions, or are feeling suicidal.
  • You are pregnant or breastfeeding
  • You have a history of: inadequately controlled diabetes; heart disease; narrow angle glaucoma; low white blood cell or platelet count; have a positive test result for human immunodeficiency virus (HIV+); or any other serious, unstable illnesses as judged by the study physician.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00094549


Locations
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United States, Arizona
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Scottsdale, Arizona, United States, 85251
United States, California
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Beverly Hills, California, United States, 90211
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Costa Mesa, California, United States, 92626
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Escondido, California, United States, 92025
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Orange, California, United States, 92868
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Pico Rivera, California, United States, 90660
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San Diego, California, United States, 92108
United States, District of Columbia
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Washington, District of Columbia, United States, 20016
United States, Florida
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Boyton Beach, Florida, United States, 33426
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Deland, Florida, United States, 32720
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North Miami, Florida, United States, 33161
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Tampa, Florida, United States, 33613
United States, Georgia
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Decatur, Georgia, United States, 30033
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Marietta, Georgia, United States, 30060
United States, Idaho
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Eagle, Idaho, United States, 83616
United States, Illinois
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Chicago, Illinois, United States, 60631
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Joliet, Illinois, United States, 60435
United States, Kansas
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Wichita, Kansas, United States, 67207
United States, Maryland
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Baltimore, Maryland, United States, 21285
United States, New York
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Brooklyn, New York, United States, 11223
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Buffalo, New York, United States, 14215
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Rochester, New York, United States, 14624
United States, Oklahoma
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Oklahoma City, Oklahoma, United States, 73120
United States, Pennsylvania
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Media, Pennsylvania, United States, 19063
United States, Tennessee
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Memphis, Tennessee, United States, 38119
United States, Texas
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Austin, Texas, United States, 78756
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Dallas, Texas, United States, 74234
United States, Virginia
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Charlottesville, Virginia, United States, 22903
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Virginia Beach, Virginia, United States, 23452
United States, Washington
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Bellevue, Washington, United States, 98004
United States, West Virginia
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Charleston, West Virginia, United States, 25301
Lithuania
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Klaipeda, Lithuania, 91251
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Siauliai, Lithuania, 76231
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Vilnius, Lithuania, 11205
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Ziegzdriu K, Lithuania, 53136
Puerto Rico
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Caguas, Puerto Rico, 00725
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Ponce, Puerto Rico, 00731
Romania
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Bucharest, Romania, 050042
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Targu Mures, Romania, 540139
Russian Federation
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Lipetsk, Russian Federation, 399007
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Moscow, Russian Federation, 107076
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Saint Petersburg, Russian Federation, 190021
Sponsors and Collaborators
Eli Lilly and Company
Investigators
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Study Director: Call1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon-Fri 9 AM - 5 PM Eastern time (UTC/GMT - 5 hours, EST) Eli Lilly and Company

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
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ClinicalTrials.gov Identifier: NCT00094549    
Other Study ID Numbers: 7029
F1D-MC-HGKQ
First Posted: October 21, 2004    Key Record Dates
Last Update Posted: January 26, 2007
Last Verified: January 2007
Additional relevant MeSH terms:
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Bipolar Disorder
Bipolar and Related Disorders
Mental Disorders
Valproic Acid
Olanzapine
Antiemetics
Autonomic Agents
Peripheral Nervous System Agents
Physiological Effects of Drugs
Gastrointestinal Agents
Antipsychotic Agents
Tranquilizing Agents
Central Nervous System Depressants
Psychotropic Drugs
Serotonin Uptake Inhibitors
Neurotransmitter Uptake Inhibitors
Membrane Transport Modulators
Molecular Mechanisms of Pharmacological Action
Neurotransmitter Agents
Serotonin Agents
Anticonvulsants
Enzyme Inhibitors
GABA Agents
Antimanic Agents