Bipolar DisorderPhase 3NCT01113541
One-Year Trial of Oral Ziprasidone in Bipolar Patients With Metabolic Syndrome
A Phase 3 study testing Ziprasidone HCL (oral) in people with Bipolar Disorder, run by Pfizer's Upjohn has merged with Mylan to form Viatris Inc. at 10 sites in Canada.
Trial summary
The purpose of this study is to explore the impact of Ziprasidone HCl on the distribution of metabolic syndrome (MS) risk factors in a population of Bipolar patients presenting with glucose intolerance, dyslipidemia and/or elevated waist circumference associated with their current antipsychotic medication. Read more about this study
- Who is it for?
- Ages 18 to 65 years
- Conditions the study is for
- Bipolar Disorder
- What is being tested?
- Ziprasidone HCL (oral)
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 13 participants
- Where
- 10 sitesCanada
- Study dates
- Jul 2010to Feb 2011
- Phase
- Phase 3
- Are there results?
- Yes, posted in the registrySummary in the doctors' view
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 65 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Subject must present at least 2 of the following risk factors of MS at screening: Elevated waist circumference: >102 cm in men and >88 cm in women; Elevated triglycerides (TGs): ≥1.7 mmol/L (≥150 mg/dL); Reduced HDL-Cholesterol: <1.03 mmol/L (<40 mg/dL) in men and <1.3 mmol/L (<50 mg/dL) in women; Elevated fasting glucose: ≥ 5.6 mmol/L.
- According to the clinical judgment of the investigator, the risk factors for MS have developed in close temporal relationship to starting an antipsychotic medication.
- Substitution to a less metabolically disruptive antipsychotic medication is considered
Who cannot join
- Subjects with contraindication(s) to the use of Ziprasidone according to Canadian prescribing information.
- Subjects with a history of treatment resistance.
- Subjects with any medical condition (e.g. pre-existing diabetes, pre-existing dyslipidemia, thyroid pathology) or taking any concomitant medication (e.g. topiramate or other weight loss-promoting agents, hypoglycemic agents, hypolipemic agents), that may confound the evaluation of the study drug.
- Body mass index ≥ 40 at baseline.
Trial locations and contacts
10 sites in 1 country.
10 sites in 1 country
Canada10 sites
Foothills Medical Centre, Department of Psychiatry
Calgary, Alberta, T2N 2T9
Mental Health Centre for Research and Education
Calgary, Alberta, T2N 2T9
Capital, Health Authority, QE II Health Sciences Centre, Mood Disorder Clinic
Halifax, Nova Scotia, B3H 2E2
Centre de recherche Fernand-Seguin de l'hopital Louis H. Lafontaine
Montreal, Quebec, H1N 3V2
Clinique St-Leonard
Montreal, Quebec, H1P 3K2
Dr. Alexander McIntyre Inc.
Penticton, British Columbia, V2A 4M4
Diex Research Sherbrooke Inc.
Sherbrooke, Quebec, J1H 1Z1
Office of Dr. A. K. Munshi
Sydney, Nova Scotia, B1S 2E8
Country Club Plaza
Winnipeg, Manitoba, R3K 2E2
Edgeland Medical, Dr. Alla Kirshner Medical Corporation
Winnipeg, Manitoba, R3P 0N5
About this study
Official title: A One-year, Phase III, Open-label, Non-comparative Trial of the Effect of Ziprasidone HCl on Metabolic Syndrome Risk Factors in Patients With Bipolar Disorder
The purpose of this study is to explore the impact of Ziprasidone HCl on the distribution of metabolic syndrome (MS) risk factors in a population of Bipolar patients presenting with glucose intolerance, dyslipidemia and/or elevated waist circumference associated with their current antipsychotic medication.
Read the detailed description
The trial was terminated prematurely on December 14, 2010, due to inability to recruit the planned number of subjects and shifting organizational priorities. The decision to terminate the trial was not based on any safety or efficacy concerns.
- Conditions
- Bipolar Disorder
- Being tested
- Ziprasidone HCL (oral)
- Keywords
- Ziprasidone, Bipolar Disorder, Metabolic Syndrome
- Medical subject headings
- Bipolar Disorder, Metabolic Syndrome
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Ziprasidone HCL (oral)Drug
Also called Zeldox, Geodon
Ziprasidone Hydrochloride 20 to 80 mg administered orally twice a day (40-160 mg total daily dose) for up to 1 year.
| Study group | Role | What they receive |
|---|---|---|
| Active treatment (switch to oral Ziprasidone) | Experimental | Not described Receives: Drug: Ziprasidone HCL (oral) |
What is being measured
The primary outcome is the main question the study is designed to answer.
Percentage of Participants Who Achieved a Reduction From Baseline of at Least 1 Risk Factor for Metabolic Syndrome (MS) at Week 52 or Premature Discontinuation
MS risks factors: elevated (el) waist circumference: ≥102 centimeters (cm) in men and ≥88 cm in women (Asian origin: ≥90 cm [men] and ≥80 cm [women]); el triglycerides: ≥1.7 millimoles per liter (mmol/L) (1≥50 milligrams per deciliter [mg/dL]); reduced high-density lipoprotein cholesterol (HDL-C): <1.03 mmol/L (<40 mg/dL) in men and <1.3 mmol/L (<50 mg/dL) in women; el fasting glucose: ≥5.6 mmol/L (≥100 mg/dL); and el systolic/diastolic blood pressure: systolic ≥130 millimeters of mercury (mmHg) and/or diastolic ≥85 mmHg. Responder = at least 1 less risk factor at endpoint than baseline.
Measured: Week 52 or Early Termination
Secondary outcomes (29)
Mean Change From Baseline in the Number of Risk Factors of Metabolic Syndrome (MS)
MS risks factors: elevated waist circumference: ≥102 cm in men and ≥88 cm in women (Asian origin: ≥90 cm [men] and ≥80 cm [women]); elevated triglycerides: ≥1.7 mmol/L (1≥50 mg/dL); reduced HDL-C: <1.03 mmol/L (<40 mg/dL) in men and <1.3 mmol/L (<50 mg/dL) in women; elevated fasting glucose: ≥5.6 mmol/L (≥100 mg/dL); and elevated systolic/diastolic blood pressure: systolic blood pressure ≥130 mm Hg and/or diastolic blood pressure ≥85 mm Hg.
Measured: Baseline, Week 52
Metabolic Syndrome (MS) Prevalence
Percentage of participants at each visit defined as having metabolic syndrome (MS) based on the National Cholesterol Education Program (NCEP) Adult Treatment Panel III. MS = 3 or more of 5 characteristics: abdominal obesity, hypertriglyceridemia, low high-density lipoprotein (HDL) cholesterol, high blood pressure, and high fasting glucose.
Measured: Baseline through Week 52
Change From Baseline in the Percentage of Participants With Each Individual Metabolic Syndrome (MS) Risk Factor
MS risks factors: elevated waist circumference: ≥102 cm in men and ≥88 cm in women (Asian origin: ≥90 cm [men] and ≥80 cm [women]); elevated triglycerides: ≥1.7 mmol/L (1≥50 mg/dL); reduced HDL-C: <1.03 mmol/L (<40 mg/dL) in men and <1.3 mmol/L (<50 mg/dL) in women; elevated fasting glucose: ≥5.6 mmol/L (≥100 mg/dL); and elevated systolic/diastolic blood pressure: systolic blood pressure ≥130 mm Hg and/or diastolic blood pressure ≥85 mm Hg.
Measured: Baseline through Week 52
Percentage of Participants With Individual Metabolic Syndrome (MS) Risk Factors
MS risks factors = elevated waist circumference: ≥102 cm in men and ≥88 cm in women (Asian origin: ≥90 cm [men] and ≥80 cm [women]); elevated triglycerides: ≥1.7 mmol/L (1≥50 mg/dL); reduced HDL-C: <1.03 mmol/L (<40 mg/dL) in men and <1.3 mmol/L (<50 mg/dL) in women; elevated fasting glucose: ≥5.6 mmol/L (≥100 mg/dL); and elevated systolic/diastolic blood pressure: systolic blood pressure ≥130 mm Hg and/or diastolic blood pressure ≥85 mm Hg.
Measured: Baseline through Week 52
Change From Baseline in Individual Risk Factors of Metabolic Syndrome (MS): Elevated Waist Circumference
MS risk factor elevated waist circumference defined as ≥102 centimeters (cm) in men and ≥88 cm in women (Asian origin: ≥90 cm [men] and ≥80 cm [women]).
Measured: Baseline, Week 4, Week 12, Week 52
Change From Baseline in Individual Risk Factors of Metabolic Syndrome (MS): Elevated Systolic/Diastolic Blood Pressure
MS risk factor elevated systolic/diastolic blood pressure defined as systolic blood pressure ≥130 millimeters of mercury (mm Hg) and/or diastolic blood pressure ≥85 mm Hg.
Measured: Baseline, Week 4, Week 12, Week 52
Change From Baseline in Individual Risk Factors of Metabolic Syndrome (MS): Elevated Fasting Glucose
MS risk factor elevated fasting glucose defined as ≥5.6 millimoles per liter (mmol/L) (≥100 mg/dL).
Measured: Baseline, Week 4, Week 12, Week 52
Change From Baseline in Individual Risk Factors of Metabolic Syndrome (MS): Reduced High-density Lipoprotein Cholesterol (HDL-C)
MS risk factor reduced HDL-C defined as <1.03 millimoles per liter (mmol/L) (<40 mg/dL) in men and <1.3 mmol/L (<50 mg/dL) in women.
Measured: Baseline, Week 4, Week 12, Week 52
Change From Baseline in Individual Risk Factors of Metabolic Syndrome (MS): Elevated Triglycerides
MS risk factor elevated triglycerides defined as ≥1.7 millimoles per liter (mmol/L) (1≥50 mg/dL).
Measured: Baseline, Week 4, Week 12, Week 52
Change From Baseline in Ten-year Coronary Heart Disease (CHD) Risk According to Framingham Scoring System
Framingham scoring system risk factors: age (risk points range: -9 to 16), cholesterol (risk points range: 0 to 13), HDL cholesterol (risk points range: -1 to 2), smoking (risk points range: 0 to 9), and systolic blood pressure (risk points range: 0 to 6); total risk points range <0 to ≥25, higher score indicates higher 10 year risk (range <1% to ≥30% 10 year risk).
Measured: Baseline, Week 4, Week 52
Change From Baseline in Total Cholesterol and Low-density Lipoprotein (LDL) Cholesterol Levels
Measured: Baseline, Week 52 or Early Termination
Change From Baseline in Weight
Measured: Baseline, Week 4, Week 12, Week 52 or Early Termination
Change From Baseline in Body Mass Index (BMI)
Body mass index = weight in kilograms (kg) / height in meters (m)^2 .
Measured: Baseline, Week 4, Week 12, Week 52 or Early Termination
Change From Baseline in Glycosylated Hemoglobin (HbA1c)
Measured: Baseline, Week 52 or Early Termination
Change From Baseline in Insulin Levels
Measured: Baseline, Week 52 or Early Termination
Change From Baseline in Corrected QT Interval (QTc): Fridericia's Heart Rate Correction Formula (QTcF)
QT interval is the time between the start of the Q wave and the end of the T wave in the cardiac electrical cycle. QTc is the QT interval corrected for heart rate. Corrected QT interval using Fridericia's heart rate correction formula: QTcF = QT/RR^1/3, where RR=RR interval in seconds.
Measured: Baseline, Week 4, Week 52 or Early Termination
Change From Baseline in Apolipoprotein B (ApoB) Levels
Measured: Baseline, Week 52 or Early Termination
Change From Baseline in Leptin
Measured: Baseline, Week 52 or Early Termination
Change From Baseline in Physical Activity Index
Physical activity (exercise) score derived for each participant based on the frequency and intensity of physical activities: regular walking, recreational activity, cycling, and sporting activity. Six categories of total score: inactive (range: 0-2), occasional (range: 3-5), light (range: 6-8), moderate (range: 9-12), moderately vigorous (range: 13-20), and vigorous (≥21). Higher score = higher frequency and intensity of physical activity.
Measured: Baseline, Week 28, Week 52 or Early Termination
Change From Baseline in Montgomery-Asberg Depression Rating Scale (MADRS) - Total Score
Measures the overall severity of depressive symptoms. The MADRS has a 10-item checklist. Items are rated on a scale of 0-6, for a total score range of 0 (low severity of depressive symptoms) to 60 (high severity of depressive symptoms).
Measured: Baseline, Week 4, Week 12, Week 28, Week 52 or Early Termination
Change From Baseline in Young Mania Rating Scale (YMRS)
11-item scale that measures the severity of manic episodes from subject reported symptoms over previous 48 hours and clinical observation during interview. Four items (irritability, speech, thought content, disruptive-aggressive behaviour) are rated on a scale from 0 (symptom not present) to 8 (symptom extremely severe). The remaining 7 items (elevated mood, increased motor activity-energy, sexual interest, sleep, language-thought disorder, appearance, insight) are rated on a scale from 0 (symptom not present) to 4 (symptom extremely severe). YMRS total score range = 0 to 60.
Measured: Baseline, Week 4, Week 12, Week 28, Week 52 or Early Termination
Change From Baseline in Clinical Global Impression - Severity (CGI-S) Subscale
CGI-S: 7-point clinician rated scale to assess severity of participant's current illness state; range: 1 (normal - not ill at all) to 7 (among the most extremely ill patients). Higher score = more affected.
Measured: Baseline, Week 4, Week 12, Week 28, Week 52 or Early Termination
Clinical Global Impression - Improvement (CGI-I) Subscale Score
CGI-I: 7-point clinician rated scale ranging from 1 (very much improved) to 7 (very much worse). Improvement is defined as a score of 1 (very much improved), 2 (much improved), or 3 (minimally improved) on the scale. Higher score = more affected.
Measured: Week 52 or Early Termination
Change From Baseline in Drug Attitude Inventory (DAI)
DAI, a 10-item scale to assess how the attitude of schizophrenia participants toward their medications may affect compliance. Respondents indicate 'true' or 'false' for each item. An overall calculated score ranged from -10 to 10, where a positive score indicated a positive subjective response (compliant), a negative score indicated non-compliance. Change: score at observation minus score at baseline.
Measured: Week 28, Week 52 or Early Termination
Change From Baseline in Social and Occupational Functioning Assessment Scale (SOFAS)
0-100 single score scale focusing exclusively on participant's level of social and occupational functioning; not directly influenced by overall severity of participant's psychological symptoms; higher score = higher level of functioning. 1 to 10 = persistent inability to maintain minimal personal hygiene; unable to function without harming self or others or without considerable external support; 91 to 100 = superior functioning in a wide range of activities.
Measured: Baseline, Week 28, Week 52 or Early Termination
Change From Baseline in EuroQoL Index (EQ-I)
EQ-5D: subject rated questionnaire to assess health-related quality of life in terms of a single utility score. Health State Profile component assesses level of current health for 5 domains: mobility, self-care, usual activities, pain and discomfort, and anxiety and depression; 1 indicates better health state (no problems); 3 indicates worst health state (confined to bed). Scoring formula developed by EuroQol Group assigns a utility value for each domain in the profile. Score is transformed and results in a total score range -0.594 to 1.000; higher score indicates a better health state.
Measured: Baseline, Week 28, Week 52 or Early Termination
Change From Baseline in European Quality of Life (EuroQol) Visual Analogue Scale (EQ-5D VAS): Current Health State Score
EQ-5D: subject rated questionnaire to assess health-related quality of life in terms of a single index value. The VAS component rates current health state on a scale from 0 (worst imaginable health state) to 100 (best imaginable health state); higher scores indicate a better health state.
Measured: Baseline, Week 28, Week 52 or Early Termination
Change From Baseline in Impact of Weight on Quality of Life-Lite Version (IWQOL-Lite) Scale
31-item self report inventory to assess impact of weight on quality of life. Five subscales: physical functioning, self-esteem, sexual life, public distress, and work, with categories in each subscale scored 1 (no trouble or difficulty) to 5 (persistent trouble or difficulty). The rescaled IWQoL-Lite score is determined by the sum of scores on all 31 items and rescaling this sum to a 1 to 100 scoring with 0=the poorest and 100=the best quality of life.
Measured: Baseline, Week 28, Week 52 or Early Termination
Number of Participants With Suicidal Tendencies (Columbian-Suicide Severity Rating Scale, [C-SSRS], Mapped to C-CASA [Columbia Classification Algorithm For Suicide Assessment])
C-SSRS is a participant rated questionnaire to assess suicidal ideation, suicidal behavior, actual attempts (yes or no responses), and intensity of ideation (rated 1=low severity to 5=high severity). Yes/No responses are mapped to Columbia Classification Algorithm of Suicide Assessment (C-CASA) categories: Completed suicide, suicide attempt, preparatory acts toward imminent suicidal behavior, suicidal ideation, and self-injurious behavior, or no suicidal intent. A participant could have a yes or no response in more than one category.
Measured: Baseline, Week 1 through Week 52 or Early Termination
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted30 Apr 2010 (estimated)
- Study startJul 2010
- Primary completionFeb 2011
- Study completionFeb 2011
Why it stopped: See termination reason in detailed description.
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Other trials for Bipolar DisorderStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 3
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 13 participants (actual)
Sponsor and investigators
- Lead sponsor
- Pfizer's Upjohn has merged with Mylan to form Viatris Inc.
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Pfizer CT.gov Call Center, Study director, Pfizer
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01113541
- Sponsor's protocol ID
- A1281190
- Status last verified
- Mar 2021
- First submitted
- 28 Apr 2010
- Last updated
- 3 Mar 2021
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 3 Mar 2021. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A One-year, Phase III, Open-label, Non-comparative Trial of the Effect of Ziprasidone HCl on Metabolic Syndrome Risk Factors in Patients With Bipolar Disorder
- ClinicalTrials.gov ID
- NCT01113541
- Acronym / sponsor ID
- A1281190
- Conditions
- Bipolar Disorder
- Keywords
- Ziprasidone, Bipolar Disorder, Metabolic Syndrome
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- TerminatedReason stopped: See termination reason in detailed description.
- Enrolment
- 13 participants (actual)
- Lead sponsor
- Pfizer's Upjohn has merged with Mylan to form Viatris Inc.Industry (pharma, biotech, devices)
- Study start
- Jul 2010
- Primary completion
- Feb 2011 (actual)
- Study completion
- Feb 2011 (actual)
- First posted
- 30 Apr 2010 (estimated)
- Results
- Posted 9 Jul 2012
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The purpose of this study is to explore the impact of Ziprasidone HCl on the distribution of metabolic syndrome (MS) risk factors in a population of Bipolar patients presenting with glucose intolerance, dyslipidemia and/or elevated waist circumference associated with their current antipsychotic medication.
Detailed description
The trial was terminated prematurely on December 14, 2010, due to inability to recruit the planned number of subjects and shifting organizational priorities. The decision to terminate the trial was not based on any safety or efficacy concerns.
Study design
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Active treatment (switch to oral Ziprasidone) | Experimental | Drug: Ziprasidone HCL (oral) |
Who may qualify
- Ages
- 18 to 65 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- Subject must present at least 2 of the following risk factors of MS at screening: Elevated waist circumference: >102 cm in men and >88 cm in women; Elevated triglycerides (TGs): ≥1.7 mmol/L (≥150 mg/dL); Reduced HDL-Cholesterol: <1.03 mmol/L (<40 mg/dL) in men and <1.3 mmol/L (<50 mg/dL) in women; Elevated fasting glucose: ≥ 5.6 mmol/L.
- According to the clinical judgment of the investigator, the risk factors for MS have developed in close temporal relationship to starting an antipsychotic medication.
- Substitution to a less metabolically disruptive antipsychotic medication is considered
Key exclusion criteria (4 listed)
- Subjects with contraindication(s) to the use of Ziprasidone according to Canadian prescribing information.
- Subjects with a history of treatment resistance.
- Subjects with any medical condition (e.g. pre-existing diabetes, pre-existing dyslipidemia, thyroid pathology) or taking any concomitant medication (e.g. topiramate or other weight loss-promoting agents, hypoglycemic agents, hypolipemic agents), that may confound the evaluation of the study drug.
- Body mass index ≥ 40 at baseline.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Ziprasidone HCL (oral)Also: Zeldox, GeodonZiprasidone Hydrochloride 20 to 80 mg administered orally twice a day (40-160 mg total daily dose) for up to 1 year. | Drug | Active treatment (switch to oral Ziprasidone) |
Primary outcome
Percentage of Participants Who Achieved a Reduction From Baseline of at Least 1 Risk Factor for Metabolic Syndrome (MS) at Week 52 or Premature Discontinuation
Time frame: Week 52 or Early Termination
MS risks factors: elevated (el) waist circumference: ≥102 centimeters (cm) in men and ≥88 cm in women (Asian origin: ≥90 cm [men] and ≥80 cm [women]); el triglycerides: ≥1.7 millimoles per liter (mmol/L) (1≥50 milligrams per deciliter [mg/dL]); reduced high-density lipoprotein cholesterol (HDL-C): <1.03 mmol/L (<40 mg/dL) in men and <1.3 mmol/L (<50 mg/dL) in women; el fasting glucose: ≥5.6 mmol/L (≥100 mg/dL); and el systolic/diastolic blood pressure: systolic ≥130 millimeters of mercury (mmHg) and/or diastolic ≥85 mmHg. Responder = at least 1 less risk factor at endpoint than baseline.
29 secondary outcomes
Mean Change From Baseline in the Number of Risk Factors of Metabolic Syndrome (MS)
Time frame: Baseline, Week 52
Metabolic Syndrome (MS) Prevalence
Time frame: Baseline through Week 52
Change From Baseline in the Percentage of Participants With Each Individual Metabolic Syndrome (MS) Risk Factor
Time frame: Baseline through Week 52
Percentage of Participants With Individual Metabolic Syndrome (MS) Risk Factors
Time frame: Baseline through Week 52
Change From Baseline in Individual Risk Factors of Metabolic Syndrome (MS): Elevated Waist Circumference
Time frame: Baseline, Week 4, Week 12, Week 52
Change From Baseline in Individual Risk Factors of Metabolic Syndrome (MS): Elevated Systolic/Diastolic Blood Pressure
Time frame: Baseline, Week 4, Week 12, Week 52
Change From Baseline in Individual Risk Factors of Metabolic Syndrome (MS): Elevated Fasting Glucose
Time frame: Baseline, Week 4, Week 12, Week 52
Change From Baseline in Individual Risk Factors of Metabolic Syndrome (MS): Reduced High-density Lipoprotein Cholesterol (HDL-C)
Time frame: Baseline, Week 4, Week 12, Week 52
Change From Baseline in Individual Risk Factors of Metabolic Syndrome (MS): Elevated Triglycerides
Time frame: Baseline, Week 4, Week 12, Week 52
Change From Baseline in Ten-year Coronary Heart Disease (CHD) Risk According to Framingham Scoring System
Time frame: Baseline, Week 4, Week 52
Change From Baseline in Total Cholesterol and Low-density Lipoprotein (LDL) Cholesterol Levels
Time frame: Baseline, Week 52 or Early Termination
Change From Baseline in Weight
Time frame: Baseline, Week 4, Week 12, Week 52 or Early Termination
Change From Baseline in Body Mass Index (BMI)
Time frame: Baseline, Week 4, Week 12, Week 52 or Early Termination
Change From Baseline in Glycosylated Hemoglobin (HbA1c)
Time frame: Baseline, Week 52 or Early Termination
Change From Baseline in Insulin Levels
Time frame: Baseline, Week 52 or Early Termination
Change From Baseline in Corrected QT Interval (QTc): Fridericia's Heart Rate Correction Formula (QTcF)
Time frame: Baseline, Week 4, Week 52 or Early Termination
Change From Baseline in Apolipoprotein B (ApoB) Levels
Time frame: Baseline, Week 52 or Early Termination
Change From Baseline in Leptin
Time frame: Baseline, Week 52 or Early Termination
Change From Baseline in Physical Activity Index
Time frame: Baseline, Week 28, Week 52 or Early Termination
Change From Baseline in Montgomery-Asberg Depression Rating Scale (MADRS) - Total Score
Time frame: Baseline, Week 4, Week 12, Week 28, Week 52 or Early Termination
Change From Baseline in Young Mania Rating Scale (YMRS)
Time frame: Baseline, Week 4, Week 12, Week 28, Week 52 or Early Termination
Change From Baseline in Clinical Global Impression - Severity (CGI-S) Subscale
Time frame: Baseline, Week 4, Week 12, Week 28, Week 52 or Early Termination
Clinical Global Impression - Improvement (CGI-I) Subscale Score
Time frame: Week 52 or Early Termination
Change From Baseline in Drug Attitude Inventory (DAI)
Time frame: Week 28, Week 52 or Early Termination
Change From Baseline in Social and Occupational Functioning Assessment Scale (SOFAS)
Time frame: Baseline, Week 28, Week 52 or Early Termination
Change From Baseline in EuroQoL Index (EQ-I)
Time frame: Baseline, Week 28, Week 52 or Early Termination
Change From Baseline in European Quality of Life (EuroQol) Visual Analogue Scale (EQ-5D VAS): Current Health State Score
Time frame: Baseline, Week 28, Week 52 or Early Termination
Change From Baseline in Impact of Weight on Quality of Life-Lite Version (IWQOL-Lite) Scale
Time frame: Baseline, Week 28, Week 52 or Early Termination
Number of Participants With Suicidal Tendencies (Columbian-Suicide Severity Rating Scale, [C-SSRS], Mapped to C-CASA [Columbia Classification Algorithm For Suicide Assessment])
Time frame: Baseline, Week 1 through Week 52 or Early Termination
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 3 Mar 2021.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- To obtain contact information for a study center near you, click here.Link provided by the sponsor.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Pfizer CT.gov Call Center study director
Pfizer
10 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 3 study testing Ziprasidone HCL (oral) in people with Bipolar Disorder, run by Pfizer's Upjohn has merged with Mylan to form Viatris Inc. at 10 sites in Canada.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: stopped early, as of the sponsor's last update on 3 Mar 2021. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 10 sites in Canada. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
Yes. Results are posted in the registry (first posted 9 Jul 2012). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Percentage of Participants Who Achieved a Reduction From Baseline of at Least 1 Risk Factor for Metabolic Syndrome (MS) at Week 52 or Premature Discontinuation (time frame: Week 52 or Early Termination). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 3 Mar 2021.