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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT00396448
Registration number
NCT00396448
Ethics application status
Date submitted
6/11/2006
Date registered
7/11/2006
Date last updated
7/11/2012
Titles & IDs
Public title
Effect of 2-year Administration of CP-945,598 on Weight Loss Efficacy and Safety.
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Scientific title
A 2-Year, Randomized, Double-Blind, Placebo-Controlled Phase 3 Study To Evaluate The Long-Term Efficacy And Safety Of CP-945,598 In The Treatment Of Obese Subjects
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Secondary ID [1]
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A5351019
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Obesity
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Condition category
Condition code
Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Treatment: Drugs - CP-945,598 Treatment B
Treatment: Drugs - CP-945,598 Treatment A
Treatment: Drugs - Placebo
Experimental: CP-945,598 Treatment B -
Experimental: CP-945,598 Treatment A -
Placebo comparator: Placebo -
Treatment: Drugs: CP-945,598 Treatment B
Subjects receive CP-945,598 plus dietary, physical activity, and behavioral counseling.
Treatment: Drugs: CP-945,598 Treatment A
Subjects receive CP-945,598 plus dietary, physical activity, and behavioral counseling.
Treatment: Drugs: Placebo
Subjects receive placebo plus dietary, physical activity, and behavioral counseling.
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Intervention code [1]
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Treatment: Drugs
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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Change in body weight and proportion of subjects with 5% weight loss
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Assessment method [1]
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Timepoint [1]
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1 year
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Secondary outcome [1]
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Waist circumference, blood lipids and glucose, prevalence of metabolic syndrome, patient reported outcomes, population PK
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Assessment method [1]
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Timepoint [1]
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1-2 years
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Eligibility
Key inclusion criteria
* Obese adults with a body mass index > or = 30 kg/m ; > or = 27 kg/m2 for those with obesity-related comorbidities including hypertension and dyslipidemia
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Minimum age
18
Years
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Maximum age
70
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
* Pregnancy
* Diabetes
* Adults with serious or unstable current or past medical conditions
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
The people receiving the treatment/s
The people analysing the results/data
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Intervention assignment
Parallel
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Other design features
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Phase
Phase 3
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Stopped early
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
1/02/2007
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
1/02/2009
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Sample size
Target
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Accrual to date
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Final
1253
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Recruitment in Australia
Recruitment state(s)
NSW,QLD,VIC
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Recruitment hospital [1]
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Pfizer Investigational Site - Caringbah
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Recruitment hospital [2]
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Pfizer Investigational Site - Miranda
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Pfizer Investigational Site - Wollongong
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Recruitment hospital [4]
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Pfizer Investigational Site - Caboolture
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Recruitment hospital [5]
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Pfizer Investigational Site - Kippa Ring
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Recruitment hospital [6]
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Pfizer Investigational Site - Clayton
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Recruitment hospital [7]
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Pfizer Investigational Site - Heidelberg
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Recruitment postcode(s) [1]
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2229 - Caringbah
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Recruitment postcode(s) [2]
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2228 - Miranda
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Recruitment postcode(s) [3]
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2500 - Wollongong
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Recruitment postcode(s) [4]
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4510 - Caboolture
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Recruitment postcode(s) [5]
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4020 - Kippa Ring
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Recruitment postcode(s) [6]
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3168 - Clayton
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Recruitment postcode(s) [7]
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3081 - Heidelberg
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Recruitment outside Australia
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United States of America
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Arizona
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California
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Luton
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Northwood, Middlesex
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Funding & Sponsors
Primary sponsor type
Commercial sector/industry
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Name
Pfizer
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Address
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Country
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Ethics approval
Ethics application status
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Summary
Brief summary
The purpose of this study is to examine the long-term weight loss and safety of CP-945,598 in obese adults
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Trial website
https://clinicaltrials.gov/study/NCT00396448
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Pfizer CT.gov Call Center
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Address
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Pfizer
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Contact person for scientific queries
No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
No documents have been uploaded by study researchers.
Results not provided in
https://clinicaltrials.gov/study/NCT00396448
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