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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT00625612
Registration number
NCT00625612
Ethics application status
Date submitted
12/02/2008
Date registered
28/02/2008
Date last updated
1/11/2015
Titles & IDs
Public title
Study of Denufosol Tetrasodium Inhalation Solution in Patients With Cystic Fibrosis (CF) Lung Disease
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Scientific title
A Phase 3, International, Multi-Center, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Efficacy and Safety Study of Denufosol Tetrasodium Inhalation Solution in Patients With Cystic Fibrosis Lung Disease and FEV1 Greater Than or Equal to 75% Predicted But Less Than or Equal to 110% Predicted
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Secondary ID [1]
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08-110
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Secondary ID [2]
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P08640
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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:
Cystic Fibrosis
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Condition category
Condition code
Human Genetics and Inherited Disorders
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Cystic fibrosis
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Respiratory
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Other respiratory disorders / diseases
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Oral and Gastrointestinal
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Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon
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Inflammatory and Immune System
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Connective tissue diseases
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Inflammatory and Immune System
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Other inflammatory or immune system disorders
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Treatment: Drugs - Denufosol Tetrasodium (INS37217) Inhalation Solution
Treatment: Drugs - Placebo
Placebo comparator: 2 -
Experimental: 1 - Denufosol Tetrasodium (INS37217) Inhalation Solution
Treatment: Drugs: Denufosol Tetrasodium (INS37217) Inhalation Solution
Drug: Denufosol Tetrasodium (INS37217) Inhalation Solution, Denufosol 60 mg is administered as an inhalation solution, three times daily for twelve months.
Treatment: Drugs: Placebo
Placebo - 0.9% w/v sodium chloride solution, three times daily for twelve months.
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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 lung function
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Assessment method [1]
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Timepoint [1]
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48 weeks
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Secondary outcome [1]
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Pulmonary Exacerbation, Antibiotic Use, Incidence of Hospitalization/ER visits, Health resource utilization, Quality of Life
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Assessment method [1]
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Timepoint [1]
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48 weeks
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Eligibility
Key inclusion criteria
* Have confirmed diagnosis of cystic fibrosis
* Have FEV1 of greater than or equal to 75% but less than or equal to 110%predicted normal for age, gender and height
* Be able to reproducibly perform spirometry
* Be clinically stable for at least 4 weeks before screening
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Minimum age
5
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Maximum age
No limit
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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
* Have abnormal renal or liver function
* Have lung transplant
* Unable to discontinue use of hypertonic saline
* Participated in Inspire trial 08-108
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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
Completed
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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
1/02/2008
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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
1/10/2010
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Sample size
Target
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Accrual to date
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Final
466
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Recruitment in Australia
Recruitment state(s)
NSW,QLD,SA,VIC,WA
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Recruitment hospital [1]
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John Hunter Hospital - Adults - New Lambton
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Westmead Adults - Westmead
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Prince Charles Hospital - Chermside
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Royal Brisbane Children's Hospital - Herston
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Royal Adelaide Hospital - Adelaide
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Monash Medical Centre - Clayton
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Alfred Hospital - Melbourne
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Respiratory Medicine - Parkville
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Sire Charles Gairdner Hospital - Nedlands
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Princess Margaret Hospital for Children - Perth
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The Children's Hospital of Westmead - Westmead
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2305 - New Lambton
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Recruitment postcode(s) [2]
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2145 - Westmead
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4032 - Chermside
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4029 - Herston
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5000 - Adelaide
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3168 - Clayton
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3004 - Melbourne
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3052 - Parkville
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6009 - Nedlands
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Recruitment postcode(s) [10]
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6840 - Perth
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Recruitment postcode(s) [11]
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NSW 2145 - Westmead
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Recruitment outside Australia
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United States of America
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Alabama
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Auckland
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Funding & Sponsors
Primary sponsor type
Commercial sector/industry
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Name
Merck Sharp & Dohme LLC
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Address
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Ethics approval
Ethics application status
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Summary
Brief summary
The purpose of this trial is to evaluate the safety and effectiveness of one dose strength of Denufosol compared to placebo in patients with CF and a predicted FEV1 of greater than or equal to 75% but less than or equal to 110% predicted.
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Trial website
https://clinicaltrials.gov/study/NCT00625612
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Trial related presentations / publications
Ratjen F, Durham T, Navratil T, Schaberg A, Accurso FJ, Wainwright C, Barnes M, Moss RB; TIGER-2 Study Investigator Group. Long term effects of denufosol tetrasodium in patients with cystic fibrosis. J Cyst Fibros. 2012 Dec;11(6):539-49. doi: 10.1016/j.jcf.2012.05.003. Epub 2012 Jun 8.
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Public notes
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Contacts
Principal investigator
Name
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Felix Ratjen, MD, PhD
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Address
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Toronto, Canada
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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/NCT00625612
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