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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/ct2/show/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
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
Secondary ID [1] 0 0
08-110
Secondary ID [2] 0 0
P08640
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Cystic Fibrosis 0 0
Condition category
Condition code
Human Genetics and Inherited Disorders 0 0 0 0
Cystic fibrosis
Respiratory 0 0 0 0
Other respiratory disorders / diseases
Oral and Gastrointestinal 0 0 0 0
Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon
Inflammatory and Immune System 0 0 0 0
Connective tissue diseases
Inflammatory and Immune System 0 0 0 0
Other inflammatory or immune system disorders

Intervention/exposure
Study type
Interventional
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.
Intervention code [1] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Change in lung function
Timepoint [1] 0 0
48 weeks
Secondary outcome [1] 0 0
Pulmonary Exacerbation, Antibiotic Use, Incidence of Hospitalization/ER visits, Health resource utilization, Quality of Life
Timepoint [1] 0 0
48 weeks

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
Minimum age
5 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
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

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?
The people receiving the treatment/s


The people analysing the results/data
Intervention assignment
Parallel
Other design features
Phase
Phase 3
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
1/02/2008
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
1/10/2010
Sample size
Target
Accrual to date
Final
466
Recruitment in Australia
Recruitment state(s)
NSW,QLD,SA,VIC,WA
Recruitment hospital [1] 0 0
John Hunter Hospital - Adults - New Lambton
Recruitment hospital [2] 0 0
Westmead Adults - Westmead
Recruitment hospital [3] 0 0
Prince Charles Hospital - Chermside
Recruitment hospital [4] 0 0
Royal Brisbane Children's Hospital - Herston
Recruitment hospital [5] 0 0
Royal Adelaide Hospital - Adelaide
Recruitment hospital [6] 0 0
Monash Medical Centre - Clayton
Recruitment hospital [7] 0 0
Alfred Hospital - Melbourne
Recruitment hospital [8] 0 0
Respiratory Medicine - Parkville
Recruitment hospital [9] 0 0
Sire Charles Gairdner Hospital - Nedlands
Recruitment hospital [10] 0 0
Princess Margaret Hospital for Children - Perth
Recruitment hospital [11] 0 0
The Children's Hospital of Westmead - Westmead
Recruitment postcode(s) [1] 0 0
2305 - New Lambton
Recruitment postcode(s) [2] 0 0
2145 - Westmead
Recruitment postcode(s) [3] 0 0
4032 - Chermside
Recruitment postcode(s) [4] 0 0
4029 - Herston
Recruitment postcode(s) [5] 0 0
5000 - Adelaide
Recruitment postcode(s) [6] 0 0
3168 - Clayton
Recruitment postcode(s) [7] 0 0
3004 - Melbourne
Recruitment postcode(s) [8] 0 0
3052 - Parkville
Recruitment postcode(s) [9] 0 0
6009 - Nedlands
Recruitment postcode(s) [10] 0 0
6840 - Perth
Recruitment postcode(s) [11] 0 0
NSW 2145 - Westmead
Recruitment outside Australia
Country [1] 0 0
United States of America
State/province [1] 0 0
Alabama
Country [2] 0 0
United States of America
State/province [2] 0 0
Alaska
Country [3] 0 0
United States of America
State/province [3] 0 0
Arizona
Country [4] 0 0
United States of America
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California
Country [5] 0 0
United States of America
State/province [5] 0 0
Connecticut
Country [6] 0 0
United States of America
State/province [6] 0 0
Delaware
Country [7] 0 0
United States of America
State/province [7] 0 0
District of Columbia
Country [8] 0 0
United States of America
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Florida
Country [9] 0 0
United States of America
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Georgia
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United States of America
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Illinois
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Indiana
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Kansas
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United States of America
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Kentucky
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United States of America
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Louisiana
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United States of America
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Maine
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United States of America
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Maryland
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Massachusetts
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Michigan
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Minnesota
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Missouri
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Nebraska
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Nevada
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New Jersey
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New York
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North Carolina
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North Dakota
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Ohio
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Oklahoma
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Oregon
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Pennsylvania
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South Carolina
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South Dakota
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United States of America
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Tennessee
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Texas
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Utah
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Virginia
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West Virginia
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United States of America
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Wisconsin
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Canada
State/province [39] 0 0
Alberta
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Canada
State/province [40] 0 0
British Columbia
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Canada
State/province [41] 0 0
Newfoundland and Labrador
Country [42] 0 0
Canada
State/province [42] 0 0
Nova Scotia
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Canada
State/province [43] 0 0
Ontario
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Canada
State/province [44] 0 0
Quebec
Country [45] 0 0
New Zealand
State/province [45] 0 0
Auckland

Funding & Sponsors
Primary sponsor type
Commercial sector/Industry
Name
Merck Sharp & Dohme LLC
Address
Country

Ethics approval
Ethics application status

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.
Trial website
https://clinicaltrials.gov/ct2/show/NCT00625612
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Felix Ratjen, MD, PhD
Address 0 0
Toronto, Canada
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for scientific queries



Summary Results

For IPD and results data, please see https://clinicaltrials.gov/ct2/show/NCT00625612