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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT02576847
Registration number
NCT02576847
Ethics application status
Date submitted
13/10/2015
Date registered
15/10/2015
Date last updated
19/07/2022
Titles & IDs
Public title
Study to Evaluate the Long-term Safety of a Once-Daily Omiganan Topical Gel
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Scientific title
A Phase 3 Open-Label Extension Study to Evaluate the Long-Term Safety of Omiganan Topical Gel in Subjects With Rosacea
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Secondary ID [1]
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CLS001-CO-PR-006
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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:
Rosacea
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Condition category
Condition code
Skin
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Dermatological conditions
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Skin
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Other skin conditions
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Treatment: Drugs - Omiganan
Experimental: Treatment - Omiganan gel applied once daily
Treatment: Drugs: Omiganan
Topical gel
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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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Number of Subjects With 1 or More Treatment-related Treatment-Emergent Adverse Events
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Assessment method [1]
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Number of subjects with 1 or more treatment-related Treatment-Emergent Adverse Events
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Timepoint [1]
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Up to 12 months
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Eligibility
Key inclusion criteria
1. Healthy, male and nonpregnant female subjects, 18 years of age or older.
2. A diagnosis of severe papulopustular rosacea using the Investigator Global Assessment grading scale at baseline
3. Subjects with the presence of telangiectasia at Baseline
4. Subjects with the presence of facial erythema associated with their rosacea at Baseline
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Minimum age
18
Years
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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?
Yes
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Key exclusion criteria
1. Subjects with steroid rosacea or subtype 3 (phymatous rosacea).
2. Subjects with nodular rosacea
3. Standard exclusion criteria.
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Study design
Purpose of the study
Treatment
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Allocation to intervention
NA
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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
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Single group
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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
1/10/2015
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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
8/02/2018
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Sample size
Target
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Accrual to date
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Final
307
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Recruitment in Australia
Recruitment state(s)
NSW,QLD
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Recruitment hospital [1]
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- Sydney
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Recruitment hospital [2]
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- Woolloongabba
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Recruitment postcode(s) [1]
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- Sydney
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Recruitment postcode(s) [2]
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- Woolloongabba
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Recruitment outside Australia
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United States of America
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California
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Florida
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Illinois
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Indiana
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Massachusetts
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New York
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Tennessee
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Texas
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Canada
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British Columbia
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Canada
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Manitoba
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Canada
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Quebec
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France
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Cannes
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France
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Nice
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Netherlands
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Bergen Op Zoom
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New Zealand
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Hamilton
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New Zealand
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Wellington
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Sweden
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Gothenburg
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United Kingdom
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Lanarkshire
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United Kingdom
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State/province [20]
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Manchester
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Funding & Sponsors
Primary sponsor type
Commercial sector/industry
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Name
Maruho Co., Ltd.
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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
This study evaluates the long-term safety of once-daily application of Omiganan topical gel in subjects with severe papulopustular rosacea.
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Trial website
https://clinicaltrials.gov/study/NCT02576847
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
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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
Type
Other Details
Attachment
Study protocol
https://cdn.clinicaltrials.gov/large-docs/47/NCT02576847/Prot_000.pdf
Statistical analysis plan
https://cdn.clinicaltrials.gov/large-docs/47/NCT02576847/SAP_001.pdf
Results publications and other study-related documents
No documents have been uploaded by study researchers.
Results are available at
https://clinicaltrials.gov/study/NCT02576847
Download to PDF