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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT02576860
Registration number
NCT02576860
Ethics application status
Date submitted
13/10/2015
Date registered
15/10/2015
Date last updated
2/08/2022
Titles & IDs
Public title
Study to Evaluate the Safety and Efficacy of a Once-Daily CLS001 Topical Gel Versus Vehicle
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Scientific title
A Phase 3, Randomized, Vehicle-Controlled, Double-Blind, Multicenter Study to Evaluate the Safety and Efficacy of Once-Daily CLS001 Topical Gel Versus Vehicle Administered for 12 Weeks to Subjects With Papulopustular Rosacea With a 4 Week Follow-up Period
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Secondary ID [1]
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CLS001-CO-PR-005
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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 - CLS001 (Omiganan)
Treatment: Drugs - Vehicle
Experimental: Treatment - CLS001 (Omignan) gel applied once daily
Placebo comparator: Vehicle Gel - Vehicle gel applied once daily
Treatment: Drugs: CLS001 (Omiganan)
Topical gel
Treatment: Drugs: Vehicle
Vehicle 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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Efficacy Absolute Change in Inflammatory Lesion Count
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Assessment method [1]
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Absolute change in inflammatory lesion count from baseline to Week 12.
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Timepoint [1]
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12 weeks
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Primary outcome [2]
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Efficacy IGA: 2 Grade Reduction
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Assessment method [2]
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Proportion of Subjects Who Achieved 2 Grade IGA Reduction at Week 12. IGA scores are from 0 to 5 (Clear, Almost Clear, Mild, Moderate and Severe).
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Timepoint [2]
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12 weeks
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Secondary outcome [1]
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Efficacy The Absolute Change in Inflammatory Lesions
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Assessment method [1]
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The absolute change in inflammatory lesions from baseline to Week 9.
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Timepoint [1]
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9 weeks
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Secondary outcome [2]
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Efficacy The Absolute Change in Inflammatory Lesions
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Assessment method [2]
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The absolute change in inflammatory lesions from baseline to Week 6.
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Timepoint [2]
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6 weeks
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Secondary outcome [3]
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Efficacy IGA: 2 Point Reduction
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Assessment method [3]
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Proportion of Subjects Who Achieved 2 Grade IGA Reduction at Week 9. IGA scores are from 0 to 5 (Clear, Almost Clear, Mild, Moderate and Severe).
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Timepoint [3]
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9 Weeks
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Secondary outcome [4]
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Efficacy IGA: 2 Point Reduction
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Assessment method [4]
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Proportion of Subjects Who Achieved 2 Grade IGA Reduction at Week 6. IGA scores are from 0 to 5 (Clear, Almost Clear, Mild, Moderate and Severe).
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Timepoint [4]
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6 Weeks
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Eligibility
Key inclusion criteria
1. Healthy, male and non-pregnant female subjects, 18 years of age or older.
2. A diagnosis of papulopustular rosacea with =30 inflammatory facial lesions at Baseline. Subjects must have no more than 2 nodular lesions, at Baseline.
3. Subjects with the presence of telangiectasia at Baseline.
4. Subjects with an erythema score of at least 2 on the Investigator Assessment of Erythema scale at Baseline.
5. Subjects with severe rosacea on the Investigators Global Assessment scale 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
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
1/10/2015
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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
5/09/2017
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Sample size
Target
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Accrual to date
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Final
263
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Recruitment in Australia
Recruitment state(s)
ACT,NSW,VIC
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Recruitment hospital [1]
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- Phillip
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Recruitment hospital [2]
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- Kogarah
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- Liverpool
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Recruitment hospital [4]
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- Box Hill
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- Phillip
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Recruitment postcode(s) [2]
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- Kogarah
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Recruitment postcode(s) [3]
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- Liverpool
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Recruitment postcode(s) [4]
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- Box Hill
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Recruitment outside Australia
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United States of America
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Arkansas
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California
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District of Columbia
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Ontario
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France
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Grenoble
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Nantes
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France
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Quimper
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Berlin
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Bonn
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Friedrichshafen
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Hamburg
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Koeln
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Lingen
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Monchengladbach
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Osnabruck
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Schweinfurt
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Auckland
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Sweden
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Halmstad
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England
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Birmingham
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United Kingdom
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London
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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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Ethics approval
Ethics application status
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Summary
Brief summary
This study evaluates the safety and efficacy of once-daily application of CLS001 topical gel compared to vehicle gel in subjects with severe papulopustular rosacea.
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Trial website
https://clinicaltrials.gov/study/NCT02576860
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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/60/NCT02576860/Prot_000.pdf
Statistical analysis plan
https://cdn.clinicaltrials.gov/large-docs/60/NCT02576860/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/NCT02576860
Download to PDF