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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT04564755
Registration number
NCT04564755
Ethics application status
Date submitted
21/09/2020
Date registered
25/09/2020
Date last updated
21/06/2024
Titles & IDs
Public title
Abrocitinib Expanded Access Protocol in Adolescents and Adults With Moderate to Severe Atopic Dermatitis
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Scientific title
ABROCITINIB EXPANDED ACCESS PROTOCOL FOR THE TREATMENT OF ADOLESCENTS AND ADULTS WITH MODERATE TO SEVERE ATOPIC DERMATITIS
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Secondary ID [1]
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2020-003610-12
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Secondary ID [2]
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B7451064
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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:
Atopic Dermatitis
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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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Inflammatory and Immune System
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Other inflammatory or immune system disorders
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Intervention/exposure
Study type
Expanded Access
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Description of intervention(s) / exposure
Treatment: Drugs - abrocitinib
Treatment: Drugs: abrocitinib
Participants will receive abrocitinib 100 mg or 200 mg orally once a day as directed by the investigator's clinical judgement
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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
Eligibility
Key inclusion criteria
* 12 years of age or older
* Clinical diagnosis of chronic atopic dermatitis for at least 6 months
* Inadequate treatment options with available, approved medicated topical and systemic therapies for moderate to severe atopic dermatitis
* Moderate to severe atopic dermatitis as indicated by at least one of the following: IGA =3; EASI =16
* Not eligible for participation in any ongoing clinical trial of abrocitinib, including lack of access due to geographical limitations
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Minimum age
12
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?
No
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Key exclusion criteria
* Medical, psychiatric, or laboratory abnormality that may increase the risk associated with study participation
* Medical history including thrombocytopenia, coagulopathy or platelet dysfunction, malignancies, current or history of certain infections, lymphoproliferative disorders and other medical conditions at the discretion of the investigator
* Require treatment with prohibited medications during the study
* Discontinued prior treatment with any systemic JAK inhibitor due to safety or tolerability issues
* 12 to <18 years old without documented evidence of having received at least one dose of the varicella vaccine or without evidence of prior exposure to varicella zoster virus based on serological test
* Pregnant or breastfeeding women or women of childbearing potential who are sexually active and unwilling to use contraception
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Study design
Purpose of the study
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Allocation to intervention
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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?
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Intervention assignment
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Phase
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Statistical methods / analysis
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Recruitment
Recruitment status
NO_LONGER_AVAILABLE
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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
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
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Actual
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Sample size
Target
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
ACT,NSW,QLD,VIC
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Recruitment hospital [1]
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Woden Dermatology - Phillip
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Recruitment hospital [2]
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Royal North Shore Hospital - St Leonards
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Recruitment hospital [3]
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The Skin Centre - Benowa
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Recruitment hospital [4]
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Dr Rodney Sinclair Pty Ltd - Melbourne
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Recruitment hospital [5]
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Sinclair Dermatology - Melbourne
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Recruitment hospital [6]
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Paratus Clinical Research Woden - Philip
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Recruitment postcode(s) [1]
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2606 - Phillip
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Recruitment postcode(s) [2]
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2065 - St Leonards
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Recruitment postcode(s) [3]
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4217 - Benowa
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Recruitment postcode(s) [4]
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3995 - Melbourne
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Recruitment postcode(s) [5]
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2606 - Philip
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Recruitment outside Australia
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United States of America
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Alabama
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California
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Florida
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Illinois
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Indiana
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Kentucky
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Michigan
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Ohio
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Texas
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West Virginia
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Austria
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Wien
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Kaohsiung
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Taiwan
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Taipei
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Funding & Sponsors
Primary sponsor type
Commercial sector/industry
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Name
Pfizer
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Ethics approval
Ethics application status
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Summary
Brief summary
This is a multi-center, expanded access protocol to provide access to the investigational product, abrocitinib, to adolescent and adult patients with moderate to severe atopic dermatitis who have inadequate treatment options with available and approved medicated topical and systemic therapies and who are otherwise ineligible for participation in clinical studies with abrocitinib.
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Trial website
https://clinicaltrials.gov/study/NCT04564755
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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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Pfizer CT.gov Call Center
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Address
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Phone
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1-800-718-1021
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Email
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[email protected]
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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/NCT04564755
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