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Delgocitinib Cream for the Treatment of Moderate to Severe Atopic Dermatitis During 8 Weeks in Adults, Adolescents, and Children

Primary Purpose

Atopic Dermatitis

Status
Completed
Phase
Phase 1
Locations
International
Study Type
Interventional
Intervention
delgocitinib
Sponsored by
LEO Pharma
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Atopic Dermatitis focused on measuring adults, pediatric

Eligibility Criteria

2 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Key Inclusion criteria (Part 1: adults and adolescents; 12 years and above)

  • Diagnosis of atopic dermatitis (AD) as defined by the Hanifin and Rajka (1980) criteria for AD
  • Age 12 years and above at baseline
  • AD involvement of 25-50% treatable body surface area (BSA) at screening and at baseline
  • Moderate to severe AD (Validated Investigator Global Assessment scale for Atopic Dermatitis [vIGA-AD] score of at least 3) at screening and at baseline

Key Inclusion criteria (Part 2: children; 2-11 years)

  • Diagnosis of AD as defined by the Hanifin and Rajka (1980) criteria for AD
  • Age 2-11 years at baseline
  • History of AD for at least 3 months (children aged 2-5 years), and at least 12 months (children aged 6-11 years)
  • AD involvement of ≥35% treatable BSA at screening and at baseline
  • Moderate to severe AD (vIGA-AD score of at least 3) at screening and at baseline

Key Exclusion criteria (Part 1 and 2: subjects aged 2 years and above)

  • Active dermatologic conditions that may interfere with the diagnosis of AD
  • Use of tanning beds or phototherapy within 4 weeks prior to baseline
  • Systemic treatment with immunosuppressive/modulating drugs or corticosteroids within 4 weeks prior to baseline or 3 or more bleach baths any week within 4 weeks prior to baseline
  • Treatment with topical corticosteroids (TCS), topical calcineurin inhibitors (TCIs), topical phosphodiesterase-4, or oral antibiotics within 1 week prior to baseline
  • Clinically significant infection (systemic infection or serious skin infection requiring parenteral treatment) within 4 weeks prior to baseline
  • Any disorder, which is not stable, and in the investigator's opinion could affect the safety of the subject, influence the results of the trial or impede the subject's ability to complete the trial

Sites / Locations

  • LEO Pharma investigational site
  • LEO Pharma investigational site
  • LEO Pharma investigational site
  • LEO Pharma investigational site
  • LEO Pharma investigational site
  • LEO Pharma investigational site
  • LEO Pharma investigational site
  • LEO Pharma investigational site
  • LEO Pharma investigational site
  • LEO Pharma investigational site
  • LEO Pharma investigational site
  • LEO Pharma investigational site
  • LEO Pharma investigational site
  • LEO Pharma investigational site
  • LEO Pharma investigational site
  • LEO Pharma investigational site

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Part 1: adults and adolescents (12 years and above)

Part 2: children (2-11 years)

Arm Description

Delgocitinib cream (dosage: A mg/g).

Delgocitinib cream (dosage: B mg/g).

Outcomes

Primary Outcome Measures

Adverse events (AEs)
Number of AEs and number of subjects with AEs

Secondary Outcome Measures

PK parameter - Cmax
Cmax
PK parameter - AUC
AUC
PK parameter - tmax
tmax

Full Information

First Posted
January 30, 2019
Last Updated
November 24, 2021
Sponsor
LEO Pharma
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1. Study Identification

Unique Protocol Identification Number
NCT03826901
Brief Title
Delgocitinib Cream for the Treatment of Moderate to Severe Atopic Dermatitis During 8 Weeks in Adults, Adolescents, and Children
Official Title
A Phase 1 Open-label, Multi-centre, Single-arm Trial to Evaluate the Safety and Pharmacokinetics (Including MUsT) of Twice Daily Topical Application of Delgocitinib Cream for 8 Weeks in Adults, Adolescents, and Children With Moderate to Severe Atopic Dermatitis
Study Type
Interventional

2. Study Status

Record Verification Date
November 2021
Overall Recruitment Status
Completed
Study Start Date
February 20, 2019 (Actual)
Primary Completion Date
October 29, 2021 (Actual)
Study Completion Date
October 29, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
LEO Pharma

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This is a multi-center, open-label trial to evaluate safety and pharmacokinetics of topical delgocitinib cream applied to pediatric subjects (2-17 years) and adult subjects (18 years and above) with atopic dermatitis.
Detailed Description
A phase 1 open-label, multi-centre, single-arm trial to evaluate the safety and pharmacokinetics (including MUsT) of twice daily topical application of delgocitinib cream for 8 weeks in adults, adolescents, and children with moderate to severe atopic dermatitis

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atopic Dermatitis
Keywords
adults, pediatric

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
46 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Part 1: adults and adolescents (12 years and above)
Arm Type
Experimental
Arm Description
Delgocitinib cream (dosage: A mg/g).
Arm Title
Part 2: children (2-11 years)
Arm Type
Experimental
Arm Description
Delgocitinib cream (dosage: B mg/g).
Intervention Type
Drug
Intervention Name(s)
delgocitinib
Other Intervention Name(s)
LEO 124249
Intervention Description
Cream for topical application
Primary Outcome Measure Information:
Title
Adverse events (AEs)
Description
Number of AEs and number of subjects with AEs
Time Frame
Week 0 to Week 8
Secondary Outcome Measure Information:
Title
PK parameter - Cmax
Description
Cmax
Time Frame
at Day 8
Title
PK parameter - AUC
Description
AUC
Time Frame
at Day 8
Title
PK parameter - tmax
Description
tmax
Time Frame
at Day 8

10. Eligibility

Sex
All
Minimum Age & Unit of Time
2 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Key Inclusion criteria (Part 1: adults and adolescents; 12 years and above) Diagnosis of atopic dermatitis (AD) as defined by the Hanifin and Rajka (1980) criteria for AD Age 12 years and above at baseline AD involvement of 25-50% treatable body surface area (BSA) at screening and at baseline Moderate to severe AD (Validated Investigator Global Assessment scale for Atopic Dermatitis [vIGA-AD] score of at least 3) at screening and at baseline Key Inclusion criteria (Part 2: children; 2-11 years) Diagnosis of AD as defined by the Hanifin and Rajka (1980) criteria for AD Age 2-11 years at baseline History of AD for at least 3 months (children aged 2-5 years), and at least 12 months (children aged 6-11 years) AD involvement of ≥35% treatable BSA at screening and at baseline Moderate to severe AD (vIGA-AD score of at least 3) at screening and at baseline Key Exclusion criteria (Part 1 and 2: subjects aged 2 years and above) Active dermatologic conditions that may interfere with the diagnosis of AD Use of tanning beds or phototherapy within 4 weeks prior to baseline Systemic treatment with immunosuppressive/modulating drugs or corticosteroids within 4 weeks prior to baseline or 3 or more bleach baths any week within 4 weeks prior to baseline Treatment with topical corticosteroids (TCS), topical calcineurin inhibitors (TCIs), topical phosphodiesterase-4, or oral antibiotics within 1 week prior to baseline Clinically significant infection (systemic infection or serious skin infection requiring parenteral treatment) within 4 weeks prior to baseline Any disorder, which is not stable, and in the investigator's opinion could affect the safety of the subject, influence the results of the trial or impede the subject's ability to complete the trial
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Medical Expert
Organizational Affiliation
LEO Pharma
Official's Role
Study Director
Facility Information:
Facility Name
LEO Pharma investigational site
City
Birmingham
State/Province
Alabama
ZIP/Postal Code
35209
Country
United States
Facility Name
LEO Pharma investigational site
City
Phoenix
State/Province
Arizona
ZIP/Postal Code
85006
Country
United States
Facility Name
LEO Pharma investigational site
City
Fountain Valley
State/Province
California
ZIP/Postal Code
92708
Country
United States
Facility Name
LEO Pharma investigational site
City
Irvine
State/Province
California
ZIP/Postal Code
92697
Country
United States
Facility Name
LEO Pharma investigational site
City
Los Angeles
State/Province
California
ZIP/Postal Code
90027
Country
United States
Facility Name
LEO Pharma investigational site
City
Centennial
State/Province
Colorado
ZIP/Postal Code
80112
Country
United States
Facility Name
LEO Pharma investigational site
City
New Haven
State/Province
Connecticut
ZIP/Postal Code
06519
Country
United States
Facility Name
LEO Pharma investigational site
City
Indianapolis
State/Province
Indiana
ZIP/Postal Code
46250
Country
United States
Facility Name
LEO Pharma investigational site
City
Ypsilanti
State/Province
Michigan
ZIP/Postal Code
48197
Country
United States
Facility Name
LEO Pharma investigational site
City
Tulsa
State/Province
Oklahoma
ZIP/Postal Code
74136
Country
United States
Facility Name
LEO Pharma investigational site
City
Medford
State/Province
Oregon
ZIP/Postal Code
97504
Country
United States
Facility Name
LEO Pharma investigational site
City
San Antonio
State/Province
Texas
ZIP/Postal Code
78218
Country
United States
Facility Name
LEO Pharma investigational site
City
Red Deer
State/Province
Alberta
ZIP/Postal Code
46-37535
Country
Canada
Facility Name
LEO Pharma investigational site
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8S 1G5
Country
Canada
Facility Name
LEO Pharma investigational site
City
Montreal
State/Province
Quebec
ZIP/Postal Code
H3T 1C5
Country
Canada
Facility Name
LEO Pharma investigational site
City
Montréal
State/Province
Quebec
ZIP/Postal Code
H2K 4L5
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
De-identified IPD can be made available to researchers in a closed environment for a specified period of time. Data-sharing is subject to approved scientifically sound research proposal and signed data-sharing agreement.
IPD Sharing Time Frame
Data is available to request after approval of the studied indication.
IPD Sharing URL
http://leopharmatrials.com/for-professionals

Learn more about this trial

Delgocitinib Cream for the Treatment of Moderate to Severe Atopic Dermatitis During 8 Weeks in Adults, Adolescents, and Children

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