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CompletedNCT03826901Updated Feb 24, 2025

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

A Phase 1 interventional study of delgocitinib in Atopic Dermatitis, sponsored by LEO Pharma. Completed at 16 sites in 2 countries. Open to participants aged 2 Years and older. Per ClinicalTrials.gov, last updated 2025-02-24.

Sponsored by LEO Pharma · Phase 1, Interventional, and Treatment

From the registry’s dates

  • Primary completion was Oct 2021, 4 years 11 months ago, and no results have been posted to the registry.
Phase
Phase 1
Study type
Interventional
Enrollment
46
Allocation
Non-randomized
Ages
2 Years and older
Sex
All
01

Study 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.

Read the 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

02

Conditions studied

  • Atopic Dermatitis

Keywords

  • adults, pediatric
03

In context

Dermatitis, Atopic

1,419 studies on the registry are indexed under Dermatitis, Atopic; 258 are open to participants now.

This study's enrollment of 46 is below the median of 83 across 1,125 interventional studies indexed under Dermatitis, Atopic.

Browse Dermatitis, Atopic studies →

Lead sponsor

LEO Pharma is the lead sponsor of 221 studies on the registry; 5 are open to participants now.

Of its 31 completed or terminated interventional studies of FDA-regulated products, 24 (77%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
2 Years and older
Sexes eligible
All
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
05

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Single group
Masking
None (open label)
Enrollment
46 participants (actual)

Study arms

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

    Delgocitinib cream (dosage: A mg/g).

    Drug: delgocitinib

  • Experimental
    Part 2: children (2-11 years)

    Delgocitinib cream (dosage: B mg/g).

    Drug: delgocitinib

Interventions

  • Drugdelgocitinib

    Cream for topical application

    Also known as: LEO 124249

06

What researchers measure

Primary outcomes

  1. Adverse events (AEs)

    Number of AEs and number of subjects with AEs

    Time frame: Week 0 to Week 8

Secondary outcomes

  1. PK parameter - Cmax

    Cmax

    Time frame: at Day 8

  2. PK parameter - AUC

    AUC

    Time frame: at Day 8

  3. PK parameter - tmax

    tmax

    Time frame: at Day 8

07

Study locations

16 sites
  • LEO Pharma investigational site
    Birmingham, Alabama 35209, United States
  • LEO Pharma investigational site
    Phoenix, Arizona 85006, United States
  • LEO Pharma investigational site
    Fountain Valley, California 92708, United States
  • LEO Pharma investigational site
    Irvine, California 92697, United States
  • LEO Pharma investigational site
    Los Angeles, California 90027, United States
  • LEO Pharma investigational site
    Centennial, Colorado 80112, United States
  • LEO Pharma investigational site
    New Haven, Connecticut 06519, United States
  • LEO Pharma investigational site
    Indianapolis, Indiana 46250, United States
  • LEO Pharma investigational site
    Ypsilanti, Michigan 48197, United States
  • LEO Pharma investigational site
    Tulsa, Oklahoma 74136, United States
  • LEO Pharma investigational site
    Medford, Oregon 97504, United States
  • LEO Pharma investigational site
    San Antonio, Texas 78218, United States
  • LEO Pharma investigational site
    Red Deer, Alberta 46-37535, Canada
  • LEO Pharma investigational site
    Hamilton, Ontario L8S 1G5, Canada
  • LEO Pharma investigational site
    Montreal, Quebec H3T 1C5, Canada
  • LEO Pharma investigational site
    Montréal, Quebec H2K 4L5, Canada
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 24, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03826901
Lead sponsor
LEO Pharma
Responsible party
Sponsor
First posted
Feb 1, 2019
Start date
Feb 20, 2019
Primary completion
Oct 29, 2021
Completion
Oct 29, 2021
Last update
Feb 24, 2025

Study contacts

Medical Expert
study director · LEO Pharma

Oversight

Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Nov 2021. You cannot join it, but the record below documents what was studied.

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