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CompletedNCT03257644Updated Nov 10, 2020

A Pharmacokinetic Study of Ruxolitinib Phosphate Cream in Pediatric Subjects With Atopic Dermatitis

A Phase 1 interventional study of Ruxolitinib phosphate cream in Atopic Dermatitis, sponsored by Incyte Corporation. Completed at 23 sites in United States. Open to participants aged 2 Years to 17 Years. Per ClinicalTrials.gov, last updated 2020-11-10.

Sponsored by Incyte Corporation · Phase 1, Interventional, and Treatment

Phase
Phase 1
Study type
Interventional
Enrollment
70
Allocation
Non-randomized
Ages
2 Years to 17 Years
Sex
All
01

Study summary

The purpose of this study is to evaluate the safety, tolerability and the pharmacokinetics (PK) of topical ruxolitinib cream applied to pediatric subjects (age ≥ 2 to 17 years) with atopic dermatitis (AD).

Read the detailed description

Study has been modified to include younger pediatric subjects (age ≥2 to 11) in four additional cohorts.

02

Conditions studied

  • Atopic Dermatitis

Keywords

  • Atopic dermatitis
  • Janus kinase (JAK) inhibitor
  • pediatric
  • inflammation
03

Who can participate

Ages eligible
2 Years to 17 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Pediatric subjects aged ≥ 2 to 17 years, inclusive
  • Subjects diagnosed with AD as defined by the Hanifin and Rajka criteria.
  • Subjects with active inflammation associated with AD.
  • Subjects with an Investigator's Global Assessment (IGA) score of at least 2 at screening and baseline.
  • Subjects with body surface area (BSA) of AD involvement of 8% to 20% at screening and baseline.
  • Subjects who agree to discontinue all agents used to treat AD from screening through the final follow-up visit.
  • Subjects of childbearing potential must agree to take appropriate precautions to avoid pregnancy or fathering a child for the duration of study participation.
  • Written informed consent of the parent(s) or legal guardian and a verbal or written assent from the subject when possible.

Exclusion criteria

Exclusion Criteria:

  • Unstable course of AD (spontaneously improving or rapidly deteriorating) as determined by the investigator over the previous 4 weeks before baseline.
  • Use of topical treatments for AD (other than bland moisturizer such as Eucerin® cream) within 2 weeks of baseline.
  • Concurrent conditions and history of other diseases:

    • Presence of AD lesions only on the hands or feet without a history of involvement of other classical areas of involvement such as the face or the flexural folds.
    • Other types of eczema.
    • Any other concomitant skin disorder (eg, generalized erythroderma such as Netherton Syndrome, or psoriasis), pigmentation, or extensive scarring that in the opinion of the investigator may interfere with the evaluation of AD lesions or compromise subject safety.
    • Immunocompromised (eg, lymphoma, acquired immunodeficiency syndrome, Wiskott-Aldrich syndrome) or have a history of malignant disease within 5 years before the baseline visit.
    • Chronic or acute infection requiring treatment with systemic antibiotics, antivirals, antiparasitics, antiprotozoals, or antifungals within 4 weeks before the baseline visit.
    • Active acute bacterial, fungal, or viral (eg, herpes simplex, herpes zoster, chicken pox) skin infection within 1 week before the baseline visit.
    • Chronic asthma requiring more than 880 μg of inhaled budesonide or equivalent high dose of other inhaled corticosteroids.
  • Subjects with cytopenias at screening per protocol-defined criteria.
  • Use of the following medications:

    • Systemic immunosuppressive or immunomodulating drugs (eg, oral or injectable corticosteroids, methotrexate, cyclosporine, mycophenolate mofetil, azathioprine) within 4 weeks or 5 half-lives of baseline (whichever is longer).
    • Subjects taking potent systemic cytochrome P450 3A4 inhibitors or fluconazole within 2 weeks or 5 half lives, whichever is longer, before the baseline visit (topical agents with limited systemic availability are permitted).
    • Subjects who have previously received JAK inhibitors, systemic or topical (eg, ruxolitinib, tofacitinib, baricitinib, filgotinib, lestaurtinib, pacritinib).
    • Current treatment or treatment within 30 days or 5 half-lives (whichever is longer) before the baseline visit with another investigational medication or current enrollment in another investigational drug protocol.
    • Use of any prohibited medications within 14 days or 5 half-lives (whichever is longer) of the baseline visit.
  • Parent or legal guardian who, in the opinion of the investigator, is unable or unlikely to comply with the administration schedule and study evaluations or are unable or unwilling to apply the study drug.
04

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
70 participants (actual)

Study arms

  • Experimental
    Cohort 1

    Ruxolitinib phosphate cream 0.5%.

    Drug: Ruxolitinib phosphate cream

  • Experimental
    Cohort 2

    Ruxolitinib phosphate cream 1.5%.

    Drug: Ruxolitinib phosphate cream

  • Experimental
    Cohort 3

    Ruxolitinib phosphate cream 0.75%.

    Drug: Ruxolitinib phosphate cream

  • Experimental
    Cohort 4

    Ruxolitinib phosphate cream 1.5%.

    Drug: Ruxolitinib phosphate cream

  • Experimental
    Cohort 5

    Ruxolitinib phosphate cream 0.75%.

    Drug: Ruxolitinib phosphate cream

  • Experimental
    Cohort 6

    Ruxolitinib phosphate cream 1.5%.

    Drug: Ruxolitinib phosphate cream

Interventions

  • DrugRuxolitinib phosphate cream

    Ruxolitinib phosphate cream at the protocol-defined dose strength based on cohort assignment.

    Also known as: INCB018424

05

What researchers measure

Primary outcomes

  1. Participants with treatment-emergent adverse events (TEAEs)

    A TEAE is any adverse event (AE) either reported for the first time or worsening of a pre-existing event after first application of study drug.

    Time frame: Screening through 30-37 days after end of treatment, up to approximately 12 weeks.

Secondary outcomes

  1. Plasma concentrations of ruxolitinib for Cohorts 1 and 2

    Venous blood samples will be collected to assess the PK of ruxolitinib .

    Time frame: Day 1, Day 15, and Day 29

  2. Plasma concentrations of ruxolitinib for Cohorts 3, 4, 5 and 6

    Venous blood samples will be collected to assess the PK of ruxolitinib .

    Time frame: Day 1, Day 10, and Day 29

06

Study locations

23 sites
  • Cahaba Dermatology
    Hoover, Alabama 35244, United States
  • Desert Sky Dermatology
    Gilbert, Arizona 85295, United States
  • Applied Research Center of Arkansas
    Little Rock, Arkansas 72212, United States
  • Orange County Research Center
    Anaheim, California 92801, United States
  • Children'S Hospital Los Angeles Specialt
    Los Angeles, California 90027, United States
  • Rady Children'S Hospital - San Diego
    San Diego, California 92123, United States
  • National Jewish Health
    Denver, Colorado 80206, United States
  • Olympian Clinical Research
    Largo, Florida 33770, United States
  • Acevedo Clinical Research
    Miami, Florida 33142, United States
  • Floridian Research Institute Llc
    Miami, Florida 33145, United States
  • Rm Medical Research Inc
    Miami, Florida 33174, United States
  • Olympian Clinical Research
    Tampa, Florida 33609, United States
  • Iact Health
    Columbus, Georgia 31904, United States
  • Advanced Clinical Research
    Boise, Idaho 83713, United States
  • Northwestern University
    Chicago, Illinois 60611, United States
  • The Indiana Clincal Trials Center
    Plainfield, Indiana 46168, United States
  • David Fivenson, Md, Pllc
    Ann Arbor, Michigan 48103, United States
  • Wake Research Associates Llc
    Raleigh, North Carolina 27612, United States
  • Ohio Pediatric Research Association
    Dayton, Ohio 45414, United States
  • Cyn3Rgy Research - Clinedge - Ppds
    Gresham, Oregon 97030, United States
  • Penn State Hershey Medical Center
    Hershey, Pennsylvania 17033, United States
  • Progressive Clinical Research
    San Antonio, Texas 78213, United States
  • Texas Dermatology and Laser Specialists
    San Antonio, Texas 78218, United States
07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT03257644
Lead sponsor
Incyte Corporation
Responsible party
Sponsor
First posted
Aug 22, 2017
Start date
Sep 21, 2017
Primary completion
Oct 7, 2020
Completion
Oct 7, 2020
Last update
Nov 10, 2020

Study contacts

Michael Kuligowski, MD, PhD, MBA
study director · Incyte Corporation

Oversight

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

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