Mode
Text Size
Log in / Sign up
Phase 1 Completed N=32 Randomized Triple-blind Basic Science

A Study of Crisaborole Ointment 2% in Adult Japanese Healthy Subjects and Adult Japanese Subjects With Mild To Moderate Atopic Dermatitis

Source: ClinicalTrials.gov NCT03260595 ↗
Enrolled (actual)
32
Serious AEs
0.0%
Results posted
Mar 2019
Primary outcomePrimary: Cohort 1: Skin Irritation Index — 40.0; 5.0 scores on a scale

Summary

This is a Phase 1 parallel-cohort study of crisaborole ointment 2% to evaluate the skin irritation potential in adult Japanese healthy subjects in Cohort 1, and to evaluate the safety, tolerability and PK in adult Japanese subjects with mild to moderate AD in Cohort 2.

Outcome Measures

OutcomeResultp-value
PRIMARY
Cohort 1: Skin Irritation Index
40.0; 5.0
PRIMARY
Cohort 2: Number of Participants With Treatment-Emergent Adverse Events (AEs) And Serious Adverse Events (SAEs)
9; 2; 0; 0
PRIMARY
Cohort 2: Number of Participants With Clinically Significant Vital Signs Abnormalities
0; 0
PRIMARY
Cohort 2: Number of Participants With Laboratory Tests Abnormalities
7; 1
PRIMARY
Cohort 2: Number of Participants With Clinically Significant Electrocardiogram (ECG) Abnormalities
0; 0
SECONDARY
Cohort 1: Number of Participants With Treatment-Emergent Adverse Events (AEs) And Serious Adverse Events (SAEs)
0; 0
SECONDARY
Cohort 2: Maximum Observed Plasma Concentration (Cmax) of Crisaborole and Its Identified Main Oxidative Metabolites
163.7; 164.9; 94.97; 68.83; 3064; 8080
SECONDARY
Cohort 2: Time to Reach Maximum Observed Plasma Concentration (Tmax) of Crisaborole and Its Metabolites
3.000; 3.000; 3.000; 3.000; 3.000; 3.000
SECONDARY
Cohort 2: Area Under the Plasma Concentration-Time Curve From Time Zero Until the Last Measurable Concentration (AUClast) of Crisaborole and Its Identified Main Oxidative Metabolites
1171; 1527; 601.9; 565.5; 57560; 169100
SECONDARY
Cohort 2: Area Under the Plasma Concentration-Time Curve From Time Zero to the 24 Hours Post-Dose (AUC24) of Crisaborole and Its Identified Main Oxidative Metabolites (AN7602 and AN8323)
1171; 1527; 601.9; 565.5; 57560; 169100
SECONDARY
Cohort 2: Area Under the Plasma Concentration-Time Curve From Time Zero to Tau (12 Hours Dosing Interval) (AUCtau) of Crisaborole and Its Identified Main Oxidative Metabolites
928.9; 1123; 500.4; 434.9; 29360; 90360
SECONDARY
Cohort 2: Accumulation Ratio for Cmax (Rac [Cmax]) of Crisaborole and Its Identified Main Oxidative Metabolites
1.007; 0.7247; 2.638
SECONDARY
Cohort 2: Accumulation Ratio for AUCtau (Rac [AUCtau]) of Crisaborole and Its Identified Main Oxidative Metabolites
1.209; 0.8688; 3.080

Eligibility Criteria

Inclusion Criteria

Cohort 1

  • Healthy male Japanese subjects who, at the time of screening, are between the ages of 20 and 55 years, inclusive.
  • Healthy skin on which reddening can be easily recognized in the area of the test fields.

Cohort 2

  • Male or female Japanese subjects aged 20 years to 55 years (inclusive) at the time of screening, and in generally good health except for AD.
  • Diagnosis of AD based on the criteria of Hanifin and Rajka (1980).
  • Has at least 25% Treatable %BSA on Day 1 (excluding the scalp and designated venous access areas).
  • Has an Investigator's static global assessment (ISGA) score of Mild (2) or Moderate (3) on Day 1.

Exclusion Criteria

Cohort 1

  • Subjects who have any visible skin disease at the application site which, in the opinion of the investigative personnel, will interfere with the evaluation of the test site reaction.
  • Subjects who have psoriasis and/or active AD/eczema.
  • Subjects who have a history of AD.
  • Subjects who have damaged skin in or around the test sites, including sunburn, excessively deep tans, uneven skin tones, tattoos, scars, excessive hair, numerous freckles, or other disfigurations of the test site.
  • Known sensitivity to any of the components of the investigational products.
  • History of the rash to the adhesive plaster, contact dermatitis to metal, or cosmetic and household articles.

Cohort 2

  • Has any clinically significant medical disorder, condition, disease (including active or potentially recurrent dermatological conditions other than AD), significant physical examination or laboratory findings that may interfere with study objectives, in the Investigator's opinion.
  • Has unstable AD or a consistent requirement for strong to strongest potency topical corticosteroids to manage AD signs and symptoms.
  • Has a significant active systemic or localized infection, including known actively infected AD.
  • Has a history or evidence of clinically significant or severe allergies (eg, seasonal, pet dander, environmental, food) requiring acute or chronic treatment.
  • Has recent or anticipated concomitant use of topical or systemic therapies that might alter the course of AD.
  • Has a history of recent (within 4 weeks of Day 1) sunbathing, tanning bed use, or ultraviolet (UV) light B therapy (UVB) or psoralen plus UVA [PUVA]).
  • Has a known sensitivity to any of the components of crisaborole ointment 2%.
  • Pregnant female subjects; breastfeeding female subjects; female subjects of childbearing potential who are unwilling or unable to use a highly effective method of contraception as outlined in this protocol for the duration of the study and for at least 28 days after the last dose of investigational product.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03260595). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

Back to search