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Phase 3 Completed N=763 Randomized Quadruple-blind Treatment

Safety and Efficacy of AN2728 Topical Ointment, 2% in Children, Adolescents, and Adults (Ages 2 Years and Older) With Atopic Dermatitis

Dermatitis, Atopic
Source: ClinicalTrials.gov NCT02118766 ↗
Enrolled (actual)
763
Serious AEs
0.8%
Results posted
Mar 2017
Primary outcomePrimary: Percentage of Participants Who Achieved Treatment Success Based on Investigator's Static Global Assessment (ISGA) at Day 29 — 32.8; 25.4 percentage of participants — p=0.038
◆ Published Evidence
Emerging
19citations · ~5 / year
Subgroup Analysis of Crisaborole for Mild-to-Moderate Atopic Dermatitis in Children Aged 2 to < 18 Years.
Paediatric drugs · 2022 · Open access · Likely link

Summary

The purpose of this study is to investigate the safety and efficacy of AN2728 Topical Ointment, 2% in children, adolescents, and adults (ages 2 years and older) with atopic dermatitis.

Linked Publications (5)

  • Subgroup Analysis of Crisaborole for Mild-to-Moderate Atopic Dermatitis in Children Aged 2 to < 18 Years.
    Paediatric drugs · 2022 · 19 citations · Open access · Likely link
  • Efficacy and Safety Trends with Continuous, Long-Term Crisaborole Use in Patients Aged ≥ 2 Years with Mild-to-Moderate Atopic Dermatitis.
    Dermatology and therapy · 2021 · 11 citations · Open access · Likely link
  • Translating the Investigator's Static Global Assessment to the Eczema Area and Severity Index in Studies of Crisaborole for Atopic Dermatitis.
    Dermatology and therapy · 2021 · 7 citations · Open access · Likely link
  • Impact of Crisaborole in Treatment-Experienced Patients With Mild-to-Moderate Atopic Dermatitis.
    Dermatitis : contact, atopic, occupational, drug · 2024 · 6 citations · Open access · Likely link
  • Demographics and Baseline Disease Characteristics of Early Responders to Crisaborole for Atopic Dermatitis.
    Journal of drugs in dermatology : JDD · 2020 · 0 citations · Likely link

Outcome Measures

OutcomeResultp-value
PRIMARY
Percentage of Participants Who Achieved Treatment Success Based on Investigator's Static Global Assessment (ISGA) at Day 29
32.8; 25.4 0.038 sig
PRIMARY
Number of Participants With Treatment-Emergent Adverse Events (AEs) And Serious Adverse Events (SAEs)
147; 50; 5; 1
PRIMARY
Number of Participants With Clinically Significant Change From Baseline in Vital Signs at Day 29
0; 0
PRIMARY
Number of Participants With Clinically Significant Change From Baseline in Laboratory Values at Day 29
0; 0
SECONDARY
Percentage of Participants With an Investigator's Static Global Assessment (ISGA) Score of Clear (0) or Almost Clear (1) at Day 29
51.7; 40.6
SECONDARY
Time to Achieve Treatment Success Based on Investigator's Static Global Assessment (ISGA)
NA; NA
SECONDARY
Change From Baseline in Signs of Atopic Dermatitis (AD) at Day 29
1.7; 1.6; -0.7; -0.4; 1.8; 1.9

Eligibility Criteria

Inclusion Criteria

  • Males or females 2 years and older
  • Has a clinical diagnosis of AD according to the criteria of Hanifin and Rajka
  • Has AD involvement ≥ 5% Treatable %BSA (excluding the scalp)
  • Has an ISGA score of Mild (2) or Moderate (3) at Baseline/Day 1
  • All female subjects of childbearing potential must use acceptable methods of contraception from the Screening Visit continuously until 30 days after stopping study drug

Exclusion Criteria

  • As determined by the study doctor, a medical history that may interfere with study objectives
  • Unstable AD or any consistent requirement for high potency topical corticosteroids
  • History of use of biologic therapy (including intravenous immunoglobulin)
  • Recent or anticipated concomitant use of systemic or topical therapies that might alter the course of AD
  • Recent or current participation in another research study
  • Females who are breastfeeding, pregnant, or with plans to get pregnant during the participation in the study
  • Participation in a previous AN2728 clinical trial
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02118766) and the linked publication. 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.

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