A Study to Evaluate the Safety and Efficacy of PAC-14028 Cream in Atopic Dermatitis
Primary Purpose
Atopic Dermatitis
Status
Completed
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
PAC-14028 cream 1.0%
PAC-14028 cream vehicle
Elidel cream 1%
Sponsored by
About this trial
This is an interventional treatment trial for Atopic Dermatitis
Eligibility Criteria
Inclusion Criteria:
- Male or female patients aged between 20 and 65 years old
- Patients with atopic dermatitis, diagnosed according to Hanifin and Rajka diagnostic criteria
- SCORAD (SCORing Atopic Dermatitis) Score less than 40
Exclusion Criteria:
- Patients presenting symptoms of systemic infection at screening
- Patients who had been treated with oral steroids, oral antibiotics, systemic phototherapy, or immunosuppressants within the last 1 month prior to the investigational product administration
- Patients who had been treated with topical steroids or antibiotics within the last 2 weeks prior to the investigational product administration
- Pregnant women or breastfeeding women
- Women of childbearing potential or women who are planning a pregnancy during the study
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Placebo Comparator
Active Comparator
Arm Label
PAC-14028 cream 1.0%
PAC-14028 cream vehicle
Elidel cream 1%
Arm Description
PAC-14028 cream 1.0%, Twice daily for 4 weeks
PAC-14028 cream vehicle, Twice daily for 4 weeks
Elidel cream 1%, Twice daily for 4 weeks
Outcomes
Primary Outcome Measures
SCORing Atopic Dermatitis (SCORAD) index
Secondary Outcome Measures
Visual Analogue Scale (VAS) score
Success rate to pruritus treatment
Eczema Area and Severity Index (EASI) score
Each SCORAD index
Transepidermal Water Loss (TEWL) level
Skin Hydration level
Skin hydration was measured using the Corneometer
Full Information
NCT ID
NCT02583022
First Posted
September 30, 2015
Last Updated
October 20, 2015
Sponsor
Amorepacific Corporation
1. Study Identification
Unique Protocol Identification Number
NCT02583022
Brief Title
A Study to Evaluate the Safety and Efficacy of PAC-14028 Cream in Atopic Dermatitis
Official Title
A Randomized, Open-label, Single Center, Investigator-initiated Clinical Study to Evaluate the Safety and Efficacy of PAC-14028 Cream in Subjects With Mild to Moderate Atopic Dermatitis
Study Type
Interventional
2. Study Status
Record Verification Date
October 2015
Overall Recruitment Status
Completed
Study Start Date
June 2013 (undefined)
Primary Completion Date
January 2014 (Actual)
Study Completion Date
August 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Amorepacific Corporation
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The study is a Phase II, single center, randomized, open-label, placebo-controlled study in male and female subjects, aged ≥ 20 years with mild to moderate atopic dermatitis. All subjects will receive BID topical applications of PAC-14028 cream or vehicle or Elidel cream for up to 4 weeks.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atopic Dermatitis
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
74 (Actual)
8. Arms, Groups, and Interventions
Arm Title
PAC-14028 cream 1.0%
Arm Type
Experimental
Arm Description
PAC-14028 cream 1.0%, Twice daily for 4 weeks
Arm Title
PAC-14028 cream vehicle
Arm Type
Placebo Comparator
Arm Description
PAC-14028 cream vehicle, Twice daily for 4 weeks
Arm Title
Elidel cream 1%
Arm Type
Active Comparator
Arm Description
Elidel cream 1%, Twice daily for 4 weeks
Intervention Type
Drug
Intervention Name(s)
PAC-14028 cream 1.0%
Intervention Description
Topical application
Intervention Type
Drug
Intervention Name(s)
PAC-14028 cream vehicle
Intervention Description
Topical application
Intervention Type
Drug
Intervention Name(s)
Elidel cream 1%
Intervention Description
Topical application
Primary Outcome Measure Information:
Title
SCORing Atopic Dermatitis (SCORAD) index
Time Frame
Change from baseline at Day 28
Secondary Outcome Measure Information:
Title
Visual Analogue Scale (VAS) score
Time Frame
Change from baseline at Day 7, 14 and 28
Title
Success rate to pruritus treatment
Time Frame
Change from baseline at Day 7, 14 and 28
Title
Eczema Area and Severity Index (EASI) score
Time Frame
Change from baseline at Day 7, 14 and 28
Title
Each SCORAD index
Time Frame
Change from baseline at Day 7, 14 and 28
Title
Transepidermal Water Loss (TEWL) level
Time Frame
Change from baseline at Day 7, 14 and 28
Title
Skin Hydration level
Description
Skin hydration was measured using the Corneometer
Time Frame
Change from baseline at Day 7, 14 and 28
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Male or female patients aged between 20 and 65 years old
Patients with atopic dermatitis, diagnosed according to Hanifin and Rajka diagnostic criteria
SCORAD (SCORing Atopic Dermatitis) Score less than 40
Exclusion Criteria:
Patients presenting symptoms of systemic infection at screening
Patients who had been treated with oral steroids, oral antibiotics, systemic phototherapy, or immunosuppressants within the last 1 month prior to the investigational product administration
Patients who had been treated with topical steroids or antibiotics within the last 2 weeks prior to the investigational product administration
Pregnant women or breastfeeding women
Women of childbearing potential or women who are planning a pregnancy during the study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
BeomJoon Kim, Professor
Organizational Affiliation
Department of Dermatology, Chungang University Hospital
Official's Role
Principal Investigator
12. IPD Sharing Statement
Learn more about this trial
A Study to Evaluate the Safety and Efficacy of PAC-14028 Cream in Atopic Dermatitis
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