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Study of Generic Pimecrolimus Cream, 1% in the Treatment of Mild to Moderate Atopic Dermatitis

Primary Purpose

Atopic Dermatitis

Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Pimecrolimus Cream, 1%
Elidel® (pimecrolimus) Cream
Placebo of Pimecrolimus Cream, 1%
Sponsored by
Glenmark Pharmaceuticals Ltd. India
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Atopic Dermatitis focused on measuring Mild to moderate

Eligibility Criteria

12 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Male or non-pregnant, non-lactating female subjects 12 years of age and older.
  • Non-immunocompromised, with a clinical diagnosis of mild to moderate AD that has failed to respond adequately to other topical prescription treatments for atopic dermatitis, or for whom those treatments are not advisable.
  • Confirmed diagnosis of AD for at least 3 months using the diagnostic features as described by Hanifin and Rajka.
  • IGA score of 2 (mild) or 3 (moderate) and ≥ 5% BSA affected at baseline.

Exclusion Criteria:

  • Active cutaneous bacterial, viral or fungal infection in any treatment area at baseline (e.g., clinically infected AD).
  • Sunburn, extensive scarring or pigmented lesion(s) in any treatment area at baseline and history or presence of skin conditions that would interfere with evaluations.
  • History or presence of Netherton's Syndrome, immunological deficiencies or diseases, organ transplant, HIV, diabetes, malignancy, malignant or pre-malignant skin conditions, serious active or recurrent infection, systemic immunosuppressive regimens, clinically significant severe renal insufficiency or severe hepatic disorders.
  • Use within one month before baseline of 1) oral or intravenous corticosteroids, 2) UVA/UVB therapy, 3) psoralen plus ultraviolet A therapy (PUVA), 4) tanning booths, 5) non-prescription ultraviolet (UV) light sources, 6) immunomodulators or immunosuppressive therapies, 7) interferon, 8) cytotoxic drugs, 9) tacrolimus or 10) pimecrolimus.
  • Use within 14 days before baseline of: 1) systemic antibiotics, 2) calcipotriene or other vitamin D preparations, or 3) retinoids.
  • Use within 7 days before baseline of: 1) antihistamines, 2) topical antibiotics, 3) topical corticosteroids or 4) other topical drug products.

Sites / Locations

  • Investigational Site 4
  • Investigational Site 22
  • Investigational Site 20
  • Investigational Site 13
  • Investigational Site 26
  • Investigational Site 17
  • Investigational Site 9
  • Investigational Site 16
  • Investigational Site 18
  • Investigational Site 19
  • Investigational Site 25
  • Investigational Site 8
  • Investigational Site 12
  • Investigational Site 3
  • Investigational Site 7
  • Investigational Site 10
  • Investigational Site 24
  • Investigational Site 14
  • Investigational Site 1
  • Investigational Site 21
  • Investigational Site 2
  • Investigational Site 11
  • Investigational Site 27
  • Investigational Site 5
  • Investigational Site 23
  • Investigational Site 15
  • Investigational Site 6

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

Placebo Comparator

Arm Label

Pimecrolimus Cream, 1%

Elidel®

Placebo

Arm Description

Pimecrolimus Cream, 1 % (Glenmark Pharmaceuticals Ltd) topical application

Elidel® (Valeant Pharmaceuticals North America LLC) topical application

Placebo of Pimecrolimus Cream, 1% (Glenmark Pharmaceuticals Ltd) topical application

Outcomes

Primary Outcome Measures

The proportion of subjects in each treatment group with treatment success (i.e., a grade of clear or almost clear; a score of 0 or 1, within the treatment area) based on the IGA of Disease Severity at the end of treatment (Visit 3; Day 15 ± 3).

Secondary Outcome Measures

Change in severity score from baseline to Visit 3 of the four individual signs and symptoms of AD (i.e., erythema, induration/papulation, lichenification and pruritus).

Full Information

First Posted
September 6, 2016
Last Updated
July 29, 2019
Sponsor
Glenmark Pharmaceuticals Ltd. India
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1. Study Identification

Unique Protocol Identification Number
NCT02896101
Brief Title
Study of Generic Pimecrolimus Cream, 1% in the Treatment of Mild to Moderate Atopic Dermatitis
Official Title
A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Multiple-Site Study to Evaluate the Therapeutic Equivalence of a Generic Pimecrolimus Cream, 1% (Glenmark Pharmaceuticals Ltd) to the Marketed Product ELIDEL® (Pimecrolimus) Cream, 1% (Valeant Pharmaceuticals North America LLC) in the Treatment of Mild to Moderate Atopic Dermatitis (AD).
Study Type
Interventional

2. Study Status

Record Verification Date
July 2019
Overall Recruitment Status
Completed
Study Start Date
August 2016 (undefined)
Primary Completion Date
June 2017 (Actual)
Study Completion Date
June 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Glenmark Pharmaceuticals Ltd. India

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This is a Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Multiple-Site Study to Evaluate the Therapeutic Equivalence of a Generic Pimecrolimus Cream, 1% (Glenmark Pharmaceuticals Ltd) to the Marketed Product ELIDEL® (pimecrolimus) Cream, 1% (Valeant Pharmaceuticals North America LLC) in the Treatment of Mild to Moderate Atopic Dermatitis (AD).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atopic Dermatitis
Keywords
Mild to moderate

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
755 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Pimecrolimus Cream, 1%
Arm Type
Experimental
Arm Description
Pimecrolimus Cream, 1 % (Glenmark Pharmaceuticals Ltd) topical application
Arm Title
Elidel®
Arm Type
Active Comparator
Arm Description
Elidel® (Valeant Pharmaceuticals North America LLC) topical application
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo of Pimecrolimus Cream, 1% (Glenmark Pharmaceuticals Ltd) topical application
Intervention Type
Drug
Intervention Name(s)
Pimecrolimus Cream, 1%
Intervention Type
Drug
Intervention Name(s)
Elidel® (pimecrolimus) Cream
Intervention Type
Drug
Intervention Name(s)
Placebo of Pimecrolimus Cream, 1%
Primary Outcome Measure Information:
Title
The proportion of subjects in each treatment group with treatment success (i.e., a grade of clear or almost clear; a score of 0 or 1, within the treatment area) based on the IGA of Disease Severity at the end of treatment (Visit 3; Day 15 ± 3).
Time Frame
Day 15
Secondary Outcome Measure Information:
Title
Change in severity score from baseline to Visit 3 of the four individual signs and symptoms of AD (i.e., erythema, induration/papulation, lichenification and pruritus).
Time Frame
Day 15

10. Eligibility

Sex
All
Minimum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male or non-pregnant, non-lactating female subjects 12 years of age and older. Non-immunocompromised, with a clinical diagnosis of mild to moderate AD that has failed to respond adequately to other topical prescription treatments for atopic dermatitis, or for whom those treatments are not advisable. Confirmed diagnosis of AD for at least 3 months using the diagnostic features as described by Hanifin and Rajka. IGA score of 2 (mild) or 3 (moderate) and ≥ 5% BSA affected at baseline. Exclusion Criteria: Active cutaneous bacterial, viral or fungal infection in any treatment area at baseline (e.g., clinically infected AD). Sunburn, extensive scarring or pigmented lesion(s) in any treatment area at baseline and history or presence of skin conditions that would interfere with evaluations. History or presence of Netherton's Syndrome, immunological deficiencies or diseases, organ transplant, HIV, diabetes, malignancy, malignant or pre-malignant skin conditions, serious active or recurrent infection, systemic immunosuppressive regimens, clinically significant severe renal insufficiency or severe hepatic disorders. Use within one month before baseline of 1) oral or intravenous corticosteroids, 2) UVA/UVB therapy, 3) psoralen plus ultraviolet A therapy (PUVA), 4) tanning booths, 5) non-prescription ultraviolet (UV) light sources, 6) immunomodulators or immunosuppressive therapies, 7) interferon, 8) cytotoxic drugs, 9) tacrolimus or 10) pimecrolimus. Use within 14 days before baseline of: 1) systemic antibiotics, 2) calcipotriene or other vitamin D preparations, or 3) retinoids. Use within 7 days before baseline of: 1) antihistamines, 2) topical antibiotics, 3) topical corticosteroids or 4) other topical drug products.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dr. Nikhil Sawant
Organizational Affiliation
Glenmark Pharmaceuticals Ltd.
Official's Role
Study Director
Facility Information:
Facility Name
Investigational Site 4
City
Hot Springs
State/Province
Arkansas
Country
United States
Facility Name
Investigational Site 22
City
Little Rock
State/Province
Arkansas
Country
United States
Facility Name
Investigational Site 20
City
Anaheim
State/Province
California
Country
United States
Facility Name
Investigational Site 13
City
Fremont
State/Province
California
Country
United States
Facility Name
Investigational Site 26
City
Norco
State/Province
California
Country
United States
Facility Name
Investigational Site 17
City
Doral
State/Province
Florida
Country
United States
Facility Name
Investigational Site 9
City
Hialeah
State/Province
Florida
Country
United States
Facility Name
Investigational Site 16
City
Miami
State/Province
Florida
Country
United States
Facility Name
Investigational Site 18
City
Miami
State/Province
Florida
Country
United States
Facility Name
Investigational Site 19
City
Miami
State/Province
Florida
Country
United States
Facility Name
Investigational Site 25
City
Miami
State/Province
Florida
Country
United States
Facility Name
Investigational Site 8
City
Miami
State/Province
Florida
Country
United States
Facility Name
Investigational Site 12
City
North Miami Beach
State/Province
Florida
Country
United States
Facility Name
Investigational Site 3
City
Ormond Beach
State/Province
Florida
Country
United States
Facility Name
Investigational Site 7
City
South Miami
State/Province
Florida
Country
United States
Facility Name
Investigational Site 10
City
Tampa
State/Province
Florida
Country
United States
Facility Name
Investigational Site 24
City
Tampa
State/Province
Florida
Country
United States
Facility Name
Investigational Site 14
City
West Palm Beach
State/Province
Florida
Country
United States
Facility Name
Investigational Site 1
City
Arlington Heights
State/Province
Illinois
Country
United States
Facility Name
Investigational Site 21
City
Lake Charles
State/Province
Louisiana
Country
United States
Facility Name
Investigational Site 2
City
Silver Spring
State/Province
Maryland
Country
United States
Facility Name
Investigational Site 11
City
Saint Joseph
State/Province
Missouri
Country
United States
Facility Name
Investigational Site 27
City
East Windsor
State/Province
New Jersey
Country
United States
Facility Name
Investigational Site 5
City
High Point
State/Province
North Carolina
Country
United States
Facility Name
Investigational Site 23
City
Raleigh
State/Province
North Carolina
Country
United States
Facility Name
Investigational Site 15
City
Cincinnati
State/Province
Ohio
Country
United States
Facility Name
Investigational Site 6
City
Nashville
State/Province
Tennessee
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Study of Generic Pimecrolimus Cream, 1% in the Treatment of Mild to Moderate Atopic Dermatitis

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