Overview
Study of Generic Pimecrolimus Cream, 1% in the Treatment of Mild to Moderate Atopic Dermatitis
Status:
Completed
Completed
Trial end date:
2017-06-01
2017-06-01
Target enrollment:
0
0
Participant gender:
All
All
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).Phase:
Phase 3Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Glenmark Pharmaceuticals Ltd. IndiaTreatments:
Pimecrolimus
Tacrolimus
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.