Study of Generic Pimecrolimus Cream, 1% in the Treatment of Mild to Moderate Atopic Dermatitis
Status: | Completed |
---|---|
Conditions: | Psoriasis, Dermatology, Dermatology, Dermatology |
Therapuetic Areas: | Dermatology / Plastic Surgery |
Healthy: | No |
Age Range: | 12 - Any |
Updated: | 6/30/2017 |
Start Date: | August 2016 |
End Date: | June 2017 |
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).
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).
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).
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.
We found this trial at
22
sites
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials