A Study of the Efficacy and Safety of DFD-06 Cream in the Treatment of Moderate to Severe Plaque Psoriasis

Completed · Phase 3

Conditions studied: Psoriasis

In brief

This study will compare the efficacy and safety of DFD-06 Cream to Vehicle Cream for topical treatment of moderate to severe plaque psoriasis after 3, 7, and 14 days of treatment.

Key facts

Study ID

NCT02635204

Run by

Promius Pharma, LLC

People needed

267

Starts

2015-12-01

Expected to finish

2016-07-01

Last updated by the study team

2018-05-15

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subject understands the study procedures and agrees to participate by giving written informed consent. Subjects must be willing to authorize use and disclosure of protected health information collected for the study.
• Subject must be at least 18 years of age.
• Subject must present with a clinical diagnosis of stable (at least 3 months) plaque-type psoriasis.
• Subject with psoriasis involving 3% or greater BSA, not including the face, scalp, groin, axillae and other intertriginous areas.
• Subject must have an IGA grade of 3 or 4 (moderate to severe) at the Baseline Visit.
• Female subjects of childbearing potential must agree to use contraception during the study which can include abstinence with an adequate secondary option should the subject become sexually active. All women of childbearing potential must complete a urine pregnancy test (test must have a sensitivity of at least 25mIU/ml for human chorionic gonadotropin) at the Baseline Visit (Visit 2) and the test result must be negative to be eligible for enrollment.
• Subject must be in good general health as determined by the investigator and supported by the medical history and normal or not clinically significant abnormal vital signs (blood pressure and pulse).

You may not qualify if…

• Current diagnosis of unstable forms of psoriasis including guttate, erythrodermic, exfoliative or pustular psoriasis.
• Other inflammatory skin disease that may confound the evaluation of the plaque psoriasis (e.g., atopic dermatitis, contact dermatitis, tinea corporis).
• Presence of pigmentation, extensive scarring, or pigmented lesions or sunburn which could interfere with the rating of efficacy parameters.
• History of psoriasis unresponsive to biological or topical treatments.
• History of organ transplant requiring immunosuppression, HIV, or other immunocompromised state.
• Use within 180 days prior to Baseline Visit of biologic treatment for psoriasis (e.g., infliximab, adalimumab, etanercept, ustekinumab, secukinumab, or alefacept).
• Have received treatment for any type of cancer within 5 years of the Baseline Visit except skin cancer and cervical cancer (in situ) are allowed if at least 1 year before the Baseline Visit.
• Use within 60 days prior to the Baseline Visit of: 1) systemic or topical immunosuppressive drugs (e.g., tacrolimus, pimecrolimus), 2) systemic antipsoriatic treatment (e.g., methotrexate, cyclosporine, hydroxyurea) or 3) oral retinoids (e.g., acitretin, isotretinoin).
• Use within 30 days prior to the Baseline Visit of: 1) systemic steroids, 2) PUVA therapy, 3) systemic anti-inflammatory agents (e.g., mycophenolate mofetil, sulfasalazine, 6-thioguanine), or 4) UVB therapy. Inhaled, intraocular, and intranasal steroids are allowed.
• Use within 14 days prior to the Baseline Visit of: 1) topical antipsoriatic drugs (e.g., salicylic acid, anthralin, coal tar, calcipotriene), 2) topical retinoids (e.g., tazarotene, tretinoin) or 3) topical corticosteroids.
• Subjects who have participated in a study of an investigational drug 60 days prior to the Baseline Visit.

Where it is running

• Site 116 — Glendale, Arizona, United States
• Site 111 — Rogers, Arkansas, United States
• Site 124 — Fountain Valley, California, United States
• Site 120 — Laguna Hills, California, United States
• Site 122 — San Diego, California, United States
• Site 123 — San Diego, California, United States
• Site 113 — Denver, Colorado, United States
• Site 117 — New Haven, Connecticut, United States
• Site 108 — Brandon, Florida, United States
• Site 112 — Coral Gables, Florida, United States
• Site 106 — Jacksonville, Florida, United States
• Site 110 — Pinellas Park, Florida, United States
• 130 — West Palm Beach, Florida, United States
• Site 103 — Arlington Heights, Illinois, United States
• Site 115 — Overland Park, Kansas, United States
• Site 127 — Beverly, Massachusetts, United States
• Site 119 — Quincy, Massachusetts, United States
• 129 — Henderson, Nevada, United States
• Site 114 — New York, New York, United States
• Site 104 — Rocky Mount, North Carolina, United States
• Site 105 — Wilmington, North Carolina, United States
• Site 126 — Cincinnati, Ohio, United States
• Site 121 — Warwick, Rhode Island, United States
• Site 107 — Nashville, Tennessee, United States
• 128 — Arlington, Texas, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.