Efficacy and Safety of Prurisol Administered Orally for Active Mild to Moderate Chronic Plaque Psoriasis

Completed · Phase 2 · Has a placebo group

Conditions studied: Plaque Psoriasis

In brief

This study is designed to evaluate the efficacy and safety of Prurisol using three different oral daily dose regimens administered to subjects with active mild to moderate chronic plaque psoriasis.

Key facts

Study ID

NCT02494479

Run by

Cellceutix Corporation

People needed

115

Starts

2015-08-01

Expected to finish

2016-05-01

Last updated by the study team

2017-07-19

Who can join

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

You may qualify if…

• Male or non-pregnant female adults aged 18 years with a clinical diagnosis of stable (at least 6 months) plaque psoriasis, not including scalp or intertriginous areas.
• The extent of psoriasis must meet all of the following three (3) criteria:
• Total Body Surface Area (BSA) affected by plaque psoriasis of 10% to 20% inclusive
• Investigator's Global Assessment (IGA) score of the severity of psoriasis of 2 or 3 (5- point ordinal scale)
• Identification of a target psoriatic lesion with a score of 3 on the Target Lesion Assessment scale (5-point ordinal scale) for Scaling. (Other psoriatic lesions may have lower scaling scores.)
• Females of reproductive potential must not be pregnant
• Female subjects with reproductive potential, if sexually active, must agree to use reliable means of contraception
• The subject must agree to avoid prolonged exposure to the sun and avoid the use of tanning booths or other ultraviolet light sources during the study.
• The subject must provide signed and dated written informed consent to participate in the clinical study.

You may not qualify if…

• 1. Females of reproductive potential who are not using reliable contraception.
• Presence of any non-psoriatic uncontrolled (in the Investigator's medical opinion) systemic disease. i
• Unstable forms of psoriasis, e.g. guttate, erythrodermic, exfoliative, palmoplantar, nail, or pustular.
• Use within 6 months of biologic treatment for psoriasis
• Use within 24 months of chemotherapy or radiation therapy.
• Use within 2 months of any systemic immunosuppressive therapy.
• Use within 1 month of (1) systemic corticosteroids, (2) systemic antibiotics, (3) systemic antipsoriasis treatments (e.g. methotrexate, corticosporin, hydroxyurea), (4) PUVA therapy, (5) UVB, (6) systemic anti-inflammatory treatment.
• Use within 2 weeks of topical antipsoriasis drugs or topical corticosteroids or topical retinoids.
• Presence of a condition (e.g., history of frequent consumption of substantial quantities of alcohol, or an untreated psychiatric condition) that makes it unlikely that the requirements of the protocol will be completed.
• History of any previous use of a Tumor Necrosis Factor (TNF) blocker or other immunomodulating drug as therapy for psoriasis within the 6 months prior to screening.
• History of any allergic reaction to any formulation of abacavir.
• Previous treatment with any abacavir-containing product, e.g., Ziagen®, Epzicom®, or Trizivir®.

Where it is running

• Cellceutix Study Center — Huntsville, Alabama, United States
• Cellceutix Study Center — Encino, California, United States
• Cellceutix Study Center — Coral Gables, Florida, United States
• Cellceutix Study Center — Hialeah, Florida, United States
• Cellceutix Study Center — Kissimmee, Florida, United States
• Cellceutix Study Center — Miami, Florida, United States
• Cellceutix Study Center — Miami, Florida, United States
• Cellceutix Study Center — Pembroke Pines, Florida, United States
• Cellceutix Study Center — Las Vegas, Nevada, United States

Full record on ClinicalTrials.gov

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