Study of the Efficacy of Cloderm® Cream in the Treatment of Moderate Plaque Psoriasis

NCT ID: NCT01714544

Last Updated: 2014-07-23

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE4
• Total Enrollment: 60 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2012-10-31

Brief Summary

The purpose of this study is to determine whether Cloderm Cream is effective for topical treatment of moderate psoriasis over 28 days.

Detailed Description

The objective of this study is to estimate the efficacy of Cloderm Cream for topical treatment of moderate plaque psoriasis over 28 days using current standards for evaluation.

Conditions

Psoriasis

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Cloderm Cream

Cloderm (clocortolone pivalate) Cream 0.1%, twice daily for 28 days

Group Type: EXPERIMENTAL

Cloderm Cream

Intervention Type: DRUG

Interventions

Cloderm Cream

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Subject understands the study procedures and agrees to participate by giving written informed consent.

2. Subjects must be at least 18 years of age.

3. Subjects must present with a clinical diagnosis of stable (at least 3 months) plaque-type psoriasis.

4. Subjects with psoriasis involving 2 to 20% BSA, not including the face, scalp and intertriginous areas.

5. Subjects must have an IGA Grade of 3 at the Baseline Visit.

6. Female subjects of childbearing potential must have a negative urine pregnancy test result at Baseline (Visit 2) (test will have a sensitivity of at least 25mIU/ml for human chorionic gonadotropin) and practice a reliable method of contraception or remain sexually inactive throughout the study.

All women of childbearing potential must be willing to undergo a urine pregnancy test at Visit 2 (Day 0), at Visit 4 (Day 14), and at Visit 5 (Day 28).

7. Subjects 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).

Exclusion Criteria

1. Current diagnosis of unstable forms of psoriasis including guttate, erythrodermic, exfoliative or pustular psoriasis.

2. Other inflammatory skin disease that may confound the evaluation of the plaque psoriasis (e.g., atopic dermatitis, contact dermatitis, tinea corporis).

3. Presence of pigmentation, extensive scarring, pigmented lesions or sunburn which could interfere with the rating of efficacy parameters.

4. History of psoriasis unresponsive to topical treatments.

5. History of organ transplant requiring immunosuppression, HIV, or other immunocompromised state.

6. Use within 180 days prior to Baseline Visit of biologic treatment for psoriasis (e.g., infliximab, adalimumab, etanercept, ustekinumab, or alefacept).

7. Have received treatment for any type of cancer within 5 years of the Baseline Visit except for non-melanoma skin cancer and cervical cancer (in situ) are allowed within 1 year of the Baseline Visit.

8. Use within 60 days prior to the Baseline Visit of: 1) immunosuppressive drugs (e.g., tacrolimus, pimecrolimus), 2) systemic antipsoriatic treatment (e.g., methotrexate, cyclosporine, hydroxyurea) or 3) oral retinoids (e.g., acitretin, isotretinoin).

9. 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. Note: Inhaled, intraocular and intranasal steroids are allowed.

10. 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.

11. Subjects with known hypersensitivity to clocortolone pivalate or any component of Cloderm Cream.

12. Subjects who have participated in a study of an investigational drug 60 days prior to the Baseline Visit.

13. Subjects unable to comply with study requirements.

14. Female subjects who are pregnant (or planning to become pregnant) or breast-feeding.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Promius Pharma, LLC

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Joanne M Fraser, PhD

Role: STUDY_DIRECTOR

Promius Pharma

Locations

Radiant Research, Inc.

Cincinnati, Ohio, United States

Oregon Medical Research

Portland, Oregon, United States

DermResearch, Inc.

Austin, Texas, United States

Research Across America

Dallas, Texas, United States

Madison Skin and Research, Inc.

Madison, Wisconsin, United States

Countries

United States

Other Identifiers

CDC1201

Identifier Type: -

Identifier Source: org_study_id