Bexarotene With Narrow-Band UVB for Psoriasis

NCT ID: NCT00151008

Last Updated: 2008-08-07

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 35 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2003-11-30
• Study Completion Date: 2005-08-31

Brief Summary

To determine if bexarotene gel with NBUVB phototherapy is more effective than placebo plus NBUVB for moderate to severe plaque-type psoriasis.

Detailed Description

Subjects will be applying active gel or placebo to target lesions to each side of the body in a blinded manner. They will start at three times a week and increase to daily or even twice a day regimen if tolerated. After 2 weeks of application, NBUVB will be added to treatment regimen (whole body, three times a week). Total study time is 10 weeks.

Conditions

Psoriasis

Keywords

psoriasis; bexarotene; narrow band; UVB

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Interventions

Bexarotene/NBUVB vs placebo NBUVB

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Patient must be a male or female aged 18 years or older
• Patient must have moderate to severe psoriasis vulgaris of at least 3% body surface area involvement
• Patient must have failed prior topical therapy
• Patient must be willing to minimize sun exposure, to use sun blockers if deemed necessary by the Investigator and to avoid use of tanning booths or other ultraviolet (UV) light sources
• Women of childbearing potential must have a negative urine ß-HCG pregnancy test with a sensitivity of at least 50 mIU/mL within seven days prior to starting of study gels and repeated every four weeks while patient remains on the study gels. All females of childbearing potential must agree to use 2 effective contraceptive methods or remain sexually abstinent one month prior to initiation of study drug, during the entire study period, and for one month after the last application of Targretin® gel 1%. Acceptable methods of birth control include: condoms with spermicide; diaphragm with spermicide; cervical cap with spermicide; spermicidal sponge; intrauterine device (IUD), oral contraceptives, Depo-Provera; contraceptive implants; vasectomy; or abstinence.
• Male patients must agree to use condoms with sexual partners of childbearing potential during the entire period of treatment and for at least one month after treatment is discontinued.
• Patients who are not sexually active and are not using contraception, must agree to use an approved method of contraception (as described above) should they become sexually active during the study

Exclusion Criteria

• Failure to understand the consent form
• Inability to comply with protocol requirements
• Pregnancy
• Inadequate birth control method
• Lactation
• Contraindication to use of topical retinoids
• Concomitant psoriasis therapies except for emollients and OTC shampoos
• Systemic psoriasis therapies, systemic Vitamin A in doses > 15,000IU/day, PUVA, (psoralen plus ultraviolet A irradiation), UVB, topical psoriasis therapies (other than emollients and OTC shampoos), other retinoid class drugs or investigational drugs within the past 1 month
• Current skin cancer
• History of previous melanoma
• History of skin sensitizing diseases (such as SLE)
• Concurrent medical illness that would make participation in this clinical trial ill-advised
• Patient unwilling or unable to avoid prolonged exposure to the sun or other UV light sources

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

Sponsors

Ligand Pharmaceuticals

INDUSTRY

Sponsor Role: collaborator

University of Medicine and Dentistry of New Jersey

OTHER

Sponsor Role: lead

Principal Investigators

Melissa Magliocco, MD

Role: PRINCIPAL_INVESTIGATOR

Rutgers, The State University of New Jersey

Other Identifiers

4405

Identifier Type: -

Identifier Source: org_study_id