Bexarotene With Narrow-Band UVB for Psoriasis

University of Medicine and Dentistry of New Jersey

Status and phase

Completed

Phase 2

Conditions

Psoriasis

Treatments

Drug: Bexarotene/NBUVB vs placebo NBUVB

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT00151008

4405

Details and patient eligibility

About

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

Full 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.

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion 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