Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Rockefeller University
Age
18–any
Sex
ALL
Healthy volunteers
Accepted
You may be eligible if
Signed informed consent
Normal volunteers with no evidence of skin disease OR diagnosis of plaque type psoriasis for at least 6 months
18 years of age or greater
For women of childbearing potential or in men whose partners may become pregnant, willingness to use an acceptable method of contraception to prevent pregnancy for the duration of the study. Acceptable methods of contraception include use of a condom; abstinence; use by sexual partner of oral implantable or injectable contraceptives, IUD, female condom, diaphragm with spermicide, cervical cap; or a sterile sexual partner
You may not be if
Guttate, erythrodermic, or pustular psoriasis as sole or predominant form of psoriasis
Clinically significant psoriasis flare during screening or on the first treatment day
Hypersensitivity to IFN-g or E. coli derivatives
Pre-existing, uncontrolled myelosuppression, cardiac disease, seizure disorders, compromised central nervous system function or multiple sclerosis
History of malignancy, clinically significant renal insufficiency, poorly controlled medical conditions that would increase the risks
Presence of malignancy within the past 5 years, including lymphoproliferative disorders. Subjects with a history of fully resolved basal cell or squamous cell skin cancer may be enrolled.
Pregnancy or lactation. As the risk of IFN-g in pregnancy is unknown, pregnant women will be excluded from the study.
Any medical condition that, in the judgment of the investigator, would jeopardize the subject's safety following exposure to study drug
