About this trial
Psoriasis is a skin disorder that is chronic proliferative and inflammatory in nature. Extensor surfaces, scalp, and lumbosacral area are covered in erythematous plaques with silvery scales. The disease can also impair the eyes and joints. It has no cure. Because of their low quality of life, many psoriasis patients experience depression. In addition to the cutaneous manifestations, it is associated with an increased risk of psoriatic arthritis, depression and cardiovascular disease.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
None
Disqualifiers
Patients with other autoimmune or inflammatory conditions (e.g., rheumatoid arthritis, lupus).
Pregnancy and lactation.
Patients currently undergoing any treatment other than Humira.
Patients with known genetic disorders affect immune system function.
Trial design
Parallel
Treatments tested in this trial
Humira
DrugAssess the response of psoriasis and psoriatic arthritis to Humira and also Assessing the pharmacogenetic association between IL 12B genetic polymorphism (rs3213094) in psoriatic and psoriatic arthritis patients taking Humira.
Treatment groups
Trial outcomes
Primary outcomes
Treatment of Psoriasis and Psoriatic Arthritis
Treatment the patients whom suffering from Psoriasis and Psoriatic arthritis and Assessment of clinical improvement to Humira therapy according to: PASI score into PASI 50: means 50% reduction in PASI score - an acceptable measure of efficacy for secondary endpoints in psoriasis clinical trials PASI 75: means 75% reduction in PASI score - standard efficacy measure used in most psoriasis clinical studies1 PASI 90: means 90% reduction in PASI score (almost clear skin) PASI 100: means Completely clear skin.
Secondary outcomes
Evaluate the effect of treatment with Humira
Evaluate the effect of treatment with Humira therapy on the level of serum IL12B genetic polymorphism (rs3213094) on the Participants whom suffering from Psoriasis and Psoriatic arthritis.
Sponsors and contacts
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