First approved in Germany |
2004 (Psoriasis arthritis)/2005 (psoriasis vulgaris) |
Recommended control parameters |
Prior to therapy exclusion of tuberculosis, during therapy: leukocyte and platelet counts, liver value controls, signs of clinical infection |
Recommended initial dosage |
5 mg/kg BW at week 0, 2, 6 |
Recommended maintenance dosage |
5 mg/kg BW in dosage intervals of 8 weeks |
Expected beginning of clinical effect |
After 1–2 weeks |
Response rate |
PASI 75 in ≥80% of the patients with moderate to severe psoriasis vulgaris (LE 1) |
Important contraindications (limited selection) |
Acute or chronic infections, tuberculosis, cardiac failure NYHA III–IV, pregnancy and nursing |
Important ADRs (limited selection) |
Infusion reactions, severe infections, progression of heart failure NYHA III–IV, very rare liver failure, autoimmune phenomena |
Important drug interactions (limited selection) |
Anakinra (IL-1 receptor antagonist) |
Other |
– |