First approved in Germany |
2002 (Psoriasis arthritis )/2004 (psoriasis vulgaris) |
Recommended control parameters |
Prior to therapy exclusion of tuberculosis, complete blood count, liver and renal values, urinanalysis |
Recommended initial dosage |
Twice 25 mg per week or 2× 50 mg/week |
Recommended maintenance dosage |
Twice 25 mg per week |
Expected beginning of clinical effect |
After 4–8 weeks, at the latest after 12 weeks |
Response rate |
PASI 75 in 34% (2 × 25 mg) or 49% (2 × 50 mg) of the patients at the end of the induction phase (12 weeks) (LE 1) |
Important contraindications (limited selection) |
Infections, pregnancy, nursing, heart failure NYHA III–IV |
Important ADRs (limited selection) |
Local reactions, infections |
Important drug interactions (limited selection) |
Anakinra (IL-1 receptor antagonist) |
Other |
– |