First approved in Germany |
September 2004 (psoriasis vulgaris) |
Recommended control parameters |
Prior to therapy exclusion of significant infections, complete blood count, liver values |
Recommended initial dosage |
0.7 mg/kg body weight (BW) per week |
Recommended maintenance dosage |
1 mg/kg BW per week |
Expected beginning of clinical effect |
After 4–8 weeks |
Response rate |
PASI 75 for approximately 30% of the patients after 12 weeks (LE 1) |
Important contraindications (limited selection) |
Chronic or acute infections, pregnancy, malignant diseases, immune deficiencies, no vaccinations before or during treatment |
Important ADRs (limited selection) |
Flu-like injection reactions, leukocytosis and lymphocytosis, rebound, exacerbation and arthralgia, thrombocytopenia |
Important drug interactions |
Not known |
Other |
Stop therapy due to the risk of exacerbation and rebound if a PASI reduction of 50% is not achieved after 12 weeks |