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. 2007 May 12;299(3):111–138. doi: 10.1007/s00403-007-0744-y

Table 8.

Tabular summary

Efalizumab
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