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Raptiva

Active Substance: efalizumab
Common Name: efalizumab
ATC Code: L04AA21
Marketing Authorisation Holder: Serono Europe Limited
Active Substance: efalizumab
Status: Withdrawn
Authorisation Date: 2004-09-20
Therapeutic Area: Psoriasis
Pharmacotherapeutic Group: Immunosuppressants

Therapeutic Indication

Treatment of adult patients with moderate to severe chronic plaque psoriasis who have failed to respond to, or who have a contraindication to, or are intolerant to other systemic therapies including ciclosporin, methotrexate and PUVA (see section 5.1 - Clinical Efficacy).

The marketing authorisation for Raptiva has been withdrawn at the request of the marketing authorisation holder.

Source: European Medicines Agency

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