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Amevive (ALEFACEPT)

Astellas Pharma · FDA-approved approved Recombinant protein Quality 21/100

Amevive (Alefacept) is a CD2-directed LFA-3/Fc Fusion Protein developed by Astellas, targeting T-cell surface antigen CD2. It is a small molecule drug class, FDA-approved in 2003 for the treatment of plaque psoriasis. Amevive works by binding to CD2 on T-cells, leading to their depletion and subsequent reduction in inflammation. The commercial status of Amevive is patented, and it is currently owned by Astellas. Key safety considerations include potential infections and allergic reactions.

At a glance

Generic nameALEFACEPT
SponsorAstellas Pharma
Drug classCD2-directed LFA-3/Fc Fusion Protein
TargetT-cell surface antigen CD2
ModalityRecombinant protein
Therapeutic areaImmunology
PhaseFDA-approved
First approval2003

Approved indications

Common side effects

No common side effects on file.

Key clinical trials

Primary sources

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SourceUsed for
FDA labelMechanism, indications, dosing, boxed warnings, drug interactions
ClinicalTrials.govTrial enrolment, design, endpoints, results

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