ANDEMBRY

This brand name is authorized in Estonia, France, Lithuania, UK.

Active ingredients

The drug ANDEMBRY contains one active pharmaceutical ingredient (API):

1
UNII 32W6AJL0DY - GARADACIMAB
 

Garadacimab is a fully human IgG4/lambda recombinant monoclonal antibody which binds to the catalytic domain of activated Factor XII (FXIIa and βFXIIa) and inhibits its catalytic activity. The inhibition of FXIIa, the first factor activated in the contact system, prevents HAE attacks by blocking the activation of prekallikrein to kallikrein and the generation of bradykinin, which is associated with inflammation and swelling in HAE attacks.

 
Read more about Garadacimab

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 ANDEMBRY Solution for injection MPI, EU: SmPC European Medicines Agency (EU)

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC Group Classification
B06AC07 B Blood and blood forming organs → B06 Other hematological agents → B06A Other hematological agents → B06AC Drugs used in hereditary angioedema
Discover more medicines within B06AC07

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
EE Ravimiamet 3108518, 3108529, 3108596, 3108608
FR Base de données publique des médicaments 63003892, 68937264
LT Valstybinė vaistų kontrolės tarnyba 1102710, 1102711, 1102712, 1102713

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