MedPath
EMA Product

Andembry

Product approved by European Medicines Agency (EU)

Basic Information

Andembry

Regulatory Information

EMEA/H/C/006116

Authorised

February 10, 2025

December 12, 2024

March 11, 2025

Company Information

Germany

Emil-von-Behring-Strasse 76 D-35041 Marburg

Csl Behring Gmbh

Drug Classification

Additional Monitoring

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Andembry is indicated for routine prevention of recurrent attacks of hereditary angioedema (HAE) in adult and adolescent patients aged 12 years and older.

Overview Summary

Andembry is used for routine prevention of recurrent attacks of hereditary angioedema (HAE) in adults and adolescents aged 12 years and older. Patients with hereditary angioedema have rapid swelling under the skin in areas such as the face, throat, gut, arms and legs. Attacks of HAE can be life threatening when the swelling around the throat presses against the airway. Andembry contains the active substance garadacimab.

© Copyright 2025. All Rights Reserved by MedPath