Adverse Event reporting and Prescribing Information can be found via the links above

Featured content

Featured content

Get leading HAE expert opinions
HAE EXPERT HUB

Get leading HAE expert opinions

Hear HAE experts discuss the clinical evidence supporting the approval of ANDEMBRY®, as well as real-world patient case studies.


More resources

More resources

Learn how ANDEMBRY® is changing the path in HAE

Review key clinical data and the mechanism of action for ANDEMBRY®.

Tools

Access helpful tools and resources to support patients with HAE

Explore new ways to help your patients navigate their treatment with ANDEMBRY® and BERINERT®.

Access e-learning via the HAE Academy

Access CPD-accredited training materials and e-learning content on the diagnosis, treatment and management of HAE.

Explore More

Explore More

Explore HAE attack reduction with ANDEMBRY® (VANGUARD)

Review key efficacy data from the pivotal phase 3 VANGUARD trial for ANDEMBRY®.

Review the safety and tolerability profile of ANDEMBRY®

View safety data from the VANGUARD trial and OLE.


Explore how to administer ANDEMBRY®

Discover convenient and consistent dosing with ANDEMBRY®.


AbbreviationsCPD, Continuing Professional Development; HAE, hereditary angioedema; OLE, open-label extension.

References:
1. ANDEMBRY® (garadacimab). Summary of Product Characteristics.
2. BERINERT® 2000 IU (C1-esterase inhibitor, human). Summary of Product Characteristics.
3. BERINERT® 3000 IU (C1-esterase inhibitor, human). Summary of Product Characteristics.

Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple store. Adverse events should also be reported to CSL Behring UK Ltd. on 01444 447405.

GBR-AND-0314 | May 2026.