Photo does not depict actual patient

ANDEMBRY Provides Significant Reduction in HAE Attacks

A median reduction of >99% was calculated because at least half of the ANDEMBRY-treated patients experienced a complete reduction in monthly HAE attack rates compared to placebo. Patients receiving ANDEMBRY in the clinical trial experienced an adjusted average of 89% (LS; least squares) reduction in monthly HAE attack rate compared to placebo.

* With all HAE medications, attacks can still occur. Patients should always have a rescue medication.
† At 6 months.
LS, least squares

ANDEMBRY, THE FIRST AND ONLY ONCE-MONTHLY HAE PROPHYLAXIS TREATMENT FROM THE START FOR ALL PATIENTS

  • Monthly dosing from the start for all patients 12 years and older
  • Subcutaneous self-injection delivered in ≤15 seconds via a convenient autoinjector
  • No reports of injection-site pain§

§ In the VANGUARD pivotal phase 3 trial. Patients in the pivotal study and open-label extension study experienced injection-site redness, itching, and bruising.

Resources

Downloadable resources that can provide additional information about ANDEMBRY

Personalized Support

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Innovation in Action

Only ANDEMBRY, a monoclonal antibody, 
inhibits FXIIa at the top of the HAE pathway

Safety Information

Important Safety Information