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Get your patients started
with EKTERLY.
EKTERLY
Resources
Actor portrayal
HCP resources
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Data overviewA concise clinical overview of the
KONFIDENT trial and key data. -
In-office product onboarding checklistA helpful checklist for your office staff to ensure easy onboarding.
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Patient discussion guideA tool for learning about your patients’ experience with HAE and starting a conversation about EKTERLY.
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HAEA treatment guidelinesReview the full US HAEA Medical Advisory Board 2020 Guidelines for the management of HAE.
Resources for patients and caregivers
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Patient brochureA clear, comprehensive guide to all things EKTERLY.
Patient advocacy groups
Help your patients get information
and build community.
Hereditary Angioedema Association
The US Hereditary Angioedema Association (HAEA) is a 501(c)(3) nonprofit advocacy and research organization serving people living with the rare genetic condition HAE and their families.
National Organization for Rare Disorders
The National Organization for Rare Disorders (NORD) is a 501(c)(3) nonprofit dedicated to supporting individuals with rare diseases through advocacy, research, and patient assistance programs. It connects patients, caregivers, and researchers to advance treatment access and policy improvements.
HAE=hereditary angioedema; US HAEA=US Hereditary Angioedema Association.
