THE RIGHT THERAPY MATTERS
HAE ATTACKS MAY IMPACT YOUR PATIENTS MORE THAN YOU THINK
86% of patients said that 3 in 4 untreated or inadequately controlled attacks were severe enough to negatively impact quality of life.1
97% of patients agree nothing could be more convenient than a medication that allows them to live attack free.2
* These findings are the result of an online survey conducted by The Harris Poll, sponsored by CSL Behring LLC, involving 100 US adults aged 18+ who have been diagnosed by a healthcare professional with hereditary angioedema (HAE) ("people living with HAE") and 150 licensed allergists/immunologists in the US who have treated/managed at least 2 HAE patients in the past 12 months ("physicians").
BUILD AND MAINTAIN STEADY‑STATE C1‑INH FUNCTIONAL LEVELS

HAEGARDA replaces missing or dysfunctional C1‑INH with functional C1‑INH, which regulates the normal production of bradykinin
- The root cause of HAE is deficient or dysfunctional C1-INH
- Functional C1-INH levels ≥40% of normal are proposed to reduce the risk of HAE attacks3
- Steady-state C1-INH functional activity is expected within 3 to 4 doses4
What made me try HAEGARDA? It’s the same protein my body is lacking.
-Zahra, HAEGARDA Advocate
C1-INH=C1 inhibitor.
HAE=hereditary angioedema.
The 2021 World Allergy Organization Guidelines recommend use of C1 esterase inhibitors for first-line, long-term prophylaxis.6
The right therapy matters to get to steady state quickly
- Quick acting: steady-state C1‑INH functional levels achieved in approximately the first 2 weeks†
- Subcutaneous C1-INH builds and maintains steady-state C1‑INH functional activity3-5‡
Administered subcutaneously, HAEGARDA 60 IU/kg maintained steady-state C1‑INH functional levels above 40%3-5
† Steady state is expected within 3 to 4 doses.
‡ The plasma levels of C1-INH functional activity were evaluated in patients with type 1 or type 2 HAE in a Phase 3, placebo-controlled, crossover study. Patients received twice-weekly subcutaneous injections of HAEGARDA 40 IU/kg or 60 IU/kg for 16 weeks. The model-derived outcome is the steady-state C1-INH functional activity vs time.4
What makes HAEGARDA different?
HAEGARDA is the HAE product that reduced HAE attacks by 95%.‡
‡ Median reduction in the number of attacks with HAEGARDA 60 IU/kg vs placebo.
WORLD ALLERGY ORGANIZATION (WAO) GUIDELINES RECOMMENDATIONS AND TREATMENT GOALS6
C1‑INH has been used for 35 years and is the WAO-recommended first-line therapy
- The WAO recommends C1‑INH as first-line preventive therapy for HAE for long-term prophylaxis6
- C1‑INH is the preferred therapy for pregnant or breastfeeding HAE patients6
On‑demand treatment goals§
- Shorter time to resolution of symptoms
- Shorter total attack duration regardless of attack severity
§ Short-term or preprocedural prophylaxis can also be administered before an event that may trigger an HAE attack (eg, medical or invasive dental procedure).
Long-term prophylaxis (LTP) treatment goals
- Achieve full control of disease burden
- Attempt to minimize treatment burden and side effects
See on-demand treatment of acute HAE attacks
EXPLORE ON-DEMANDWorld Allergy Organization/European Academy of Allergy and Clinical Immunology guidelines on prophylaxis
"We recommend that HAE patients are evaluated for long-term prophylaxis at every visit. Disease burden and patient preference should be taken into consideration. Evidence Grade D; strength of recommendation strong, 96% agreement."