New Harris Poll findings reveal HAE patients are unsatisfied with current prophylactic treatment options, with over 90% interested in trying new therapies

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Hereditary angioedema (HAE) burden of illness survey results
Hereditary angioedema (HAE) burden of illness survey results

– Despite currently available treatment options, the majority of surveyed adults with HAE reported making tradeoffs in their daily lives due to the unexpected and unpredictable nature of HAE attacks –

Opportunity exists for more consistent use of tools to support transparent communications between patients and their doctors, as HCPs may underestimate the full burden of HAE –

CARLSBAD, Calif., April 29, 2025--(BUSINESS WIRE)--Ionis Pharmaceuticals, Inc. (Nasdaq: IONS) today announced results from a new survey showing that 91% of surveyed adults living with hereditary angioedema (HAE) were interested in trying a new prophylactic therapy, with nearly two-thirds (65%) reporting they haven’t yet found the best treatment option for them. The Ionis-sponsored survey was conducted online by The Harris Poll among 150 adults living with HAE and 228 allergists/immunologists who see HAE patients in the U.S.

HAE is a rare and potentially life-threatening genetic condition that involves recurrent attacks of severe swelling (angioedema) in various parts of the body, including the hands, feet, genitals, stomach, face and/or throat. A majority (72%) of patients in the survey said they made tradeoffs in their daily lives because they were not able to predict when they might have an attack. Despite most (85%) HCPs reporting that they understood how much HAE impacts their patients’ day-to-day lives, 60% of patients who have seen an HCP for their HAE wished their HCPs better understood this impact.

"These survey findings shed light on the holistic experience of living with HAE, as patients continue to experience painful and unpredictable attacks with a significant impact on their day-to-day lives, despite available treatments. We see that patients may be hesitant to share the full extent of their disease burden with their doctor, and as a result HCPs may be overestimating patients’ level of disease control," said Dr. William Lumry, M.D., clinical professor of internal medicine, University of Texas Southwestern Medical School. "In my practice, I've found that using a standardized questionnaire can help aid in these discussions, providing a simple way for patients to objectively evaluate and communicate their disease burden, and thus supporting more informed conversations about treatment considerations."

The use of standardized disease control tools, such as the Angioedema Control Test (AECT), can be an effective way to evaluate disease control and understand the full impact of HAE on people living with this serious disease. Only about a third (36%) of patients surveyed reported using a standardized tool with their HCP to regularly assess their level of HAE control, suggesting these resources may be underutilized.