hereditary
angioedema
Research is at the heart of advancing our knowledge of Hereditary Angioedema.
without people like you, we would not be where we are today.
Do you or a loved one suffer from Hereditary Angioedema?
You may be eligible to participate in a clinical study here in Columbus, Ohio.
HEREDITARY ANGIOEDEMA (HAE)
Hereditary angioedema (HAE) is a very rare and potentially life threatening genetic condition that causes severe swelling (angioedema). Swelling often occurs without a known trigger. The most common areas of the body to develop swelling are the limbs, face, intestinal tract, and airway. The frequency and duration of swelling vary greatly and episodes often cause excruciating pain. Up to 25% of HAE cases result from a spontaneous mutation of a blood factor gene called the C1-inhibitor.
We have many trials for HAE. Contact us to see if you meet the criteria for any of our current trials.
Click below to visit the sponsor provided website for the HAErmony1 clinical trial for HAE:
