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FDA approves Haegarda (subcutaneous C1-esterase inhibitor) for subcutaneous administration to prevent hereditary angioedema (HAE) attacks in adolescent and adult patients.-CSL Behring

Read time: 1 mins
Last updated: 24th Jun 2017
Published: 24th Jun 2017
Source: Pharmawand

The FDA has approved Haegarda, the first C1 Esterase Inhibitor (Human) for subcutaneous (under the skin) administration to prevent Hereditary Angioedema (HAE) attacks in adolescent and adult patients. The subcutaneous route of administration allows for easier at-home self-injection by the patient or caregiver, once proper training is received.

HAE, which is caused by having insufficient amounts of a plasma protein called C1-esterase inhibitor (or C1-INH), affects approximately 6,000 to 10,000 people in the U.S. People with HAE can develop rapid swelling of the hands, feet, limbs, face, intestinal tract or airway. These attacks of swelling can occur spontaneously, or can be triggered by stress, surgery or infection.

Comment:The subcutaneous formulation allows patients to administer the product at home to help prevent attacks.

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