MENTALIST – Unmet needs in hereditary angioedema – a global physician perspective
Aim: To identify and rank unmet needs in hereditary angioedema (HAE) including HAE due to C1INH deficiency and HAE with normal C1INH values with known or unknown causative mutations.
Background: In recent years, new scientific findings on HAE and the establishment of international treatment guidelines have contributed to a broader understanding of the disease and improved the quality of life of patients with HAE. Therefore, it is important to understand, from the physician perspective, what the current unmet needs in HAE globally are and to raise awareness on specifics with updated supporting data.
This study will only run for 30 days, from September 1 to September 30 and is open to all HAE treating physicians.
The survey takes about 15 minutes to complete.
To take part, please reach out to Dr. Thomas Buttgereit: thomas.buttgereitATcharite.de
The study is supported by CSL Behring.
Read more news from ACARE
- February 23, 2024
Topic: HAE WITH NORMAL C1 INHIBITOR: HOW TO CORRECTLY DIAGNOSE AND TREAT THIS RARE TYPE OF RECURRENT ANGIOEDEMA Date: April 4, 2024 Time: 4:00 to 5:00 pm CEST Click HERE [...]
- December 21, 2021
We are pleased to invite you to participate in the 6th Bradykinin Symposium at Charité from Thursday to Friday, 15-16 September 2022 in Berlin. International experts in the field of bradykinin [...]
- October 13, 2023
Dr Thomas Buttgereit is joined by Dr Carolina Vera to discuss the use of attenuated androgens in the treatment of hereditary angioedema and their associated risks and side effects. Both [...]
