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Clinical Trial Summary

The main aim of this study is to compare the HAE attack rate before and after lanadelumab treatment was started in persons with Hereditary Angioedeme Type I or II. Data from participants will be collected for at least 24 months. Participants will report information in a smartphone application at study start and then every 3 months until the study ends; data will also be collected by the study doctor during routine clinic visits.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03845400
Study type Observational
Source Takeda
Contact
Status Completed
Phase
Start date March 30, 2019
Completion date October 22, 2022

See also
  Status Clinical Trial Phase
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