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A Survey of Lanadelumab in Participants With Hereditary Angioedema
Sponsor: Takeda
Summary
This study is a survey in Japan of Lanadelumab used to treat people with hereditary angioedema (HAE). The study sponsor will not be involved in how the participants are treated but will provide instructions on how the clinics will record what happens during the study. The main aim of the study is to check for side effects related from Lanadelumab and to check if Lanadelumab improves symptoms of HAE. During the study, participants with HAE will take Lanadelumab subcutaneous injection according to their clinic's standard practice. The study doctors will check for side effects from Lanadelumab for 12 months.
Official title: Specific Use-Results Survey of TAKHZYRO Subcutaneous Injection 300 mg Syringe for Hereditary Angioedema With Long-term Administration
Key Details
Gender
All
Age Range
Any - Any
Study Type
OBSERVATIONAL
Enrollment
155
Start Date
2022-05-30
Completion Date
2026-06-25
Last Updated
2026-04-13
Healthy Volunteers
No
Conditions
Interventions
Lanadelumab
Lanadelumab 300 mg, subcutaneous injection every 2 weeks
Locations (1)
Takeda selected site
Tokyo, Tokyo, Japan