A Study of Lanadelumab (SHP643) in Chinese Participants With Hereditary Angioedema (HAE)
NCT05460325 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 20
Last updated 2024-12-13
Summary
The main aim of this study is to evaluate the safety of lanadelumab in Chinese participants with HAE.
Participants will be treated with lanadelumab for 26 weeks.
Conditions
- Hereditary Angioedema (HAE)
Interventions
- DRUG
-
Lanadelumab
Lanadelumab subcutaneous injection
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Study Director · Takeda
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 12 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2022-06-22
- Primary Completion
- 2023-11-28
- Completion
- 2023-11-28
Countries
- China
Study Locations
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