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ACTIVE NOT RECRUITING
NCT05397431

A Survey of Lanadelumab in Participants With Hereditary Angioedema

Sponsor: Takeda

View on ClinicalTrials.gov

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

Interventions

DRUG

Lanadelumab

Lanadelumab 300 mg, subcutaneous injection every 2 weeks

Locations (1)

Takeda selected site

Tokyo, Tokyo, Japan