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Study identifier: NCT05509569 Synced from ClinicalTrials.gov · August 07, 2026
● Study status: Completed

A Survey of Icatibant in Pediatric Participants With Hereditary Angioedema

Condition: Hereditary Angioedema (HAE)  ·  Sponsor: Takeda

PhaseN/A
Planned participants32
Who can joinAll sexes, 2 Years to 17 Years
Healthy volunteersNo

Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.

About this study

This study is a survey in Japan of Icatibant subcutaneous injection 30 mg syringe used to treat children or teenagers with acute attacks of 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 Icatibant subcutaneous injection 30 mg syringe and to check if Icatibant subcutaneous injection 30 mg syringe improves acute attacks of HAE. During the study, pediatric participants with HAE will take Icatibant subcutaneous injection 30mg syringe according to their clinic's standard practice. The study doctors will check for side effects from Icatibant subcutaneous injection 30 mg syringe for 3 months.

This description comes directly from the study's public registry record.

Talk to the study team

No contact information is available for this study as per the public registry record.

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Locations (1)

Takeda selected siteTokyo, Tokyo, Japan

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