Open-label, Single-arm Study to Assess the Pharmacokinetics, Safety, and Tolerability of a Single Subcutaneous Dose of Icatibant in Healthy Japanese Volunteers

Completed · Phase 1

Conditions studied: Hereditary Angioedema (HAE)

In brief

This is a single-dose study to evaluate the pharmacokinetics, safety, and tolerability of icatibant administered to adult Japanese subjects.

Key facts

Study ID
NCT02045264
Run by
Shire
People needed
12
Starts
2014-02-21
Expected to finish
2014-02-27
Last updated by the study team
2021-06-03

Who can join

Age: 18 and older, up to 55. Sex: any. Healthy volunteers: accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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