drugset / Trial / NCT06806657

Safety Study in Subjects ≥ 12 Years of Age With Hereditary Angioedema Switching to Garadacimab

NCT06806657 ↗

Phase 4 Active not recruiting 18 enrolled CSL Behring
NaSingle-groupOpen-labelPrevention

Summary

This study is designed to evaluate the safety after switching to garadacimab from another prophylactic hereditary angioedema (HAE) treatment (marketed kallikrein \[KK\] inhibitor or plasma-derived C1-esterase inhibitor \[pdC1INH\]prophylactic) when administered once monthly for approximately 3 months in participants aged greater than or equal to (\>=) 12 years with HAE.

Timeline

Start
2025-04-28
Primary completion
2026-06-23
Completion
2026-06-23

Drugs

EvaluationDrugModalityDoseRoute
Subject CSL312 Monoclonal antibody — Subcutaneous

Indications