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

Completed · Phase 4 · NCT06806657

Conditions: Hereditary Angioedema

At a glance

Research payments reported, 2025
$168,962
U.S. investigators named
5
Sites paid
6
Planned or actual enrollment
18

About the trial

Sponsor
CSL Behring
Tested
Garadacimab (biological)
Dates
Started 2025-04-28; completion 2026-06-29
Results posted
Not yet

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.

From ClinicalTrials.gov, last updated 2026-07-23. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Csl Behring reported $168,962 in research payments for this study in 2025 (51 payments).

Products named: Andembry

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

  • $62,041
  • Research Solutions of Arizona (dcrpi) $44,214
  • Bernstein Clinical Research Center $40,239
  • Chronicle Bio Inc $16,040
  • Donald Levy $2,707
  • Aire Medical of Los Angeles $2,707
  • Metrodora Institute LLC $1,015

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.