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Completed Phase 3 Interventional Results available

C1 Esterase Inhibitor in Hereditary Angioedema (HAE)(Extension Study)

ClinicalTrials.gov ID: NCT00292981

Public ClinicalTrials.gov record NCT00292981. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 23, 2026, 1:23 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Open-label Extension Study of CE1145 (Human Pasteurized C1 Esterase Inhibitor Concentrate) in Subjects With Congenital C1-INH Deficiency and Acute HAE Attacks

Study identification

NCT ID
NCT00292981
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
CSL Behring
Industry
Enrollment
57 participants

Conditions and interventions

Interventions

  • C1 Esterase Inhibitor Drug

Drug

Eligibility (public fields only)

Age range
6 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 31, 2005
Primary completion
Jan 31, 2010
Completion
Apr 30, 2010
Last update posted
May 6, 2015

2005 – 2010

United States locations

U.S. sites
13
U.S. states
13
U.S. cities
13
Facility City State ZIP Site status
Contact CSL Behring for facility details Weston Florida 33331
Contact CSL Behring for facility details Atlanta Georgia 30342
Contact CSL Behring for facility details Idaho Falls Idaho 83404
Contact CSL Behring for facility details Chicago Illinois 60612-3244
Contact CSL Behring for facility details Shreveport Louisiana 71130
Contact CSL Behring for facility details Boston Massachusetts 02115
Contact CSL Behring for facility details Plymouth Minnesota 55446
Contact CSL Behring for facility details Omaha Nebraska 69131
Contact CSL Behring for facility details Tulsa Oklahoma 74133
Contact CSL Behring for facility details Eugene Oregon 97401
Contact CSL Behring for facility details Hershey Pennsylvania 17033
Contact CSL Behring for facility details Rapid City South Dakota 57702
Contact CSL Behring for facility details Dallas Texas 75230

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00292981, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 6, 2015 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00292981 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →