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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01108848
Other study ID # CE1145_5002
Secondary ID 1500
Status Completed
Phase N/A
First received April 12, 2010
Last updated June 5, 2014
Start date April 2010
Est. completion date April 2014

Study information

Verified date June 2014
Source CSL Behring
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Observational

Clinical Trial Summary

The objective of this patient registry is to collect data on the safety of Berinert® in normal clinical practice in the United States. The patient registry will be maintained for a period of at least 3 years. The duration of individual patient participation will vary and is determined by the frequency of hereditary angioedema (HAE) attacks and the patient's need for Berinert® treatment.


Recruitment information / eligibility

Status Completed
Enrollment 318
Est. completion date April 2014
Est. primary completion date April 2014
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Any patient receiving CSL Behring's C1-esterase inhibitor

- Written informed consent (may not be required for some retrospective chart review cases)

Exclusion Criteria:

- Any patient participating in an HAE study using other C1-inhibitors than Berinert®

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Biological:
Berinert® (C1 Esterase Inhibitor)
Berinert® is marketed as a lyophilized concentrate available in a single-use vial to be reconstituted with sterile water before administration as described in the prescribing information.

Locations

Country Name City State
Denmark Denmark, Odense C Odense C
Germany Germany, Berlin Berlin
Germany Germany, Frankfurt Frankfurt
Germany Germany, Mainz Mainz
Germany Germany, München München
Switzerland Switzerland, Luzern 16 Luzern 16
United States United States, Pennsylvania Altoona Pennsylvania
United States United States, Georgia Atlanta Georgia
United States United States, Massachusetts Boston Massachusetts
United States United States, New Jersey Branchburg New Jersey
United States United States, Ohio Centerville Ohio
United States United States, Maryland Chevy Chase Maryland
United States United States, Ohio Cincinnati Ohio
United States United States, Maryland Columbia Maryland
United States United States, South Carolina Columbia South Carolina
United States United States, Texas Dallas Texas
United States United States, North Carolina Durham North Carolina
United States United States, New Jersey Edison New Jersey
United States United States, California Granada Hills California
United States United States, Pennsylvania Hershey Pennsylvania
United States United States, Idaho Idaho Falls Idaho
United States United States, New Jersey Iselin New Jersey
United States United States, Missouri Kansas City Missouri
United States United States, Oregon Lake Oswego Oregon
United States United States, California Los Angeles California
United States United States, Louisiana New Orleans Louisiana
United States United States, New York New York New York
United States United States, New York North Syracuse New York
United States United States, New Jersey Ocean New Jersey
United States United States, Oklahoma Oklahoma City Oklahoma
United States United States, Pennsylvania Pittsburgh Pennsylvania
United States United States, Minnesota Plymouth Minnesota
United States United States, South Dakota Rapid City South Dakota
United States United States, California Redding California
United States United States, California San Diego California
United States United States, Arizona Scottsdale Arizona
United States United States, Washington Spokane Washington
United States United States, Missouri St. Louis Missouri
United States United States, Washington Tacoma Washington
United States United States, Oklahoma Tulsa Oklahoma

Sponsors (2)

Lead Sponsor Collaborator
CSL Behring Chiltern International Inc.

Countries where clinical trial is conducted

United States,  Denmark,  Germany,  Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence of thrombotic and thrombo-embolic events Within 30 days of treatment with Berinert® Yes
Primary Occurrence of suspected viral transmission Duration of the study, at least 3 years Yes
Primary Use of concomitant medications and plasma products Duration of the study, at least 3 years No