Ceprotin Treatment Registry

Completed

Conditions studied: Protein C Deficiency

In brief

The overall objective is to collect and assess data on the treatment, safety, and treatment outcomes of subjects prescribed, receiving and participating in the Ceprotin treatment registry.

Key facts

Study ID

NCT01127529

Run by

Baxalta now part of Shire

People needed

43

Starts

2010-06-23

Expected to finish

2015-06-22

Last updated by the study team

2021-03-17

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Participants for whom CEPROTIN therapy has been indicated and meeting the following criteria may be enrolled in this study:
• Signed and dated informed consent from either the participant or the participant's legally authorized representative prior to enrollment, as applicable
• Males and females of any age, including neonates, children, adolescents and adults
• Participant who received CEPROTIN or is initiating/receiving CEPROTIN treatment

You may not qualify if…

• None

Where it is running

• Study site — Phoenix, Arizona, United States
• Study site — Orange, California, United States
• Study site — Aurora, Colorado, United States
• Study site — Indianapolis, Indiana, United States
• Study site — Boston, Massachusetts, United States
• Study site — Grand Rapids, Michigan, United States
• Study site — Lebanon, New Hampshire, United States
• Study site — Cincinnati, Ohio, United States
• Study site — Columbus, Ohio, United States
• Study site — Dayton, Ohio, United States
• Study site — Fort Worth, Texas, United States
• Study site — Houston, Texas, United States
• Study site — Innsbruck, Austria
• Study site — Vienna, Austria
• Study site — Bonn, Germany
• Study site — Frankfurt, Germany
• Study site — Hanover, Germany
• Study site — Heidelberg, Germany
• Study site — Magdeburg, Germany
• Study site — Magstadt, Germany
• Study site — Milan, Italy
• Study site — Palermo, Italy
• Study site — Rome, Italy
• Study site — Vicenza, Italy
• Study site — Nijmegen, Netherlands

Full record on ClinicalTrials.gov

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