Ceprotin Treatment Registry



Status:Completed
Conditions:Metabolic
Therapuetic Areas:Pharmacology / Toxicology
Healthy:No
Age Range:Any
Updated:1/20/2018
Start Date:June 23, 2010
End Date:June 22, 2015

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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.


Inclusion Criteria:

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

Exclusion Criteria:
We found this trial at
13
sites
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Grand Rapids, MI
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Aurora, CO
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Boston, MA
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Cincinnati, OH
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Columbus, OH
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Dayton, OH
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Fort Worth, TX
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Houston, TX
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Indianapolis, IN
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Innsbruck,
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Lebanon, NH
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Orange, CA
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Phoenix, AZ
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