Last updated on August 2016

Kineret CAPS Post Authorisation Study


Brief description of study

A non-interventional, post authorization safety study to evaluate the safety of Kineret in the treatment of Cryopyrin Associated Periodic Syndromes (CAPS) in routine clinical care with regard to serious infections, malignancies, injection site reactions, allergic reactions and medication errors, including re-use of syringe.

Clinical Study Identifier: NCT02326376

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Elisa Patrone

Swedish Orphan Biovitrum Investigational Site
Lille, France
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Elisa Patrone

Swedish Orphan Biovitrum Investigational Site
Paris, France
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Elisa Patrone

Swedish Orphan Biovitrum Investigational Site
Groningen, Netherlands
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Elisa Patrone

Swedish Orphan Biovitrum Investigational Site
Utrecht, Netherlands
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Elisa Patorne

Swedish Orphan Biovitrum Investigational Site
London, United Kingdom
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