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Clinical Trial Summary

The objective of this extension protocol is to collect safety data (serious and non-serious adverse events) and to provide continuous canakinumab to patients in France who completed study CACZ885G2301E1(NCT00891046), CACZ885G2306 (NCT02296424) or CACZ885N2301 (NCT02059291) until a decision regarding reimbursement in France is effective for canakinumab (Ilaris®) in these indications.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02334748
Study type Interventional
Source Novartis
Contact
Status Completed
Phase Phase 3
Start date November 3, 2014
Completion date August 31, 2018

See also
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