Clinical Outcomes and Safety: A Registry Study of Ilaris (Canakinumab) Patients
NCT01213641 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 288
Last updated 2016-03-28
Summary
The purpose of this observational study is to collect additional information regarding long-term safety and effectiveness of Ilaris in the treatment of CAPS patients in clinical practice.
Conditions
- Cryopyrin-associated Periodic Syndromes (CAPS)
- Familial Cold Autoinflam Syn (FCAS)
- Muckle-wells Syn (MWS)
- Neonatal Onset Multisystem Inflam Disease (NOMID)
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Novartis Pharmaceuticals · Novartis Pharmaceuticals
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2009-11-30
- Primary Completion
- 2015-12-31
- Completion
- 2015-12-31
Countries
- United States
- Austria
- Germany
- Norway
- Switzerland
Study Locations
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