Clinical Outcomes and Safety: A Registry Study of Ilaris (Canakinumab) Patients

NCT01213641 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 288

Last updated 2016-03-28

No results posted yet for this study

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

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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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01213641 on ClinicalTrials.gov