Cryopyrin-Associated Periodic Syndromes Clinical Trial
Official title:
An Open-label, Long-term Safety and Efficacy Study of ACZ885 (Anti-interleukin-1β Monoclonal Antibody) Administered for at Least 6 Months in Patients With the Following Cryopyrin-associated Periodic Syndromes: Familial Cold Autoinflammatory Syndrome, Muckle-Wells Syndrome, or Neonatal Onset Multisystem Inflammatory Disease
This will provided long-term safety and efficacy data for ACZ885 (a fully human
anti-interleukin-1β [anti-IL-1β] monoclonal antibody) given as an injection subcutaneously
in patients who participated in the CACZ885A2102 (NCT00487708), CACZ885D2201 (NCT00685373)
or CACZ885D2304(NCT00465985) studies or newly identified patients with the following
cryopyrin-associated periodic syndromes: Familial Cold Autoinflammatory Syndrome,
Muckle-Wells Syndrome or Neonatal Onset Multisystem Inflammatory Disease.
The duration of this study was 6 months with a maximum duration of 2 years
n/a
Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Status | Clinical Trial | Phase | |
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Completed |
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