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Clinical Trial Summary

This is a Phase 2 study to investigate the safety and efficacy of ATI-450 for the Maintenance of Remission in Patients with Cryopyrin-Associated Periodic Syndrome (CAPS) Previously Managed with Anti-IL-1 Therapy.


Clinical Trial Description

This is a Phase 2a, Open-Label, Single-Arm Study to Investigate the Safety and Efficacy of ATI-450 for the Maintenance of Remission in Patients with Cryopyrin-Associated Periodic Syndrome (CAPS) Previously Managed with Anti-IL-1 Therapy. The study will consist of up to an 8-week screening period, a 12-week treatment period, and a 4-week safety follow-up period. The total duration of the study for patients remaining until their final follow-up assessment will be up to 24 weeks. ;


Study Design


Related Conditions & MeSH terms

  • Cryopyrin-Associated Periodic Syndrome
  • Cryopyrin-Associated Periodic Syndromes
  • Syndrome

NCT number NCT04524858
Study type Interventional
Source Aclaris Therapeutics, Inc.
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Status Terminated
Phase Phase 2
Start date October 23, 2020
Completion date February 25, 2021