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NCT04524858

Study of ATI-450 in Patients With Cryopyrin-Associated Periodic Syndrome (CAPS)

Terminated Phase 2 Results posted Last updated 21 September 2023
What this trial tests

Phase 2 trial testing ATI-450 in Cryopyrin-Associated Periodic Syndrome in 1 participant. Terminated before completion.

Timeline
23 October 2020
Primary endpoint
25 February 2021
25 February 2021

Quick facts

Lead sponsorAclaris Therapeutics, Inc.
PhasePhase 2
StatusTerminated
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment1
Start date23 October 2020
Primary completion25 February 2021
Estimated completion25 February 2021
Sites2 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Aclaris Therapeutics, Inc. — full company profile →

Who can join

18 and older, any sex, with Cryopyrin-Associated Periodic Syndrome. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

2 peer-reviewed publications reference this trial (live from Europe PMC):

  1. Diversity and versatility of p38 kinase signalling in health and disease.
    Canovas B, Nebreda AR. · · 2021 · cited 466× · PMID 33504982 · DOI 10.1038/s41580-020-00322-w
  2. IL-1 and autoinflammatory disease: biology, pathogenesis and therapeutic targeting.
    Broderick L, Hoffman HM. · · 2022 · cited 112× · PMID 35729334 · DOI 10.1038/s41584-022-00797-1

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Other trials of ATI-450

Trials testing the same drug.

Other Aclaris Therapeutics, Inc. trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04524858.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing