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NCT04524858
Study of ATI-450 in Patients With Cryopyrin-Associated Periodic Syndrome (CAPS)
Phase 2 trial testing ATI-450 in Cryopyrin-Associated Periodic Syndrome in 1 participant. Terminated before completion.
25 February 2021
Quick facts
| Lead sponsor | Aclaris Therapeutics, Inc. |
|---|---|
| Phase | Phase 2 |
| Status | Terminated |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 1 |
| Start date | 23 October 2020 |
| Primary completion | 25 February 2021 |
| Estimated completion | 25 February 2021 |
| Sites | 2 locations across United States |
Drugs / interventions tested
- ATI-450 — full drug profile →
Conditions studied
- Cryopyrin-Associated Periodic Syndrome — all drugs for Cryopyrin-Associated Periodic Syndrome →
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):
-
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 -
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
Verify or expand the search:
- PubMed search for NCT04524858
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of ATI-450
Trials testing the same drug.
- NCT05511519 — Study of ATI-450 vs Placebo in Patients With Moderate to Severe Psoriatic Arthritis · Phase 2 · terminated
- NCT05216224 — ATI-450 vs Placebo in Participants With Moderate to Severe Hidradenitis Suppurativa (HS) · Phase 2 · completed
- NCT04481685 — A Trial of Aclaris Therapeutics, Inc. (ATI)-450 in Patients With Moderate-severe Novel Coronavirus Disease 2019 (COVID-1 · Phase 2 · completed
- NCT04247815 — Study of ATI-450 Plus Methotrexate (MTX) vs MTX Alone in Patients With Moderate to Severe RA · Phase 2 · completed
Other Aclaris Therapeutics, Inc. trials
Trials by the same sponsor.
- NCT06585202 — Study of ATI-2138 in Adult Participants With Moderate to Severe Atopic Dermatitis · Phase 2 · completed
- NCT05511519 — Study of ATI-450 vs Placebo in Patients With Moderate to Severe Psoriatic Arthritis · Phase 2 · terminated
- NCT05432596 — Study of ATI-1777 in Patients 12 to 65 Years Old With Mild to Severe Atopic Dermatitis · Phase 2 · completed
- NCT05279417 — ATI-450 Plus Methotrexate (MTX) Versus Placebo Plus MTX in Participants With Moderate to Severe Active Rheumatoid Arthri · Phase 2 · completed
- NCT05216224 — ATI-450 vs Placebo in Participants With Moderate to Severe Hidradenitis Suppurativa (HS) · Phase 2 · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT04524858 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Aclaris Therapeutics, Inc.
- Last refreshed: 21 September 2023
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