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Cryopyrin-Associated Periodic Syndromes (CAPS)

2
Pipeline Programs
3
Companies
3
Clinical Trials
1 recruiting
0
Approved Products

Pipeline by Development Stage

Preclinical
Phase 1
Phase 1/2
Phase 2
Phase 2/3
Phase 3
On Market
0
1
0
1
0
0
0
Early DiscoveryClinical DevelopmentMarket

Competitive Landscape

3 companies ranked by most advanced pipeline stage

Handok
HandokKorea - Seoul
1 program
1
HL2351Phase 21 trial
Active Trials
NCT02853084Terminated8Est. Jan 2019
Akros Pharma
Akros PharmaNJ - Princeton
1 program
1
JTE-162Phase 11 trial
Active Trials
NCT07247266Recruiting5Est. Dec 2026
Sandoz
SandozAustria - Kundl
1 program
Clinical Outcomes and Safety: A Registry Study of Ilaris (Canakinumab) PatientsN/A1 trial
Active Trials
NCT01213641Completed288Est. Dec 2015

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
HandokHL2351
Akros PharmaJTE-162
SandozClinical Outcomes and Safety: A Registry Study of Ilaris (Canakinumab) Patients

Clinical Trials (3)

Total enrollment: 301 patients across 3 trials

HL2351 CAPS Phase II Study

Start: Oct 2015Est. completion: Jan 20198 patients
Phase 2Terminated

Study to Evaluate the Safety, Tolerability, Efficacy and Pharmacokinetics of JTE-162 in Subjects With Cryopyrin-Associated Periodic Syndrome (CAPS)

Start: Feb 2026Est. completion: Dec 20265 patients
Phase 1Recruiting
NCT01213641SandozClinical Outcomes and Safety: A Registry Study of Ilaris (Canakinumab) Patients

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

Start: Nov 2009Est. completion: Dec 2015288 patients
N/ACompleted

Phase Legend

PreclinicalLab & animal studies
Phase 1Safety & dosing
Phase 2Efficacy testing
Phase 3Large-scale trials
On MarketApproved & available

Key Insights

1 actively recruiting trials targeting 301 patients
3 companies competing in this space

The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.