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NCT02326376
Kineret CAPS Post Authorisation Study
trial testing anakinra (Kineret) in Cryopyrin-Associated Periodic Syndromes in 12 participants. Completed in 12 September 2019.
12 September 2019
Quick facts
| Lead sponsor | Swedish Orphan Biovitrum |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 12 |
| Start date | 24 April 2015 |
| Primary completion | 12 September 2019 |
| Estimated completion | 12 September 2019 |
| Sites | 2 locations across United Kingdom, Netherlands |
Drugs / interventions tested
- anakinra (Kineret)
Conditions studied
- Cryopyrin-Associated Periodic Syndromes — all drugs for Cryopyrin-Associated Periodic Syndromes →
Sponsor
Swedish Orphan Biovitrum — full company profile →
Who can join
Eligibility, any sex, with Cryopyrin-Associated Periodic Syndromes. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
A non-interventional, post authorization safety study to evaluate the safety of Kineret in the treatment of Cryopyrin Associated Periodic Syndromes (CAPS) in routine clinical care with regard to serious infections, malignancies, injection site reactions, allergic reactions and medication errors, including re-use of syringe.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT02326376
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Cryopyrin-Associated Periodic Syndromes
Currently open trials in the same condition.
- NCT06974877 — Repeat PET/CT Imaging in People With CAPS and Anakinra-Induced Amyloidosis Using an Amyloid-Reactive Peptide to Measure · Phase 1 · recruiting
Other Swedish Orphan Biovitrum trials
Trials by the same sponsor.
- NCT06666335 — A Study to Evaluate Efficacy and Safety of Anakinra in Chinese Patients With Colchicine-resistent FMF · Phase 4 · not yet recruiting
- NCT06992505 — Assessment of Macrophage Activation syndromE in STill's Disease in Italy · completed
- NCT06782373 — A Study to Assess the Effectiveness and Safety of Pacritinib in Patients With VEXAS Syndrome (PAXIS) · Phase 2 · recruiting
- NCT06579144 — Pharmacokinetic Comparison of Efanesoctocog Alfa vs Other EHL-rFVIII Products in Participants With Severe Haemophilia A · Phase 1 · recruiting
- NCT06405152 — Assessment of Macrophage Activation syndromE in STill's Disease · 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 NCT02326376 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Swedish Orphan Biovitrum
- Last refreshed: 18 January 2020
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/NCT02326376.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing