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NCT02326376

Kineret CAPS Post Authorisation Study

Completed Last updated 18 January 2020
What this trial tests

trial testing anakinra (Kineret) in Cryopyrin-Associated Periodic Syndromes in 12 participants. Completed in 12 September 2019.

Timeline
24 April 2015
Primary endpoint
12 September 2019
12 September 2019

Quick facts

Lead sponsorSwedish Orphan Biovitrum
StatusCompleted
Study typeOBSERVATIONAL
Enrollment12
Start date24 April 2015
Primary completion12 September 2019
Estimated completion12 September 2019
Sites2 locations across United Kingdom, Netherlands

Drugs / interventions tested

Conditions studied

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:

Other recruiting trials for Cryopyrin-Associated Periodic Syndromes

Currently open trials in the same condition.

Other Swedish Orphan Biovitrum trials

Trials by the same sponsor.

Verify against primary sources

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/NCT02326376.

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