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Phase 2/3 Study of Participants With Recurrent Pericarditis Evaluating the Efficacy and Safety of KPL-387

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NCT07010159 · readout in 499 d

Sponsored by Kiniksa Pharmaceuticals International, plc (industry) · KNSA — their whole pipeline →. With Kiniksa Pharmaceuticals, GmbH.

Phase
Phase 2/3
Status
Recruiting
Study type
Interventional
Design
Randomized · Triple · Treatment
Enrollment
325estimated
Sites
62
Countries
Canada, France, Germany +7

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2025-07-25actualWhen the study began enrolling
Primary completion2027-12-31estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2029-12-31estimatedThe whole study's end, after follow-up
First posted2025-06-08actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-08-11actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Pericarditis
  • Pericarditis Acute
  • Recurrent Pericarditis

Interventions

  • Drug: KPL-387
  • Drug: Placebo

Primary outcomes

what the primary-completion date above is the date OF
Phase 2: Time to Treatment Response by Week 24
measured From Baseline up to Week 24
Phase 3: Time to Pericarditis Recurrence
measured From Baseline in the RW Period
Long-Term Extension: Annualized rate of Pericarditis Recurrence
measured Up to 24 Months

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