CI

At a glance

ClinicalIndex Comparison Record
Early Ph 1Completed· 13 target
Drug / intervention
Kineretdrug
Likely dose
Kineret 8 mg/kgfrom record
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Search/NCT04136028
NCT04136028Early Ph 1Completed

A Retrospective Analysis of Efficacy and Safety of Interleukin-1 Receptor Inhibitor for the Treatment of Granulomatous Complications in Patients With Chronic Granulomatous Disease

Federal Research Institute of Pediatric Hematology, Oncology and Immunology·interventional·Posted Oct 23, 2019·Updated Apr 7, 2020

In Brief

A Early Phase 1 clinical trial evaluating Kineret for Chronic Granulomatous Disease. Completed, enrolled 13 participants across 1 site.

Detailed Summary

"Kineret" (INN: Anakinra) neutralizes the biological activity of interleukin-1α (IL-1α) and interleukin-1β (IL-1β) by the concurrent inhibition of binding to interleukin-1 receptor I (IL-1RI). Interleukin-1 (IL-1) is the main pro-inflammatory cytokine that mediates many cellular responses. Anakinra inhibits the reactions caused by IL-1 in vitro, including the induction of nitric oxide and prostaglandin E2 and / or the formation of collagenase by synovial cells, fibroblasts and chondrocytes. According to published data, patients with the chronic granulomatous disease have an increased secretion of interleukin-1, which contributes to the development of granulomatous inflammation. Blocking interleukin-1 reduces the activity of the main pro-inflammatory complex - the inflammasomes, and also restores the autophagy process impaired in patients with chronic granulomatous disease. In this way, inhibition of the IL-1 receptor prevents the activation of innate immunity cells and prevents the maintenance of pathological pro-inflammatory signaling in conditions of IL-1 overproduction. The efficacy and safety of therapy with the above drug is based on the results of international studies on the using of anakinra in patients with chronic granulomatous disease.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesRussia
Collaborators--

Timeline

Early Ph 1CompletedFinished
20162017201820192020202120222023202420252026
First PostedOct 23, 2019
Enrollment StartSep 25, 2015
Primary CompletionJan 16, 2019
Study CompletionJan 1, 2020
TodayJul 2, 2026
Enrollment to primary: 3.3 yearsPosted 6.7 years ago

Interventions

Kineretdrug

Kineret at a dose of 8 mg/kg per day subcutaneously daily, every day at the same time