drugset / Trial / NCT01817959

Study to Assess Efficacy & Safety of Reparixin in Pancreatic Islet Transplantation

NCT01817959 ↗

Phase 3 Completed 51 enrolled Dompé Farmaceutici S.p.A
RandomizedParallel-groupDouble-blindPrevention

Summary

The objective of this clinical trial was: \- to assess whether Reparixin leads to improved transplant outcome as measured by glycaemic control following intra-hepatic infusion of pancreatic islets in patients with Type 1 diabetes (T1D). The safety of Reparixin in the specific clinical setting was also evaluated. Background: The chemokine CXCL8 plays a key role in the recruitment and activation of polymorphonuclear neutrophils in post-ischemia reperfusion injury after organ transplantation. Reparixin is the first low molecular weight blocker of CXCL8 biological activity in clinical development. Thus, the use of reparixin may emerge as a potential key component in the sequentially integrated approach to immunomodulation and control of non specific inflammatory events surrounding the early phases of pancreatic islet transplantation in T1D patients.

Timeline

Start
2012-10
Primary completion
2016-12
Completion
2017-12

Outcome

Missed primary endpoint

registry analysis (superiority test); Reparixin Group vs Placebo Group; p = 0.9863 NCT01817959 ↗

registry analysis (superiority test); Reparixin Group vs Placebo Group; p = 0.7115 NCT01817959 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Reparixin Small molecule — Intravenous