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Evaluation of the Safety of Use of Anti-IL6 Receptor Antibodies to Reduce Allo-sensitization Post Allograft Nephrectomy (RAIPONS)

T

Toulouse University Hospital

Status and phase

Enrolling
Phase 2

Conditions

Graft Failure
Kidney Transplantation

Treatments

Drug: Tocilizumab

Study type

Interventional

Funder types

Other

Identifiers

NCT04779957
RC31/19/0511

Details and patient eligibility

About

Graft nephrectomy is associated with massive allo-sensitization following this event. The occurrence of anti-HLA antibodies is a major barrier to perform a second kidney transplantation. Investigators propose here to evaluate in a phase II pilot study, the safety of the use of a single dose of Tocilizumab immediately before or after graft nephrectomy. The primary endpoint evaluated here is the occurrence of serious infectious complications following graft nephrectomy, with a treatment by Tocilizumab. Secondary endpoints evaluated here are - to evaluate all complications after graft nephrectomy, - and the Tocilizumab effectiveness to reduce anti-HLA antibodies at one year post nephrectomy.

Full description

Background: graft nephrectomy is associated with massive allo-sensitization following this event The occurrence of anti-HLA antibodies is a major barrier to perform a second kidney transplantation. Moreover, a systemic inflammatory response syndrome can occur which could lead to serious patient's complications, in case of early graft thrombosis. To date, no treatment or strategy is available to reduce these risks, after graft nephrectomy. IL-6 is a key cytokine in inflammation, but also in the development of T and B cells activation. This treatment previously demonstrated a major role in the occurrence of allo-antibodies. Tocilizumab is a monoclonal antibody blocking IL6 receptor, previously used with success in kidney transplantation to reduce anti-HLA antibodies mediated rejection.

Objectives: Investigators hypothesize that Tocilizumab is useful to prevent allo-sensitization post graft nephrectomy. They propose here to evaluate in a phase II pilot study, the safety of the use of a single dose of Tocilizumab immediately before or after graft nephrectomy.

Enrollment

18 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult recipients,
  • affiliated to the social security
  • requiring a graft nephrectomy, with a project to retransplantation

Exclusion criteria

  • combined transplantations, PRA >20%.
  • Patient under protective measures,
  • Rituximab used for immunosuppression induction
  • Previous transplants not removed,
  • Active infectious complications at graft nephrectomy, need for immunosuppressive treatments after graft nephrectomy,
  • Participation to another interventional studies using Rituximab, polyclonal antibodies, Eculizumab, or Tocilizumab.
  • adults under guardianship or other legal protection, deprived of their liberty by judicial or administrative decision,
  • pregnancy or breastfeeding.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

18 participants in 1 patient group

Tocilizumab
Experimental group
Description:
Evaluation of the use of Tocilizumab after allograft nephrectomy.
Treatment:
Drug: Tocilizumab

Trial contacts and locations

1

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Central trial contact

Arnaud DEL BELLO, MD

Data sourced from clinicaltrials.gov

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