Assessment of T-cell Response and In-vitro Proof-of-concept of T-cell Engineering in Chronic ESKD Patients.

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorCentre Hospitalier Régional d'Orléans

About this trial

This is a comparative, prospective, non-interventional study to evaluate immune response in patients with chronic kidney disease. The primary objective is to define immunodeficiency (phenotype and function of T cells) in patients with end-stage kidney disease. The second objective is to provide an in-vitro proof-of-concept of T-cell engineering in the context of end-stage kidney disease.

The study population was patients with chronic kidney disease.

Eligibility criteria

Qualifiers

Male or female ≥ 18 years

Informed participants who did not object to participating in the study

Disqualifiers

Chronic progressive infections

Prior organ transplantation (including bone marrow transplantation)

Previous treatment with immunosuppressive agents (such as Rituximab, Eculizumab, Tacrolimus or Ciclosporin, Cellcept or Imurel) within 2 years prior to inclusion

Participant under guardianship, curatorship or deprived of liberty

Trial design

Treatments tested in this trial

  • 1 blood sample for each participant

Treatment groups

100 Participants
are divided into 3 treatment groups