Immunological Reset to Allow Access to HLA Compatible Transplantation in Highly Sensitized Kidney Transplant Candidates Through Non-myeloablative Autologous Stemm Cell Transplantation (RESET TRIAL)

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This is a study for hypersensitized patients who have been waiting for more than 3 years for an offer for a kidney transplant. The objective is to perform a transplant of autologous hematopoietic precursors with the aim of producing what we call an immunological reset to make the maximum number of anti-HLA antibodies disappear and thus increase the chances of the patient receiving an offer for a kidney transplant.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
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• The patient must be able to understand and give written consent.

• Women and men between 18 and 65 years old.

• Patients with chronic kidney disease who are on renal therapy replacement with dialysis.

• Patient who is on the waiting list for kidney transplant from a death donor and who has not received an offer for a compatible transplant in the last 3 years within the national PATHI prioritization program.

• cPRA calculated of more than 97% and having been in the program of prioritization for more than 3 years

• Positive IgG serologies for Cytomegalovirus and Epstein Barr.

• Women of childbearing potential must have a negative pregnancy test upon entry to the study and must agree to use safe contraceptive methods according to the guideline CTFG recommendations on contraception in clinical trials during duration of the study (condoms are considered safe methods male and female, oral contraceptives, etc.).

• Patients vaccinated against tetanus, influenza, pneumococcus and herpes zoster

Locations
Other Locations
Spain
Hospital Universitari Vall d'Hebron
RECRUITING
Barcelona
Contact Information
Primary
Oriol Bestard, MD, PhD
oriol.betsard@vallhebron.cat
932746000
Backup
Delphine Kervella, MD, PhD
delphine.kervella@vallhebron.cat
932746000
Time Frame
Start Date: 2024-04-05
Estimated Completion Date: 2026-12
Participants
Target number of participants: 10
Treatments
Experimental: hypersensitive patients undergoing aHSCT
hypersensitive patients undergoing aHSCT. All patients in this study participate in this arm.
Related Therapeutic Areas
Sponsors
Leads: Hospital Universitari Vall d'Hebron Research Institute

This content was sourced from clinicaltrials.gov