The Safety/Efficacy Of Daratumumab With Belatacept In Highly HLA-Sensitized Patients Awaiting Kidney Transplantation

NARecruitingINTERVENTIONAL
Enrollment

12

Participants

Timeline

Start Date

January 19, 2022

Primary Completion Date

December 1, 2024

Study Completion Date

November 2, 2025

Conditions
SensitisationHighly Sensitised Dialysis Patients
Interventions
COMBINATION_PRODUCT

Each patient will undergo in the first step of the study belatacept treatment and in the second apheresis and daratumumab

"Four consecutive cohorts each comprising 3 patients are planned. STEP I: Patients receive Belatacept 10mg/kg, administered on days 1, 5, end of week 2, 4 and 8 .~Patients without a significant decrease in the global cPRA (cPRA or TGI ≥99%) or significant reduction of anti-HLA Ab MF will continue to the second step.~STEP II: (15 weeks) One week after the last injection of belatacept, patients will undergo 4 sessions of apheresis (plasmapheresis (PF) or Immunoadsorption (IA)) which will be given every 48h. At week 11, patients will receive 4 doses of daratumumab (8mg/kg) every two weeks until week 17. Daratumumab will be alternated with 4 additional doses of belatacept 5 mg/kg FOLLOW-UP (24 weeks) All patients exiting the study, either having completed all treatment courses or exiting prematurely (transplanted or not), will be proposed monthly follow-up visits"

Trial Locations (1)

38700

RECRUITING

Chu Grenoble, La Tronche

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Bristol-Myers Squibb

INDUSTRY

lead

University Hospital, Grenoble

OTHER

NCT05145296 - The Safety/Efficacy Of Daratumumab With Belatacept In Highly HLA-Sensitized Patients Awaiting Kidney Transplantation | Biotech Hunter | Biotech Hunter