Imlifidase for Highly Sensitized Kidney Transplant Recipients With a posItive crossmAtch Against a Deceased Donor: Results of Kidney Transplantations Performed in Accordance to the French Guidelines.

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity Hospital, Bordeaux

About this trial

Imlifidase is a recombinant cysteine protease derived from Streptococcus pyogenes and produced in Escherichia coli, which has the ability to cleave and degrade all human IgGs. Four to six hours after imlifidase infusion, the entire IgG pool is degraded into F(ab')2 and Fc fragments. In vitro, imlifidase inhibits HLA antibody-mediated NK cell activation and antibody-dependent cell-mediated cytotoxicity. Imlifidase degrades also the IgG of the B cell Receptor (BCR), inhibiting BCR-mediated cell signal, transiently preventing memory B cell response to antigenic stimulation and their transition into antibody-producing cells.

Two clinical studies have been designed to determine whether imlifidase could inactivate IgG donor-specific antibodies as a desensitization strategy in highly sensitized candidates for kidney transplantation. In the phase I/II study, 25 patients were transplanted in Sweden and United States. Among them, 18 had a positive flow cytometry crossmatch (FCXM) and 2 a positive complement-dependent cytotoxicity crossmatch (CDCXM). In the phase II study (Highdes Trial), 19 patients with an incompatible living or deceased donor from the United States, Sweden, and France were included. Among them, 7, 18, 2, and 8 had respectively a positive T-cell FCXM, positive B-cell FCXM, positive T-cell CDCXM, and positive B-cell CDCCXM. The primary efficacy endpoint was the ability of Imlifidase to convert a positive XM to a negative one. Conversion of baseline positive XM to negative within 24 h after Imlifidase treatment occurred in 89.5% (n=17) of the 19 patients. In the follow-up study including all the patients transplanted after Imlifidase desensitization, the antibody-mediated rejection rate (AMR) was at 39%, most of them occurring during the first month post-transplantation. Three-year death-censored graft survival was 93% in patients with AMR and 77% in the others. Three-year patient survival was 85% in patients with AMR and 94% in the others. No safety signal was reported.

Based on these data, Imlifidase is now indicated as a desensitization agent of highly sensitized adult kidney transplant patients with positive crossmatch against an available ABO-compatible deceased donor. It should be reserved for patients unlikely to be transplanted under the available kidney allocation system including the prioritization program for highly sensitized patients (https://www.ema.europa.eu). Therefore, the French Society of Transplantation (SFT), the French-speaking Society of Nephrology, Dialysis and Transplantation (SFNDT) and the French Society of Histocompatibility and Immunogenetics (SFHI) have proposed French recommendations for patient selection, choice of antibodies characteristics, treatment and follow-up in order to homogenize practices.

Although this new treatment addressed an unmet medical need, its authorization was based on only two small-scale studies. Therefore, additional data on long-term graft function and survival are required in patients treated by imlifidase.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Highly sensitized adult kidney transplant candidates

Eligible to imlifidase (patient with a delisting of at least one A, B, DR, DQ HLA antibody)

Disqualifiers

Age < 18 years-old

Trial population

When a kidney transplant candidate eligible to imlifidase is identified in a transplant center in France, HLA antibodies are delisted by the HLA laboratory, according to the French guidelines. Following this delisting, the patients can be transplanted with or without imlifidase or stay on dialysis. Bordeaux University Hospital will establish agreements with the 20 other university hospitals who have patients eligible to imlifidase. An implementation visit will be carried out at each CHU to: 1. identify patients already eligible for imlifidase, 2. set up a system to inform the Bordeaux CHU, as the coordinating center, when new incident patients eligible for imlifidase are identified, 3. offer all identified patients' inclusion in the ISKIA study

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

450 Participants
are grouped into 3 trial groups
Group A: Patient eligible for Imlifidase
Group B: Patient eligible for imlifidase and transplanted with
Group C: Patient eligible for imlifidase but transplanted without

Trial outcomes

Primary outcomes

1

Percentage of transplantations performed with or without imlifidase among the eligible patients

CRISTAL register

Time frame
Year 1, year 2 and year 3 after kidney transplantation

Secondary outcomes

1

Incidence of HLA donor-specific antibodies (DSA) rebound after transplantation

DSA analysis on a Luminex platform

Time frame
Days 3, 5, 7, 10, and month 1, month 3 and month 12, after kidney transplantation
2

Timing of HLA donor-specific antibodies (DSA) rebound after transplantation

DSA analysis on a Luminex platform

Time frame
Days 3, 5, 7, 10, and month 1, month 3 and month 12, after kidney transplantation
3

Incidence of antibody-mediated rejection

Protocol and indication biopsies

Time frame
Day 10, month 3 and month 12 after kidney tranplantation
4

eGFR

Estimated eGFD based on serum creatinine (CKD-epi formula)

Time frame
Days 7, 14, month 1, month 3 and month 12 after kidney transplantation

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: