Imlifidase in Living Donor Renal Transplantation Highly Sensitized Recipients

Kidney Transplant Candidates Clinical Trial

— LIVEDES  

Official title:

Imlifidase in Living Donor Renal Transplantation Highly Sensitized Recipients (LIVEDES)

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT06461546
• Other study ID #: LIVEDES study
• Secondary ID: 2024-513607-14-0
• Status: Not yet recruiting
• Phase: Phase 2
• Start date: November 2024
• Est. completion date: December 2026

Study information

• Verified date: June 2024
• Source: Fundacion Clinic per a la Recerca Biomédica
• Contact: Anna Cruceta, Phd
• Phone: +34 932275400
• Email: acruceta[@]recerca.clinic.cat
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a Phase II, pilot, prospective, unicentric trial, to evaluate Imlifidase could improve the transplantability of the highly sensitized patients with good outcomes respect to survival and functionality of the graft.

Description:

The patients between 18 and 65 years will be flow cytometry crossmatch (FC-XM) positive against an available living donor. The imlifidase treatment will turn the crossmatch test negative prior to transplantation. A second dose of imlifidase can be given within 24 hours if the first dose is considered not to have sufficient effect. If a second dose is given, a confirmatory FCXM test will be performed pre-second imlifidase dosing and between 2-6 hours following the second dose.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 10
• Est. completion date: December 2026
• Est. primary completion date: July 2026
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:Inclusion Criteria To be eligible to participate in this study, candidates must meet the following elegibility criteria. Currently, at the Hospital Clinic of Barcelona, up to 10 highly sensitized patients would meet the following inclusion criteria.

• Participant Inclusion Criteria

• Sensitized (cPRA = 50%) kidney transplant candidates between 18 and 65 years.

• Low probability to get a transplant in a kidney exchange program (KEP) from a living donor.

• Included in the living donor program, with an accepted potential living donor.

• Donor and recipient must meet the eligibility criteria for donation and kidney transplantation respectively at the Hospital Clinic of Barcelona and the national guidelines.

• Presence of donor-specific antibody/crossmatch positive (DSA/FC-XM+) non-HLA identical donor.

• at least one DSA with MFI >3.000.

• and DSA MFI <10.000 (in serum samples diluted 1/64).

• and maximum two Class II DSAs.

• and maximum 17 points in Jordan RIS Score (DSA 2500-5000: 2 points; DSA MFI 5001-10000: 5 points; DSA MFI > 10000: 10 points)

• Women of childbearing age must take contraceptive measures because Imlifidase is not recommended during pregnancy.

• Must have given written informed consent (signed and dated) and any authorizations required by local law and be able to comply with all study requirements.

Exclusion Criteria

Participants who meet any of the following criteria will be excluded from participation in this study:

• Participant Exclusion Criteria

1. Known contraindications for therapy with IVIG, Rituximab, plasma exchange (PLEX) or Imlifidase.

2. Recipients of Deceased Donors (DBD, Extended Criteria Donors (ECD) or DCD).

3. A positive Complement-Dependent Cytotoxicity (CDC) Crossmatch against the living donor.

4. HIV-positive subjects.

5. Subjects who test positive for HBV infection [positive HBVsAg or HBVeAg/DNA] or HCV infection [RNA+].

6. Subjects with active TB.

7. Subjects with selective IgA deficiency, those who have known anti-IgA antibodies, and those with a history of anaphylaxis or severe systemic responses to any part of the clinical trial material.

8. Subjects who have received or for whom multiple organ transplants are planned.

9. A significantly abnormal general serum screening lab result defined as WBC<3.0x103/ml, Hgb<8.0 g/dL, platelet count <100x103/ml, SGOT>3xupper limit.

10. Subjects with active CMV or EBV infection as defined by positive PCR.

11. Subjects with a known history of previous myocardial infarction within one year of screening.

12. Subjects with a history of clinically significant thrombotic episodes, and subjects with active peripheral vascular disease.

13. Patients with a kidney disease with high risk of recurrence and/or complement-associated kidney disease (aHUS, etc).

14. Subjects with Protein C and Protein S deficiency.

15. Pregnant and lactating women

16. Current diagnosis or history of thrombotic thrombocytopenic purpura (TTP), or known familial history of TTP.

17. Known allergy to Imlifidase or excipient of the drug preparation

Related Conditions & MeSH terms

• Kidney Transplant Candidates

Intervention

Drug:
• Imlifidase
Imlifidase (POD0, pre-transplantation), imlifidase, 0.25 mg/kg over a period of 15 minutes, prior to transplantation. Dose Adjustment Criteria FC-XM screening and single antigen will be performed after 6 hours of imlifidase infusion, It will take 3 hours to obtain the results, respectively: NEGATIVE (FC-XM) - renal transplantation will be performed as soon as possible. POSITIVE (FC-XM) - 2nd Imlifidase infusion will be required (imlifidase dose: 0.25mg/Kg). FC-XM screening and single antigen will be performed after 2 hours of the 2nd Imlifidase infusion: NEGATIVE (FC-XM) - renal transplantation will be performed as soon as possible. POSITIVE (FC-XM) - The scheduled kidney transplant will be canceled.

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Fundacion Clinic per a la Recerca Biomédica

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	• Proportion of patients with conversion of a positive virtual crossmatch to negative within 6 hours after imlifidase treatment (up to two doses).	The fraction of patients with a conversion of a positive FC-XM within 6 hours of treatment with imlifidase.	6 hours
Secondary	1. Proportion of patients that require a second dose of imlifidase	To evaluate flow cytometry T-cell crossmatch conversion within 24 hours of imlifidase treatment, requirement of a second dose of imlifidase.	24 hours
Secondary	2. To evaluate the rebound of preexisting donor specific antibodies (DSA) (difference between MFI of each DSA daily - until D+14 - compared to pre-imlifidase administration)	Pre-existing DSA appearance measured daily until D+14	daily, from day 0 to day 14
Secondary	3. De novo DSA appearance over 14 days after imlifidase treatment	To evaluate the appearance of de novo DSAs (any DSA no present in pre-transplant or historical) daily - until D+14. To be considered positive the bead MFI should be over 750 and to be above the bead specific threshold related to the lowest bead of the same locus.	daily, from day 0 to day 14
Secondary	4. To evaluate HLA/DSA antibody levels up to 1 year after transplantation	HLA/DSA antibody levels at several time points between pre-dose imlifidase and 2 weeks, and at 1, 3 and 6 months and 1 year after imlifidase treatment	time points between pre-dose imlifidase and 2 weeks, and at 1, 3 and 6 months and 1 year after imlifidase treatment
Secondary	5. To evaluate renal function up to 1 year after transplantation	by estimated glomerular filtration rate (eGFR) and serum/plasma creatinine levels	time points between 24 hours and 2 weeks and at 1, 3 and 6 months and 1 year after transplantation as assessed
Secondary	6. To evaluate patient survival 1 year after transplantation	Patient survival at 12 months after transplantation	at 12 months after transplantation
Secondary	7. To evaluate the graft survival at 12 months	To evaluate the graft survival at 12 months (both overall and death-censored analysis).	at 12 months after transplantation
Secondary	8. Proportion of patients with biopsy confirmed rejection, either cell-mediated or antibody-mediated rejection, over 1 year	To evaluate the incidence of acute allograft rejection within 12 months (overall and stratified by type: cell mediated rejection or antibody-mediated rejection	within 12 months
Secondary	9. To evaluate safety of Imlifidase treatment with regards to infusion related reactions occurring within 48 hours of Imlifidase infusion	Proportion of patients with infusion-related reactions within 48 hours of Imlifidase infusion	within 48 hours of Imlifidase infusion
Secondary	10.adverse events within 30 days after transplantation	Proportion of patients with adverse events within 30 days after transplantation	30 days after transplantation
Secondary	11. Proportion of patients with severe or serious infections	To evaluate the adverse events ( infectious disease that required hospitalization) at 6 and 12 months.	6 months and 12 months
Secondary	12. To evaluate safety of Imlifidase treatment with regards to reported serious adverse events (SAEs)	Safety over 1 year as measured by reported SAEs	12 months