Safety & Tolerability of Berinert® (C1 Inhibitor) Therapy to Prevent Rejection

Study Results

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE1/PHASE2

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2011-08-31

Study Completion Date

2013-11-30

Brief Summary

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Organ transplantation offers the only hope for a normal life for patients with end-stage renal disease on dialysis (ESRD). For the highly-sensitized patient, patients with antibodies to human leukocyte antigens (HLA), transplantation is extremely difficult or impossible since pre-formed antibodies will cause severe rejection and loss of transplanted organs. Approximately 30% of the transplant list in the U.S. is considered sensitized (have detectable antibodies to HLA antigens). These anti-HLA (anti-Human Leukocyte Antigen antibodies) pose a significant barrier to transplantation that has recently been successfully addressed using desensitization therapies with IVIG, rituximab and/or plasmapheresis (PE). Despite the success of these therapies, post-transplant antibody mediated rejection (AMR) and chronic Antibody Mediated Rejection (CAMR) remain significant problems. Recent data suggests that addition of Berinert (C1 Inhibitor) to post-transplant treatment regimen may significantly reduce incidence of Antibody Mediation Rejection.

Twenty highly-sensitized patients who have undergone desensitization treatment and are awaiting kidney transplant will be enrolled in the study. Once transplanted these patients will be started on the standard of care post-transplant immunosuppressive protocol. In addition patients will receive Berinert 20 units/ kg daily x 3 days, then twice weekly x 3 weeks. At the end of Berinert treatment a kidney biopsy will be performed. Subjects will be followed for 6 months to assess safety and efficacy of the study protocol.

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Detailed Description

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Single center, Phase I/II, randomized The trial will examine the safety and efficacy of human C1 INH given post-transplant to reduce or prevent complement-dependent, antibody-mediated rejection (AMR) in 20 subjects (adult) who are highly-HLA sensitized (HS),(Panel Reactive Antibodies \>30% (PRA), have undergone desensitization with intravenous immunoglobin (IVIG) + rituximab and/or plasmapheresis and are awaiting Living donor (LD)/ Deceased Donor (DD) kidney transplant. Once transplant offers are entertained, a donor-specific crossmatch will be performed to detect anti-HLA antibodies and donor-specific anti-HLA antibodies (DSA) which are associated with acute rejection or graft loss. (These anti-HLA (anti-Human Leukocyte Antigen antibodies) antibodies may result naturally or from previous pregnancy, transfusions, or prior transplants.) If acceptable crossmatches and Donor Specific Antibody levels are seen after desensitization, the patients will proceed to Living Donor/Deceased Donor transplantation. Patients receiving transplants will have pre-transplant labs obtained for C1 INH levels, Complement 3 (C3) and Complement 4 (C4) at transplant. In addition to the standard post-transplant immunosuppressive protocol, participating patients will receive placebo or 20 Units/kg C1 INH twice weekly X 4 weeks. At the end of the treatment, a protocol biopsy will be performed to assess the allograft for evidence of Antibody Mediated Rejection, including C4d staining. Since \~25% of highly sensitized patients experience Antibody Mediated Rejection post-transplant and 85% of these Antibody Mediated Rejection episodes occur in the 1st post-transplant month, we feel the assessment of the potential impact of C1 INH therapy is best assessed in this time period. After completion of the C1 INH therapy, patients will be followed for an additional 6 month to assess allograft function and Antibody Mediated Rejection episodes as well as Donor Specific Antibodies.

The subjects will be followed to determine the proportion who develop evidence of Antibody Mediated Rejection within 6 month of completion of the study. In addition we will asses the transplanted patients to determine the number who sustain a viable and functioning kidney allograft for 6 months. All subjects will be evaluated on an intent-to-treat basis. The subject accrual rate will be limited to no more than five subjects per month in the initial three months to assure safety to all subjects. Repeat laboratories will be performed at the completion of C1 INH therapy to determine effect on levels and correlation with any potential events.

Conditions

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Kidney Transplantation

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Participants Caregivers Investigators

Study Groups

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C1 esterase inhibitor

10 subjects will receive C1 esterase inhibitor in addition to standard of care immunosuppressive therapy.

Group Type EXPERIMENTAL

C1 Esterase Inhibitor

Intervention Type DRUG

C1 Esterase Inhibitor 20 units/kg twice weekly x 4 weeks

Placebo

10 subjects placebo \[normal saline\] in addition to standard of care immunosuppressive therapy.

Group Type PLACEBO_COMPARATOR

Placebos

Intervention Type DRUG

NS (comparable volume as intervention) twice weekly x 4wks

Interventions

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C1 Esterase Inhibitor

C1 Esterase Inhibitor 20 units/kg twice weekly x 4 weeks

Intervention Type DRUG

Placebos

NS (comparable volume as intervention) twice weekly x 4wks

Intervention Type DRUG

Other Intervention Names

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Berinert

Eligibility Criteria

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Inclusion Criteria

* End-stage renal disease.
* No known contraindications for therapy with Immune Globuillin Intravenous 10%/Rituximab or C1 INH.
* Age 18-65 years at the time of screening.
* Panel Reactive Antibody \[PRA\] \> 50% demonstrated on 3 consecutive samples, Patient highly-HLA (Human Leukocyte Antigen) sensitized and a candidate for Living Donor/Deceased Donor transplantation after desensitization at Cedars Sinai Medical Center.
* At transplant, patient must have Donor Specific Antibody /Cross match + non-HLA (Human Leukocyte Antigen) identical donor.

Subject/Parent/Guardian must be able to understand and provide informed consent.

Exclusion Criteria

* Lactating or pregnant females.
* Women of child-bearing age who are not willing or able to practice Food and Drug Administration \[FDA\]-approved forms of contraception.
* HIV-positive subjects.
* Subjects who test positive for Hepatitis B Virus infection \[positive Hepatitis B Virus surface Antigen, Hepatitis B Virus core Antigen, or Hepatitis B Virus e Antigen/DNA\] or Hepatitis C Virus infection \[positive Anti-Hepatitis C Virus (EIA) and confirmatory Hepatitis C Virus Recombinant ImmunoBlot Assay (RIBA)\].
* Subjects with active Tuberculosis.
* Subjects with selective Immunoglobulin A deficiency, those who have known anti-Immunoglobulin A antibodies, and those with a history of anaphylaxis or severe systemic responses to any part of the clinical trial material.
* Subjects who have received or for whom multiple organ transplants are planned.
* Recent recipients of any licensed or investigational live attenuated vaccine(s) within two months of the screening visit (including but not limited to any of the following:
* Adenovirus \[Adenovirus vaccine live oral type 7\] Varicella \[Varivax\] Hepatitis A \[VAQTA\] Rotavirus \[Rotashield\] Yellow fever \[Y-F-Vax\] Measles and mumps \[Measles and mumps virus vaccine live\] Measles, mumps, and rubella vaccine \[M-M-R-II\] Sabin oral polio vaccine Rabies vaccines \[IMOVAX Rabies I.D., RabAvert\])
* A significantly abnormal general serum screening lab result defined as a White Blood Cell \< .0 X 103/ml, a Hemoglobin \< 8.0 g/dL, a platelet count \< 100 X 103/ml, , an Serum Glutamic Oxaloacetic Transaminase \[SGOT\] \> 5X upper limit of normal, and an Serum Glutamic Pyruvic Transaminase \[SGPT\] \>5X upper limit of normal range.
* Individuals deemed unable to comply with the protocol.
* Subjects with active Cytomegalovirus or Epstein Barr Virus infection as defined by Cytomegalovirus-specific serology (Immunoglobulin G or Immunoglobulin M) and confirmed by quantitative Polymerase Chain Reaction with or without a compatible illness.
* Subjects with a known history of previous myocardial infarction within one year of screening.
* Subjects with a history of clinically significant thrombotic episodes, and subjects with active peripheral vascular disease.
* Use of investigational agents within 4 weeks of participation.
* Know allergy/sensitivity to C1 INH infusions

Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No