Clazakizumab for the Treatment of Chronic Active Antibody Mediated Rejection in Kidney Transplant Recipients (IMAGINE)

Overview

About this study

The purpose of this study is to investigate whether clazakizumab (an anti-interleukin (IL)-6 monoclonal antibody (mAb)) may be beneficial for the treatment of CABMR in recipients of a kidney transplant by inhibiting the production of Donor Specific Antibodies (DSA) and re-shaping T cell alloimmune responses.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

- Inclusion criteria:

1. Age 18-75 years.

2. Living donor/deceased donor kidney transplant recipients ≥6 months from time of
transplant.

3. Diagnosis of CABMR determined by kidney biopsy and the presence of HLA DSA using
single-antigen bead-based assays.

NOTE: If conducted within 12 months (+3 weeks) prior to the start of the
screening period, and no intervening treatments have been administered, the
biopsy does not need to be repeated at Screening. If conducted within 6 months (+
3 weeks) prior to the start of Screening, the DSA analysis does not need to be
repeated at screening. To be considered for determination of study eligibility,
the biopsy and DSA analysis must be performed at least 2 months ± 2 weeks after
the end of any prior treatment for ABMR (including CABMR) or TCMR, in order to
show continuing CABMR and presence of HLA DSA. In addition, with the exception of
steroids, treatments for ABMR or TCMR are not allowed within 3 months prior to
the start of screening.

The following histopathologic and serologic diagnostic criteria (based on Banff
2015 criteria [Loupy et al, 2017]) must be met for inclusion:

- Morphologic evidence of chronic tissue injury, as demonstrated by TG (cg>0).
Biopsies without evidence of chronic tissue injury on light microscopy, but
with glomerular basement membrane double contours on electron microscopy
(cg1a) are eligible.

- Evidence of current/recent antibody interaction with vascular endothelium,
including 1 or more of the following.

- Linear C4d staining in peritubular capillaries or medullary vasa recta (C4d2
or C4d3 by immunofluorescence on frozen sections, or C4d > 0 by
immunohistochemistry on paraffin sections).

- At least moderate microvascular inflammation ([g + ptc] ≥ 2) in the absence
of recurrent or de novo glomerulonephritis, although in the presence of
acute TCMR, borderline infiltrate, or infection, ptc ≥ 2 alone is not
sufficient and g must be ≥ 1.

NOTE: The local pathologist's diagnosis must be reviewed by a central pathologist
to confirm eligibility for entry into the study. Biopsies with other
histopathologic changes (eg, BKV nephropathy or recurrent glomerulonephritis) may
be eligible if concurrent CABMR changes (as detailed above) are present and
determined to be the predominant cause of renal dysfunction.

4. Serologic evidence of circulating DSA to HLA. NOTE: The local laboratory DSA
results must be reviewed and confirmed by the central HLA reviewer during the
screening period.

- Exclusion criteria:

1. Multi-organ transplant recipient (except for simultaneous kidney-pancreas or
previous multiple kidney transplants) or cell transplant (islet, bone marrow,
stem cell) recipient.

2. Treatment for ABMR (including CABMR) or TCMR within 3 months prior to the start
of screening with the exception of steroids.

3. Received T cell depleting agents (e.g., alemtuzumab, anti-thymocyte globulin)
within 3 months prior to the start of screening.

4. Pregnant, breastfeeding, or unwillingness to practice adequate contraception.

5. Active tuberculosis (TB) or history of active TB.

6. History of human immunodeficiency virus (HIV) infection or positive for HIV.

7. Seropositive for hepatitis B surface antigen (HBsAg)

8. Hepatitis C virus (HCV) RNA positive.

9. History of anaphylaxis or known hypersensitivity to clazakizumab or to any constituent of the drug product.

10.  Active infection with coronavirus disease 2019 (COVID-19):

a. Subject not known to have been previously infected with COVID-19 must have a negative PCR test result during the Screening Period as near to the Day 1 Baseline Visit (Visit 2) as possible. If the subject is unwell with symptoms suggestive of COVID-19 but PCR test result is negative, other causes for symptoms must be ruled out to determine subject eligibility. Note: If the subject was not previously known to have been infected with COVID-19 and has a positive PCR test result at Screening, criterion

b. Subject known to have been previously infected with COVID-19 must meet all the following conditions:

i. Must be without symptoms attributable to COVID-19 for at least 1 month prior tothe start of Screening.

ii. Must be re-established on background immunosuppressants for at least 2 weeks prior to the start of Screening.

11. For subjects receiving anti-hypertensive agents (eg, ACEIs or ARBs), the dose of the agent should be stable for at least 2 months prior to the start of Screening and not planned to be increased.

Note: Other protocol defined Inclusion/Exclusion Criteria may apply.

Eligibility last updated 1/31/24. Questions regarding updates should be directed to the study team contact.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status

Rochester, Minn.

Mayo Clinic principal investigator

Carrie Schinstock, M.D.

Closed for enrollment

Scottsdale/Phoenix, Ariz.

Mayo Clinic principal investigator

Carrie Schinstock, M.D.

Closed for enrollment

More information

Publications

Publications are currently not available
.
CLS-20471585

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