A Study of the Activity of Eculizumab for Prevention of Delayed Graft Function In Deceased Donor Kidney Transplant

Based on experimental data and supportive observations in humans associating complement gene
upregulation with ischemic reperfusion injury, it is hypothesized that C5 cleavage is a key
step in the pathogenesis of ischemic reperfusion injury following transplantation. It is
further hypothesized that eculizumab, an antibody that blocks C5 cleavage in humans will be
an effective prophylactic agent to prevent ischemic reperfusion injury in high risk
recipients. To test this hypothesis, this study is a pilot prospective, randomized study to
test the efficacy of eculizumab vs. placebo given once at the time of transplantation in
preventing delayed graft function in first adult recipients of deceased donor kidneys.

Inclusion Criteria:

- Age 18 or older

- Weight > 40 kg

- Male or Female

- Recipients of first deceased donor kidneys

- Able to provide written informed consent

- Transplant candidate as per site specific guidelines

- Dialysis dependent renal failure (initiated more than 2 months prior to transplant)

- Novartis Delayed Graft Function Score 3-8

- Extended criteria donor with brain death, or standard criteria donor with cold
ischemic time < 24 hours

Exclusion Criteria:

- Planned to receive multi-organ transplant

- Kidneys from donors < 6 years of age

- Dual kidney transplant (from same donor, including en bloc)

- Living donor kidney

- Highly sensitized recipients (PRA > 50%)

- Previous transplant

- Participation in another investigational trial

- Recipient BMI > 40

- ABO incompatible

- DCD Donor

- Preemptive kidney transplant

- Recipients with DGF scores < 3 or > 8

- Women who are pregnant or breast feeding

- Women of child bearing potential who are unable or unwilling to use a medically
acceptable form of contraception

- Patients infected with HIV, HCV or HBV

- Active bacterial or other infection which is clinically significant in the opinion of
the investigator

- Patients with history of splenectomy

- Patients with history of meningococcal disease

- Patients with known or suspected hereditary complement deficiency

- Patients with history of cancer (other than non-melanoma skin cancers) within the
last 5 years