Placebo-Controlled Study to Evaluate the Safety and Efficacy of OPN-305 in Preventing Delayed Renal Graft Function

Completed · Phase 2 · Has a placebo group

Conditions studied: Delayed Graft Function

In brief

When a patient receives a kidney transplant particularly if the kidney is from an older donor or one who has had the kidney removed after their heart has stopped, there is a risk that the newly transplanted kidney may not function immediately. If the delay in function means that dialysis is needed in the first 7 days after the transplantation then this is known as delayed graft function or dDGF. Also delayed graft function that does not require dialysis but is present because the serum creatinine does not fall sufficiently is known as functional delayed graft function or fDGF. This problem is often due to an excessive inflammatory reaction to not having had a blood supply between the time of donation and transplant. OPN-305 is a monoclonal antibody that blocks Toll-like Receptor 2 which is thought to be partly responsible for increasing the risk of this inflammation. It is hoped that the effects of the inflammation will be reduced and therefore prevent dDGF and fDGF from occurring. The purpose of the study is to explore how effective OPN-305 is in preventing dDGF and fDGF as well as improving other measures of kidney function and the overall safety of the antibody. In the first part of the study, each patient received an Infusion of one of three possible doses of OPN-305 or a placebo and in the second part the most suitable dose of OPN-305 and a placebo would be used. The purpose of this second part of the study is to find out if a dose of OPN-305 which has already been tested in an earlier part of this study can prevent kidney graft dysfunction. For the purposes of this study, kidney function will be assessed using the composite of delayed graft function (dDGF) because dialysis is necessary in the first 7 days and functional delayed graft function that does not require dialysis but is present because the serum creatinine, a key measure of renal function, does not fall sufficiently (fDGF) in the first 7 days post-transplant. Protocol OPN305-103 follows out to 12 months post-transplant the clinical status and graft function of patients who have completed the 6-month post-transplant period under Part A or Part B of OPN305-102.

Key facts

Study ID

NCT01794663

Run by

Opsona Therapeutics Ltd.

People needed

252

Starts

2012-10-01

Expected to finish

2016-06-30

Last updated by the study team

2017-02-16

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• INCLUSION CRITERIA FOR TRANSPLANT RECIPIENTS
• First or second renal transplant recipient - for second renal transplantations;
• The second transplant should NOT be due to rejection
• Panel Reactive Antibody (PRA) should be <10%
• Minimum 3 months since the loss of the first transplanted kidney
• Dialysis-dependent at the time of transplantation as documented by:
• Requirement for at least 2 dialysis sessions/week in the 56 days before transplantation
• INCLUSION CRITERIA FOR DONOR KIDNEY:
• The donor kidney must be considered compatible according to local transplant guidelines
• An ECD donor defined as:
• o Extended Criteria Donor defined as:
• Donor ≥60 years of age
• Donor 50-59 years of age with two of three of the following criteria present:
• Death due to cerebrovascular accident
• Pre-existing history of systemic hypertension
• Terminal creatinine > 1.5mg/dL (132.6 µmol/L)
• Kidney allograft maintained in cold storage with or without machine perfusion

You may not qualify if…

• EXCLUSION CRITERIA FOR TRANSPLANT RECIPIENTS:
• Use of an investigational drug in the 30 days before Study Day 1
• Participation in any other research
• Known hypersensitivity to human monoclonal antibodies or any of the study-drug excipients
• Previous hypersensitivity to basiliximab or anti-thymocyte globulin (ATG)
• History or known HIV, HBV, or HCV-positive
• History of malignancy within the last five years, except excised squamous or basal cell carcinoma of the skin or cervical intraepithelial neoplasia
• Scheduled to undergo multi-organ transplantation
• Planned dual kidney transplantation
• Presence of clinically significant infections requiring continued therapy
• Active tuberculosis
• Existence of any surgical or medical condition, other than the current transplantation which, in the opinion of the investigator, might significantly alter the distribution, metabolism or excretion of study medication
• Presence of uncontrolled diabetes mellitus.
• Current drug and/or alcohol abuse
• History or presence of a medical condition or disease that in the investigator's assessment would place the patient at an unacceptable risk for study participation
• Lactating or pregnant woman
• Patient institutionalized by administrative or court order
• EXCLUSION CRITERIA FOR ALL DONOR KIDNEYS
• DCD or SCD donor kidney
• Terminal creatinine >3mg/dL
• Donor who is known to have received an investigational drug for I-R injury or graft rejection (immunosuppressant) in the 48h before organ recovery
• Participation in any other research (drug or non-drug)
• Kidney donor <5 years of age or <20kg body weight
• Living donor allograft
• HLA or ABO incompatible kidney as defined by a negative cytotoxic crossmatch

Where it is running

• Research Site — Los Angeles, California, United States
• Research Site — Washington D.C., District of Columbia, United States
• Research Site — Tampa, Florida, United States
• Research Site — Chicago, Illinois, United States
• Research Site — New Orleans, Louisiana, United States
• Research Site — New Orleans, Louisiana, United States
• Research Site — Livingston, New Jersey, United States
• Research Site — New York, New York, United States
• Research Site — The Bronx, New York, United States
• Research Site — Harrisburg, Pennsylvania, United States
• Research Site — Charleston, South Carolina, United States
• Research Site — Dallas, Texas, United States
• Research Site — Fort Worth, Texas, United States
• Research Site — Richmond, Virginia, United States
• Research Site — Linz, Austria
• Research Site — Brussels, Belgium
• Research Site — Ghent, Belgium
• Research Site — Leuven, Belgium
• Research Site — Liège, Belgium
• Research Site — Prague, Czechia
• Research Site — Bordeaux, France
• Research Site — Paris, France
• Research Site — Toulouse, France
• Research Site — Berlin, Germany
• Research Site — Berlin, Germany

Full record on ClinicalTrials.gov

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