YSPSL for Prevention of Ischemic Reperfusion Injury in Patients Undergoing Cadaveric Orthotopic Liver Transplantation
Keywords
Abstract
Description
YSPSL-0003 is an extension into 36 patients of the previous 12 patient pilot study YSPSL-0002 under an almost identical study protocol with extended inclusion criteria. Like YSPSL-0002, YSPSL-0003 is a single-center (UCLA), randomized, placebo-controlled, double-blind study. Patients are randomly assigned to either active study drug (Active group) or placebo (Control group) prior to transplantation. The active study drug dose includes both a 1 mg/kg IV infusion for the recipient and a 20 mg [approximately 0.27 mg/kg] as an ex vivo flush. The doses are administered via 2 separate infusions of study agent: one 20 mg dose into the portal vein of the liver prior to implantation as an ex vivo flush with Viaspan®; and the second infusion of 1 mg/kg intravenously into the recipient, when technically feasible, prior to the hepatic artery anastomosis. Placebo of a volume equivalent to active study drug is prepared for administration to the control group to help maintain the blind. Those patients that experience an intraoperative blood loss of >10 units, receive an additional 1 mg/kg IV infusion of study agent (or placebo equivalent) at the end of the transplant surgery. The Investigator/Sponsor is blinded to the treatment assignment for each patient. Randomization assignment is maintained by UCLA's clinical pharmacist.
Dates
| Last Verified: | 03/31/2009 |
| First Submitted: | 04/02/2009 |
| Estimated Enrollment Submitted: | 04/05/2009 |
| First Posted: | 04/06/2009 |
| Last Update Submitted: | 04/05/2009 |
| Last Update Posted: | 04/06/2009 |
| Actual Study Start Date: | 04/30/2008 |
| Estimated Primary Completion Date: | 02/28/2009 |
| Estimated Study Completion Date: | 09/30/2009 |
Condition or disease
Intervention/treatment
Drug: 1
Drug: 2
Phase
Arm Groups
| Arm | Intervention/treatment |
|---|---|
| Experimental: 1 Active Group: (18 subjects) YSPSL administered as an ex vivo flush (20 mg YSPSL in Viaspan® 200 mL total volume) into the portal vein prior to transplant at the back table; YSPSL 1 mg/kg administered IV to the transplant recipient PRIOR to arterial reperfusion of the liver. One extra IV dose of 1 mg/kg will be given at the end of the procedure only to patients that have experienced an intraoperative blood loss of greater than 10 units. | Drug: 1 The active study drug dose includes both a 1 mg/kg IV infusion for the recipient and a 20 mg [approximately 0.27 mg/kg] as an ex vivo flush. The doses will be administered via 2 separate infusions of study agent: one 20 mg dose into the portal vein of the liver prior to implantation as an ex vivo flush with Viaspan®; and the second infusion of 1 mg/kg intravenously into the recipient, when technically feasible, prior to the hepatic artery anastomosis. Those patients that experience an intraoperative blood loss of >10 units, will receive an additional 1 mg/kg IV infusion of study agent at the end of the transplant surgery. |
| Placebo Comparator: 2 Placebo Control: (18 subjects) Ex vivo flush of placebo control (200 mL Viaspan®) into the portal vein prior to transplant and 0.1 mL/kg placebo control (saline) IV to the transplant recipient PRIOR to arterial reperfusion of the liver. One additional infusion of 0.1 mL/kg placebo control (saline) will be given at the end of the procedure to patients that have experienced an intraoperative blood loss of greater than 10 units. | Drug: 2 Placebo of a volume equivalent to active study drug will be prepared for administration to the control group to help maintain the blind. Those patients that experience an intraoperative blood loss of >10 units, will receive an additional 1 mg/kg IV infusion of placebo equivalent at the end of the transplant surgery. |
Eligibility Criteria
| Ages Eligible for Study | 18 Years To 18 Years |
| Sexes Eligible for Study | All |
| Accepts Healthy Volunteers | Yes |
| Criteria | Inclusion Criteria: - Patient will be a recipient of a primary (first) ABO compatible cadaveric liver allograft - Patient's age is less than 18 years - Patient is not a recipient of a multivisceral transplant or simultaneous kidney transplant - Patient has not undergone prior organ or cellular transplant of any type - Patient has a Model for End Stage Liver Disease (MELD) score of ≤38 - Cold ischemia time (CIT) anticipated to be less than 14 hours - Donor liver procured by UCLA liver team - Veno-veno bypass is not planned to be used for the patient (e.g. no prior surgery or other factor that indicates a risk for excessive blood loss and therefore a need for veno-veno bypass +/- autologous recovery during surgery) - For patients who are women of childbearing potential, patient has a negative pregnancy test (either urine or serum) within 48 hours prior to transplant - Patient (male and female) is willing to use an acceptable form of birth control for at least 3 months post-treatment - Patient is willing and able to sign informed consent. Exclusion Criteria: - Patient has a prior organ transplant of any type - Patient has known allergic or intolerance reactions to human immune globulins, antibodies, or components of the formulation or known contraindication to administration of YSPSL - Patient has an uncontrolled active infection (on antibiotics with controlled infection is not an exclusion) - Patient has active Hepatitis B virus (HBV)/transplant for HBV related cirrhosis - Patient has previously participated in this study or another study with YSPSL - Patient has received investigational therapy within 90 days prior to the transplant procedure - Patient has current drug or alcohol abuse or, in the opinion of the investigator, is at risk for poor compliance with the visits in this protocol (no drug testing required) - Patient is a pregnant or nursing female, a female of childbearing potential planning to become pregnant within the duration of this study, or is not practicing birth control - Patient is planned to receive a living donor liver transplant - Patient lives >200 miles away or otherwise is not able to participate in study follow-up visits - Donor body mass index >40 - Donor liver biopsy >40% macrosteatotic fat - Donor age >70. |
Outcome
Primary Outcome Measures
1. Safety will be evaluated by clinical and laboratory assessments, an abbreviated pharmacokinetic (PK) profile of the administered dose of YSPSL, and graft function and patient and graft survival through 6 months post-transplant. [6 months post trasplant]
Secondary Outcome Measures
1. To evaluate the potential efficacy of prophylaxis with YSPSL on ischemia reperfusion injury (IRI) as assessed by proposed efficacy evaluations of IRI in liver transplants, in patients who meet eligibility criteria for the trial. [6 months post transplant]
