Status:
TERMINATED
A Pilot Study to Assess the Safety and Efficacy of Alefacept in de Novo Kidney Transplant Recipients
Lead Sponsor:
Northwestern University
Collaborating Sponsors:
Astellas Pharma Inc
Conditions:
Transplant; Failure, Kidney
Eligibility:
All Genders
18+ years
Phase:
PHASE1
Brief Summary
The purpose of this study is to assess Alefacept in combination with alemtuzumab induction and calcineurin inhibitor and corticosteroid withdrawal.
Detailed Description
This is a single center, investigator initiated, pilot study to assess the safety and efficacy of Alefacept in combination with Alemtuzumab induction and Myfortic with rapid steroid and calcineurin in...
Eligibility Criteria
Inclusion
- Institutional Review Board (IRB) approved written Informed Consent and Health Insurance Portability and Accountability Act (HIPAA) Authorization for U.S. sites, or equivalent privacy language as per national regulations, obtained from the subject or legally authorized representative prior to study-related procedures (including withdrawal of prohibited medication, if applicable)
- Recipient of a kidney from a non-HLA identical related living donor, a non- related living donor, or deceased donor
- Recipient of a de novo kidney transplant
- ≥ 18 years of age
- Anticipated to receive first oral dose of tacrolimus within 48 hours of transplant procedure
- Female subjects of child bearing potential must have a negative urine or serum pregnancy test, and must agree to maintain effective birth control during the study
- Healthy donor is eligible for the blood draw if:
- Institutional Review Board (IRB) approved written Informed Consent and Health Insurance Portability and Accountability Act (HIPAA) Authorization for U.S. sites, or equivalent privacy language as per national regulations, is obtained from subject prior to any study-related procedures
- Subject is a donor to a de novo kidney transplant subject who is enrolled in the study or a self declared healthy volunteer who is not a kidney donor for a subject enrolled in the study
- ≥ 18 years of age
Exclusion
- Previously received or is receiving an organ transplant other than a kidney
- Sensitivity to iodine
- Will receive a transplant from a non-heart beating donor (donation after cardiac death - DCD)
- Receives a transplant from an HLA identical related living donor
- Will receive a solitary kidney from a deceased donor \< 5 years of age
- Will receive a kidney with an anticipated cold ischemia time (CIT) of \> 30 hours
- Will receive an ABO incompatible donor kidney
- Recipient or donor is known to be seropositive for human immunodeficiency virus (HIV)
- Recipient has a positive T or B cell crossmatch by investigational site's standard method of determination. For recipients where a flow cytometry crossmatch is performed and is positive in either T or B cell testing, recipients are excluded only if donor specific, anti-HLA antibody is detected by flow cytometry based, specific anti-HLA antibody testing.
- Current malignancy or a history of malignancy (within the past 5 years), except non-metastatic basal or squamous cell carcinoma of the skin that has been treated successfully
- Significant liver disease
- Serologically negative for cytomegalovirus (CMV) with serologically positive CMV donor
- Serologically negative for Epstein Barr virus
- Has received intravenous immunoglobulin (IVIG) therapy in the three months prior to first dose of study drug
- Uncontrolled concomitant infection or any other unstable medical condition that could interfere with the study objectives
- Concurrently participating in another drug study or has received an investigational drug within 28 days prior to transplant
- Known hypersensitivity to alefacept, alemtuzumab, tacrolimus, mycophenolic acid, corticosteroids, or any of their components
- Any form of substance abuse, psychiatric disorder, or a condition that in the opinion of the Investigator could invalidate communication with the Investigator
- Subject is pregnant or lactating
- Subject is unlikely to comply with the visits scheduled in the protocol
- Subject will receive a kidney transplant from an expanded criteria donor (ECD)
- Will receive a kidney transplant from a CDC high risk donor
- Healthy donor subject will be excluded from participation if any of the following apply:
- Unable to comprehend the investigational nature of the protocol participation
- Complete blood count results determined to be outside the normal ranges
Key Trial Info
Start Date :
July 1 2010
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
August 1 2012
Estimated Enrollment :
9 Patients enrolled
Trial Details
Trial ID
NCT01163799
Start Date
July 1 2010
End Date
August 1 2012
Last Update
May 3 2013
Active Locations (1)
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1
Northwestern Memorial Hospital
Chicago, Illinois, United States, 60611