A single center, open-label, randomized, controlled pilot trial to evaluate the efficacy and safety of everolimus conversion versus standard immunosuppression in liver transplant recipients
Study for liver transplant recipients using drug (Everolimus)
Sponsor: Tomoaki Kato MD
Enrolling: Male and Female Patients
Study Length: 24 Days
Clinic Visits: 15
IRB Number: AAAL1602
U.S. Govt. ID: NCT01998789
Contact: Theresa Lukose: 212-305-3839 / tt2103@columbia.edu
Additional Study Information: The primary objective of this exploratory study is to compare the change in renal function from baseline to 12 months post liver transplantation, in subjects maintained on an everolimus conversion regimen versus those maintained on a standard tacrolimus based regimen. The study consists of a screening period that must take place up to 90 days prior to, or within 10 days post liver transplantation. Participants will be randomized at baseline visit to either an everolimus conversion arm or the standard immunosuppression arm.
This study is closed
Investigator
Tomoaki Kato, MD
Do You Qualify?
Have you received a liver transplant? Yes No
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For more information, please contact:
Theresa Lukose
tt2103@columbia.edu
212-305-3839