Your session is about to expire
← Back to Search
Immunosuppressant
1 for Liver Disease (thymo Trial)
Phase 4
Waitlist Available
Led By Wendy Grant, MD
Research Sponsored by University of Nebraska
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up post op days 1-6, months 3,6, 9, and 12
Awards & highlights
thymo Trial Summary
The purpose of this study is to compare kidney function, long term patient and graft survival, and incidence of acute rejection in liver transplant recipients between one group receiving thymoglobulin induction and delayed initiation of tacrolimus and another group of liver transplant recipients having immediate administration of tacrolimus without any induction immunosuppression.
Eligible Conditions
- Liver Disease
- Liver Transplant
- Immunosuppression
thymo Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ post op days 1-6, months 3,6, 9, and 12
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~post op days 1-6, months 3,6, 9, and 12
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Evaluation of renal function via Glo-Fil nuclear medicine scan and laboratory parameters
Secondary outcome measures
patient and graft survival, incidence of acute rejection, incidence of active CMV disease, incidence of other infections, any adverse events or serious adverse events associated with the use of thymo induction therapy
thymo Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: 1Experimental Treatment1 Intervention
Patients in arm 1 will receive induction with thymoglobulin at time of transplant with delayed initiation of tacrolimus
Group II: 2Active Control1 Intervention
patients in arm 2 will not receive thymo induction at time of transplant and will have immediate initiation of tacrolimus
Find a Location
Who is running the clinical trial?
University of NebraskaLead Sponsor
537 Previous Clinical Trials
1,143,854 Total Patients Enrolled
Genzyme, a Sanofi CompanyIndustry Sponsor
524 Previous Clinical Trials
85,530 Total Patients Enrolled
Wendy Grant, MDPrincipal InvestigatorUniversity of Nebraska
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Recent research and studies
Share this study with friends
Copy Link
Messenger