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Clinical Trial Summary

The purpose of this study is to transition patients who have been stable on Belatacept for one year after kidney transplant from standard 4-week to an investigational 8-week belatacept dosing schedule. The investigators hypothesize that renal function and acute rejection rates will be non-inferior with 8-week belatacept dosing.


Clinical Trial Description

The current dosing protocol for patients who have undergone a kidney transplant requires that Belatacept be given as an infusion every 4 weeks. The investigator wants to assess if the patients who have been stable for one year after transplant can be safely transitioned to an 8-week Belatacept infusion schedule. Renal function and any episodes of acute rejection will be closely monitored. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02560558
Study type Interventional
Source Emory University
Contact
Status Completed
Phase Phase 4
Start date September 2015
Completion date August 29, 2019

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