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Clinical Trial Summary

This is a randomized, multicenter, open-label, active control, non-inferiority study to assess the safety and efficacy of AT-1501 compared with tacrolimus in the incidence of BPAR events through 6 months post-transplant.


Clinical Trial Description

This is a randomized, multicenter, open-label, active control, non-inferiority study to assess the safety and efficacy of AT-1501 compared with tacrolimus. Approximately 120 de novo kidney transplant recipients will receive rabbit anti-thymoglobulin (rATG) (Thymoglobulin®) induction, corticosteroid maintenance, mycophenolate, and will be randomized 1:1. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04819880
Study type Interventional
Source Eledon Pharmaceuticals
Contact Jennifer Areh
Phone 6175952605
Email jareh@eledon.com
Status Not yet recruiting
Phase Phase 2
Start date June 2021
Completion date March 30, 2025

See also
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