drugset / Trial / NCT05669001

A Study of TCD601 in de Novo Renal Transplant Recipients

NCT05669001

Phase 2 Completed 76 enrolled ITB-Med LLC
RandomizedParallel-groupOpen-labelPrevention

Summary

The purpose of this study is to evaluate the safety and efficacy of TCD601 in combination with Belatacept when compared to standard of care immunosuppression therapy in de novo renal transplant patients.

Timeline

Start
2023-12-28
Primary completion
2026-04-10
Completion
2026-04-10

Drugs

EvaluationDrugModalityDoseRoute
Comparator ATG Unknown
Subject Belatacept Protein / enzyme biologic
Subject Siplizumab Monoclonal antibody
Comparator TAC Unknown
Background MPA Unknown
Background Prednisone Other / unclassified

Indications

No indication recorded.