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Clinical Trial Summary

The purpose of this study is to evaluate the long-term safety of up to two gelatin-hydrogel formulation REACT injections given 3 to 6 months apart and delivered percutaneously into same kidney on renal function in participants with chronic kidney disease (CKD).


Clinical Trial Description

This observational extension study is a multi-center, prospective, non-therapeutic study, where up to 80 participants who have been enrolled and dosed with Renal Autologous Cell Therapy in previous interventional clinical studies (RMCL-002, REGEN-003, REGEN-004) will be monitored for up to five years with alternating in clinic and phone visits. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05918523
Study type Observational
Source Prokidney
Contact Beth Hilburger
Phone 336-999-7031
Email info@prokidney.com
Status Recruiting
Phase
Start date December 11, 2023
Completion date March 2028

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