drugset / Trial / NCT01846715

Study of an Autologous Neo-Kidney Augment in Patients With Chronic Kidney Disease

NCT01846715 ↗

Phase 1 Terminated 6 enrolled Tengion
NaSingle-groupOpen-labelTreatment

Summary

The primary purpose of this study is to assess the safety and optimal delivery of the Neo-Kidney Augment (NKA) when implanted at one site in a recipient kidney. NKA is made from expanded autologous, homologous, selected renal cells (SRC) obtained from the patient's kidney biopsy.

Timeline

Start
2013-04
Primary completion
2014-12
Completion
2014-12

Outcome

Outcome not reported

Stopped (Business): “lack of funding”

Drugs

EvaluationDrugModalityDoseRoute
Subject NKA Cell therapy — Other