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NCT02836574CompletedPhase 2

A Study of Renal Autologous Cell Therapy (REACT) in Type 2 Diabetics With Chronic Kidney Disease

A Phase 2 Prospective, Randomized, Double-Arm, Deferred Treatment, Open Label, Repeat Dose, Safety and Efficacy Study of Renal Autologous Cell Therapy (REACT) in Subjects With Type 2 Diabetes and Chronic Kidney Disease

Source: ClinicalTrials.gov · Last updated 24 Aug 2025

Brief summary (registry, in English)

To assess the safety and efficacy of up to two REACT injections given 6 months (+4 weeks) apart and delivered into the biopsied kidney using a percutaneous approach in participants with Type 2 Diabetes Mellitus (T2DM) and Chronic Kidney Disease (CKD).

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
83 (actual)
First submitted
22 Jun 2016
Start date
1 Sept 2016
Primary completion date
31 Dec 2023
Lead sponsor
Prokidney
NCT number
NCT02836574

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 83
  • From 1 Sept 2016 to the primary completion date, 31 Dec 2023
  • 16 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • 1\. The subject is currently receiving renal dialysis.

Other illness

  • The subject has a history of type 1 diabetes mellitus.
  • The subject has a history of renal transplantation.
  • The subject has uncontrolled diabetes (defined as metabolically unstable by the Investigator).

Lab values

  • The subject has a serum Hemoglobin A1c (HbA1c) level greater than 10% at the Screening Visit.
  • The subject has hemoglobin levels less than 9 g/dL prior to each Renal Autologous Cell Therapy (REACT) injection.

Who the study is looking for

  • The subject is male or female, 30 to 80 years of age on the date of informed consent.
  • The subject has an established diagnosis of Type 2 Diabetes Mellitus.
  • The subject has an established diagnosis of diabetic nephropathy as the underlying cause of renal disease.
  • The subject has an established diagnosis of Chronic Kidney Disease not requiring renal dialysis, defined as having an Estimated Glomerular Filtration Rate (eGFR) between 20 and 50 mL/min/1.73m².
  • The subject has blood pressure less than 150/90 at the Screening Visit.
  • The subject has stable blood pressure and is maintained on a stable anti-hypertensive medication regimen.
  • A minimum of 2 measurements of Estimated Glomerular Filtration Rate (eGFR) or serum creatine ratio (sCr) should be obtained at least 3 months apart prior to the Screening Visit or within the previous 18 months to define the rate of progression of Chronic Kidney Disease (CKD).
  • The subject is willing and able to provide signed informed consent.
  • The subject was enrolled into Part 1 of the study and received at least one Renal Autologous Cell Therapy (REACT) injection.

Age in the registry: 30 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (16)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Lehigh Valley Health Network
Coordinator of this site? Confirm its status
AllentownUnited StatesUnknown status
University of Michigan
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Ann ArborUnited StatesUnknown status
Renal Associates of Baton Rouge
Coordinator of this site? Confirm its status
Baton RougeUnited StatesUnknown status
University of North Carolina, Chapel Hill
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Chapel HillUnited StatesUnknown status
University of Chicago Medical Center
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ChicagoUnited StatesUnknown status
Kidney Associates of Colorado
Coordinator of this site? Confirm its status
DenverUnited StatesUnknown status
University of Florida
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GainesvilleUnited StatesUnknown status
Paragon Health
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KalamazooUnited StatesUnknown status
University of Louisville
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LouisvilleUnited StatesUnknown status
University of Wisconsin - Madison
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MadisonUnited StatesUnknown status
Boise Kidney and Hypertension Institute
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MeridianUnited StatesUnknown status
Vanderbilt University
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NashvilleUnited StatesUnknown status
Yale Univeristy
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New HavenUnited StatesUnknown status
Mt Sinai Hospital
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New YorkUnited StatesUnknown status
University of Arizona
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TucsonUnited StatesUnknown status
Nephrology & Hypertension Associates
Coordinator of this site? Confirm its status
TupeloUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.