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
- Diseases
- Chronic kidney disease, Type 2 diabetes
- 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
Sites (16)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Lehigh Valley Health Network Coordinator of this site? Confirm its status | Allentown | United States | Unknown status |
| University of Michigan Coordinator of this site? Confirm its status | Ann Arbor | United States | Unknown status |
| Renal Associates of Baton Rouge Coordinator of this site? Confirm its status | Baton Rouge | United States | Unknown status |
| University of North Carolina, Chapel Hill Coordinator of this site? Confirm its status | Chapel Hill | United States | Unknown status |
| University of Chicago Medical Center Coordinator of this site? Confirm its status | Chicago | United States | Unknown status |
| Kidney Associates of Colorado Coordinator of this site? Confirm its status | Denver | United States | Unknown status |
| University of Florida Coordinator of this site? Confirm its status | Gainesville | United States | Unknown status |
| Paragon Health Coordinator of this site? Confirm its status | Kalamazoo | United States | Unknown status |
| University of Louisville Coordinator of this site? Confirm its status | Louisville | United States | Unknown status |
| University of Wisconsin - Madison Coordinator of this site? Confirm its status | Madison | United States | Unknown status |
| Boise Kidney and Hypertension Institute Coordinator of this site? Confirm its status | Meridian | United States | Unknown status |
| Vanderbilt University Coordinator of this site? Confirm its status | Nashville | United States | Unknown status |
| Yale Univeristy Coordinator of this site? Confirm its status | New Haven | United States | Unknown status |
| Mt Sinai Hospital Coordinator of this site? Confirm its status | New York | United States | Unknown status |
| University of Arizona Coordinator of this site? Confirm its status | Tucson | United States | Unknown status |
| Nephrology & Hypertension Associates Coordinator of this site? Confirm its status | Tupelo | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.