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RECRUITING

A Long-Term Follow-Up Study of Participants Exposed to REACT

NCT05918523 · View on ClinicalTrials.gov ↗

Study 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).

Interventions

  • BIOLOGICAL Renal Autologous Cell Therapy (REACT)

Study Locations (1)

Idaho

  • Boise Kidney & Hypertension Institute — Meridian

Trial Details

FieldValue
Enrollment Target 80 participants
Start Date 2023-12-11
Est. Completion 2028-03

Sponsor

Prokidney

3 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05918523

The ClinicalTrials.gov registry entry for NCT05918523 describes a study currently listed as recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 80 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Prokidney, which has 3 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Chronic Kidney Diseases appearing as the primary indexed condition, and to 1 intervention — of which Renal Autologous Cell Therapy (REACT) is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT05918523 reports 1 study location spanning 1 distinct geographic area — top geographies include Idaho. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT05918523 about?

NCT05918523 is a clinical study titled "A Long-Term Follow-Up Study of Participants Exposed to REACT". 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).

What is the current status of trial NCT05918523?

This trial is currently recruiting. The enrollment target is 80 participants. The study started on 2023-12-11. Estimated completion is 2028-03.

What conditions does trial NCT05918523 study?

This clinical trial studies the following conditions: Chronic Kidney Diseases, Diabetic Kidney Disease. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05918523?

The interventions under investigation include: Renal Autologous Cell Therapy (REACT) (BIOLOGICAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05918523?

This trial is sponsored by Prokidney, which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05918523 being conducted?

This trial has 1 study location across Idaho. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial