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RecruitingDiabetic Kidney DiseaseChronic Kidney Diseases

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

Eligible age

30–80 yrs

Accepts

All genders

Locations

1 state

Healthy volunteers

No

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About this study

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).

Sponsor: Prokidney

You may qualify if…

  • The participant must have received gelatin-hydrogel formulation REACT in a previous trial (RMCL-002, REGEN-003, REGEN-004) for the treatment of chronic kidney disease and completed an end of study visit in their parent trial per protocol.

You may not qualify if…

  • The participant did not receive REACT in a previous trial for the treatment of chronic kidney disease.

Where it's recruiting

Idaho

Meridian

Source: ClinicalTrials.gov · NCT05918523 · last updated 2025-05-28