Safety and Efficacy of Mesenchymal Stromal Cells (Amimestrocel ) in Diabetic Kidney Disease

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-80
SponsorChinese PLA General Hospital

About this trial

This trial is to evaluate the efficacy and safety of umbilical cord-derived mesenchymal stromal cells (Amimestrocel ) in study subjects with progressive diabetic kidney disease (DKD), to investigate whether Amimestrocel can improve renal function or proteinuria of DKD patients.

Eligibility criteria

Qualifiers

Men and women who are ≥18 and ≤ 80 years old.

Diagnosed with type 2 diabetes mellitus.

Diagnosed with diabetic kidney disease based on renal pathology within the past 10 years.

The 24-hour urine protein quantification is continuously ≥ 3.5 g, or the urine albumin-to-creatinine ratio (UACR) > 1000 mg/g.

Disqualifiers

Patients with kidney diseases not caused by diabetes mellitus.

Patients who have received treatment with systemic immunosuppressants (such as cyclosporine A, tacrolimus, mycophenolate mofetil, etc.) within 30 days before enrollment and the duration of treatment exceeds one week.

Severe cardiovascular diseases, such as congenital heart diseases, atrial fibrillation, NYHA class Ⅲ-IV, unstable angina pectoris, etc.

A history of cerebral hemorrhage or cerebral infarction within the past six months (except for those with a history of lacunar cerebral infarction without residual limb movement disorders, cognitive and language function disorders).

Trial design

Treatments tested in this trial

  • Amimestrocel

Treatment groups

120 Participants
are divided into 1 treatment group

Sponsors and collaborators