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NCT06969807RecruitingPhase 2

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

Clinical Study to Evaluate the Efficacy and Safety of Mesenchymal Stromal Cell (Amimestrocel ) in Patients With Diabetic Kidney Disease

Source: ClinicalTrials.gov · Last updated 14 Jul 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
120 (estimated)
First submitted
24 Apr 2025
Start date
9 Jun 2025
Primary completion date
15 Aug 2026
Lead sponsor
Chinese PLA General Hospital
NCT number
NCT06969807

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 120
  • From 9 Jun 2025 to the primary completion date, 15 Aug 2026
  • 6 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

  • 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.
  • Active infection within one week before enrollment and requiring treatment with intravenous antibiotics.
  • Patients who have participated in other interventional clinical trials within three months before enrollment.

Other illness

  • Patients with kidney diseases not caused by diabetes mellitus.
  • 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).
  • Patients with active infections of hepatitis B or hepatitis C viruses (the copy number of HBV DNA or HCV RNA exceeds the upper limit of the normal value); patients with active tuberculosis; patients with severe immunodeficiency diseases, human immunodeficiency virus (HIV) infection, etc.
  • Patients with a history of malignant tumors within the past five years.
  • Patients with a known history of severe allergy to component blood or blood products, or patients with a history of allergy to heterologous proteins.
  • The research physician deems that the patient's condition is not suitable for participating in this clinical study.

Lab values

  • Patients with severe hyperlipidemia: (serum triglyceride ≥ 6.2 mmol/L, serum low-density lipoprotein cholesterol ≥ 4.1 mmol/L).
  • Hyperkalemia that cannot be controlled through diet or potassium-lowering treatment.

Other

  • Lactating women, or female patients who have a pregnancy plan or an egg donation plan from the start of the study to the follow-up period, and male patients (or their partners) who have a childbearing plan or a sperm donation plan from the start of the study to the follow-up period and are unwilling to take contraceptive measures.

Who the study is looking for

  • 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.
  • The estimated glomerular filtration rate (eGFR) ≥ 15 ml/min/1.73m² (calculated according to the CKD-EPI formula).
  • The blood pressure can be controlled at BP ≤ 160/100 mmHg.
  • Glycated hemoglobin (HbA1c) \< 9%.
  • Willing and able to provide written informed consent.

Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (6)

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

SiteCityCountrySite status
Xuanwu Hospital, Capital Medical University
Coordinator of this site? Confirm its status
BeijingChinaRecruiting
Beijing Hospital
Coordinator of this site? Confirm its status
BeijingChinaRecruiting
Chinese PLA General Hospital
Coordinator of this site? Confirm its status
BeijingChinaRecruiting
China-Japan Friendship Hospital
Coordinator of this site? Confirm its status
BeijingChinaRecruiting
Beijing Tsinghua Changgung Hospital, Medical Center, Tsinghua University
Coordinator of this site? Confirm its status
BeijingChinaNot yet recruiting
Capital Medical University Affiliated Beijing Friendship Hospital
Coordinator of this site? Confirm its status
BeijingChinaRecruiting

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