Clinical Study on the Safety and Preliminary Efficacy of hUC-MSCs Intravenous Infusion Therapy for ARDS

NCT ID: NCT06505941

Last Updated: 2024-07-17

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 60 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-07-20
• Study Completion Date: 2027-02-20

Brief Summary

The object of this study is to observe the safety of umbilical cord mesenchymal stem cell therapy for acute respiratory distress syndrome, consisting with two phases.

Detailed Description

The secondary objectives are to observe the preliminary efficacy of umbilical cord mesenchymal stem cell therapy for acute respiratory distress syndrome. Phase One is an open-label, dose-escalation clinical study. Following safety and tolerability conclusions from Phase One, and upon evaluation and approval by the data safety committee and ethics committee, conduct Phase Two study, which will be a randomized, double-blind, placebo-controlled study. Dosage selection will be based on the safest and most effective dosage determined from Phase One results.

Conditions

Acute Respiratory Distress Syndrome

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

placebo

1 intravenous infusion of an equal volume of cell-free placebo.

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

non-cell-containing placebo

MSC

Name：Human umbilical cord mesenchymal stem cells Specification: 30 ml/bag Dosage: 1×106cells/kg, 5×106cells/kg, 10×106cells/kg Usage: Intravenous infusion The stem cells used in this study are human umbilical cord mesenchymal stem cells (hUC-MSCs), which are derived from umbilical cords donated by healthy mothers who have given birth in maternity hospitals. hUC-MSCs are extracted, processed, cultured and harvested from umbilical cord donors recruited by laboratories complying with the GMP standards. hUC-MSCs cell suspensions that have passed the quality control will be put into bags and transported to the hospitals for use by the subjects of the present clinical study.

Group Type: EXPERIMENTAL

umbilical cord mesenchymal stem cell

Intervention Type: DRUG

umbilical cord mesenchymal stem cell

Interventions

umbilical cord mesenchymal stem cell

umbilical cord mesenchymal stem cell

Intervention Type: DRUG

Placebo

non-cell-containing placebo

Intervention Type: DRUG

Other Intervention Names

cell

Eligibility Criteria

Inclusion Criteria

1. Age greater than 18 years, regardless of gender;

2. Meeting the ARDS Berlin diagnostic criteria;

3. Definite diagnosis within 72 hours;

4. P/F < 150mmHg;

5. Understanding and signing informed consent.

Exclusion Criteria

1. Women of childbearing potential with a positive serum pregnancy test before medication, pregnant women, or lactating women;

2. ARDS directly caused by physical or chemical factors;

3. Moderate to severe liver damage (Child-Pugh score >12);

4. Chronic heart failure, New York Heart Association functional class IV;

5. Severe kidney disease undergoing renal replacement therapy;

6. Severe lung disease, Grade III or IV pulmonary hypertension, receiving oxygen therapy or ventilator support for more than one month in the six months prior to screening, end-stage lung disease, or severe physical limitations due to chest wall deformity;

7. Immunodeficiency, receiving immunosuppressive therapy within 2 weeks (except for low-dose corticosteroids), or with lymphoma, leukemia, or acquired immune deficiency syndrome; history of organ transplantation, bone marrow transplantation, or autologous hematopoietic stem cell suppression;

8. Expected survival time of less than 48 hours due to terminal illness;

9. Patients diagnosed with deep vein thrombosis (DVT) or pulmonary embolism (PE) in the past three months;

10. Patients receiving ECMO therapy;

11. Hepatitis B, hepatitis C, syphilis, or HIV infection.

12. eGFR < 30ml/min/BSA;

13. ALT > 5 × ULN;

14. Absolute neutrophil count < 1500/μL;

15. Subjects who have participated in other clinical studies within the past month (excluding those who have not received intervention), or are currently participating in other experimental treatments;

16. Subjects deemed unlikely to benefit from the study by the investigator, or deemed unsuitable for participation in this study.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Zhongda Hospital

OTHER

Sponsor Role: collaborator

Yinguan Biologics, Shenzheng

UNKNOWN

Sponsor Role: collaborator

Southeast University, China

OTHER

Sponsor Role: lead

Responsible Party

Jianfeng Xie

deputy director

Responsibility Role: PRINCIPAL_INVESTIGATOR

Other Identifiers

2019ZDSYLL077-P06

Identifier Type: -

Identifier Source: org_study_id