Autologous Adipose-derived Stem Cells (AdMSCs) for COVID-19

COVID-19 Clinical Trial

Official title:

Clinical Study for the Prophylactic Efficacy of Autologous Adipose Tissue-Derived Mesenchymal Stem Cells (AdMSCs) Against Coronavirus 2019 (COVID-19)

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT04428801
• Other study ID #: CTX0020-003
• Status: Not yet recruiting
• Phase: Phase 2
• Start date: September 2023
• Est. completion date: September 2026

Study information

• Verified date: April 2023
• Source: Celltex Therapeutics Corporation
• Contact: Jane Young
• Phone: 7135901000
• Email: jyoung[@]celltexbank.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a phase 2 multi-center, double-blind, randomized, placebo-control clinical trial with 200 subjects who have never been infected by COVID-19 (SARS-Cov-2 virus screen test negative, no blood SARS-Cov-2 IgM and IgG antibodies detected during enrollment) followed by a pilot study of 5 subjects to demonstrate the safety of proposed three-dose regimen of autologous AdMSCs infusions. The 100 study subjects who have previously banked their AdMSCs with Celltex, will receive three doses of autologous AdMSCs (approximately 200 million cells) intravenous infusion every three days. The 100 subjects in the control group who have previously banked their AdMSCs with Celltex will not receive any Celltex's AdMSC therapy but placebo treatments. All subjects are monitored for safety (adverse events/severe adverse events), COVID-19 symptoms, SARS-Cov-2 virus test, blood SARS-Cov-2 IgM and IgG antibodies tests, blood cytokine and inflammatory (CRP, IL_6, IL-10, TNFα) tests and disease severity evaluation for 6 months after the last dose of AdMSC infusion for the study group and 6 months after the enrollment for the control group.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 200
• Est. completion date: September 2026
• Est. primary completion date: September 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Age above 18 years.

• Male or female

• Subjects should have banked AdMSCs in Celltex (already passed communicable disease screen tests for HIV, syphilis, Hepatitis B and C during banking stage)

• Must understand and voluntarily sign an Informed Consent for study participation obtained prior to undergoing any study-specific procedures

• Highly susceptible to SARS-Cov-2 infections, such as obesity (BMI = 40), early to middle stage of hypertension (systolic pressure ranging above 140 Hg or a diastolic pressure ranging from 90 mm Hg), diabetic mellitus hemoglobin A1c >8%), chronic heart disease (one or more conditions including previously diagnosed as coronary artery disease, chronic heart arrhythmia, cardiomyopathy…) chronic pulmonary disease (COPD, fibrosis), chronic liver disease (Hepatic impairment, defined as any of ALT, AST, LDH or bilirubin > 2 x the upper limit of normal (ULN) range according to local laboratory standards) and kidney diseases (serum creatinine > 133 mmol/L (1.5 mg/dL). No terminal stages of the above medical conditions.

• No previous COVID-19 history

• SARS-CoV-2 RT-PCR or equivalent tests negative in respiratory tract specimen

• Blood test for SARS-Cov-2 IgM and IgG negative

Exclusion Criteria:

• Participation in another clinical study (with use of another Investigational Medical Product) within 3 months prior to study treatment start

• Unwillingness or inability to comply with study procedures

• Blood test for SARS-Cov-2 antibodies IgM and IgG positive

• Patients with serious basic diseases that affect survival, including blood diseases, cachexia, active bleeding, severe malnutrition, etc.

• Clinically active malignant disease

• Previous thrombotic disorder

• History of known pulmonary embolism or known secondary anti-phospholipid syndrome

• Known or suspected hypersensitivity to any components used to culture the AdMSCs, e.g. BSA and sulfur-containing products (e.g., DMSO)

• Major trauma or surgery within 14 days of study treatment start

• Mental condition rendering the subject (or the subject's legally acceptable representative[s]) unable to understand the nature, scope and possible consequences of the study

• Alcohol, drug, or medication abuse within one year prior to study treatment start

• Any condition in the Investigator's opinion that is likely to interfere with evaluation of the AdMSC therapy or satisfactory conduct of the study

• Irreversible severe end-organ failures, such as heart failure/attack, stroke, liver and renal failure due to other disease conditions

• Patients or family history with hypercoagulable states, such as protein C/protein S deficiency, factor V Leiden, prothrombin gene mutation, dysfibrinogenemia, etc.

• History of long-term use of immunosuppressive agents

• Organ transplant in the past 6 months

• Pregnant, breastfeeding, or desire to become pregnant or unwilling to practice birth control during participation in the study duration, unless surgically sterilized or postmenopausal during the study

• Patients with severe pulmonary obstructive pneumonia, severe pulmonary interstitial fibrosis, alveolar proteinosis, allergic alveolitis, and other known viral pneumonia or bacterial pneumonia. This includes patients with pulmonary imaging that reveals interstitial lung damage before contracting COVID-19.

• QT interval shows greater than 450 ms in males and 470 ms in females in the medical histories or during screen EKG test.

Related Conditions & MeSH terms

• COVID-19

Intervention

Biological:
• autologous adipose-derived stem cells
Culture expanded mesenchymal stem cells isolated from a patient's own abdominal fat tissue

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Celltex Therapeutics Corporation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Tolerability and acute safety of AdMSC infusion by assessment of the total number of AEs/SAEs related and non-related with the medication	adverse events and severe adverse events	6 months
Primary	The overall proportion of subjects who develop any AEs/SAEs related and non-related with the AdMSC infusions as compared to the control group	adverse events and severe adverse events	6 months
Primary	COVID-19 incidence rates in both the study and control groups	efficacy	6 months
Secondary	The proportion of subjects who are infected by SARS-Cov-2 measured by PCR or other nuclear level-based SARS-Cov-2 virus testing in respiratory tract specimens (oropharyngeal samples) collected by oropharyngeal swab using the CDC standard method.	efficacy	6 months
Secondary	The proportion of subjects who are infected by SARS-Cov-2 virus develop symptoms including mild, classic, severe and critical sever cases between study group and control group.	efficacy	6 months
Secondary	Change of proportion of subjects who are infected by SARS-Cov-2 and develop IgM/IgG antibodies against SARS-Cov-2 between study group and control group.	efficacy	6 months
Secondary	Change of lymphocyte count in white blood cell counts from the baseline	efficacy	6 months
Secondary	Change of PaO2 arterial blood gases from the baseline	efficacy	6 months
Secondary	Compare the proportion of subjects who develop severe COVID-19 pneumonia cases for both study and control groups	efficacy	6 months
Secondary	COVID-19 mortality rates for both study and control groups	efficacy	6 months
Secondary	Change of C-reactive protein (CRP) (mg/L) from the baseline	efficacy	6 months
Secondary	Change of D-dimer (mg/L) from the baseline	efficacy	6 months
Secondary	Change of Procalcitonin (ug)/L from the baseline	efficacy	6 months
Secondary	Change of pro-type B natriuretic peptide (pro-BNP) (pg/mL) from the baseline	efficacy	6 months
Secondary	Change of Bilirubin (mg/dL) from the baseline	efficacy	6 months
Secondary	Change of Creatinine (mg/dL) from the baseline	efficacy	6 months
Secondary	Change in blood test values for cytokine panels (IL-1ß, IL-6, IL-8, IL-10, TNFa) from the baseline	efficacy	6 months
Secondary	The proportion of subjects from SARS-CoV-2 RT-PCR positive to negativity in respiratory tract specimens (oropharyngeal samples) collected by oropharyngeal swab using the CDC standard method. as compared to control group	efficacy	6 months
Secondary	Quantifying viral RNA in stool for baseline and final follow-up.	efficacy	6 months