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Study of Intravenous Administration of Allogeneic Adipose Stem Cells for COVID-19

This study is designed rapidly assess safety and preliminary efficacy in hospitalized patients with COVID-19 respiratory distress to provide clinical guidance for possible wider use in treating patients in this pandemic environment. This data will be used for FDA IND filings and pursuit of a BLA.

Purpose of Study

This study is single arm, non-randomized Phase 1 study of the safety and preliminary efficacy of PSC-04, an adipose-derived allogeneic mesenchymal stem cell. The outcome data will be compared to contemporaneous non-enrolled patients at the same clinical site(s) as the enrolled patients.

Study Objectives:

Primary: To evaluate the safety of intravenous infusion of allogeneic adipose stem cells in patients with COVID-19 disease and respiratory distress.

Secondary: To evaluate a set of secondary safety and efficacy outcome variables to give guidance in assessing the risk/benefit ratio in patients with COVID-19 respiratory distress.

Eligibility

Age:
18 - 80
Sex:
All

Key Inclusion / Exclusion Criteria

Inclusion Criteria:

Admitted to hospital as in-patient (ward or ICU)
Respiratory distress – respiratory rate ≥ 30/minute (or PaO2:FiO2 <300) Bilateral lung infiltrates (CT or frontal X-ray) Supplemental oxygen started but NOT intubated or ventilated COVID-19 (SARS-CoV-2) antigen test positive (FDA-approved test); CDC confirmation not necessary Time from Enrollment to treatment must be less than 24 hours Age: 18-80 years Gender: any Suitability for cellular therapy: In the opinion of the Investigator or the Sponsor the patient is suitable for cellular therapy Cognitive function: Able to understand and willing to sign informed consent form or legally authorized representative or surrogate Exclusion

Exclusion Criteria:

Intubation / ventilation Current therapy is working, and patient is clinically improving Disease Conditions: Heart failure severe (NY Heart Association Classification IV); Clinical evidence of left heart failure or volume overload as a primary explanation for the bilateral pulmonary infiltrates; Any disease or condition other than current respiratory COVID-19 disease for which 6-month mortality is estimated to be greater than 50%; Moderate to severe liver failure; Severe chronic respiratory disease or the use of home oxygen use prior to this current illness; Currently receiving extracorporeal life support (ECLS/ECMO) Past Disease Conditions: Any history of malignancy within the last 2 years (except for patients in remission or cured of the malignancy); Lung transplant patient or lobectomy; Deep venous thrombosis or pulmonary embolism within past 3 months; History of splenectomy Other Experimental Conditions: Currently enrolled or treated in last 60 days in another clinical study Consent Issues: Do not resuscitate (DNR) order in place; Not willing to follow lung protective ventilation strategy, if needed Concurrent disease or circumstances that Investigator or Sponsor judges to be an unacceptable risk to patient health or a confounding variable to assessment or problem in completion of trial.

Conditions:

COVID-19

Status:

Completed

Phase:

Phase 1

Study ID

NCT04486001

Read Detailed Summary

Start Date / End Date:

15/12/2020 -

Enrollment:

10

Full Details:

https://clinicaltrials.gov/ct2/show/NCT04486001

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1 Study Locations

United States

Fresno Community Hospital
Fresno, California, 93710
United States


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