Treatment of Coronavirus COVID-19 Pneumonia (Pathogen SARS-CoV-2) With Cryopreserved Allogeneic P_MMSCs and UC-MMSCs

NCT04461925 — Phase 1 / Phase 2, Unknown, 30 participants, Institute of Cell Therapy

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Treatment of Coronavirus COVID-19 Pneumonia (Pathogen SARS-CoV-2) With Cryopreserved Allogeneic Multipotent Mesenchymal Stem Cells of the Placenta and Umbilical Cord

RegistryNCT04461925
StatusUnknown
PhasePhase 1 / Phase 2
Study typeInterventional; non randomized, parallel, masking: none, treatment
Enrollment30 (Estimated)
SponsorInstitute of Cell Therapy (Industry); collaborators: Kyiv City Clinical Hospital # 4
ConditionsCOVID-19 Pneumonia
InterventionsPlacenta-Derived MMSCs; Cryopreserved Placenta-Derived Multipotent Mesenchymal Stromal Cells, Antibiotics, Hormones, Anticoagulant Therapy, Оxygen therapy (Procedure, drug, device)
Datesstart 2020-05-02, primary completion 2021-05-02 (estimated), completion 2021-12-01 (estimated), first posted 2020-07-08, last updated 2020-07-08
Locations1 site in Ukraine

Related Papers Related Patents Related Grants Related Experts
All trials for COVID-19 Pneumonia All trials of Placenta-Derived MMSCs; Cryopreserved Placenta-Derived Multipotent Mesenchymal Stromal Cells All trials of Antibiotics

-Summary

Assessment of the clinical effects of infusions of cryopreserved allogeneic multipotent mesenchymal stem cells of the placenta and umbilical cord for COVID-19 patients with acute respiratory distress syndrome.

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+Detailed description

Currently, cell-based therapy and especially stem cell therapy has become a promising therapeutic field, in which many see opportunities to cure incurable diseases. Severe respiratory consequences of the COVID-19, the disease caused by the novel SARS-CoV-2 coronavirus, have prompted urgent need for novel therapies.

Cell-based approaches, primarily using mesenchymal stem cells (MSCs), have demonstrated safety and efficacy in patients with the acute respiratory distress syndrome (ARDS) - common manifestation of cytokine storms, and the cause of death in many COVID-19 patients.

Mesenchymal stem cells are a powerful immunomodulator, they secrete many anti-inflammatory biologically active substances (cytokines) that reduce the inflammatory process in the lungs. Also mesenchymal stem cells secrete numerous growth factors that contribute to the recovery of not only the affected lung tissue but also other organs.

+Arms and interventions

ArmTypeInterventionsDescription
Experimental groupExperimentalProcedure: Placenta-Derived MMSCs; Cryopreserved Placenta-Derived Multipotent Mesenchymal Stromal Cells; Drug: Antibiotics; Drug: Hormones; Drug: Anticoagulant Therapy; Device: Оxygen therapyOn the basis conventional symptomatic treatment and supportive therapy, P-MMSCs were given at 1 million cells/kg body weight/ time, once every 3 days for a total of 3 times: Day "1", Day "4", Day "7".
Control GroupActive comparatorDrug: Antibiotics; Drug: Hormones; Drug: Anticoagulant Therapy; Device: Оxygen therapyConventional symptomatic treatments such as antibacterial (ceftriaxone, azithromycin), anticoagulants, hormones, oxygen therapy, mechanical ventilation and other supportive therapies
  • Placenta-Derived MMSCs; Cryopreserved Placenta-Derived Multipotent Mesenchymal Stromal Cells (Procedure), also known as P-MMSCs: i/v infusions
  • Antibiotics (Drug), also known as ceftriaxone and azithromycin capsules: per os
  • Hormones (Drug), also known as dexamethasone: a moderate amount of dexamethasone i/v
  • Anticoagulant Therapy (Drug), also known as Еnoxaparin: Sub-Q
  • Оxygen therapy (Device), also known as Оxygen insufflation: Оxygen therapy, mechanical ventilation and other supportive therapies

+Outcome measures

Primary outcomes

  • Changes of oxygenation index PaO2/FiO2, most conveniently the P/F ratio. [up to 28 days]: Improvement of pulmonary function. Arterial oxygen tension PaO2 (in mmHg)/fractional inspired oxygen FiO2 (expressed as a fraction, not a percentage), most conveniently the P/F ratio. The normal P/F ratio is \~ 400-500 mmHg (\~55-65 kPa). P/F ratio <300mmHg - sign of Acute Respiratory Distress Syndrome (ARDS)
  • Changes in length of hospital stay [up to 28 days]: Length of Hospital Stay
  • Changes in mortality rate [up to 28 days]: Marker for efficacy of treatment

Secondary outcomes

  • Changes of С-reactive protein (CRP, mg/L) [At baseline, Day 1, Week 1, Week 2, Week 4, Week 8]: Infection biomarker. Serum CRP levels can be used for early diagnosis of pneumonia, patients with severe pneumonia had high CRP levels.
  • Evaluation of Pneumonia Improvement [At baseline, Day 1, Week 1, Week 2, Week 4, Week 8]: CT assessment of pulmonary lesions and lung tissue changes
  • Duration of respiratory symptoms (difficulty breathing, dry cough, fever, etc.) [At baseline, Day 1, Week 1, Week 2, Week 4, Week 8]: Indirect response to lung function
  • Peripheral blood count recovery time [At baseline, Day 1, Week 1, Week 2, Week 4, Week 8]: Degree of infection

+Eligibility

Sex: All, ages: 18 Years to 75 Years

Inclusion Criteria:

* Male or female, aged at 18 years (including) - 75 years old.
* Laboratory confirmation of SARS-CoV-2 infection by reverse-transcription polymerase chain reaction (RT-PCR) from any diagnostic sampling source.
* Pneumonia that is judged by X-ray imaging.

In accordance with any one of the following:

* dyspnea (RR ≥ 30 times / min);
* finger oxygen saturation ≤ 93% in resting state;
* arterial oxygen partial pressure (PaO2) / oxygen absorption concentration (FiO2) ≤ 300MMHG (if possible);
* invasive ventilation< 48 h.

Exclusion Criteria:

* Male or female, aged at <18 years and > 75 years old.
* Pregnancy, lactation and those who are not pregnant but do not take effective contraceptives measures.
* Patients with malignant tumor, other serious systemic diseases and psychosis.
* Patients who are participating in other clinical trials.
* Inability to provide informed consent or to comply with test requirements.
* Co-Infection of HIV, syphilis.
* Invasive ventilation > 48 h.
* Combined with other organ failure (need organ support).

+Locations (1)

FacilityCityCountryStatus
Institute of Cell TherapyKyivUkraineRecruiting

+Investigators