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Phase 2 N=25 Treatment

Inhalation Low Dose Radionuclide Therapy in Treatment COVID-19

Covid19 · Pneumonia, Viral

Enrolled (actual)
25
Serious AEs
0.0%
Results posted
Jul 2021
Primary outcome: Primary: Count of White Blood Cells (WBC) After 99mTc-pertechnetate Aerosol Inhalation for Adverse Events Monitoring as Evaluation Safety of This Procedure in Patients With COVID-19 Viral Pneumonia. — 11.2; 9.8; 9.7; 8.7 x 1000 cells/microL

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
99mTc-pertechnetate aerosol (Radiation); 99mTc-pertechnetate aerosol (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
National Medical Research Radiological Centre of the Ministry of Health of Russia
Primary completion
Feb 2021

Outcome Measures

OutcomeResultp-value
PRIMARY
Count of White Blood Cells (WBC) After 99mTc-pertechnetate Aerosol Inhalation for Adverse Events Monitoring as Evaluation Safety of This Procedure in Patients With COVID-19 Viral Pneumonia.
11.2; 9.8; 9.7; 8.7; 8.8; 9.3
PRIMARY
Count of Red Blood Cells (RBC) After 99mTc-pertechnetate Aerosol Inhalation for Adverse Events Monitoring as Evaluation Safety of This Procedure in Patients With COVID-19 Viral Pneumonia.
4.5; 4.5; 4.3; 4.4; 4.2; 4.4
PRIMARY
Hemoglobin Count (Hb) After 99mTc-pertechnetate Aerosol Inhalation for Adverse Events Monitoring as Evaluation Safety of This Procedure in Patients With COVID-19 Viral Pneumonia.
140.5; 132; 137.5; 130.6; 135.3; 131
PRIMARY
Percentage of Neutrophils (N) After 99mTc-pertechnetate Aerosol Inhalation for Adverse Events Monitoring as Evaluation Safety of This Procedure in Patients With COVID-19 Viral Pneumonia.
76.3; 72.2; 68.8; 72.2; 68.4; 71.5
PRIMARY
Absolute Neutrophil Count (ANC) After 99mTc-pertechnetate Aerosol Inhalation for Adverse Events Monitoring as Evaluation Safety of This Procedure in Patients With COVID-19 Viral Pneumonia.
8.8; 7.4; 6.8; 6.6; 6.2; 6.9
PRIMARY
Absolute Lymphocyte Count (ALC) After 99mTc-pertechnetate Aerosol Inhalation for Adverse Events Monitoring as Evaluation Safety of This Procedure in Patients With COVID-19 Viral Pneumonia.
1.6; 1.6; 2.1; 1.4; 1.64; 1.73
PRIMARY
Level of Lactate in the Blood After 99mTc-pertechnetate Aerosol Inhalation for Adverse Events Monitoring as Evaluation Safety of This Procedure in Patients With COVID-19 Viral Pneumonia.
5; 4.11; 4.4; 4.6; 4.28; 4.81
PRIMARY
Level of D-dimer in Blood After 99mTc-pertechnetate Aerosol Inhalation for Adverse Events Monitoring as Evaluation Safety of This Procedure in Patients With COVID-19 Viral Pneumonia.
1737; 1284; 843; 685; 383; 859
SECONDARY
Level of CD4+ T-cells in Blood After 99mTc-pertechnetate Aerosol Inhalation for Evaluation of Cellular Immune Response After This Procedure in Patients With COVID-19 Viral Pneumonia
761; 614; 1100; 832; 845; 718
SECONDARY
Level of NK-cells in Blood After 99mTc-pertechnetate Aerosol Inhalation for Evaluation of Cellular Immune Response After This Procedure in Patients With COVID-19 Viral Pneumonia
153; 164; 188; 149; 219; 181

Summary

Coronavirus disease (COVID-19) is a pandemic of unprecedented proportions with an exponential increase in incidence. Airway epithelium infection caused by coronavirus (SARS-CoV-2) triggers a cascade of difficult-to-control reactions, a so-called "cytokine storm". In contrast to the previously used method of external beam radiation therapy for patients at high risk of a cytokine storm, in present study a different dose delivery mechanism through inhalation of 99mTc-labeled carbon ultrafine aerosol obtained from a TechnegasPlus generator is used. By utilizing anthropometric phantoms the dosimetric characteristics of the applied technique and obtained the coefficients of the transition from the count rate over the area of interest to the activity contained in this area (in kBq) were studied. By observing a group of healthy volunteers after inhalation of 99mTc-labeled carbon ultrafine aerosol, the accumulated dose in the human lungs under internal irradiation of 99mTc was determined. A novel technique has been developed and the possibility of using inhaled low-dose radionuclide therapy in the complex treatment of patients with COVID-19 - associated pneumonia has been studied. As a result, a significant improvement of hematological parameters in the group of patients after inhalation of 99mTc-labeled carbon ultrafine aerosol as compared to the control group is expected.

Eligibility Criteria

Inclusion Criteria

  • Positive SARS-Cov-2 polymerase chain reaction (PCR)
  • CT confirmed pneumonia
  • Men and non-pregnant women ≥ 18 y/o with early laboratory signs of cytokine storm
  • Men and non-pregnant women <65 y/o and/or with early laboratory signs of cytokine storm
  • Informed consent obtained for participation

Exclusion Criteria

  • Age ≤ 18
  • Severe course of COVID-19
  • Pregnant or breast-feeding females
  • Severe concomitant pathology
  • Previous and/or present treatment of oncology disease (e.g. immunotherapy)
  • Autoimmune diseases, severe cardiac disease, bone marrow and/or visceral transplantation
  • Surgical treatment and/or radiotherapy of chest pathology
  • Treatment with specific antiviral and anticytokine agents a day before inhalation procedure
  • Absence of informed consent obtained for participation
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04724538). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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