Condition: SARS-CoV-2 · Influenza, Human · Respiratory Syncytial Virus Infections · Sponsor: PEACHES BIOTECH
The purpose of this clinical trial is to evaluate the safety, tolerability and efficacy of two doses (dose A and dose B) of Standardized Conditioned Medium Obtained by Coculture of M2-macrophages and fat-derived Mesenchymal Stromal Cells (PRS CK STORM) in the modulation of the cytokine storm in participants with acute respiratory infection caused by SARS-Cov-2, influenza A, influenza B and respiratory syncytial virus (RSV) in need for oxygen therapy. The main questions it aims to answer are: * Are both doses of PRS CK STORM (dose A and dose B) safe as an intravenous drug to modulate inflammatory processes, such as the cytokine storm in participants with SIRS caused by SARS-Cov-2, influenza A, influenza B and RSV? * Are both doses of PRS CK STORM (dose A and dose B) effective as an intravenous drug to modulate SIRS-associated cytokine storm caused by SARS-Cov-2, influenza A, influenza B and RSV compared to the control group? * What are the anti-inflammatory and pro-inflammatory cytokine profiles after treatment with two different doses of PRS CK STORM in participants with SIRS caused by SARS-Cov-2, influenza A, influenza B and RSV? Researchers will compare both doses of PRS CK STORM with the control group to test whether the anti-inflammatory action of PRS CK STORM is safe and effective in modulating the cytokine storm for the treatment of SIRS caused by SARS-Cov-2, influenza A, influenza B and RSV. In addition, the anti-inflammatory and pro-inflammatory cytokine profiles a…
This description comes directly from the study's public registry record.
Francesca Sarno, Dr. · +34 674 747 199 · francesca.sarno@livingcells.org
Juan Carlos de Gregorio · +34 607964152 · jcg@peaches.es
Always discuss trial participation with your own doctor first.
| Hospital Universitario Príncipe de Asturias | Alcalá de Henares, Madrid, Spain | Recruiting |
| Hospital Universitario de Fuenlabrada | Fuenlabrada, Madrid, Spain | Recruiting |
| Hospital Universitario Reina Sofía | Córdoba, Spain | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06684379