COVID-19 is causing a serious viral pandemic in terms of health and social impact. To date, no treatment has yet demonstrated Strong efficacy in treating the infectious disease (COVID-19). Pulmonary administration of Interferon (IFN) type I is a therapeutic strategy with high potential,due to higher local concentrations and minimal adverse effects. Type I interferons (including IFN-α and IFN-β) are antiviral defence cytokines and also have the potential to negatively modulate IFN Type II and IL-6 dependent cytokine storm, the latter being induced in the late forms of COVID-19. In vitro, IFN-β were more effective on COVID-19 than IFN-α. In existing preliminary studies, only patients receiving IFN type I modulators have a decrease in viral carriage and a rapid reversal. The purpose of this project is to assess in hospitalized patients with oxygen for COVID 19, the clinical efficacy on oxygen requirements of the addition of inhaled Interferon type I compared to the control arm .
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
74
The interventional arm includes inhaled interferon (9.6 MUI x2/d for 48 hours, then 9.6 MUI x1/d for 8 to 16 days or discharge), in addition to standard care. In phase B, maximum treatment duration is 8 days.
The interventional arm includes a WFI water nebulization comparator.
CH d'Abbeville
Abbeville, France
CHU Amiens
Amiens, France
CH Compiègne-Noyon
Compiègne, France
CH de l'Arrondissement de Montreuil-sur-mer
Rang-du-Fliers, France
CH de Saint-Quentin
Saint-Quentin, France
CH de Tourcoing
Tourcoing, France
CH de valenciennes
Valenciennes, France
oxygen requirement score at day 0
oxygen requirement score at day 0
Time frame: day 0
oxygen requirement score at day 15
oxygen requirement score at day 15
Time frame: day 15
Variation oxygen requirement score between day 0 and day15
Variation oxygen requirement score between day 0 and day15
Time frame: at day 15
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