Phase Ib, open-label, multicenter, study of NOX66, given rectally to hospitalized patients with moderate systemic illness due to COVID-19 infection at high risk of developing severe sepsis / septic shock.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
41
NOX66 Suppository
Institute of Emergency Medicine
Chisinau, Moldova
Incidence of Treatment-Emergent Adverse Events
Routine safety monitoring during the study period
Time frame: 60 Days
Change of National Early Warning Score 2 units from baseline
Measurement of 7 clinical parameters (respiration rate, oxygen saturation, any supplemental oxygen, temperature, systolic blood pressure, heart rate, level of consciousness) to assess overall clinical condition.
Time frame: 60 Days
Change in WHO-9 point ordinal scale
Assessment of WHO-9 point ordinal scale for clinical improvement (i.e., 0 = uninfected and 8 = death) category ordinal scale of clinical status from admission.
Time frame: 60 Days
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