This study adopts a randomized, double-blind, placebo parallel control design, and is expected to include 168 eligible patients with severe novel coronavirus pneumonia.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
75mg of Jaktinib administered orally Twice daily(BID) with best available treatment.
100mg of Jaktinib administered orally Twice daily(BID) with best available treatment.
Placebo (given as two placebo tablets) administered orally BID with best available treatment.
The proportion of Participants who develop death or respiratory failure.
Respiratory failure is defined as Participants who on invasive mechanical ventilation or Extracorporeal Membrane Oxygenation(ECMO) or on non-invasive ventilation or high-flow oxygen devices.
Time frame: 28 days after randomization
The proportion of Participants who develop death or respiratory failure.
Respiratory failure is defined as Participants who on invasive mechanical ventilation or ECMO or on non-invasive ventilation or high-flow oxygen devices.
Time frame: 14 days after randomization
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