80% reduction in relative risk of invasive mechanical ventilation and/or death in patients treated with lenzilumab compared to the control group Median time to resolution of acute respiratory distress syndrome (ARDS) reduced to one day for patients treated with lenzilumab versus eight days in control group Lenzilumab patients discharged from the hospital in less than half the time compared with control group BURLINGAME, CA / ACCESSWIRE / September 1, 2020 / Humanigen, Inc. , (OTCQB:HGEN)
September 1, 2020
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