Sept 9 (Reuters) - Humanigen Inc HGEN.O :
* FDA HAS DECLINED HUMANIGEN’S EMERGENCY USE AUTHORIZATION
(EUA)
REQUEST FOR LENZILUMAB IN HOSPITALIZED COVID-19 PATIENTS
* HUMANIGEN - FDA HAS DECLINED ITS REQUEST FOR EMERGENCY USE
AUTHORIZATION OF LENZILUMAB TO TREAT NEWLY HOSPITALIZED COVID-19
PATIENTS
* NIH'S ACTIV-5/BET-B STUDY IS EXPECTED TO PROVIDE FURTHER
DATA
THAT MAY SUPPORT A NEW EUA REQUEST
* HUMANIGEN - FDA STATED IT WAS UNABLE TO CONCLUDE
KNOWN&POTENTIAL
BENEFITS OF LENZILUMAB OUTWEIGH KNOWN&POTENTIAL RISKS OF USE FOR
COVID19 TREATMENT
Source text for Eikon: ID:nBw1C3Ctqa
Further company coverage: HGEN.O
((Reuters.Briefs@thomsonreuters.com;))