May 4 (Reuters) - Cytodyn Inc CYDY.PK :
* FDA APPROVES 54 EMERGENCY INDS FOR LERONLIMAB TREATMENT OF
CORONAVIRUS – CYTODYN REQUESTS COMPASSIONATE USE FROM FDA FOR
COVID-19 PATIENTS NOT ELIGIBLE FOR PARTICIPATION IN TWO ONGOING
CLINICAL TRIALS IN U.S. – CYTODYN TARGETS ENROLLMENT COMPLETION
FOR IT
* CYTODYN INC - 49 COVID-19 PATIENTS HAVE ENROLLED FOR
TREATMENT
WITH LERONLIMAB THROUGH EIND
* CYTODYN INC - 4 OUT OF 11 CRITICALLY ILL PATIENTS WITH
PRE-EXISTING CONDITIONS SURVIVED AFTER TREATMENT WITH LERONLIMAB
* CYTODYN INC - OF NEXT 38 PATIENTS TREATED WITH LERONLIMAB,
MANY
WERE EXTUBATED, IMPROVED, OR WERE DISCHARGED
Source text for Eikon: ID:nGNX4G4LS1
Further company coverage: CYDY.PK
((Reuters.Briefs@thomsonreuters.com;))