EINDs reinstated is a positive development IMO.
Post# of 143003
Does everyone agree? Seems FDA would not do unless they think LL helps.
Dec 22 (Reuters) - Cytodyn Inc:
* FDA RESUMES EIND APPROVAL FOR SEVERE-TO-CRITICAL COVID-19 PATIENTS USE OF VYROLOGIX™ (LERONLIMAB) FOLLOWING FULL ENROLLMENT IN CYTODYN’S PHASE 3 TRIAL
* CYTODYN INC - FDA'S DECISION WILL ENABLE CYTODYN TO RESPOND TO ONGOING REQUESTS FOR LERONLIMAB UNTIL PHASE 3 TRIAL DATA IS UNBLINDED Source text for Eikon: Further company coverage: