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CytoDyn Inc CYDY
(Total Views: 746)
Posted On: 07/30/2020 1:25:25 PM
Post# of 156281
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Posted By: TechGuru
After last release of safety data for M-M CYDY said:

Quote:
39% (11 SAEs in 28 Patients) in Placebo Arm as Compared to Only 14% (8 SAEs in 56 Patients) in Leronlimab Arm Reported Serious Adverse Events (SAEs), Which Were Unrelated to Leronlimab. The Efficacy Portion of the Trial Will Be Announced Along With a Full Report as Soon as Statistical Analyses Are Completed



Can somebody think why would CYDY call for a conference call and NOT announce the efficacy portion instead of rather wait until Statistical Analyses are completed & available ???

I can't and therefore think we will be given the results.













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