Did the FDA cause this or could it be CYDY conserv

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Did the FDA cause this or could it be CYDY conserving finances?

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The "partial clinical hold" part is what is confusing me. That seems to say the overall HIV preogram is not at issue, something specific might be. The "full clinical hold on its Covid-19 program" is more routine.

My reading of what FDA states about clinical holds is that they are for 30 days and "a clinical hold is an order issued by the U.S. Food and Drug Administration (FDA) to the sponsor of an investigational new drug (IND) application to delay a proposed clinical investigation or to suspend an ongoing clinical trial. The reason for a clinical hold is concern for the safety of clinical trial participants"

There has been far too many reports from doctors using Leronlimab on Covid patients for me to believe that there is any real evidence of injury, real or perceived from using it to treat Covid-19.

Tomorrow morning will be enlightening, to say the least.