(Total Views: 475)
Posted On: 03/05/2021 11:35:25 PM
Post# of 151830
Exactly FDA and Cytodyn want more data to be able to support a full approval. I believe there is ample evidence for an Immediate EUA. These patients do not have any other viable option that to take a leronlimab a safe drug that will increase there chance of survival by 24% without putting them at risk is for SAE. All 5 countries I think will be purchasing an allotment to be used on a probably a certain criteria of severe critical that are on high oxygen or ventilation and with more data prob could get expanded to other populations when supply and manufacturing are ramped up.


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