Wang et al. & Remdesivir: did Wang's LANCET publication May 2020 blow Remdesivir out the water as ineffective & deadly yet NIH that day approved Remdesivir? Yes! Media then moved to cover up Wang!

Wang's trial should have ensured Remdesivir was DOA, but NIH & Fauci disregarded this study that was released SAME day, 'remdesivir was not associated with statistically significant clinical benefit'

You the reader should be reminded that in this LANCET Wange et al. clinical trial, Remdesivir was stopped early because of adverse events in 18 (12%) patients versus four (5%) patients who stopped placebo early. It was stopped early not ‘for benefit’, but ‘for harm’. It was deemed too harmful but that afternoon, Fauci with Trump siting there with Hahn the two-timing duplicitous sell-out ‘now working for Moderna that he just prior gave EUA for the mRNA transfection vaccine to’, all of them, save Trump, understanding the best evidence that it was DEADLY as per Wang et al.

Tell me who to hang…we need to run these people through courts and once judges give us the nod, we have to hang many of these people. And to know that Remdesivir (aka Veklury) is still be given in USA.

Hang them high!

SOURCE:

https://www.thelancet.com/journals/lancet/article/PIIS0140-6736(20)31022-9/fulltext

‘Between Feb 6, 2020, and March 12, 2020, 237 patients were enrolled and randomly assigned to a treatment group (158 to remdesivir and 79 to placebo); one patient in the placebo group who withdrew after randomisation was not included in the ITT population. Remdesivir use was not associated with a difference in time to clinical improvement (hazard ratio 1·23 [95% CI 0·87–1·75]). Although not statistically significant, patients receiving remdesivir had a numerically faster time to clinical improvement than those receiving placebo among patients with symptom duration of 10 days or less (hazard ratio 1·52 [0·95–2·43]). Adverse events were reported in 102 (66%) of 155 remdesivir recipients versus 50 (64%) of 78 placebo recipients. Remdesivir was stopped early because of adverse events in 18 (12%) patients versus four (5%) patients who stopped placebo early.

Interpretation

In this study of adult patients admitted to hospital for severe COVID-19, remdesivir was not associated with statistically significant clinical benefits.’

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