I haven’t seen any mention of the (apparent) fac
Post# of 148292
If it were just a matter of safety (and assuming that placebos are, by definition, perfectly safe), then the placebo arm of the trial could not have had a significantly greater number of adverse events than the drug arm.
The claim that patients treated with Leronlimab suffered only about half as many adverse events is therefore already a strong statement about the efficacy of Leronlimab.
If this is correct, then I guess the question is what sort of adverse events Leronlimab kept these patients from experiencing — and whether they are potentially new indications.