Per the PR, I had also noticed that the FDA purposefully excluded moderate intubated ARDS patients (mechanically ventilated with PEEP <15 cmH20 with Pa02/FiO2 >150 mmHg) from the eIND protocol. Is it because they don't consider moderate ARDS as an emergency scenario? Either they are trying to save LL for the sickest of sick or handicapping LL from achieving good results. Either way, LL will be victorious even with one hand tied behind its back!