It wasn’t a definite timeline, just his explanation of what he’s hoping transpires. Get the efficacy to submit with the safety and then ask for emergency approval based on unmet need. This is different than waiting for the results of both trials because he also talked about how the results of the P3 could be met with approval right away after it ends, based on it being a registration trial rather than an exploratory (phase2) like the mild to moderate. So I don't believe he’s waiting for both trial results first. I feel like he was expressing that the efficacy results, as soon as we have them, get immediately sent on with safety for an approval request. I’m sure it’ll be posted to listen to. See for yourself when you have a chance. It seems like others feel like the timeline of two weeks is for M/M efficacy to be released.