Cover up B v C likely failure Day 12 already. How do we know it likely failed? No early data. Pretense that must wait so many days before releasing any data- when the key data is ALREADY AVAILABLE! any key info ready right NOW!
Data now Leo?
Why do you wait for Day 29 or Day 60? Why? I get it, I get it- we should have already figured out that it failed.
COVID in Russia esp Moscow cases up a lot, as you no doubt have heard. And yet no word from company about atelier data analysis. To me this adds up to : failure. Would Putin let the cure languish in his hospitals' pharmacies and do nothing? Bound to be some extra doses available- if it worked.
1." COVID in Russia esp Moscow cases up a lot, as you no doubt have heard"...
OF COURSE...its ravaging through all of Russia, while greatly subsided in U.S. ... meaning the Covid-19 Patient Pool for Clinical Trials has been RUSSIA for the past couple of months. Great that LEO picked the right domain for filling the C.T. promptly. Had it been all U.S. we might have been lucky enough to be 1/2 full! (Glad you brought that up TIAB!)
2. "And yet no word from company about atelier data analysis."
WHY WOULD ANYONE EXPECT "data analysis" after test ended and FDA has PROHIBITED the release of Data (under C.T. protocol)...First, it is still being collected, and Secondly it is NOT PERMITTED to be unblinded...until 60th day of last patient tested... LEO has no control and even if he did...IT WOULD BE MALFEASENCE AND SUICIDE for IPIX to do so. ... BUT being a MD, YOU KNEW THAT!
3. "this adds up to : failure."...
Actually, NO...this adds up to an irrational conclusion and a failure to acknowledge the process reference in #2 above.
4. "Would Putin let the cure languish in his hospitals' pharmacies and do nothing?"...
What does Putin or anyone know about the success or failure of the trial?...So YES...PUTIN would do nothing, because WE and PUTIN know nothing ... except that BRILACIDIN did not have SAE, otherwise the trials would have been stopped!...But as an MD...you already knew that!
5. "Bound to be some extra doses available- if it worked"
If it worked or if it did not work...WHAT DO YOU THINK THEY DO WITH UNUSED DOSES AFTER A CLINICAL TRIAL...put unused Doses in a Candy Bowl for visitors to try out? (free staw provided so they can sip it up) AS AN MD in a hospital...you already know unused Scripts (doses) have to be accounted for as part of protocol...every usage requires reporting...