Pinserkr …
Yes , all that was proven million times , and there is a need to talk more . Why ???
Dr Lalezari said many times , and he is very responsive , everyone confused may email him and ask again ..
According to him , protocol for CD12 given to FDA was for 4 doses ..at 0 , 7, 14 and 21 days ..
For no apparent reason FDA refused to approve this way , first they changed to 2 doses , at 0 and at 7 days only , and primary endpoint , mortality , they moved from 14 to 28 days ..
What a perfect sabotage of the protocol , design to fail ..
FDA and Fauci are very good in that , all the studies for HCQ were design to fail .
In CD12 there were 2 official groups .,
A..severe
B..critical
All together in entire CD12 SS was not met , problems noticed later , like wrong age distribution , the oldest patients were in LL arm , and the youngest , the healthiest in placebo ..
Was that an accident , was that another sabotage , was Amarex just neglectful , or was it something more behind this ..
But with all of this we have a very good results in group B , critical patients ., unbelievable good !!!
It was 100% prove that LL saving lives , and not only without one serious side effect , but it look that LL repair some side effects due to some toxic SOC drugs ..
there was less side effects in LL arm , then placebo ( SOC)
What a drug !!
At 14 days there was 82% mortality benefit above all SOC
And even at 28 days , 21 days after the second dose , there was 31% mortality benefit ABOVE all SOC .
And this was with only 62 patients , as we know the smaller the group , the more difficult is to prove benefits , this is why most of the studies of these worthless , toxic drugs are with 1000s of patients , and even then they showing “ trending “
And what FDA do ..
Carrying for American people FDA said , they will not look at “ some “ subgroup results .
They looked and approved “ trending “ results of this toxic drug Remdesivir when Fauci told them .
They show later some positive results , but ONLY when Fauci or Gilead doing the studies , hmmm , interesting …
As FDA said in a hit letter , they will not look at some subgroup good results ..
This subgroup is a group B in CD12 , and the people in it are people on the ventilators and ECMO without one good drug approved for them ..
They all fellow Americans , our families and friends ..
FDA know ( they not stupid ) LL is the ONLY drug saving life’s ., what’s an indifference in this people , observing almost 1 mill death , and doing nothing about it ..
And soon after they approved Biogen drug for Alz..
--Drug showing no clinical significance..
--no primary endpoint,
--no p-value..
And up to 30% of patients developing as a side effect , cerebral edema and/or cerebral bleeding..
What a terrible indifference !!!
What a corruption..
All imo .,
AI
