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***** EXCELLENT POST *****
SHAME ON YOU JON, ENJOY YOUR THANKSGIVING WITH ALL YOUR PRECIOUS NEW WEALTH, because your greed and endless misleading statements have cost MANY PEOPLE to NOT HAVE LOVED ONES AT THEIR TABLES... and I’m sure caused endless financial issues for many.. but hey at least You, Your brother, your sister, and your son have wealth at the cost of the above mentioned!!!
The latest CEO UPDATE from @Jonathan_Javitt EXPOSES HIM COMPLETELY AS AN UTTER FAILURE WHO WAS MORE INTERESTED IN ENRICHING HIMSELF, HIS FAMILY AND HIS FRIENDS THAN ACTUALLY SAVING PROPLE WHO ARE FIGHTING FOR THEIR LAST BREATH...
YOU WOULD HAVE THOUGHT AFTER RECEIVING NOT ONE... BUT TWO FDA EUA DENIALS THAT THE BTD APPLICATION WOULD HAVE HAD MORE INFORMATION THAN WHAT THE FDA WANTED, NOT LESS!!!!
JAVITT HAS MISLEAD EVERYONE FOR SO LING I BET HE NOW BELIEVES HIS LIES AS TRUTH, but the FDA is harder to fool than investors who only have access to limited information!!!
SHAME ON YOU JON!!!
***** NASDAQ.COM ARTICLE HEADLINE*****
“Insiders at NRx Pharmaceuticals, Inc. (NASDAQ:NRXP) must be relieved they sold stock as market valuation descends to US$268m“
WOW!!!!
***** NASDAQ.COM ARTICLE HEADLINE*****
“Insiders at NRx Pharmaceuticals, Inc. (NASDAQ:NRXP) must be relieved they sold stock as market valuation descends to US$268m“
WOW!!!!
**** THE TRUTH COMING OUT READ BELOW****
YET MORE IN THE ENDLESS EVIDENCE THATN JAVITT MISLEAD INVESTORS...
THIS QUOTE FROM THE VP OF IQVIA (Ex NRX employee) WAS APPROVED BY JAVITT WHEN HE POSTED IN ONLINE... SEEMS THEY HIRED IQVIA BECAUSE OF FDA CONCERNS ABOUT STATISTICAL ANALYSIS OF DATA BUT THEY LED US TO BELIEVE IT WAS FOR “EUA ACTIVATION”
“We are honored by the opportunity to join with NRx on the EUA activation and compliance for ZYESAMI in treating some of the sickest patients suffering from COVID-19,” said Susan Kitlas, vice president, Precommercial Business Unit, IQVIA. [/b
**** THE TRUTH COMING OUT READ BELOW****
YET MORE IN THE ENDLESS EVIDENCE THATN JAVITT MISLEAD INVESTORS...
THIS QUOTE FROM THE VP OF IQVIA (Ex NRX employee) WAS APPROVED BY JAVITT WHEN HE POSTED IN ONLINE... SEEMS THEY HIRED IQVIA BECAUSE OF FDA CONCERNS ABOUT STATISTICAL ANALYSIS OF DATA BUT THEY LED US TO BELIEVE IT WAS FOR “EUA ACTIVATION”
“We are honored by the opportunity to join with NRx on the EUA activation and compliance for ZYESAMI in treating some of the sickest patients suffering from COVID-19,” said Susan Kitlas, vice president, Precommercial Business Unit, IQVIA.
***** MUST READ BELOW*****
NOTICE THAT THE COWARD LIAR @Jonathan_Javitt didnt even bother to address all the shareholders he ABSOLUTELY SCREWED OVER in this CEO UPDATE ABOUT HIS 3rd DENIAL FROM FDA.... NICE JOB JON 0-3 WITH FDA... I GUESS YOU CANT FOOL THEM OR MISLEAD THEM AS EASILY AS INVESTORS!!!!
***** MUST READ BELOW*****
NOTICE THAT THE COWARD LIAR @Jonathan_Javitt didnt even bother to address all the shareholders he ABSOLUTELY SCREWED OVER in this CEO UPDATE ABOUT HIS 3rd DENIAL FROM FDA.... NICE JOB JON 0-3 WITH FDA... I GUESS YOU CANT FOOL THEM OR MISLEAD THEM AS EASILY AS INVESTORS!!!!
*** BTD DENIED ALSO.. NICE JOB JAVITT****
** BTD DENIED ALSO.. NICE WORK JAVITT!!!!****
****** GOOD READ 14 PAGES*****
https://www.bgandg.com/nrxp-complaint
****** GOOD READ 14 PAGES*****
https://www.bgandg.com/nrxp-complaint
***** PROVEN RIGHT YET AGAIN****
STATED IN THE CALL TODAY THAT FDA REFUSED TO LOOK AT ANY DATA OUTSIDE OF THE RCT.... ARE WE EXPECTED TO BELIEVE IT TOOK THEM ALMOST HALF A YEAR TO LOOK AT THAT SMALL GROUP????
SOMETHING STINKS... I THINK JAVITT KNEW A LONG LONG TIME AGO TRIAL SIZE WAS AN ISSUE.... IF YOU REMEMBER I POINTED OUT THE GREAT DECEIVER’s VERBIAGE BACK WHEN THEY ANNOUNCED THE TRIAL WAS DONE ENROLLING JAVITT THE LIAR SAID THEN.. “THE TRIAL HAD REACHED THE FDA AGREED UPON NUMBER” I SAID BACK THEN THAT LANGUAGE WAS CONCERNING AS I BELIEVED THAT IT WAS DR DECEIT LAYING THE GROUNDWORK TO BLAME THE FDA FOR DENIAL BASED ON TRIAL SIZE... HMMM RIGHT YET AGAIN
***** PROVEN RIGHT YET AGAIN****
STATED IN THE CALL TODAY THAT FDA REFUSED TO LOOK AT ANY DATA OUTSIDE OF THE RCT.... ARE WE EXPECTED TO BELIEVE IT TOOK THEM ALMOST HALF A YEAR TO LOOK AT THAT SMALL GROUP????
SOMETHING STINKS... I THINK JAVITT KNEW A LONG LONG TIME AGO TRIAL SIZE WAS AN ISSUE.... IF YOU REMEMBER I POINTED OUT THE GREAT DECEIVER’s VERBIAGE BACK WHEN THEY ANNOUNCED THE TRIAL WAS DONE ENROLLING JAVITT THE LIAR SAID THEN.. “THE TRIAL HAD REACHED THE FDA AGREED UPON NUMBER” I SAID BACK THEN THAT LANGUAGE WAS CONCERNING AS I BELIEVED THAT IT WAS DR DECEIT LAYING THE GROUNDWORK TO BLAME THE FDA FOR DENIAL BASED ON TRIAL SIZE... HMMM RIGHT YET AGAIN
**** I MAY HAVE FIGURED IT OUT!!!!******
HMMMM NO WONDER THEY REFUSED TO ANSWER THESE QUESTIONS...
FUNNY THING I JUST THOUGHT OF... Remember question #5 (DID MOTLEY FOOL VERIFY WITH YOU ABOUT THE STATEMENT IN THEIR ARTICLE ABOUT NRX FILING FOR EUA IN EUROPE BEFORE PRINTING IT)...
Motley fool article From OCT 27th it states “ NRX is gearing up to submit application for an EUA for the treatment in EUROPE”
TIME LINE FITS OCT 27th (MOVING FORWARD WITH EUROPE CAUSE EUA DENIED, ON 11/4 SAID FILED FOR TYPE A REJECTION MEETING “last week” WEEK OF OCTOBER 27th ??
WE HAVE BEEN TOLD SINCE THE BEGINNING THAT WE WOULD NOT MOVE FORWARD WITH EUA IN EUROPE UNTIL FDA DECISION... DID THEY KNOW BY THE PRINT OF THIS ARTICLE (OCT 27th) THAT EUA WAS DENIED? WAS THAT PART ABOUT APPLYING FOR EUA IN EUROPE A SECRET “advisement” THE TIME LINE FITS
**** I MAY HAVE FIGURED IT OUT!!!!******
HMMMM NO WONDER THEY REFUSED TO ANSWER THESE QUESTIONS...
FUNNY THING I JUST THOUGHT OF... Remember question #5 (DID MOTLEY FOOL VERIFY WITH YOU ABOUT THE STATEMENT IN THEIR ARTICLE ABOUT NRX FILING FOR EUA IN EUROPE BEFORE PRINTING IT)...
Motley fool article From OCT 27th it states “ NRX is gearing up to submit application for an EUA for the treatment in EUROPE”
TIME LINE FITS OCT 27th (MOVING FORWARD WITH EUROPE CAUSE EUA DENIED, ON 11/4 SAID FILED FOR TYPE A REJECTION MEETING “last week” WEEK OF OCTOBER 27th ??
WE HAVE BEEN TOLD SINCE THE BEGINNING THAT WE WOULD NOT MOVE FORWARD WITH EUA IN EUROPE UNTIL FDA DECISION... DID THEY KNOW BY THE PRINT OF THIS ARTICLE (OCT 27th) THAT EUA WAS DENIED? WAS THAT PART ABOUT APPLYING FOR EUA IN EUROPE A SECRET “advisement” THE TIME LINE FITS
*** MUST READ BELOW... EYE OPENER****
WANNA KNOW HOW SHADY NRX IS AND HOW LITTLE IT CARES ABOUT ITS SHAREHOLDERS... READ THIS STATEMENT...
“The company assumes no obligation to revise any forward-looking statement, whether as a result of new information, future events, or otherwise. Accordingly, you should not place reliance on any forward-looking statement, and all forward-looking statements are herein qualified by reference to the cautionary statements set forth above.”
MEANING THEY COULD MAKE A STATEMENT THAT EXCITES SHAREHOLDERS/PUBLIC.. FIND OUT THE NEXT DAY IT WAS CATEGORICALLY INCORRECT AND NOT ADVISE ANYONE AND LET THEM BELIEVE WHAT NRX KNOWS TO BE UNTRUE!!
Good news is they just started adding this disclaimer and wasn’t on a vast majority of the earlier statements now known to be misleading/UNTRUE.
*** MUST READ BELOW... EYE OPENER****
WANNA KNOW HOW SHADY NRX IS AND HOW LITTLE IT CARES ABOUT ITS SHAREHOLDERS... READ THIS STATEMENT...
“The company assumes no obligation to revise any forward-looking statement, whether as a result of new information, future events, or otherwise. Accordingly, you should not place reliance on any forward-looking statement, and all forward-looking statements are herein qualified by reference to the cautionary statements set forth above.”
MEANING THEY COULD MAKE A STATEMENT THAT EXCITES SHAREHOLDERS/PUBLIC.. FIND OUT THE NEXT DAY IT WAS CATEGORICALLY INCORRECT AND NOT ADVISE ANYONE AND LET THEM BELIEVE WHAT NRX KNOWS TO BE UNTRUE!!
Good news is they just started adding this disclaimer and wasn’t on a vast majority of the earlier statements now known to be misleading/UNTRUE.
**** DEMAND TO SEE FDA REJECTION LETTER***
IF Jonathan Javitt and NRX REFUSE TO POST THE FDA REJECTION LETTER FOR FULL TRANSPARENCY (remember Javitt and his temper set a precedent of posting official documents when he posted Georgia letter) ISNT THAT AVAILABLE THROUGH FDA REQUEST AND/OR FOIA??
WE NEED TO ALL DEMAND TO SEE THAT FULL LETTER, the truth can be found
https://www.fda.gov/regulatory-information/freedom-information/how-make-foia-request
**** DEMAND TO SEE FDA REJECTION LETTER***
IF Jonathan Javitt and NRX REFUSE TO POST THE FDA REJECTION LETTER FOR FULL TRANSPARENCY (remember Javitt and his temper set a precedent of posting official documents when he posted Georgia letter) ISNT THAT AVAILABLE THROUGH FDA REQUEST AND/OR FOIA??
WE NEED TO ALL DEMAND TO SEE THAT FULL LETTER, the truth can be found
https://www.fda.gov/regulatory-information/freedom-information/how-make-foia-request
MAYBE NOW YOU KNOW WHY I MADE....
SUCH A HUGE DEAL ABOUT THEIR REFUSAL TO TELL US ON WHAT EXACT DAY/TIME
THEY FOUND OUT THAT THE 9/17/2020’EUA WAS DENIED
LOOKS LIKE THEY MAY HAVE HAD THIS INFO FOR A WHILE ALSO
**** THIS SEEMS LIKE PROOF OF MISLEADING****
WANT PROOF OF MISLEADING INVESTORS..... THIS IS FROM PR ON 11/2.... “On May 31, 2021, NRx submitted a request for Emergency Use Authorization to the US Food and Drug Administration (FDA) for ZYESAMI for the treatment of patients suffering from Critical Covid-19 with respiratory failure. That request remains pending.”
EUA REQUEST REMAINS PENDING!!!
YET TODAY PR SAYS THEY REQUESTED A TYPE A MEETING LAST WEEK?? A TYPE A MEETING BECAUSE OF REJECTION OF EUA DUE TO ONLY 131 PATIENTS..... SO THEY REQUESTED THAT LAST WEEK BUT PR FROM 11/2 SAYS STILL PENDING???
**** THIS SEEMS LIKE PROOF OF MISLEADING****
WANT PROOF OF MISLEADING INVESTORS..... THIS IS FROM PR ON 11/2.... “On May 31, 2021, NRx submitted a request for Emergency Use Authorization to the US Food and Drug Administration (FDA) for ZYESAMI for the treatment of patients suffering from Critical Covid-19 with respiratory failure. That request remains pending.”
EUA REQUEST REMAINS PENDING!!!
YET TODAY PR SAYS THEY REQUESTED A TYPE A MEETING LAST WEEK?? A TYPE A MEETING BECAUSE OF REJECTION OF EUA DUE TO ONLY 131 PATIENTS..... SO THEY REQUESTED THAT LAST WEEK BUT PR FROM 11/2 SAYS STILL PENDING???
JAVITT LED US ALL TO BELIEVE
THE FDA OK’d the trial size all along.... SO THE MASTER OF GETTING DRUGS APPROVED BUILT AND RAN A TRIAL DESTINED TO FAIL BECAUSE IT WAS TOO SMALL FROM THE BEGINNING????
JAVITT LED US ALL TO BELIEVE
THE FDA OK’d the trial size all along.... SO THE MASTER OF GETTING DRUGS APPROVED BUILT AND RAN A TRIAL DESTINED TO FAIL BECAUSE IT WAS TOO SMALL FROM THE BEGINNING????
SOO NOW WE KNOW WHY....
I GUESS NOW WE KNOW WHY JAVITT HAS BEEN ENDLESSLY FEEDING US Regurgitated ”saftey” PR’s..... And we are supposed to believe the FDA didn’t tell him that ONLY 131 patient safety data was a problem... THATS JUST A COINCIDENCE I GUESS...
MORE EVIDENCE OF MATERIAL INFORMATION THAT WAS WITHHELD FROM US... IMO
SOO NOW WE KNOW WHY....
I GUESS NOW WE KNOW WHY JAVITT HAS BEEN ENDLESSLY FEEDING US Regurgitated ”saftey” PR’s..... And we are supposed to believe the FDA didn’t tell him that ONLY 131 patient safety data was a problem... THATS JUST A COINCIDENCE I GUESS...
MORE EVIDENCE OF MATERIAL INFORMATION THAT WAS WITHHELD FROM US... IMO
SO THEY REQUESTED THE TYPE A MEETING LAST WEEK??????
SO THEY NEW IT GOT REJECTED LAST WEEK??????
Last week, NRx requested a Type A meeting with FDA officials, a request endorsed by key study investigators, to discuss the development of ZYESAMI.
SO THEY REQUESTED THE TYPE A MEETING LAST WEEK??????
SO THEY NEW IT GOT REJECTED LAST WEEK??????
Last week, NRx requested a Type A meeting with FDA officials, a request endorsed by key study investigators, to discuss the development of ZYESAMI.
SO THEY REQUESTED THE TYPE A MEETING LAST WEEK??????
SO THEY NEW IT GOT REJECTED LAST WEEK??????
Last week, NRx requested a Type A meeting with FDA officials, a request endorsed by key study investigators, to discuss the development of ZYESAMI.
ONLY 131 patients??????
WHAT HAPPENED TO THE 600 JAVITT WAS TOUTING IN LAST PUMP SAFETY PR??
the FDA noted that so far, it has reviewed safety in only 131 randomized patients treated with ZYESAMI
Only 131 patients reviewed??????
ONLY 131 patients?????? WHAT HAPPENED TO THE 600 JAVITT WAS TOUTING IN LAST PUMP SAFETY PR??
the FDA noted that so far, it has reviewed safety in only 131 randomized patients treated with ZYESAMI
*** 1/150 ADR SPLIT.... *****
Screw job for shareholders
**** MUST READ ARTICLE BELOW****
Recognize the author?? Wow
https://investorsprism.com/death-by-fda/
*** ABSOLUTELY MUST READ ARTICLE!!!***
WOW!!!!
https://investorsprism.com/death-by-fda/
Recognize the AUTHOR????
WOULDNT THEY BE MANDATED TO....
Tell us if FDA is waiting for one of the other trial data??
There is ZERO chance in my opinion if that’s the case that it hasn’t been communicated to Javitt!!
****** GREAT POST... MAKES YA THINK****
Seriously... take a step back and do an HONEST assessment... DO YOU REALLY THINK, OR CAN WE REALLY BELIEVE that the FDA has taken OVER 5 MONTHS for EUA decision and NOT COMMUNICATED to Dr Javitt the REASON for the MASSIVE delay in what he himself , the CEO OF THIS PUBLICLY TRADED COMPANY told us ON THE RECORD to “expect” (prompt response, usually within 60 days, SUMMER 2021)
Remember this is the SAME CEO who on video made it a point to advise shareholders about how the FDA WAS BENDING RULES FOR HIM AND “EMAILING HIM BACK RESPONSES AT 02:00”
COME ON..... ITS NOT BELIEVABLE..ITS IMPOSSIBLE NOT TO FEEL AS IF WE ARE NOT BEING TOLD MATERIAL INFO
****** GREAT POST... MAKES YA THINK****
Seriously... take a step back and do an HONEST assessment... DO YOU REALLY THINK, OR CAN WE REALLY BELIEVE that the FDA has taken OVER 5 MONTHS for EUA decision and NOT COMMUNICATED to Dr Javitt the REASON for the MASSIVE delay in what he himself , the CEO OF THIS PUBLICLY TRADED COMPANY told us ON THE RECORD to “expect” (prompt response, usually within 60 days, SUMMER 2021)
Remember this is the SAME CEO who on video made it a point to advise shareholders about how the FDA WAS BENDING RULES FOR HIM AND “EMAILING HIM BACK RESPONSES AT 02:00”
COME ON..... ITS NOT BELIEVABLE..ITS IMPOSSIBLE NOT TO FEEL AS IF WE ARE NOT BEING TOLD MATERIAL INFO
HERES THE LINK....NRX APPLY IN EUROPE
NRX APPLYING FOR EUA IN EUROPE.... (RELIEF TERRITORY)
SO IF IM RIGHT THEY WITHHELD DATA SO RELIEF COULDNT DO ANYTHING AND THEN THEY (NRX) APPLY THERE??
https://www.google.com/amp/s/www.fool.com/amp/investing/2021/10/27/1-small-cap-stock-with-10x-potential/
PER MOTLEY FOOL NRX APPLYING FOR EUA IN EUROPE
READING THIS ONLINE.... HUH... EUROPE
****** MUST READ********
https://stocktwits.com/PerpetuallyDazed/message/395283809
Nation of Georgia saying NO EUA FOR ZYESAMI
THIS CONTRADICTS NRX JULY 27th PR AND WHAT DR J SAID RINGING BELL AT NASDAQ....