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Impossible to disagree with you on this point.
A "no response" by NRXP to a lawsuit like this is deafening quiet and reflects very poorly on NRXP. Trust, honor, reputation, and reliability are in question now for those at the top of this business.
thanks PennyWorld, A very good summary.
DISHONEST AND UNTRUSTWORTHY !!!
the non response to the lawsuit speaks volumes.
BOARD OF DIRECTORS AT NRXP SHOULD OUT THOSE IN CHARGE OF THIS FRAUD UNLESS THEY ARE ALSO PART OF THIS FRAUD
Companies or People that TRUST/HONOR the agreements/words/contracts of NRXP and would be willing to work with a company like NRXP might be very limited going forward.
One would need to ask why any contract or agreement signed today would have any greater meaning than what was agreed to yesterday to NRXP.
Going forward why would NRXP honor anything agreed to with anyone or any business, based on what is their past obligations being pretty much completely ignored. ???
It appears very clear right now, that those that had signed contracts and or agreements with RLFTF had NO intention of honoring any of them, and that was, no doubt, even before the involvement of what was eventually big rock/ and then NRXP .
Sad to say, the moral fiber of some is absolutely sickening.
Might explain the attempted vaccine tie in with Israel.
Hope they makes lots on the vaccines so they will be able to pay RLFTF lots of damage awards and penalties.
Vermont — 76% of September Covid deaths were Fully Vaccinated…
https://citizenfreepress.com/breaking/vermont-76-of-september-covid-deaths-were-fully-vaccinated/
THE MOST HIGHLY VAXXED STATE IN THE NATION AND COVID IS SURGING. GO FIGURE. !!!
MAYBE THE FDA NEEDS TO TRIPLE AND QUADRUPLE VAX BY MANDATE IN VERMONT................
VAXX THE POOR FOLKS TO DEATH, AND THE CASE COUNT WILL DROP AFTER ALL DIE OF COVID, AND MAYBE, JUST MAYBE SOMEONE IN THE GOVERNMENT WILL
ACTUALLY ACQUIRE SOME LOGIC AND SOME HONEST SCIENCE.
A LOT BETTER TO APPROVE AVIPTADIL AND ZYESAMI IF THE FDA IS ACTUALLY FOLLOWING THE SCIENCE....SO FAR ITS A BAD NIGHTMARE WITH THE VAX.
Now a rational logical person might ask why does the FDA approve BP shots that are being mandated to be taken in some areas and companies, when it is known to cause serious side effects and deaths, it is ineffective longer term, charts and evidence indicate it increases the viral load count spreading the virus further, it may degrade the natural immune system longer term, the long term side effects are unknown, and it may require semiannual/annual injections for antibody dependent enhancement, plus the BP companies have proven to have millions of doses of product made defectively.
And these BP companies are exempted from any and all liability, death or serious injury.
At best it has known problems with massive numbers of serious side effects and deaths documented on rumble.com and bitchute.com, plus being listed on openvaers, the gov vaccine adverse event reporting system, not to mention other documentation.
YET, the FDA has still has not approved a perfectly safe very effective treatment option in AVIPTADIL and ZYESAMI.
Time to ask WHY !!!!! Call your senators and congressmen. Demand approval for RLFTF and NRXP.
Evidently still problems with Merkmectin, and hot on its heels Fizermectin, which is ANOTHER Protease Inhibitor, like Ivermectin, which is used by 1.3 BILLION people in India.
APPROVAL OF AVIPTADIL/ZYESAMI IS NEEDED QUICKLY....FDA IS STARTING TO LOOK LIKE ITS BEEN ASLEEP UP TO THIS POINT .
https://www.zerohedge.com/news/2021-10-01/mercks-therapeutics-waiting-wings-faucis-removal
Merck's Molnupiravir News
This is a drug with known mutagenicity. Ironically Merck’s inclusion criteria in ALL their clinical trials required participants to not have sex. This includes the clinical trial for prophylaxis. Perhaps they want to avoid the potential of birth defects so this drug is clearly not going to appeal to anyone building a family or engaging in intercourse.
From HIV/AIDS to COVID-19: Vaccines Fail to Impress
The government has a very flawed strategy that the vaccines will fix all.
Therapy Ignorance Costing American Lives and Trillions of Dollars
Changes IV, thanks. Very Interesting.
Penny, you are right. Time to shut up or put up some facts. Time for some evidence and proof or one can only conclude.............. that type of statement is 1) little more than mindless negative speculation intended to push prices lower for shorts, or 2) an outrageous lie, or 3) it is based on inside information and ILLEGALLY made for the benefit of shorts.
SENATOR ON NATURAL IMMUNITY PROTECTS AGAINST DELTA BETTER THAN
THE JAB.
https://www.zerohedge.com/covid-19/sen-johnson-health-agencies-are-ignoring-natural-immunity
https://www.theepochtimes.com/previous-covid-19-infection-protects-against-delta-variant-better-than-pfizer-vaccine-study_3967844.html
AND THEY WANT TO STAB THE CHILDREN
BUT HAVE NOT APPROVED SAFE MEDS LIKE
AVIPTADIL AND ZYESAMI
https://www.theblaze.com/op-ed/horowitz-cdc-endorsed-use-of-ivermectin-for-afghan-refugees
CDC endorsed use of ivermectin … for Afghan refugees!
Op-ed
WHY NOT AVIPTADIL AND OR ZYESAMI IN THE USA ???????
ONLY ENDLESS STABS AND JABS APPROVED BY THE FDA :?????
TOKYO MEDICAL ASSN RECOMMENDS THERAPEAUTICS
https://needtoknow.news/2021/09/tokyo-medical-association-recommends-ivermectin-for-covid-while-the-ama-in-the-us-discourages-its-use/?print=print
WHERE IS THE FDA ON THERAPEAUTICS........???
SAFE EFFECTIVE ONES LIKE AVIPTADIL AND ZYESAMI ?????
1.3 Billion in India Using Therapeautics With Success .........
https://www.thedesertreview.com/news/national/ivermectin-obliterates-97-percent-of-delhi-cases/article_6a3be6b2-c31f-11eb-836d-2722d2325a08.html
Why not approval of Aviptadil and Zyesami.......
Being used in India
Where is the fda ?????????
BRAZIL DEFIES "MANDATE" by useless United Nations
https://www.zerohedge.com/geopolitical/de-blasio-whines-brazils-bolsonaro-brazenly-defies-uns-vaccine-mandate
TIME FOR SAFE THERAPEUTICS.....like aviptadil and zyesami
Is the FDA sleeping or taking its orders from BP ????
doctors bombshell testimony against the jabs at the FDA
https://citizenfreepress.com/breaking/bombshell-testimony-from-doctors-at-fda-vaccine-booster-hearing/
FULL APPROVAL IS NEEDED FOR RLFTF AND NEURO LIVE SAVING PRODUCTS.
EVEN A CHILD CAN SEE THE PROBLEM AND THE NEED FOR AN ALTERNATE TREATMENT THAT ACTUALLY WORKS AND SAVES LIVES AND GET PEOPLE BACK TO WORK !!!!!!!!!!!!! . ....BUT THEY WANT TO JAB THE CHILDREN AND HAVE ENDLESS JABS UNTIL NATURAL IMMUNITY IS NOT WORKING.
AVIPTADIL AND ZYESAMI ARE SAFE AND EFFECTIVE.
BERMUDA, VERMONT, ISRAEL, SINGAPORE...same problem... JAB rates go up and covid rates go up
https://citizenfreepress.com/breaking/the-vaccine-isnt-working-in-bermuda-check-the-chart/
THE WORLD NEEDS AVIPTADIL AND ZYESAMI.
WHERE IS THE FDA ??????
NEW COVID VARIANT....a mutation termed E484K located in the spike protein of the virus, gives it an "increased resistance" to antibodies generated by the vaccine......
https://www.the-sun.com/news/3707195/new-covid-variant-kentucky-nursing-home-mutations-virus-antibodies/
and the fda sits around passing paper work back and forth, scratching their butts, while people die and can not go to work, businesses fail, and the economy tanks.
ALL THE WHILE THE FDA HAS....... A SAFE EFFECTIVE THERAPEUTIC FROM RELIEF T. AND NEURO, WHICH ARE PATIENTLY WAITING TO SOLVE THE PROBLEMS ..........
Countries are realizing the problem....and would use safe therapeutics like AVIPTADIL and or ZYESAMI
https://citizenfreepress.com/breaking/romania-shuts-down-government-vaccine-centers/
https://citizenfreepress.com/breaking/president-of-croatia-we-will-not-be-vaccinated-anymore/
WHATS THE HOLDUP AT THE FDA ?????
The higher the number of JABS the greater the Covid Rates, so its clear there is not protection with endless JABS, and its clear its not safe with massive numbers of side effects ( openvaers ) , and someone is paying for it, so its not free.
Ditto same problems with high covid rates in Singapore, Vermont, and Bermuda......
https://citizenfreepress.com/breaking/israel-updates-health-pass-4th-vaccine-will-be-required-of-all-citizens/
And Aviptadil and Zyesami are truely safe and effective and patiently waiting for FDA approval.
The Vaccinated are the superspreaders… Data shows ‘high-viral’ load…
https://citizenfreepress.com/breaking/dear-cnn-the-vaccinated-are-the-superspreaders-with-251x-times-the-viral-load/
RLFTF / NRXP needs approval
Is someone at the FDA starting to get scientific ??????
Did the bell finally ring over at the FDA ????
https://www.cnbc.com/2021/09/15/covid-booster-shots-fda-staff-declines-to-take-stance-on-pfizers-third-doses-citing-lack-of-ve
RLFTF / NRXP need approval....................
Singapore and Israel cases keep surging and they keep
on giving kill shots and the rates keep climbing....go figure.
relief thera and neuro need approval quickly
Further evidence...for FDA approval of safe and effective therapeutics like Aviptadil / zyesami...........
..............its pretty simple.
https://www.npr.org/sections/goatsandsoda/2021/08/20/1029628471/highly-vaccinated-israel-is-seeing-a-dramatic-surge-in-new-covid-cases-heres-why
The FDA needs to approve safe and effective therapeutics
like Aviptadil / zyesami...........
heres another reason why
https://sydneynewstoday.com/singapore-reports-the-largest-surge-in-covid-cases-in-a-year-despite-81-vaccination-rate-singapore/347934/
From previous post by Soli - in part.
(GEM) Global Emerging Markets owns 1,165,000,000 shares and yes that’s (billion). I don’t see them running for the door but you are trying to tell me that you are smarter and wiser than this 3.5 billion dollar company with all their well payed advisers and lawyers ? .......................... They’re staying for a reason (to make money not lose money)and it surely isn’t ....FUD reasons for getting out now!
In that case, will the Red Cross become an ally of RLFTF/NRXP
and lobby for FDA approval ?
ADDITIONAL REASONS THE FDA NEEDS TO APPROVE RLFTF/NRXP
THE LIST IS ENDLESS AT THIS POINT, but here are some new reasons
https://citizenfreepress.com/breaking/red-cross-vaccine-alert-you-gotta-hear-this/
https://citizenfreepress.com/breaking/we-have-seen-a-25-increase-in-deaths-of-people-who-are-double-vaccinated/
https://citizenfreepress.com/breaking/vaccinated-israel-records-10000-covid-cases-in-one-day/
https://www.rt.com/news/533666-moderna-vaccine-japan-supply-withdrawn/
https://www.cnbc.com/2021/09/01/who-says-it-is-monitoring-a-new-covid-variant-called-mu.html
Penny, without exact dates on the patents, and without
a lot of patent knowledge, I can only agree that the words
may create less than definite meaning. On the whole the
post answers some questions, if its all true and verified at some point. But RLFTF/NRXP are still like a moving train switching boxcars between stops.
Still believe that Relief And Neuro need to work together
and resolve any open issues to be successful. They definitely need each other, IMHO, and I am starting to feel or sense Neuro may need Relief a bit more now than initially.
Interesting Post that nots Cryptic on you know who>>>>>>>
Mav 3 hours ago
I got a reply from Relief about the Data They got the Trial report but did not get the underlying data and interestingly also about the patent. The inhaler patent for Aviptadil ( not a formulation)belongs to Relief through the acqisition of . So anyone going to inhaler need to licence it. Now you can see why Dr J is fighting
1) Relief said in a previous PR that they got the data from phase 2/3 of RLF100 from Neurorx but todays PR has a disclaimer that the data was not released to Relief. What is the truth?
Relief has not received the underlying data to the clinical study report which NRx provided to Relief, as mentioned in the June 2, 2021 press release. Relief is continuing to work with NRx to obtain the underlying data to the phase 2b/3 study of IV RLF-100.
2) How about the patent that Relief acquired through Advita? Is this patent based on a stable formulation or does it have similar stability issue like RLF100 that Neurorx mentioned?
With the acquisition, Relief has gained additional pending intellectual property rights that may cover RLF-100 inhaled formulation specifications and the potential application of inhaled aviptadil for the treatment of lung diseases such as acute respiratory distress syndrome (ARDS), pulmonary sarcoidosis and checkpoint inhibitor-induced pneumonitis (CIP).
Safe Effective Therapeutics by the FDA are needed now..
like the ones from IPIX, CYDY,and Ivermectin, and
Aviptadil, Zyesami.
https://www.zerohedge.com/covid-19/ends-debate-israeli-study-shows-natural-immunity-13x-more-effective-vaccines-stopping
Safe Effective Therapeutics by the FDA are needed now..
like the ones fronm CYDY,and Ivermectin, and
Aviptadil, Zyesami.
https://www.zerohedge.com/covid-19/ends-debate-israeli-study-shows-natural-immunity-13x-more-effective-vaccines-stopping
WHY THE FDA NEEDS TO APPROVE AVIPTADIL AND ZYESAMI.
https://www.zerohedge.com/covid-19/ends-debate-israeli-study-shows-natural-immunity-13x-more-effective-vaccines-stopping
Dr. Anthony Fauci and the rest of President Biden's COVID advisors have been proven wrong about "the science" of COVID vaccines yet again. After telling Americans that vaccines offer better protection than natural infection, a new study out of Israel suggests the opposite is true: natural infection offers a much better shield against the delta variant than vaccines.
he study was described by Bloomberg as "the largest real-world analysis comparing natural immunity - gained from an earlier infection - to the protection provided by one of the most potent vaccines currently in use." A few days ago, we noted how remarkable it was that the mainstream press was finally giving voice to scientists to criticize President Biden's push to start doling out booster jabs. Well, this study further questions the credibility of relying on vaccines, given that the study showed that the vaccinated were ultimately 13x as likely to be infected as those who were infected previously, and 27x more likely to be symptomatic.
THE FDA AND THOSE IN CHARGE NEED TO FOLLOW THE SCIENCE
And After Five Vaccines and a few more years the data many turn out the same way, or worse, with the EXPERIMENTAL JABS still having the same unfortunate results.
https://www.openvaers.com/
MASSIVE SIDE EFFECTS, AND DEATHS.
It Is Easier To Fool People, than it is To Convince Them That They Have Been Fooled. - Mark Twain.
FDA NEEDS TO FOLLOW THE SCIENCE EVIDENTLY
Ultra-Vaxxed Israel’s Crisis Is a Dire Warning to America
https://www.thedailybeast.com/ultra-vaccinated-israels-debacle-is-a-dire-warning-to-america
“I don’t want to frighten you,” Israel’s COVID czar Dr. Salman Zarka told parliament this week. “But… unfortunately, the numbers don’t lie.”
The massive surge of COVID-19 infections in Israel, one of the most vaccinated countries on earth, is pointing to a complicated path ahead for America.
In June, there were several days with zero new COVID infections in Israel. The country launched its national vaccination campaign in December last year and has one of the highest vaccination rates in the world, with 80 percent of citizens above the age of 12 fully inoculated. COVID, most Israelis thought, had been defeated. All restrictions were lifted and Israelis went back to crowded partying and praying in mask-free venues.
Fast forward two months later: Israel reported 9,831 new diagnosed cases on Tuesday, a hairbreadth away from the worst daily figure ever recorded in the country—10,000—at the peak of the third wave. More than 350 people have died of the disease in the first three weeks of August. In a Sunday press conference, the directors of seven public hospitals announced that they could no longer admit any coronavirus patients. With 670 COVID-19 patients requiring critical care, their wards are overflowing and staff are at breaking point.
“I don’t want to frighten you,” coronavirus czar Dr. Salman Zarka told the Israeli parliament this week. “But this is the data. Unfortunately, the numbers don’t lie.”
What happened?
The complex and sobering truth is that no single policy or event brought Israel to this crisis, Hagai Levine, a Hebrew University of Jerusalem professor of epidemiology, told The Daily Beast. A deadly set of circumstances came together to put Israel on the precipice, most of which can be summed up as: “We are still in the midst of a pandemic, and there is no silver bullet.”
“All the vectors have influenced the rise in morbidity,” he said.
But the principal causes of Israel’s current predicament are the dominance of the extremely infectious Delta variant, which was carried into the country by Israelis returning from foreign vacations during the weeks in which Israel dropped all restrictive measures—along with the worrisome decrease in vaccine efficacy after about six months.
Israel vaccinated its population almost exclusively with the Pfizer/BioNTech vaccine, which received full FDA approval on Monday and remains the gold standard for the prevention of severe illness due to the coronavirus.
It is not an Israeli problem. It is everywhere.
But in early July, with citizens over the age of 60 almost completely vaccinated, Israeli scientists began observing a worrisome rise in infections—if not in severe illness and death—among the double-vaccinated.
Fully vaccinated people with weakened immune systems appeared particularly vulnerable to the aggressive Delta variant.
By mid-July, Sheba Hospital Professor Galia Rahav began to experiment with booster shots for oncology patients, transplant patients, and the hospital’s own staff. A group of 70 elderly vaccinated Israelis with transplanted kidneys were the first to receive a third dose.
The success of Rahav’s trials in boosting immunity at about the sixth-month mark contributed to the Centers for Disease Control decision, announced last week, to begin offering booster shots to Americans in September.
In order to keep severe illness and the number of COVID deaths down, and avoiding a fourth national lockdown, Israel has embarked on an aggressive effort to provide all adults with boosters in a matter of weeks.
SO....THE MOST VACCINATED COUNTRY ON THE PLANET IS HAVING A HORRIBLE OUTBREAK OF COVID
WHATS NEXT.....A FOURTH AND A FIFTH JAB..EVERY SIX MONTHS???
A SAFE EFFECTIVE MED IS PATIENTLY WAITING IN RLFTF / NRXP