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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
CONTROL GROUPS NOT NEEDED BY FDA FOR APPROVAL !!!
ITS PERHAPS AN OUT DATED CONCEPT, AND NO LONGER REQUIRED.
https://www.zerohedge.com/covid-19/pfizer-just-got-full-fda-approval-its-covid-vaccine-theres-just-one-thing
THAT SHOULD MAKE APPROVAL OF RELIEF AND NEURO
MEDS VERY QUICK AND SIMPLE.
JB, My New Best Friend, have not seen you lately.......
How about sharing a few of your pearls of knowledge ?
EXCEPT FOR SOME BIG CROOKED CORRUPT CLOWNS A LOT OF GOOD
PEOPLE WORK FOR THE FDA. SOME KEEP CHANGING THE NARRATIVE
SO MUCH ITS LIKE THEY ARE FULL OF IT AND CONSTANTLY WRONG.
AND A SAFE EFFECTIVE THERAPEUTIC IS WAITING. IT IS MADE BY RELIEF THERAPEUTICS AND NEURO RX !!!!!!!!
https://citizenfreepress.com/breaking/fauci-cant-get-his-dates-right/
FDA IS NOT COMPLETELY CROOKED AND CORRUPT !!!!!!!!!!
CERTAINLY, IN A HORRIBLE PANDEMIC THE FDA WILL APPROVE RLFTF AND NRXP MEDICATIONS THAT ARE PROVEN SAFE AND EFFECTIVE AGAINST COVID AND ITS VARIANTS....
From Brady on You Know Who.......
FORMER FDA COMMISSIONER DR. HERBERT LEY’S FAMOUS QUOTE
After three long years of running the FDA in the late 1960s, former commissioner Herbert Ley resigned in utter frustration. The San Francisco Chronicle immediately interviewed him and asked why he quit, to which he replied with the following quote.
“The FDA protects the big drug companies, and is subsequently rewarded, and using the government’s police powers, they attack those who threaten the big drug companies. People think that the FDA is protecting them. It isn’t. What the FDA is doing and what the public thinks it is doing are as different as day and night.”
That was nearly 70 years ago, and things haven’t changed much since. In a Wall Street Journal article of 2006, reporter Anna Wilde-Mathews mirrored Dr. Ley’s disapproval of the FDA, and went a few steps further.
“Regulators usually don’t negotiate their budgets with the industries they oversee... For most of its history, the FDA was funded entirely by Congress. But in the early 1990s, companies unhappy with the pace of drug approvals agreed to pay the FDA millions of dollars in annual fees to help speed its performance. Because the industry and the agency renegotiate every five years over the size of fees - and what they can be used for - drug makers can have considerable input, into which programs receive funding.”
“Each time the arrangement has been renewed, the FDA has gained new funding. In return, industry has wrung concessions. In the 1997 deal, the review time for a standard application dropped from 12 months to 10 months. In 2002, the FDA agreed to a number of changes, including a new deadline for how fast the agency would respond to companies’ requests for meetings about their drug applications.”
Herein lies the problem. The U.S. government apparently sees no conflict of interest in the incestuous collaboration between the FDA and Big Pharma.
FDA’s Pfizer vaccine approval letter contains the dates of when several safety and efficacy studies (ie. Vaccine exposure during pregnancy and infant outcomes, occurrence of myocarditis + pericarditis, etc.) are set to be completed.
pic.twitter.com/zBjfiPMmEa
https://www.thegatewaypundit.com/2021/08/fda-approval-letter-pfizer-vaccine-several-key-future-dates-complete-studies-threw-garbage-approved-yesterday/
WAITING PATIENTLY FOR FDA APROVAL OF A SAFE EFFECTIVE THERAPEUTIC MEDICATION CALLED AVIPTADIL AND ZYESAMI............!!!!!!!
FDA: Rigorous testing means final vaccine approval in 2024!
Also the FDA: We work for Big Pharma so who are we kidding? It’s not like you can sue us! Let’s just approve it all right now! https://t.co/5lSnRVPkNw
https://www.thegatewaypundit.com/2021/08/fda-approval-letter-pfizer-vaccine-several-key-future-dates-complete-studies-threw-garbage-approved-yesterday/
WAAITING PATIENTLY FOR FDA APPROVAL OF A SAFE EFFECTIVE MED FROM RELIEF THERAPEUTICS AND NEURO RX
SAFETY,EFFICACY NOT NEEDED, PHASE 3 UNNECESSARY
https://www.thegatewaypundit.com/2021/08/fda-approval-letter-pfizer-vaccine-several-key-future-dates-complete-studies-threw-garbage-approved-yesterday/
with this news about BP, then RELIEF THERAPEUTICS AND NEURO RX
should be a cake walk for quick approval........!!!!!!!!!!!
GREAT NEWS...........!!!!!!!
SAFETY AND EFFICACY STUDIES MEAN NOTHING TO THE FDA ANY LONGER.
ALSO PHASE THREE STUDIES ARE UNNECESSARY FOR APPROVAL........
Yes, agreed, Aviptadil and or Zyesami might have saved even more lives than that, IMHO.
Clearly starting to look like something is upside down in the gov.
No approval yet for a perfectly safe effective therapeutic, yet full approval now for a so called "vaccine" thats not a vaccine which has been proven deathly dangerous and has proven to show massive numbers having serious adverse events.
Yet, NO liability AT ALL for any of the companies involved......
NOTHING LIKE ANYTHING IN MODERN HISTORY.
WHY APPROVALS FOR RLFTF AND NRXP ARE NEEDED RIGHT NOW
Landmark Study Proves COVID Vaccines Much Less Effective Than Advertised
https://www.zerohedge.com/markets/landmark-study-proves-covid-vaccines-much-less-effective-advertised
"Herd Immunity Is Not A Possibility": Dr. Malone Vindicated After Oxford Prof Warns Over New Variants
https://www.zerohedge.com/covid-19/herd-immunity-not-possibility-dr-malone-vindicated-after-oxford-prof-warns-over-new
mRNA Vaccine Inventor Shares Viral Thread Showing COVID Surge In Most-Vaxxed Countries
https://www.zerohedge.com/covid-19/worrying-me-quite-bit-mrna-vaccine-inventor-shares-viral-thread-showing-covid-surge-most
WHO JUST BOUGHT OVER 250,000 SHARES AND MOVED UP PRICES !!!!!
another ALL CAPS guy.......VF incognito ??
Changes, cc, SF, ......thanks, all very excellent thoughts,
and, there is NO hollow CRYPTIC FUD in your information
good points. Thanks pegs1
FROM ILKAS over on the you know who board..........
3 hours ago
Hi All,
First, a Thank You to @Pierre and @Lt Francis. Pierre's post made me go and check out the Form 10Q (I used FINTEL.IO for that) and I originally posted the extract about Liquidity earlier.
I have now read the entire Form 10Q of NRx and I advise everyone to read it for themselves as there a lot of mentions of Relief Therapeutics. I didn't know, for example, that Relief has also given a 500K loan to NRx in addition to the nearly $11 million that they have already paid in expenses.
I side with Lt Francis on this : I read many form 10Q for my other investments and this is the first time I have come across one that has question marks everywhere in its consolidated statement. Question marks in financials ring alarm bells for me, especially when they also include the 2020 financials, and that, to me, informs NRx's desire to re-draft the percentages more in NRx favour.
But going back to Relief Therapeutics : after you read that Form 10Q, you absolutely have to agree with Lt Francis - the wording will not stand a chance with Relief Therapeutics' legal team.
It also makes me thankful that I am with Relief Therapeutics.
Thanks again to @Pierre and @Lt Francis.
Ilka
VF, YOUR STATEMENT IS FALSE, WRONG, AND INCORRECT STATEMENT ABOUT RLFTF. YOU CONTINUE TO MAKE FALSE CONTENT ERRORS
quote RAM IS A DISASTER HAS DONE ABSOLUTELY NOTHING TO SUPPORT SHAREHOLDERS unquote
THAT IS ANOTHER BIG WHOPPER THAT I THINK COULD BE LIBELOUS, AND OR, EVEN HAVE YOU CONSIDERED FOR BEING BANNED FROM THIS BOARD.
PROOF OF THE AMAZING PROGRESS AND ACCOMPLISHMENTS ARE CLEAR.......... IMPOSSIBLE TO HAVE AN OUNCE OF TRUTH IN YOUR STMT
RLFTF AND NRXP NEED SOME FDA APPROVAL FOR SAFE EFFECTIVE MEDS TO HELP THE WORLD IN A PANDEMIC.
https://www.relieftherapeutics.com/apr < see pipeline
https://www.relieftherapeutics.com/pipeline
https://www.relieftherapeutics.com/partnering
https://www.nrxpharma.com/pipeline/
AMAZING, AMAZING GOOD ACCOMPLISHMENTS WITH SAFE EFFECTIVE THERAPEUTICS. WAITING ON FDA APPROVALS TO SAVE THE WORLD.