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Lawsuits are Turning into Get in Line and take a number..
Now Another.... Robbins Geller Rudman & Dowd
https://www.bloomberg.com/press-releases/2022-01-20/alert-nrx-pharmaceuticals-inc-investors-with-substantial-losses-have-opportunity-to-lead-class-action-lawsuit-nrxp-nrxpw
https://www.lawyer-monthly.com/2022/01/alert-nrx-pharmaceuticals-inc-investors-with-substantial-losses-have-opportunity-to-lead-class-action-lawsuit-nrxp-nrxpw/
Gotta wonder if DENIAL is the main defense here also.
So far not a word from the company.
https://www.businesswire.com/news/home/20220119006016/en/SHAREHOLDER-ACTION-ALERT-The-Schall-Law-Firm-Encourages-Investors-in-NRx-Pharmaceuticals-Inc.-with-Losses-of-100000-to-Contact-the-Firm
And Another. Guess that provides additional lawyers for NRX with plenty of hours to bill NRX, not to mention the possible costs of fines, judgements, and or penalties. When it rains it pours.
What assets does NRX legally own that might be sold to raise cash ??
Any ideas ?
Looking pretty grim today for NRX. New lows again.
Short of a quick and compete settlement with RLF, and quick approval
by the FDA for AVIPTADIL / ZYESAMI, it looks like NRX is in for
some heavy stormy hurricane weather.
Perhaps Brilife can manage a big win to NRX and a miraculous come back for NRX stock price. It continues down, even at this level.
Those days of double digit prices sure look long gone now.
Neuro looks to be in trouble and I think they know it.
IMHO, Neuro clearly needs to settle with RLF, but pride and or greed may be blocking that path. If Neuro stock keeps dropping, on things like old news that gets rehashed as current, the cash burn rate may not be sustainable without a new public funding source and some of the insiders may have few takers to unload their shares upon in several months. It will be interesting to see the neuro financials for this most recent reporting quarter. Quick FDA approval for neuro is critical.
Wow, Bill B, it would be great to see a link for that alleged report by some lab tech that "debunked" the UCI study, especially with this section below in the link provided, thanks to LJ Bodhi.
NeuroRx Inc., Relief Therapeutics’ U.S. partner, with operations in Radnor, Pa., is leading the Aviptadil clinical trial. In a previous trial of vasoactive intestinal polypeptide for ARDS in eight patients with sepsis, seven people on mechanical ventilation showed substantial improvement and six ultimately left the hospital, said Dr. Jonathan Javitt, CEO of NeuroRx.
https://www.ucihealth.org/news/2020/05/aviptadil-covid-clinical-trial
BY Bogo 8 hours ago --- Great Post from the Y@h@@ blog
I have not had time to do DD to seek out the alleged NRXP “lawsuit.” Normally, counterclaims are asserted in the Answer to the original Complaint by RLFTF. So, if this is truly a separate document and Action, I am “surprised” to say the least! I find most interesting, if it this is true, that NRXP is seeking “recission of the Collaboration Agreement (CA).”
Having not read the original Complaint, I am assuming Relief pled some Equitable Claims and Relief.
I posted some weeks ago, my feelings re: the CA. Two points of interest: The Agreement was executory in nature, and secondly, provides no terms for breach, nor defined “material” in terms of a breach.
Clearly, an equitable claim against NRXP is “unjust enrichment” because, even according to NRXP in the CA and I believe in post writing(s) by Dr. Javitt, Relief paid millions of dollars toward the development up to the point Relief alleged there was no accounting being provided. Secondly and as to being unjustly enriched, NRXP had full access to the IP and continued to use it and have access to it, throughout the development of “a formulation,” that Dr. Javitt now claims is proprietary to NRXP. Keenly, in my opinion, NRXP has been unjustly enriched.
The CA, as I expressed previously, is subject to an NDA which nobody knows the terms of. That NDA is certainly material to what occurs.
Lastly, the CA defines “Product” as: “[M]eans Aviptadil (also known as RLF-100 or a drug name mutually agreed upon by the Parties and approved by the FDA) for any route of administration, including intravenous and inhaled use, as long as Relief funds the research and development costs for developing such use. Relief may use a different brand name in the Relief Territory (as defined below).” This definition is pretty “all encompassing” of anything that gets created, and really sets the entire dispute. In my opinion, Dr. Javitt certainly knew this and it will be up to Relief to show and prove that they were within their right/inability to have continued funding development because of lack of accounting by NRXP. In my opinion, if it is true that NRXP did not provide the accounting, this was a purposeful way out of the CA.
Dr. Javitt was OBLIGATED to not “exceed 30% of the budget contemplated by Relief’s Board of Directors n March 22, 2020….” Parag. 4.4
Further, “[t]he Parties recognize that the March 22, 2020 budget did not contemplate the costs that have been incurred for drug formulation, manufacture, CMC, stability, etc., which costs have been funded by Relief.” Parag. 4.6
Certainly, any development(s) of the product, presumptively including budget overruns, funding from outside sources, accounting issues was/were supposed to be reported by both parties, each to the other, “regularly.” Parag. 5.6
And, NRXP “shall, as promptly as reasonably practice, provide accurate and complete vendor and other service providers invoices, along with supporting documentation and any other information reasonably requested by Relief, and Relief shall pay such invoices in accordance with the approved budget for the Project and the terms of the applicable vendor or service provider contract.” Parag. 6.1. Interestingly, “project” is not a “defined” term in the CA.
NRXP was obligated to provide the invoices and “in accordance with the APPROVED budget.”
NRXP cannot have use of the IP, develop their own product, acknowledge payment of millions of dollars toward development of the product, and then just run away from the CA, calling a product developed their own. THAT MY FRIENDS IS CALLED “UNJUST ENRICHMENT.”
Seeing it is Football playoffs are abound here in the U.S.A, the ball is coming back and a new down is going to be had with lossed yards.
Still Long and strong.
Bullish
https://www.marketscreener.com/quote/stock/RELIEF-THERAPEUTICS-HOLDI-5527488/news/Relief-Comments-on-Lawsuit-Filed-Against-It-by-NeuroRx-37523685/
My sense is that RLF is honestly working to a noble solution for a dangerous virus and to solve many other serious respiratory problems. Wish that I felt that way about neuro.
These out of the ordinary events, denial of the CA, no FDA approval, lack of cooperation with RLF, all the law firms, suits, countersuit, et al, might sadly reflect in the personality of why jj has been at so many different companies.
Wonder if jj is going to say he doesnt need to repay RLF the money loaned to neuro, and it seems jj does not honor at all his signed agreement.
Only 30 days for relief to respond ?? Or judgement to Neuro ??
And delays by neuro are ok....?? Something doesnt add up.
Lawyer nonsense ??
And thanks to all for sharing.
Bill, greatly appreciate a link to the counter suit. TIA.
https://www.americanthinker.com/blog/2022/01/new_study_of_pfizers_covid_vaccine_has_some_disturbing_findings.html
Safe, effective, and NOT FREE, is Aviptadil....
https://www.wnd.com/2022/01/pfizer-ceo-2-shots-offer-limited-protection/
https://thelibertyloft.com/2022/01/10/large-british-study-finds-risk-of-myocarditis-doubles-after-each-mrna-jab/
https://thecovidworld.com/
A few other reasons why a safe effective product by RLF in needed.
https://citizenfreepress.com/column-2/bill-gates-admits-mrna-vaccines-arent-working/
Wow, and I was hammered countless times that its safe, effective, and free.
THE world needs AVIPTADIL and its variations like Zyesami.
https://www.bloomberg.com/opinion/articles/2021-05-19/changes-in-menstruation-after-covid-19-vaccines-should-be-studied
Why we need a safe effective med like AVIPTADIL..............
https://citizenfreepress.com/breaking/dear-australia-vaccines-dont-work-check-the-chart/
https://www.thegatewaypundit.com/2022/01/massive-145-country-study-shows-sharp-increase-transmission-death-introduction-covid-vaccines/
https://www.brighteon.com/a7668819-a224-4cbe-9b19-06e743ea59d7
https://www.bitchute.com/search/?query=vaccine%20side%20effects&kind=video
https://www.bitchute.com/search/?query=openvaers&kind=video
https://openvaers.com/
Too many web sites and very very well qualified medical professionals to list on here.....do your own research......
Countless articles, too many to ignore.
https://rumble.com/search/video?q=vaccine%20side%20effects
https://rumble.com/search/video?q=vaccine%20related%20deaths
https://rumble.com/vqby92-were-approaching-a-million-vaccine-injuries-in-the-u.s..html
https://rumble.com/vs5nb1-the-government-now-admits-to-severe-vaccine-side-effects.html
https://rumble.com/vhsm3h-nobel-laureate-luc-montagnier-warns-covid-vaccine-may-lead-to-neurodegenera.html
https://rumble.com/vrrp9d-australian-government-at-least-79000-covid-19-vaccine-side-effects.html
https://rumble.com/vrj4gh-dr.-peter-mccullough-informed-consent-with-covid-jab-potential-side-effects.html
https://rumble.com/vrqhqi-dr.-robert-malone-on-joe-rogan-vaccine-side-effects-and-natural-immunity.html
https://rumble.com/vn5g77-dr.-ryan-cole-on-the-vaccine-and-potential-for-unwanted-even-dangerous-reac.html
https://rumble.com/vqdap8-japan-nhk-world-tv-health-ministry-warns-of-vaccines-side-effects.html
This is why a safe effective med like AVIPTADIL needs desperately to be approved quickly.
There is Plenty of evidence of serious side effects and deaths including the governments own data base, all reported in places like bitchute and rumble including the gov data base VAERS and OPENVAERS.
solil, Thank you, and I hope it all works VERY out well for ALL of us, but unfortunately I have lost much confidence in neuro because of what appears to me to be clearly a lack of cooperation with RLF. Even the neuro press releases seem to usually fail to mention that RLF is a partner, not to mention the previous failures in the submissions to the FDA.
Other concerns seems to be RLF is the giver and NRXP is the taker in this relationship so far.
I felt forced to divest my modest neuro position, esp when a new small company like neuro has become entangled in so many lawsuits and investigations, right out of the starting gate.
An excellent resolution and a close working relationship between the two companies, I feel, is very necessary, but my concern is the positions seem to be hardening and neuro is moving even further apart.
Seems lotsa holders bailing out on Neuro today......
Could it be what company is the most believable
related to violations of the extensive signed CA ???
Seems to me like neuro is has some real xplainin to do,
or some serious amends to make.
Appreciate any enlightening information on the subject.
Great Work PW, thank you again !!
To me, this looks like jj is still in complete denial about the CA.
Dated Jan 4, by atty.
https://iapps.courts.state.ny.us/fbem/DocumentDisplayServlet?documentId=LL5fqX/Y9WpMaUBPkXLIHQ==&system=prod
Joey 5 hours ago......on the y@h@@ threads from Joey
Dr. Javitt...I'm so confused ??. Please answer the following questions or feel free to call me when you can. I posted these publicly simply so your investors can get a clearer understanding of these issues. I WANT to believe in Zyesami, however I'm having tremendous trouble reconciling the following concerns with your position on everything.
$NRXP $RLFTF
1. I notice you've said frequently that SUNY Brook owns the patent and ODD for aviptadil, yet the FDA officially says different:
https://www.accessdata.fda.gov/scripts/opdlisting/oopd/detailedIndex.cfm?cfgridkey=180903
As does the EMA: https://www.orpha.net/consor/cgi-bin/Drugs_Search.php?lng=EN&data_id=57809&search=Drugs_Search_Simple&data_type=Status&Typ=Sub
2. Even if the Zyesami patents are successful, Bevec was a direct consultant for you, and he is under RLFTF now. Also, the announcement came after exposure to Bevec/AdVita IP that would not have been otherwise known. So, this is knowledge in addition to just NRXP's ideas plus SUNY Brook/Said. Therefore, it would seem that his IP was used in the process as well as the fact that a new formulation was either:
A) withheld at the time of signing the CA, or
B) created after signing the CA.
In either case, even if it is approved, wouldn't it be necessarily cross-licensed according to the CA? Wouldn't that alone nullify any monetary value from being exclusively NRXP and/or SUNY Brook even? In other words, even if the Zyesami patents are approved, the money gained must be under CA Agreement plus cross-licensed to RLFTF. If not, then Bevec (either alone or as an agent/extension of RLFTF via AdVita subsidiary) is entitled to claim rights. Am I Correct on this understanding?
3. By Q3 of this year, it must be proven that you have made significant grounds with the development of aviptadil and it's subsequent approval in order to be granted "exclusive" (well, proxy-exclusive, I'm sure you know what I mean by the terminology SUNY used) continuance to work on it for further diseases, correct?
4. If #3 is true, and RLFTF already holds ODD for sarcoidosis for both the FDA and the EMA, and they are breaking significant grounds already with CIP, and berryliosis, as well as other filings this year for more diseases, are you concerned that even with SUNY's blessings and Zyesami patent approval,
you still would not be able to produce Zyesami without having to adhere to Relief's market exclusivity granted under the ODD terms?
In other words, and from my understanding, if you marketed Zyesami in the EU (outside of non-EU adherence territories like Georgia) or in The US, you would be breaking the market exclusivity provisions inherent in ODD Status designation. Is this correct?
Any clarification is greatly appreciated, and thanks in advance for your response(s)! Additionally, I just replied to your last email to ensure you have my current contact information. Good luck to NRXP this year and Happy New Year!
Excellent PW, thank you for sharing.
Provisional utility applications
• A provisional application for patent (provisional application) is a U.S.
national application filed in the USPTO for utility and plant inventions.
– Design inventions are not eligible for filing provisional applications.
• Provides a low-cost way to establish an early effective filing date (priority
date) with fewer formalities.
• A provisional application does NOT issue as a patent, but only a later-filed
nonprovisional application may issue as a patent and benefit from the provisional
application filing date.
• Provides a 12-month window to file corresponding utility nonprovisional patent
application in order to benefit from the priority date of the provisional application.
• Provisional application is abandoned automatically at 12 months and is not examined.
https://www.uspto.gov/sites/default/files/documents/Basics%20of%20a%20Provisional%20Application.pdf
swordman, Actually, Penny reflects as my general understanding of situation, and so, for "swordman" it would be kindly and helpful for you to provide an answer to the question "where are you getting YOUR information from??" ... Even if I prefer your scenario swordman.
Unless of course the source is confidential and or from a fly on the wall, or something even less specific.
New VIDEO on RELIEF and ACER by Dr. Joey... EXCELLENT
World Sees Record Daily COVID Cases As Less-Lethal Omicron Displaces Delta
https://www.zerohedge.com/covid-19/world-sees-record-daily-covid-cases-less-lethal-omicron-displaces-delta
A safe effective inhaled therapeutic like AVIPTADIL would help the world in countless ways.
COVID Antiviral Pills Cause Life-Threatening Reactions With Many Common Meds......................
................AND WHY THE WORLD NEEDS AVIPTADIL.............
https://www.zerohedge.com/covid-19/covid-antiviral-pills-cause-life-threatening-reactions-many-common-meds
both Pfizer's and Merck's drugs come with some serious drawbacks, the biggest being that they can cause life-threatening reactions with widely used medications like statins - taken by people with high blood pressure - blood thinners, and even some antidepressants.
What's more, the FDA doesn't recommend Paxlovid for people who have severe liver and kidney disease.
The Merck drug hasn't even been approved because the experts are worried about potential side effects. Because of this, the FDA has restricted its use to adults, and only in scenarios in which other authorized treatments, including monoclonal antibodies produced by Regeneron and others, are inaccessible or are not "clinically appropriate."
Here's a more detailed explanation of how the Pfizer drug works, and why it might be hazardous for some (courtesy of NBC News):
The Paxlovid cocktail consists of two tablets of the antiviral nirmatrelvir and one tablet of ritonavir, a drug that has long been used as what is known as a boosting agent in HIV regimens. Ritonavir suppresses a key liver enzyme called CYP3A, which metabolizes many medications, including nirmatrelvir. In the case of Paxlovid treatment, ritonavir slows the body’s breakdown of the active antiviral and helps it remain at a therapeutic level for longer.
The boosting effect was likely to have been crucial in driving Paxlovid’s high effectiveness in clinical trials.
When Paxlovid is paired with other medications that are also metabolized by the CYP3A enzyme, the chief worry is that the ritonavir component may boost the co-administered drugs to toxic levels.
One expert chimed in to warn that these interactions involving Paxlovid are "not trivial".
"Some of these potential interactions are not trivial, and some pairings have to be avoided altogether," said Peter Anderson, a professor of pharmaceutical sciences at the University of Colorado Anschutz Medical Campus. "Some are probably easily managed. But some we’re going to have to be very careful about."
Supplies of Paxlovid and Molnupiravir are scarce - for now, at least. But the production line is roaring and the two competitors say they hope to produce millions of courses of each medication during the coming year.
Some Progress by RLFTF this week would be fabulous good news
for saving lives and improving the economy which seems headed
in the wrong direction with no sign of covid being stopped.
Seems like the higher the number of shots only equals higher
numbers of covid out breaks and a safe effective inhaler would be a miracle.
From Snow Man yesterday on the Y@H@@ boards....
$RLFTF conversation
A pair of over-the-counter compounds—diphenhydramine and lactoferrin—have been found in preliminary tests to inhibit the virus that causes COVID-19, University of Florida Health researchers have discovered. The findings by David A. Ostrov, Ph.D, an immunologist and associate professor in the UF College of Medicine’s department of pathology, immunology, and laboratory medicine and his colleagues, are published in the journal Pathogens.
What are these compounds?
An antihistamine used to treat allergy, hay fever, and the common cold, Diphenhydramine goes by well-known brand names such as Benadryl or Nytol. While Lactoferrin (LF) is a multifunctional protein, part of the transferrin family, and is widely used in various secretious fluids such as milk, saliva, tears, and nasal secretions.
Dr. Ostrov went on the record, “We found out why certain drugs are active against the virus that causes COVID-19. Then, we found an antiviral combination that can be effective, economical, and has a long history of safety.”
https://abcnews.go.com/Business/wireStory/eu-approves-5th-covid-19-vaccine-bloc-novavax-81856001
Another High Hurdle for anyone developing a potential new vax
PW....Thats a Very Interesting Question.....
We do know that some dislike following business procedures.
Penny, thank you and everyone else for the information provided...
and also the thoughts......
Looks like JJ has had at least about a full year now and right before court he throws up a half a dump of massive complex data, indicating, to me, his ethics and unwillingness to follow the signed agreements have not changed much. Like in the classic old movie with Paul Newman, Cool Hand Luke, "What we have here is a failure to communicate."
jj is still not sharing the clinical data with RLFTF, which is hampering their efforts with RLFTF 100 outside of the USA.
Another Reason for Approval of a Safe Effective Therapeutic
like AVIPTADIL....................
https://www.zerohedge.com/news/2021-12-14/covid-propaganda-roundup-american-heart-associations-vaccine-warning-censored
Endless rounds of deadly dangerous boosters or AVIPTADIL ???
changes...interesting question you ask. It seems to me, it may be even longer, or with meaningless redacted docs it may effectively be never.
With a gov payment of about $1,500 per jab, so I am told, thats a lot of jack to spread around, and many in power always have a hand out to take,
and a blind eye to look elsewhere for any problems.
Months to develop, and not in my remaining lifetime or yours to release the data.
Something stinks very badly.
https://duckduckgo.com/?q=pfizer+to+release+data+on+vaccine+in+75+years&t=h_&ia=web
Horrible thought that maybe a safe effective medication like AVIPTADIL is not what the powers that be are interested in having to save lives across the globe.
https://www.zerohedge.com/covid-19/another-study-finds-natural-immunity-protects-better-against-infection-pfizer-vaccine
https://alexberenson.substack.com/p/urgent-a-huge-israeli-study-shows
https://citizenfreepress.com/breaking/dr-peter-mccullough-blockbuster-interview-with-joe-rogan/
https://duckduckgo.com/?q=athletes+with+recent+heart+problems+or+heart+damage&t=h_&ia=web
Big mystery, is all these good athletes are dropping like bugs
going through an electric fence. But oddly they are required to have been VAXXED. But it couldn't be the VAX, as any good medical authority will tell you these are problems with PTSD from Covid 19, and oddly have nothing to do with the VAX. WHAT COULD IT BE ???
Go figure..../SAC
https://citizenfreepress.com/breaking/vaccinated-byu-starting-center-i-will-miss-the-rest-of-season-due-to-heart-damage/
FOR SURE THE WORLD NEEDS A SAFE EFFECT THERAPEUTIC LIKE AVIPTADIL
remember kids, moms n dads, teens and five year olds , take your clot shot and move along, nothing to see here..........
https://citizenfreepress.com/breaking/booster-shots-every-4-weeks-in-germany/
Some terrifying stuff out there, not just Germany.
AND WHY THE WORLD NEEDS AVIPTADIL AND RLFTF.........
https://www.blacklistednews.com/article/81370/israeli-health-official-tells-public-to-prepare-for-endless-boosters-we-will-need-to-take-the-4th.html
Endless clot shots till death or a safe effective therapeutic ?
The genius of jj....
Israel is one of the most VAXXED country on the planet, if not the most highly VAXXED of all countries, and now on their Fourth VAXX
https://stuartbramhall.wordpress.com/2021/09/27/it-never-ends-israel-says-fourth-booster-vaccine-will-be-required-to-keep-covid-green-pass-active/
And jj thinks he will insert himself on top of four or five other "vaccinations" of Israels folks and other companies doing a huge business in Israel.
On top of testing his VAXX, he will need to test it against people that have already been VAXXED with a different VAXX four or five or six times, and ya know it might just be very time consuming and very expensive on top of regular testing.
All the while dealing with a massive host of legal problems for a very young and small company, now with a history of bad behavior, or the lawyers would not be all over Neuro
Good luck.
https://rumble.com/search/video?q=bill%20gates%20population%20control&sort=date
Penny, It seems, over time, its like he has become obsessed with reducing the human population and countless videos illustrate it in places like rumble and bit chute.
https://rumble.com/search/video?q=bill%20gates%20population%20control
changes, Thats Stunning.......his own words on video
And also he wants CO2 to go to ZERO...
To kill all the plants ?
https://stockcharts.com/h-sc/ui?s=NRXP&p=D&b=5&g=0&id=p27695432074
At this rate.......Four, Three, Two, One ???
jj needs to come clean with RELIEF.... and do whatever it takes to
settle with RELIEF, esp before the need for bankruptcy lawyers.
Months to Produce a Dangerous Deadly "VAX", and
about (55) Years to release the Data on the "VAX",
would make a logical thinking person believe something is very
very wrong here, especially when AVIPTADIL has been
proven safe and effective over a long period of time.
Is that Pre Christmas News about Bankruptcy, another FDA Rejection,
Another Failed Test, an addition Violation of the Contract w Relief, A Fourth (4th) lawsuit against Neuro or perhaps something else like a concession to RELIEF and Actually abiding by the extensive terms of the signed contract???
Repayment of the $$$$$$$ owed to Relief ?