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ie if you sold a antique object, antique dealers says it's a fake and offers you $10 for it, and later he sells for $10,000 a few days later as 'authentic' it's called fraud, and the seller can sue the antique dealer for ripping him off. for buying asset with trickery and ly it was a fake when it was not.
that schmuck insurance is so if the drug is successful former sellers of the drug cannot sue Taran for ripping them off and buying the ip lenzi molecule for nothing.. it's called the asset was sold way below 'fair value' in business.
Does the schmuck insurance still apply if the hgenq shares are 'liquidated' why even have smuck insurance hgenq who sold the worthless patent gets money if the drug is commercialized?
As previous owners of the patent LENZI, if the drug doesn't work and not effective why would Taran waste time lending 2 million to bid for a 'worthless' drug called lenzi that received more than 2.5 million in ip licensing fees from research firms for testing.
if the drug has no commercial use, the the molecule 'worthless so why bid for a worthless asset?
people were infected with corvid before there was a vaccine. you don't need a vaccine if a person can be cured with lenzi or anti-viral drug. The problem is the vaccine side effects is worse than the virus itself. that is the problem and over 20 billion of the vaccine was sold and billions in profits.
it's because if the lenzi works you don't need a vaccine. because a lot of people who get infected with flue or corvid recover without a vaccine. the problem is the cure is worse than then disease for some people taking the mRNA 'vaccine'
you body cannot make enough- t-cells or white blood cells fast enough when virus spreads too fast. with injection of these lenzi, drug sor anti-bacterial drugs it's synthetic boost in body defense until your body recovers on it's own.
a lot of these drugs in pharma just micmics or copy drugs in nature. the opium plant is natural..you can make synthetic opiod but why. nature does a good job of making opium for pain relief. same with white blood cells or T-cells , your body make those cells, people with AIDS have their t-cells reduced or damaged. with anti-viral drugs it boost your t-cell or what lenzi is. that critical moment can be life and death if a anti-viral drug is not injected in patient that is infected. a patient can die in days without a drug injection if in virus overtakes the body and t-cells cannnot absorb the viral cells and overrunned.
LENZI drug is blood cancer drug, with blood cancer, you immune system is suppressed like if you have AIDS. which is what happens when you have corvid, you immune system collapse. drug like LENZI is like hemo drugs like Draculat had blood disorder and had to drink human blood. lenzi is has same molecules as in human blood or other animal blood.
If this short squeezes beyond $15,000 from $0.000001 then that is a 1.5 Billion Bagger.
"The US government, in my opinion, is keeping lenz out of the covid market, to safeguard their Moderna investment, and misplaced faith in mRNA technology."
If that is true, as I firmly believe that it is, you must ask yourself how that could possibly have come about.
This authority for the US Government to interfere with the commercial development of covid vaccines, and to curtail the development of safe and effective therapeutics to combat covid, was vested in NIAID, when it was decided to resume the manufacture of bioweapons. In fact, Fauci got a 68% pay raise to resume the development of bioweapons, and their counter-measures.
Additional funding of gain function research began to be provided by other agencies and entities. The largest of these is the United States Agency for International Development ("USAID").
If you don't want to keep and study the entire video, watch it from minute marks 35 - 45:24
Ep. 16 RFK Jr. explains Ukraine, bio-labs, and who killed his uncle pic.twitter.com/RMr5VZVqSM
— Tucker Carlson (@TuckerCarlson) August 14, 2023
" I immediately remembered that Japan has a unique non-inflammatory diet and that this may account for the difference."
The US has 4.2% of the world's population, yet accounts for 17.4% of all covid deaths.
https://www.worldometers.info/world-population/
https://www.worldometers.info/coronavirus/
The Chinese collected national DNA databases, and it was reported that this was to aid in the design of a virus specifically targeting particular nations, such as the US.
I can see diet and obesity impacting covid cases differently from country to country, but not to this extent. However, I totally agree about the third mRNA jab "wrecking" the immune response system, which is why I want to see if lenz can help to restore the immune system in these vaccinees.
The FDA has a lot of power because if a drug is approved and has a patent, you are talking about billions in profits to investors.
As they say power corrupts, and absolute power corrupts absolutely.
Just with the 5 year data of the mRNA results ,the FDA would not approve moderna mRNA vaccine.
Another reason FDA would not approve a drug is there is no condition or drug needed.
Weight loss drug is a drug that is not needed. The side effect of weight loss drug is not enough to warrant risk of health risk.
Being overweight is not a disease. people can lose weight naturally and don't need drugs.
Like plastic surgery, most people don't need plastic surgery and some are just immoral to do as the people requesting has psychological issues who want weight loss or plastic surgery. FDA is not protecting the public or have the best interest of the public. when it's mandate is to protect the health of the public, a privillege granted to it by the 'public'
Why do you think FDA didn't approve a lot of drugs.
1. Side effects are too severed
2. Not effective doesn't work only improves conditions
And public cannot sue the gov't or sue the company who makes the experimental drug which didn't have the data for 5 years. As some conditions don't occur after 5-10 years as not everyone has same side effects from a drug. ie allergic reactions are unknown. when doing clinical drugs of new molecules like Lenzi. It does not matter. HGENQ shareholders don't own the patent and is being liquidated. May not even exist as a shell company for tax purpose or trading purposes.
how do you see ask at 0.25? which platform do you use?
the 'evil plan' is to liquidate..take the money and run and shut down operations.
that $3 million dollar lawsuit, the company has not paid any to the law firm as of april 4,2024. so way anyone who sent claims would have been paid. you a fool if you think humanigen would pay you a dime as the shareholder lawsuit was part of the scam to bankrupt the company. the claimants were fake too. there was no trial. or court hearing.
The 3 million dollar lawsuit has not been paid by humanigen so none of the .047/share settlement is paid as of april 4, 2024 which is 7 days ago. Why it took 1 years of litigation for this company to payout and insurance still has not paid. you drag it longer that 3 million minus legal fees has less than 1 million left in the pot. And reason the company wants to bail and liquidate company and not pay 3 milllion settlement. why pay. Insurance company has not wired the money to the law firm who supposedly was suppose to be receiving the money. but humanigen wants it and then wire it to the law firm who is the escrow and pay the .047/share. Insurance always wire the money to the company policy holder and then policy holder unless it gets permission to wire to law firm who claim the $3 million settlement.
Howdy, mates! Or should I say 'G,day, partners?'
"Hi Jay Booth, Aka Cowtown Jay,
There's been an update on Taran Pharma (Europe) Ltd in the last 24 hours:
Shareholders/Group Structure"
Management 'expects' the class 4,5 creditor which is the shareholders to get nothing in 'evil plan' to liquidate and shut down fraud operation. and needs the permission of the fake creditors and the Courts stamp of approval.
who still owns the 100 million shares? they didn't bother to get the tax capital loss? i think they didn't sell because if they sold their 100 million shares, they lose control of the bankruptcy process. The question who owns the 100 million shares and why nobody selling that 100 million shares. if you read the latest 'plan' it says equity owners get no nothing and management is asking the 'creditors' to agree to liquidation even though creditor nothing. why you need the creditor 'permission' for .
I plan to first sell a couple cheapies in the $60-$70 range... I'm posting this now to show proof that I care about the shorts and that I am doing my part to help them with their recovery.
It's trading on the Grey Sheets and why there is no volume. Listen I have a million shares for sale @ .40 cents that you can have if you want them, or you need to cover a serious short position. I will place it good for 60 days. As for the other 3 million shares I am just going to sit on them and wait this out.
If they disappear then so be it. This was a 1-800-GAMBLER moment for me anyhow! :)))
this bankruptcy case or chapter 11 court is mockery of justice and miscarriage of justice. you've got criminals who are charged with serious stock fraud, corporate embezzlment, filing fake claims etc. the people who run this stock scam also run 100 other stock scams all run by the same people in the backrupt. guys like durrants, chappel morhner the four employees are just frontman of this stock scam
it only had less than 3 million in liability and had 3 million in cash. without the 40 million bogus lawsuit its was not bankrupt and can easily raise addditonal capital but it wanted to go bankrupt by self sabotage it's business by signing contracts and breaking them deliberately and agreed to pay $3 million to a bogus investor lawsuit. for a company with no revenue and only 2 million in cash, a 3 million dollar payout would bankrupt the company. but it wanted to go bankrupt.
if this was legitimate company, it would not have gone bankrupt, lots of companies with no revenues can easily get investment or issue more shares to raise capital but this company had no intention of continue as viable business.
The guy who owns this company wants to go bankrupt hence no selling of any shares. he gets off legally clean if this scam court bankruptcy court case is done. If he sells the stock and someone owns 51% or controlling shares, the bankruptcy will not proceed. What HGENQ did was reject offer to the ip because it wants to go bankrupt. and the lawsuits or 'breach contract of 27 million and 7 million anther 3 million a total 40 million in bogus
claims' which prevented the company from getting any investment from potential investors. even if the 40 million was bogus lawsuit no investors would touch a company that is being sued by investors and suppliers. self sabotage my the owners to go bankrupt to make the shares worthless
The shares are WORTHLESS, why is not trading and ZERO volume? nobody selling any shares below .01/share
one guy owns 110 million shares and not selling. it worthless shares. bid is like .000001
idiot didn't sell to get tax writeoff? or get capital loss
The only new filing I see from the four companies I track (Humanigen, Baudax, Novavax, and Sanofi), is from an upset an investment firm holding Novavax. The comments provided by the investment firm are legitimate, and actually reflect why I feel that Novavax really needs to use lenz as their vaccine enhancement, if the company is going to survive.
https://www.sec.gov/Archives/edgar/data/1000694/000139834424007144/fp0087987-1_ex992.htm
Recent studies indicate that Novavax has an advantage in booster antibody durability. That's a plus, especially as mRNA booster antibodies are degrading, and becoming less effective. And it is becoming evident that Serious Adverse Events are presenting after a third mRNA booster.
I hope that Humanigen and Novavax can partner, and take the majority of the US covid market, currently captured by Moderna.gov (US govt), and PfDA (Pfizer/BioNtech and their German govt and European bank ownership).
Well, another newly created account for the purpose of helping us poor HGEN holders. How nice you are. Oh, you must know biowa and a few others like yourself.....very helpful people.
Even in bankruptcy, the court or public still don't know how the real owners of this company is....
as the delusional fool either he is getting paid to post about LENZ, there is no hope in this stock. one guy owns 90% of the shares and there is no way who that person is and it's probably taran..they need shut this stock scam over by dissolving and liquidating the scam operation. and move on to the next scam with stolen assets that they paid nothing for and hire new front man. Durant, chapeelle, rohnier all just hired hands and front man in this stock scam.
The stock since it was delisted to the 'expert market' short for banned market has not been buyerable for Americans or US regulated brokerages. Americans are not allowed to buy in the xpert market only able to sell.
Anyone buying stock in the expert market or OTC market knows 99% of the equities is worthless and will be worthless. only a few are ADR like tencents but they are not equities. and don't have to report to the SEC in quarterly reports. When buying ADR your name is not in the registered shareholders list. and shares are not registered as shares with ADR. but receipts
welcome to the jungle
welcome to my evil world.
in the mean streets and lawless jungle, if your rip someone off, and you know who ripp off, you don't sue them etc. you just go buy a gun and kill them and take back what was stolen
Once the courts lose their moral authority, the court and SEC no longer have legal authority to rule anything. meaning judgements and rulings have not enforceable or valid.
American fraud has been exported to many countries like China. the capitalist greed has corrupted the justice system, SEC, and even politicians. even crypto is a scam and SEC wants to regulate it yet more than 10% of the market is now ponzi scheme cryto financial instruments. a legal pyramid scheme or MLM with state approval. Once the courts lose their moral authority, the court and SEC no longer have legal authority to rule anything.
this is my observation and complaint of the American justice system and corrupt SEC and corrupt court system in helping crooks and theives steal and rip off the american public
eb is correct, oldstocks. I moved out of Fort Worth in 2008, but just across the county line, where it is still possible to buy land, and the taxes are significantly lower.
Dude… again with the fake screen name and profile for the what?? This is the 6th or 7th one?
Why? What do you gain from it?
lots of crimes
1. corporate embezzlement by management
2. misleading investors with false FDA approval
3. insurance scam, buys insurance and commmiting investor fraud
4. fake creditor claim submission deliberately signging contracts knowing it cannot commit ausin breach of contract lawsuit.
5. stock manipulatoin of the market makers.
this bankruptcy was a fraud. to clean the hands of the shorts who shorted the sharees in 2021 and transfer the assets which was the ip of lenz and close this stock scam and walk free and no jail with assistance from the gov't and cops(SEC) as for retail investors who go robbed, you won't get dime of that 3 million dollar settlement, that was an insurances scam too. 5 million had to paid out because the company paid $250,000/annual premium in insurance policy for lawsuits of managemennt corruption.
why spends millions to declare bankruptcy?
I hope the public is not pay for the Judge time wasting his time in this bogus court case.
even the trading is scam..AI front run humans and manipulate human traders. entire operation is like watching WWF wrestling match all this drama about bankruptcy .lawsuits. FDA approval, it's was a an act an fake. they want to go bankrupt with fake lawsuits and management deliberately sabotage the company with misconducts like embezzlment to cause a bankruptcy. this company only 5 million in debt in 2022 even if FDA didn't approve there was little chance of bankrupty as it had over 5 million in cash in 2022 and management could easily raise investment in 2021 or 2022 and raise more capital with share issuance when equity was still hot..but it's 2024 nobody wants to ivnest in money losing drug companies or vaccines anymore. SPAC ipo is dead. why reddit ddin't ipo in 2021 is beyond me, right now the market for equities dried up zero bid and even trading is dead, not even a dead cat bounce now.
as for this stock scam, it's gov't assisted robbery of public investors money. technically it's not illegal. but immoral but plan was to rip of investors from the beginning. from ipo like hundreds of these stocks and things like crypto. false hope and fomo etc when it was shell game. stock picking is scam. you are to choose 1 stock from 10 stock...all 10 stocks are scam. or shell game.no winners in all 10 stocks you were told to pick. investment fraud is what it is.
the latest scam is crypto ETF. when crypto classic pyramid scheme MLM scheme. collapses Cryto ETF and itself is MLM scam very similiar.
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Humanigen, Inc. is a clinical-stage biopharmaceutical company developing its portfolio of next-generation cell and gene therapies for the treatment of cancers via its novel, GM-CSF neutralization and gene-knockout platforms. As a leader in GM-CSF pathway science, we believe that we have the ability to transform CAR-T therapy and a broad range of other T-cell engaging therapies, including both autologous and allogeneic cell transplantation. There is a direct correlation between the efficacy of CAR-T therapy and the incidence of life-threatening toxicities (referred to as the efficacy/toxicity linkage). We believe that our GM-CSF neutralization and gene-editing platform technologies have the potential to reduce the inflammatory cascade associated with serious and potentially life-threatening CAR-T therapy-related side effects while preserving and potentially improving the efficacy of the CAR-T therapy itself, thereby breaking the efficacy/toxicity linkage. Clinical correlative analysis and pre-clinical in vivo evidence points to GM-CSF as the key initiator of the inflammatory cascade resulting in CAR-T therapy’s side-effects. Pre-clinical in vivo data on the neutralization of GM-CSF using antibody or gene KO indicates that it is not required for CAR-T cell activity. Our strategy is to continue to pioneer the use of GM-CSF neutralization and GM-CSF gene knockout technologies to improve efficacy and prevent or significantly reduce the serious side-effects associated with CAR-T therapy.
We believe that our GM-CSF pathway science, assets and expertise create two technology platforms to usher in next-generation CAR-T therapies. Lenzilumab, our proprietary Humaneered® anti-GM-CSF immunotherapy, has the potential to be used in combination with any FDA-approved or development stage CAR-T therapy, as well as in combination with other cell therapies such as HSCT, to make these treatments safer and more effective. In addition, our GM-CSF knockout gene-editing platform has the potential to create next-generation CAR-T therapies that may inherently avoid any efficacy/toxicity linkage, thereby potentially preserving the benefits of the CAR-T therapy while altogether avoiding its serious and potentially life-threatening side-effects.
The company’s immediate focus is combining FDA-approved and development stage CAR-T therapies with lenzilumab, the company’s proprietary Humaneered® anti-human-GM-CSF immunotherapy, which is its lead product candidate. A clinical collaboration with Kite, a Gilead Company, was recently announced to evaluate the use of lenzilumab with Yescarta®, axicabtagene ciloleucel, in a multicenter clinical trial in adults with relapsed or refractory large B-cell lymphoma. The company is also focused on creating next-generation combinatory gene-edited CAR-T therapies using strategies to improve efficacy while employing GM-CSF gene knockout technologies to control toxicity. The company is also developing its own portfolio of proprietary first-in-class EphA3-CAR-T for various solid cancers and EMR1-CAR-T for various eosinophilic disorders. The company is also exploring the effectiveness of its GM-CSF neutralization technologies (either through the use of lenzilumab as a neutralizing antibody or through GM-CSF gene knockout) in combination with other CAR-T, T cell engaging, and immunotherapy treatments to break the efficacy/toxicity linkage including the prevention and/or treatment graft-versus-host disease (GvHD) in patients undergoing allogeneic HSCT. The company has established several partnerships with leading institutions to advance its innovative cell and gene therapy pipeline.
June 15, 2020
Phase 3 Study to Evaluate Efficacy and Safety of Lenzilumab in Hospitalized Patients With COVID-19 Pneumonia
https://clinicaltrials.gov/ct2/show/NCT04351152
Anti-GM-CSF antibodies expected to show better effect in Covid-19 than cytokine-specific targets
July 27, 2020
https://discoverysedge.mayo.edu/2021/06/22/cancer-to-covid-19/
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