Humanigen Inc (CE) (HGENQ) Quote

right . they say pilots spend all day in thin air smelling farts.
gets to you doesn’t it

So what? Again that doesn’t math does it? Logic clearly isn’t your strongest attribute.

I wouldn’t send you to your made up “reeducation camp” that Tucker tells you about. We already have a circus to send clowns like you to for entertainment.

you can go on about the virtues of mrna covid vaccines, and vaccines in general , i understand. call me names , have at it
you should study the pennsylvania dutch community. autism is unheard of .
they eschew vaccines
no its not the funny outfits and horse buggies

yes i did it on purpose, im just not a liberal pig

if you had the chance im sure you would send me to a reeducation camp

Satan Does This RIGHT When I Get to the Gospel...

Do you even read what you write?
“Clown, leftist pig” etc and you have the moronic wherewithal to accuse others of name calling when they present you with the truth and reason of logic instead of conspiracy driven rabbit holes that you go diving into.

Like you said “clown”

4 Mormons CLASH With Preacher

uh the virus was most virulent early on but im sure a pilot would know that

when a leftist pig has no argument they name call lol

No shit doofus, Covid came to the US in 2020, the same year we fired the cheetoh. He only had less than one year left in his term to screw up the initial response. Simple math and logic would clearly explain why there were more deaths the 4 years after the lying narcissist was kicked to the curb. Nice try at “alternative facts” though..

said to a preacher amen

see how you get denigrated when you have an opinion that doesn’t conform with groupthink

Yes, I talk to God daily. Spiritual war for our Soul is for real.

please stick to preaching your medical prowess to your personal flock

haha there you go being a judgmental jackass

more people died under your hero joe shitbrains that for the cheetoh.
be honest clown

Do you have someone you can talk to? .....maybe a professional?

I will never take it or get it! I personally know of several people who took it who got injured by it.

So many are asleep and will never wake up to the spells that have been placed on them by our own Government, Hollywood, the music industry, along with science.

This guy gets it:

https://www.youtube.com/@WAKEUPCALL2024/videos

ya your a vaccine clown too

i really don’t care if people wanted it . good for them .
what was not right was the ridicule of anyone that asked questions.
for the record the long term results are not in , but anyone with eyes open has seen whats gone on up to now.
“turbo cancer” is a new term
cardiac and blood clots are killing all ages
why not enhance the two leading killers of man as blueprint of a master plan . shake the trees baby
but they point you at boeing airplanes as the real people killers lmao

Very, VERY well said sosjtb.

The bullet-point reasons not enough to sign The Hope Accord?

Didn't feel like clicking on the link I provided for additional information?

https://thehopeaccord.org/

You want somebody to explain it to you?



You want to hear the truth in the prettiest way possible? I suggest:

Wow, comparing the Tuskegee Syphilis experiment to the Trump administration’s response to Covid is a stretch for even the most conspiracy driven whack job ideologue! Heck, it even belittles the racist policies of the US government at the time that allowed something like that happen, something that anyone with an ounce of decency let alone empathy would understand the horror that was inflicted on a population based on skin color.

Making any sort of false equivalence to the governments response to Covid and the vaccine with intentionally getting/letting people get infected with a disease is the projection that folks like Tucker and his pearl grasping sheeple lap up with joy! Creating a fake narrative is what makes them feel as if they are smarter than the person who can actually see through the bullshit. Reasonable people who can actually see through the bullshit is why even Fox News had to can his racist dog whistling ass, he is still there for them though, the tin foil hat wearing idiots still need someone to validate their nonsense and the internet allows them the platform for that to continue.

Science and reason is what ended the pandemic when it was killing on a daily basis. Fortunately there are more people of reason than there are conspiracy driven whack jobs, society can still continue to evolve and progress while they kick and scream nonsense that’s only validated through religious texts and mythology.

Unfortunately, our wicked rulers are not finished with getting this magic potion in our veins.
There will be something else which will be created to force people to get that magic potion injected in us.
So many sheeple are asleep as to what taking place on the world stage.

sad you have no clue what a sick experiment was performed on the sheeple .
makes the tuskegee syphilis experiment look like childs play

absolutely a better end of the trail for those that took it

Dloggold you can kick and scream all you want about the conspiracy that doesn’t exist…maybe it would have been a better evolutionary trail if we would have let Covid runs its course?

https://www.facebook.com/share/r/FaggVHr4Khw5tFeX/?mibextid=6GsUZ4

F auci the modern day gain of function resesrch Dr Mengele
of sheer evil, greed, terror and profits!!!

I signed The Hope Accord, calling for:

1. THE IMMEDIATE SUSPENSION OF THE COVID-19 mRNA VACCINE PRODUCTS

2. A COMPREHENSIVE RE-EVALUATION OF THE SAFETY AND EFFICACY OF ALL COVID-19 VACCINE PRODUCTS

3. THE IMMEDIATE RECOGNITION AND SUPPORT FOR THE VACCINE-INJURED

4. THE RESTORATION OF ETHICAL PRINCIPLES ABANDONED DURING THE COVID-19 ERA

5. ADDRESSING THE ROOT CAUSES OF OUR CURRENT PREDICAMENT

https://thehopeaccord.org/

We know all we need to know about lenzilumab's safety and efficacy. We reported the LIVE-AIR trial results. Soon, the PREACH-M trial results will also be published, and based on the interim results, we know that will lead to Australian approval and other regulatory incentives, to include a PRV.

I recall that it was 300K doses we had to trash, because the product reached the expiration date. I also know that other manufacturers got extensions of the arbitrary expiration dates.

Management will succeed in getting lenz approved. Management will accomplish this overseas, and that will lead to US authorization, especially if HIVICRON proves to be more lethal than anything we have yet seen. I only hope that lenz will be able to help to restore the innate immune response system, which has been severely damaged by the mRNA vaccines.

jay you can kick and scream all you wish, half the shareholders that were on this site thought the mrna vaccines were good for you and only pariahs went against that grain.
turns out mrna is poison, killing some before others.
if humanigen had kept up the studies with all those doses that went down the drain we might lnow more about the efficacy

How the hell do you demonstrate the graft and corruption of regulatory agencies, when THEY control the authorization of your drug, and when THEY are major investors in the mRNA vaccine manufacturers whose revenues will be smashed by lenz and the lenz-enhanced Novavax vaccine, and when THEIR scientists are receiving royalties, and when THEY are receiving the majority of their funding from their Big Pharma partners/sponsors?

Humanigen changed their primary endpoint to better align with the government's trial design.

Of course ACTIV-5 didn't meet the endpoint. The trial was designed to fail. We knew ACTIV-5 would fail, when CRP levels of the critically ill patients get >150mg/L of CRP.

Necessity, as I have always said, will lead to our authorization and approval. NOBODY believes in the mRNA vaccines, now that the truth about Serious Adverse Events are being reported. Pfizer trial patients had 36% more SAE's than the placebo group. And with a highly virulent strain of omicron (HIVICRON) expected, lenz will be the only safe and effective treatment on the market.

and there are 20 other reasons at least

jay we lost because durrant did not know how to navigate the ship against the people that pay the FDA and NIH bills .
and with respect to your diatribe..
they changed the primary endpoint with live air to meet efficacy goals number one.
number 2 activ five did not meet endpoint, and not a single word from the company about what you bitch about.
why didn’t the company rehash the data with the sicker stage cases removed?
it probably did not make a difference thats why

The Mayo Clinic case-cohort study, and Humanigen's LIVE-AIR trial, both showed durable, repeatable, safety and efficacy in patient treatment outcomes before there were vaccines. The vaccines only increased the number of patients who will subsequently need lenz.

In October of 2020, Tucker interviewed Durrant about lenzilumab being a "Potential breakthrough coronavirus treatment." This was only about 7 months after covid hit our shores. This discovery of lenzilumab's potential to treat covid was the result of a Case Cohort Study led by Mayo Clinic, and included Humanigen's Dr. Cameron Durrant, Dr. Dale Chappell, and others, as trial investigators. A matter of 'all hands on deck.'

Results of the Case Cohort Study were published in June of 2020, and showed:

"Twelve patients were treated with lenzilumab. Clinical improvement was observed in 11 out of 12 (92%), with a median time to discharge of 5 days. There was a significant improvement in oxygenation: The proportion of patients with SpO2/FiO2 < 315 at the end of observation was 8% vs. compared to 67% at baseline (p=0.00015). A significant improvement in mean CRP and IL-6 values on day 3 following lenzilumab administration was also observed (137.3 mg/L vs 51.2 mg/L, p = 0.040; 26.8 pg/mL vs 16.1 pg/mL, p = 0.035; respectively). Cytokine analysis showed a reduction in inflammatory myeloid cells two days after lenzilumab treatment. There were no treatment-emergent adverse events attributable to lenzilumab, and no mortality in this cohort of patients with severe COVID-19 pneumonia."

https://pubmed.ncbi.nlm.nih.gov/32587983/

Here's the interview.
https://www.foxnews.com/video/6197198838001

Contemporaneous to Tucker's interview, Big Pharma began reporting the efficacy of their vaccines, in which most were claiming efficacy just slightly better than lenzilumab. Of course, THOSE claims were proven false. And vaccines were redefined from "preventing infection," to reducing hospitalizations and deaths.

Tucker's second interview of Durrant, in October of 2021 (a full year after Tucker's interview to discuss how lenzilumab's efficacy was demonstrated), was intended to expose how "Treatments for Covid Are Being Ignored By FDA."

https://www.realclearpolitics.com/video/2021/10/01/humanigen_ceo_durrant_treatments_for_covid_are_being_ignored_by_fda.html

By this time, Humanigen had reported, in March of 2021, the positive topline results of their LIVE-AIR trial.

https://www.businesswire.com/news/home/20210329005301/en/

You've been here since 2015, just as I have. It's despicable that you would now claim that these results have been a scam. I have made it clear as day that the NIAID/NIH ACTIV-5 government-sponsored trial was designed to fail, by including late-stage patients in Ordinal Scales 5, 6, and 7, and excluding patients in Ordinal Scale 4, who accounted for 78% of the LIVE-AIR trial population. Humanigen included early-stage patients only in Ordinal Scales 4 and 5.

ACTIV-5 patient inclusion criteria:

Illness of any duration, and requiring, just prior to randomization, supplemental oxygen (any flow), mechanical ventilation or Extracorporeal Membrane Oxygenation (ECMO) (ordinal score 5, 6, or 7).

https://clinicaltrials.gov/study/NCT04583969?intr=lenzilumab&rank=2


LIVE-AIR patient inclusion criteria

SpO2 ≤ 94% on room air and/or require low-flow supplemental oxygen and/or require high-flow oxygen support or NIPPV

https://clinicaltrials.gov/study/NCT04351152?intr=lenzilumab&rank=3

Drugs like Lenzi if it works can generate min. 1 billion in revenues and if used with treating corvid the potential is in the billions. The question is does Lenzi work in reducing deaths from corvid 19 viral infection for people who are not vaccinated. FDA has not approved any drug that treats corvid 19 along with other drugs to treat people who are not vaccinated. The side effects of the mRNA is being under reported by the govt controlled media and homeland security to reduce public panic or sueing the the gov't for forced vaccinations. I had severe reaction to my 4th vaccine two years ago it was 1 month after the mRNA injection. This vaccine is poison to the body as warned and causing serious side effects for some people including death but is put under the news editor desk for fear of gov't raids and accused of spreading 'misinformation' Homeland security is now the new SS of the gov't. The SS were qausi gov't security agents or privately hired security agents paid by the gov't. SS in Germany were volunteers fanatics like talibans or green party activist who volunteer.

He didn't take any heed of your advice, eb, and instead, his first two posts following yours, were the two worst posts that he has written.

But I know of a guy that blew-off a chance to meet with Durrant, so what can you say? I know of another guy that should know better, but thinks our trial results were not statistically significant. We all have made regrettable decisions.

Lenzi molecule claims to cure a form of rare blood cancer, well FDA says it's snake oil and doesn't work like those fake creditor claims. as for corvid that cowtown keeps talking about, there is no emperical evidence that lenzi has any effifacy in patient survival after corvid infection and was injected with lenzi. it was all snake oil. and FDA probably knew that too. you trust a agency that approves a weight loss drug that risk so many health hazards to lose weight? beign fat isn't a disease and nor risk of death but taking these weight loss drug,,some people can die. or very serious side effects. if taken for long time. or long term use of these weight loss drugs. but FDA approves it for mass consumption. humans have evolved to gain weight and store fat to starve off times of starvation and not a disease to be fat. people who are fat based on evolution were survivals of famine when food was short in the winter.

the 'claim' that this molecule eats the virus is false because it's snake oil which is why it didn't get FDA approval. you are assuming anti-viral drugs are like anti-biotics. there are lots of way to cure cancer but for blood disorders it's much more difficult chemically speaking which is why there is no cure as far as I know. most of the supposedly cures are just artificial replication of human cells it doesn't kill the virus. it's the bodies own immune system that KILLS the virus. When you get infected with virus your body creates antidotes to KILL the virus. your body goes haywire when it detects certain chemicals like poison and that is how poison works, it's 'toxic chemical' and wrecks havoc in your bodies immune system.
LENZI is either 'snake oil' or FDA is part of the scam and if this drug works but FDA is not releasing it to the public and people are dying because it was not available.
As for cowtown, did his wife die from corvid infection or just paid actor in these forums.? either way this drug lenzi is not approved by the FDA because it doesn't work like many of these drugs.
As for assisting in corvid infection, the only way it works it helps the bodies own immune system to produce more white blood cells or T-cells or Lenzi could be T-cell molecule derived from animal blood or human blood.
eitherway, the drug doesn't work in curing cancer or blood disorders. the patient didn't have any improvements upon injecting the drug but had side effects.. side effects are expected but the patient condition didn't improve and was not cured and eventually died.

Excess deaths just go on and on and on. The most recent data for the US reflects a total of 366,894 excess deaths from the start of 2023, through week 16 of 2024. Those excess deaths are 10% higher than what would normally be expected. And this is before the projected highly virulent form of omicron (HIVICRON) begins to circulate, which I think will be more deadly than anything we have yet seen. I also think only the lenz-enhanced Novavax vaccine (if it is developed with Sanofi), will be able to prevent infections, as true vaccines are supposed to do, and that only the therapeutic version of lenz will be able to save the lives of infected patients. That's partly why I post here as often as I do. I don't want to see what happened to my wife, happen on a population scale. Also, I would like to have lenz available to treat whatever is causing my inflammation, and of course, as a small shareholder, I want to see lenz get regulatory approval and reach it's market value potential.

Here's the source data in the video. I also left a comment on Dr. Campbell's site, following the video.



@JayBooth-oj2dy
32 minutes ago
"Humanigen (Taran Therapeutics) Announces Peer-Reviewed Publication in Thorax Supporting Early Treatment of Hospitalized COVID-19 Patients with Lenzilumab Guided by C-Reactive Protein
Jul 06, 2022

Lenzilumab improved clinical outcomes in hospitalized non-mechanically ventilated hypoxic COVID-19 patients.2 The greatest benefit was observed in those with a CRP level below 150 mg/L in the LIVE-AIR study. In this sub-analysis, lenzilumab improved the likelihood of (Survival Without Ventilation) SWOV compared with placebo (HR: 2.54; p=0.0009), demonstrated reduced odds (OR 0.38; p=0.0053) and a 62% reduction in the relative risk of progressing to mechanical ventilation or death in lenzilumab-treated patients, there were more ventilator-free days (p=0.0045), fewer ICU days (p=0.0458), and improved time-to-recovery (p=0.0219).1

https://ir.humanigen.com/English/news/news-details/2022/Humanigen-Announces-Peer-Reviewed-Publication-in-Thorax-Supporting-Early-Treatment-of-Hospitalized-COVID-19-Patients-with-Lenzilumab-Guided-by-C-Reactive-Protein/default.aspx

Lenzilumab (lenz) is variant-agnostic. It binds GM-CSF, modulating the immune response, and prevents cytokine storm. I fervently hope that lenz gets regulatory approval, and saves as many lives as possible before and after the arrival of Geert's HIVICRON.

You had better educate yourself on what you are bashing before anyone will ever take you seriously.
it's mainly anti-viral effects boosting the bodies own immune system in creating more white blood cells quickly or artificially very fast before a virus can over run the bodies immune system to heal itself. Lenz does exactly the opposite of this. It tamps down the "runaway" immune system that is trying to cure the infection. It does NOT boost it. It keeps the body from "eating itself", as it eats the virus, and emulating an autoimmune activity. Crawl back under your rock ......or your mother's basement..

"As (far) as more common blood cancer like Leukemia, there is currently no cure for it..."

Last year, Humanigen, "...extended previously
reported results by presenting additional, statistically significant hematologic improvements and reductions in
inflammatory markers from lenzilumab, its investigational drug, in a Phase 2/3 trial of treatment-naïve participants
with chronic myelomonocytic leukemia and RAS-pathway mutations.
The additional data demonstrate that in all 10 participants with at least three months of treatment with both
lenzilumab and azacitidine, blood monocyte count decreased fivefold (P=0.03), the percentage of blast cells and
pro-monocytes decreased more than twofold (P=0.04), and C-reactive protein decreased more than threefold
(P=NS) with improvements noted after both 3 months and 6 months of this combination treatment. These results
suggest lenzilumab may normalize hematologic and inflammatory aberrations in CMML and improve the condition
of participants. All ten evaluable participants had a rapid clinical response...

The incidence of CMML in the US, UK, and Australia is about 1,700 patients annually.9 As an orphan disease,
lenzilumab may qualify for certain regulatory and commercial advantages that could expedite development and
potential approval. Humanigen and the Principal Investigator are assessing regulatory pathways that may enable
early results to support a regulatory submission and potential approval by the Therapeutic Goods Administration in
Australia."

https://s28.q4cdn.com/539885110/files/doc_news/Humanigen-Presents-Promising-New-Hematologic-Data-from-PREACH-M-Trial-for-Chronic-Myelomonocytic-Leukemia-Treatment-at-the-2023-Europ-OYZCQ.pdf

Regulatory incentives include a potential Priority Review Voucher, with a value of ~$125M+.

If you understand what was said about lenzilumab's Method of Action, then maybe you'll see how wrong you were about this in your post.

Paid for what??? AND Paid by Who??? In case you haven't noticed HGENQ is on the Expert Market and Nobody can buy this stock.

Only liquidation of securities is allowed and No Buying!!!

it's obvious cowtown jay is paid stock forum promoter or cheerleader. no way a normal person post on some stock forum at midnight on EST. What is cowtown purpose on constant raving and posting about Lenzi and the drug that was sold for free to Taran?

You know, ZEN, they're going to restrict you to "emoji only" if this laughable argument is the best you can do. I've had one sip of coffee, which isn't enough to give your post the shredding it deserves. Even the purists here should be able to counter your claims, if they put their minds to it.

It's not that the day is young, it's off to a false start, which is often the case for me. But I'll be back later, after I get more sleep. But thanks for your post. It will motivate me to marshal a fitting response, if no one else does before I get back to this.

The fact is Taran bought the LENZI patent for free which has a potential to have 1 billion in sales if the FDA approves it. it's like free lottery ticket. or free money if the FDA approves it to the owner of the molecule Lenzi. It even got 2.5 million in licensing from Australian division. The FDA in US didn't approve for use in US that doesn't mean other countries cannot approve it. Either the FDA is corrupt or something or was sent bad data and technically cannot approve it or the application data was sabotaged so it won't get FDA approval and need more 'data' and testing

the lenzi molecule or patent that hgenq owns is what cowtown jay is raving about and was in stage 3 clinical studies but didn't show enough efficacy to cure a very rare blood disorder or blood cancer and is only 3 in 10,000 people type of blood disorder. 341 000 000 americans x .0003= 100,000 patients at $10,000/cure is $1,000,000,000 that is where the estimate or potential market for this Lenzi MOLECULE. As for as more common blood cancer like Leukemia, there is currently no cure for it and experimental drug as far as I know. these blood cancer disease are not easy to cure without side effects. The blood contains many cells and introducing a new chemical can have unknown side effects.

As for corvid use, it's mainly anti-viral effects boosting the bodies own immune system in creating more white blood cells quickly or artificially very fast before a virus can over run the bodies immune system to heal itself. that market if it works in the 10 billion market as more people choose not to take vaccines or boosters. mRNA vaccines like astra zeneca admit to side effects and vaccines are already waning. As a result, post treatment of viral infection is only option as people don't want to take vaccines as the vaccine side effect is worse than the virus infection. Corvid infection are rising as new variants or vaccine wanes over time. There are probably lots of drugs like lenzi to treat POST infection for people are not vaccinated or no longer interested in booster shots or taking their 5 or 6 shot of mRNA shots.

I don't agree that the value of the IP was/is based upon a, "...potential for 1 billion in sales." That came from management's initial revenue estimate, which was capacity-constrained to 100K treatments, at a cost of $10K per treatment.

Is that a lost opportunity for Humanigen or Taran (HOT)? No. That opportunity was delayed, but it also created a much larger market demand. I thought that it might, as a result of our countermeasures only making matters worse.

In that regard, we have the potentially imminent arrival of HIVICRON (Highly Virulent Omicron variant). Dr. Rob Rennebohm, MD, summarized Dr. Geert Vanden Bossche’s work in this field, as seen below.

https://notesfromthesocialclinic.org/wp-content/uploads/2024/06/COVID-ANALYSIS-260-GEERTS-ANALYSIS-FINAL-13-on-6-19-24.pdf

For those that might prefer a video presentation of the information, you can see it here.



In my opinion:

HOT, working with Novavax and Sanofi, will be able to get as much of the lenz-enhanced Novavax covid vaccine into the market, as will be required. As I expect that we are likely to form a merger entity with Sanofi and/or Novavax, I will look forward to that entity launching a reformulated therapeutic version of lenz to treat non-hospitalized covid patients while their CRP levels are still low. Lenz demonstrated 8-fold improved treatment outcomes when administered early, when CRP levels were