If you can prove that the NIH and WHO got their treatment guidelines right, you could win $2M

If you can prove that the NIH and WHO got their treatment guidelines right, you could win $2M

This is the second in a series of articles arguing that obeisance to constrictive evidence-based medicine (EBM) treatment protocols in a pandemic is causing an unnecessary loss of hundreds of thousands of lives.

In my previous article, I showed that the current NIH and WHO treatment guidelines for fluvoxamine and ivermectin don’t fit the evidence at all. A FOR recommendation for both these drugs is a near-perfect fit to all the data.

In this article, I will make it clear to everyone that their recommendations are so indefensible that no qualifying enabler (see list below) will be able to come forward to support these recommendations even if I offer a million dollar incentive for them to do so.

Any drug protocol used for treating COVID early must fall into one of three categories: 

  1. helpful, 
  2. neutral, 
  3. or harmful.

I claim that there has been abundant evidence on the table for at least the past 7 months, all in plain sight, that both fluvoxamine and ivermectin when given early at an effective dose are helpful because a HELPFUL hypothesis is a near perfect fit to all the evidence and that the other two alternatives, neutral or harmful, don’t fit the evidence at all. 

To win the $1M prize, all you have to do is to provide a convincing argument that the NIH or WHO NEUTRAL and AGAINST recommendations on fluvoxamine or ivermectin (existing on May 21, 2021 when I am making this offer) are:

  1. more likely to fit the evidence than recommendations FOR these drugs, or
  2. more likely to save more lives than recommending FOR these drugs.

Either method of proof is fine: fit the facts or superior cost-benefit. You have two completely independent ways to win each prize. What could be easier?

Essentially, my contest is the embodiment of the Precautionary Principle of medicine and use all the available evidence. The failure to use these sound approaches has led to the needless loss of life of millions of people. We use the precautionary principle for masks. Why aren’t we using it for safe, repurposed drugs?

To qualify for the prize, you must be one of the key enablers of the myth:

  1. A professor at any accredited institution of higher learning anywhere in the world
  2. A licensed physician anywhere in the world
  3. An editor of any peer reviewed medical journal
  4. The executive management of Frontiers
  5. An employee of the NIH or WHO
  6. A member of the mainstream media anywhere in the world (especially in Brazil where they believe that all early treatments don’t work) including newspapers and online,
  7. An elected official anywhere in the world
  8. A public health official anywhere in the world
  9. Any employee at YouTube responsible for the ridiculous YouTube policy banning videos that claim that Ivermectin is an effective treatment for COVID-19
  10. An employee of any social network (including YouTube) who has decision authority for censoring content, suspending accounts, and banning groups related to ivermectin or fluvoxamine
  11. A fact checker in any country in the world especially Wikipedia editors who remove content saying that ivermectin works

You must also agree to allow your submission to be made public including your name since this is a matter of great public interest. Also, I request that you check that your work is correct before submitting it. For example, Adrian Hernandez, an open detractor of ivermectin for a year, recently self-published a paper showing that ivermectin didn’t work. The authors made one tiny error: they transposed the control and ivermectin numbers from the Niaee study probably hoping that nobody would notice. People’s lives are at stake; if your entry has errors like this, you will be disqualified. You only get one entry attempt per person.

The first person to submit a winning entry wins the prize, i.e. there will not be more than one winner per drug: $1M for ivermectin, $1M for fluvoxamine. To enter, submit your entry to the comments below. If I believe you met the challenge, you win INSTANTLY. If you want to appeal my decision, I agree we will go to JAMS where the loser will pay the fee (we’ll both put the fee as a deposit). This discourages frivolous entries and is a drop in the bucket compared to the $2M you stand to win if you think you are right.

The entries must consider the 23 early treatment studies of ivermectin and the two studies of fluvoxamine including the symptom data from the Seftel study. Post your entry in the comments for all to see. I probably won’t even have to respond as other readers will tear your analysis to shreds and make a mockery of you and your attempt. Public peer review.

I am not worried about losing $2M. This is an impossible task because all but one of these studies is positive and the only negative study had a p value of .526 (which is basically no confidence whatsoever and would be tossed from any serious analysis since the p-value was so insignificant and the effect size was computed by algorithm and not directly measured). The evidence also shows that the earlier these drugs are given in adequate dosages, the greater the positive effect. If the drugs are neutral or harmful, that’s impossible, a fact that seems to be lost on our experts from the WHO and NIH. 

The evidence today is simply impossible to ignore. Cases in Delhi, where Ivermectin was begun on April 20, dropped from 28,395 to just 2,260 on May 22. This represents an astounding 92% drop. Likewise, cases in Uttar Pradesh have dropped from 37,944 on April 24 to 5,964 on May 22 – a decline of 84%. If it wasn’t the ivermectin, then why aren’t the NIH and WHO all over this to find the real cause so they can let the entire world know? They aren’t investigating because they know the cause: the adoption of ivermectin. They do nothing and say nothing. It’s frustrating. More importantly, it’s costing lives because doctors in many parts of the world including Brazil and Tamil Nadu continue to blindly follow the WHO advice.

The purpose of this challenge is two fold:

  1. To draw worldwide attention to the fact that none of the enablers of the NIH and WHO are able to credibly defend the indefensible recommendations of the NIH and WHO for these drugs even if offered a huge monetary incentive to do so
  2. To show that the current recommendations of these two organizations for these two drugs have cost the unnecessary loss of life of hundreds of thousands of people.

If you qualify and would like to submit an entry, please message me on TrialSiteNews or DM me on twitter. 

The reason these absurd recommendations even exist is because the NIH and WHO insist on ignoring any evidence that is not a high quality phase 3 clinical trial published in a peer reviewed journal. Thus, in their view, all these drugs do nothing and since there is no benefit, there is no reason to recommend the drug.  This is completely outdated thinking that is inappropriate in a pandemic. They totally ignore the cost of death.

If they were smart, they would look at all available evidence and choose the hypothesis about each drug which is the closest match to all the observed evidence and maximizes the number of lives saved. Because they did not do that, we are left with the inescapable conclusion that they aren’t very smart and that their recommendations for these drugs should be ignored. QED.

Finally, why are Dr. Anthony Fauci and Dr. Francis Collins still remaining silent about the NIH guidelines for these two drugs? If a computer entrepreneur from Silicon Valley can figure all this out 7 months ago that it’s virtually impossible for these two drugs not to work, why can’t the NIH leadership? And apparently everyone agrees with me since there are no entries.

We are also left to wonder why, when David Seftel confirmed the 100% success rate in the original fluvoxamine RCT published in JAMA with a real-world study also with 100% effect size, why did they just ignore it like it never happened? Why didn’t they send a team to investigate if there were any biases or confounders? Instead, they just sat back and did nothing when the news came out. There was no investigation. There wasn’t even a phone call or email to the investigator. Even after 60 Minutes did a story on this miracle at the racetrack, they still did nothing to investigate. They could have saved hundreds of thousands of lives if they had acted earlier on the evidence that was hiding in plain sight for at least the past 7 months.

Did you ever see the movie Contagion? That was fictional, but that was a very serious virus that was very contagious and deadly. If we are as inept with evidence on that one as we are on this one, we will be all dead.

Lastly, to support my claim that this evidence has been in plain sight for over 7 months and that it was clear that the data supported action by the medical community, I offer a simple example that I am intimately familiar with: my own personal efforts to get the world’s attention to both of these drugs. For example, on October 17, 2020, I wrote about both fluvoxamine and ivermectin in a very long article on Medium — a 23-minute read. This was followed with an email to Elemental entitled “Two drugs that can dramatically reduce the hospitalization and death rate from COVID-19… perhaps to zero” and included a link to my article. However, because these recommendations were counter to the recommendations of the NIH and WHO, my Medium account was suspended for life.

And finally, if they got it wrong on ivermectin and fluvoxamine, do you think they might also have got it wrong about other drugs such as hydroxychloroquine, vitamin D, zinc, and other early treatments too? Of course they did. See Do the NIH and WHO COVID treatment recommendations need to be fixed? and Good Science Saves Lives, Bad Science Has Ruined Lives for the evidence of this. Or read this excellent article in Wired about The 60-Year-Old Scientific Screwup That Helped Covid Kill which documents how the WHO ignores expert opinion that disagrees with their narrative.

The sooner these recommendations are changed, the better. The drugs have been sitting on the shelf the whole time. The data has been available to the public for over 6 months. What we lack are leaders with the ability to clearly see the evidence that is hiding in plain sight. The NIH and WHO should either take my money or they should change their guidelines. Lives are at stake. What will they actually do? Answer: Absolutely nothing. And Congress is supporting this. It’s really very sad.

Steve Kirsch is a high-tech serial entrepreneur based in Silicon Valley. He has been a medical philanthropist for more than 20 years. When the pandemic started, he left his day job at M10 and started the COVID-19 Early Treatment Fund (CETF) which funds researchers from all over the world running outpatient clinical trials on repurposed drugs. CETF funded David Boulware’s trials on hydroxychloroquine and the Phase 2 and Phase 3 fluvoxamine trials, among many other research projects. He was recently featured on 60 Minutes which highlighted his work with fluvoxamine. He has no conflicts of interest; his objective is to help save lives. In 2003, Hillary Clinton presented him with a National Caring Award. He wrote this article to share some of what he has learned over the past year about the failure of evidence-based medicine during a pandemic in the hopes that people will realize their mistakes and change their views.

Note that views expressed in this opinion article are the writer’s and not necessarily those of TrialSite, Inc.  


  1. The case against Ivermectin:

    After much soul-searching and tons of research I have finally have finally reached a conclusion as to WHY there is such a vehement backlash against the safest, by far the best treatment in all phases of the SARS-Cov2 aka COVID-19 pandemic. My personal conclusion.

    Something called Emergency Use Authorization, under which pharmaceutical companies can virtually cut every corner in the trial safety book, get indemnity from prosecution and make plenty of money AND under the guise of this Emergency Use Authorization, venture into areas of research that would otherwise be unjustifiable, immoral and unethical.

    Because if a re-purposed safe, cheap, highly effective, alternative is found to exist, BILLIONS in profits would be lost, and Emergency Use Authorization would disappear in a puff of smoke.

    Who cares if millions lose their lives in the process, potentially millions suffer permanent and debilitating organ failure as a result of hastily concocted short term solutions?
    Of course, if you are a pharmaceutical company, would you say bye bye indemnities, bye bye incentives, bye bye short-cuts. As researcher say so-long grants, so near yet so far. As a government officials and politicians whose bread is well buttered, say cheerio to an under the table bribes. If your investors are reliant on the super profits you hope to generate. If you were a university whose BigPharma research grants are in jeopardy. If your survival is dependent on donations from so-called philanthropic organizations when you are the WHO, and you need to toe the line to stand with a begging bowl in hand, or if you are peer-review journal who stands to be ignored should you dare NOT to toe the line. If you are U-tube or F ace-book and your access to global markets could be jeopardized \. If you ere any or all of these, would you be willing to let a drug, treatment that costs NOTHING, compete with the super-profits you stand to lose?

    If you were willing to let the whole pyramid scheme of false information and disinformation described above collapse, for the sake of FEW MILLION PEOPLE, decide carefully, would you be sane or insane.

    So the question is, where does the insanity truly lie, why do we allow this to be done to us? This Emergency Use Authorization? I would rather call it Genocide, but then again, would I be called insane, a psychopathic mass-murderer, a sociopath, if I dared to think up such a hare-brained scheme and tried to suggest, let alone implement it? Or a benevolent philanthropist?

    Ivermectin CANNOT, DARE NOT do what “they” say it can do. Too much is at stake.

    1. congress can EASILY change the law if needed. not the reason. if drugs worked, fauci looks incompetent for ignoring. Outstaged by a tech entrepreneur? Fauci will have none of that. So NIH claims the drugs don’t work. Who cares if millions of people die because of it. Fauci doesn’t care. He’s not rewarded for minimizing loss of life. If he did, he’d be all over fluvoxamine and ivermectin. Fauci must go, but Congress loves him so it won’t happen because nobody in Congress will do anything. I’ve emailed many members but nothing happens. It is ridiculous and frustrating. Don’t ignore me…. if you have proof I’m wrong show me! They don’t.

  2. With 14 peer-reviewed articles published worldwide, and an e-book compiling all evidence (plus an appendix from Nobel-awarded S. Omura and a Toxicology review from Lyon University (France), I beleive there is no margin for doubt… unless big pharma provokes the worst form of blindness: voluntary blindness. If you want to receive ALL the information, just let me know. Regards. Prof. Hector Carvallo

    1. There is no doubt IVM works. Cliff Lane knows it for sure that it works. He no longer answers my emails to him telling him to do the right thing. They can even put it as “expert opinion”. Fauci and Lane need to go, but Congress is completely blind to it.

    1. Banned for life for spreading medical misinformation. Medium censors cited NO FACTS to justify their decision. Their CEO, Evan Williams, refused to talk to me.

  3. Thank you. I don’t want the money, I’m interested in the restoration of our country.

    I have the opinion that the medical PhDs at the top of administrative pyramids are unable to function as normal, compassionate house doctors anymore. The number of litigious law firms in this country says to me that any common person can make recommendations of a practical drug to a peer, but if made by a medical government employee, it will be met with threats of lawsuits.
    Weird country.
    I’m going to go back to this Ninth Amendment movement thing – if you get into legal trouble for taking or recommending drugs for diagnosis, prevention, treatment or cure of COVID-19, PLEAD the Ninth (as you would the Fifth) Amendment, and then show your evidence of benefits as Exhibits in a Circuit Court of Appeals or the Supreme Court…a precedent for putting the three-letter medical government agencies back in the role of protecting the people’s rights to be healthy and avoid death (instead of suppression of real world evidence).

  4. Gargling and swishing with an antiviral mouthwash for over a minute seems to work better than Remdesivir without liver damage. Aspirin is helpful with the inflammatory syndrome.
    Ivermectin pills are hard to get in the US, Brazil and now even in India; all day chemist is out. India is starting to ramp up production but most of the available supply is still in the livestock treatment market, like flavored horse dewormer paste and topical pesticides for cattle that have another active ingredient that I’d be afraid to be exposed to. Hopefully adequate fluox is still available. Prozac fluoxetine is very similar to fluvoxamine and has good availability.

      1. POLYETILENGLYCOL is part of the veterinarian formula. And it may be toxic. Besides, why using vet formula, if IVM is intended, manufactured and sold for humans?

    1. TV won’t run it because it would reveal that they misled the public earlier about the safety of the vaccine. So they will ignore it to continue the narrative. At some point it collapses just like when Fauci said that it’s possible it could have come from a lab.