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Whether EDTA or Emeramide or any other chelation, a decades-long pondering of mine is how can such an agent target solely that which one is trying to target, rather than binding any and all (esp. “free” ions) it encounters.
I’ve never had a cogent response.
 
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Regarding Lordstown, one single point:
I don’t consider a CEO’s lockup of 100% to Oct 2021 and a 50% to Oct 2022 any kind of lockup or vote of confidence in any known universe.
 
Great criteria. I know another stock that fits.

I recently invested in a tiny biotech company with huge potential. This is a private placement opportunity for US Accredited Investors or non-US citizens only. The minimum investment is 50k US dollars or euros, with investor intention to hold the shares for years.

The company, EmeraMed Limited, was founded by Boyd Haley, PhD, a distinguished research scientist and former Chairman of the Chemistry Department at the University of Kentucky. Dr Haley’s team is preparing to market a new drug (Emeramide, aka NBMI) that binds tightly with mercury and other toxic metals trapped in body tissues. This binding with a metal (called chelation) stops its toxicity and allows the body to safely excrete it.

There is nothing else like Emeramide. No FDA-approved treatment exists now for mercury poisoning, and the few drugs used off-label (or on-label for lead poisoning) are not very effective and often toxic. Emeramide is extremely safe, as demonstrated since 2005 by extensive animal testing, human clinical trials, and use by thousands of people when it was briefly sold as an antioxidant (which it also is). Emeramide effectively chelates many different toxic metals, because the molecule has two arms that adjust to get a double-grip on a metal ion of any size, as shown here:


The company is currently in the final stages of seeking FDA approval to market Emeramide as a mercury chelator. Personally I believe chronic mercury poisoning is far more common than government agencies acknowledge, because:
  • No practical test exists to accurately measure mercury trapped in body organs.

  • Studies suggest mercury causes or contributes to many common diseases (heart disease, cancer, depression, Alzheimer’s, autism, ADHD, chronic fatigue, hypothyroidism, leaky gut, allergies, asthma, arthritis, autoimmunity, etc.)

  • Billions of people have been, or still are, exposed to dental amalgam fillings (which are half mercury), medical products preserved with mercury (vaccines, contact lens solutions, etc.), and mercury-contaminated fish and shellfish.
Many of EmeraMed’s investors are dentists who were mercury-poisoned by their practice, and cured themselves and their patients with Emeramide when it was available as an antioxidant supplement (then called OSR#1). Around the world, enormous health problems are also caused by arsenic in drinking water, and by lead in water pipes, paint and gasoline. So global demand should be high for an effective chelator of toxic metals in the human body.

However, EmeraMed has bigger plans. After approval for mercury, they intend to seek marketing approval for the following uses, for which clinical trials are underway or planned:
  • Iron overload. Millions of people suffer excess-iron poisoning due to Hereditary Hemochromatosis or frequent blood transfusions required for diseases such as Sickle Cell Anemia and Beta-Thalassemia Major. Emeramide binds with free iron (which is toxic) but not protein-bound iron (which is essential) and has no toxicity, unlike the leading iron chelator (Deferasirox) with annual sales over $1B. Parkinson’s Disease patients have excess iron in the brain, and many have improved rapidly from oral Emeramide.

  • Chronic Obstructive Pulmonary Disease. Toxic metals are toxic partly because they displace essential metals from body proteins, releasing free iron, copper and zinc. Free iron and copper then generate large amounts of reactive molecules (free radicals) that damage body molecules. Such damage (called oxidative stress) causes many diseases, including COPD. Emeramide reduces oxidative stress, not only by chelating toxic metals and free iron and copper, but also by binding with free radicals. COPD patients have shown impressive recoveries from using Emeramide.

  • Acetaminophen (Tylenol) toxicity. Pain medications containing Acetaminophen can damage the liver because the drug metabolizes to a free radical called NAPQI. Emeramide binds and detoxifies NAPQI and other free radicals. Thus Emeramide shows promise for treating Tylenol overdose, and for combining in a pill with Acetaminophen. Such a pain pill could be safer than Tylenol, and nonaddictive unlike opioids that are causing huge addiction problems.

  • Viral infections. Your immune system fights viruses using a self-produced antioxidant and chelator called glutathione. Emeramide boosts intracellular glutathione dramatically in people with low levels (the old or sick). It may also inhibit COVID viruses by chelating free iron that the virus releases to replicate itself.

  • Animal uses. Pets and wild animals suffer metal poisoning and oxidative stress from eating contaminated food. Dr Haley has seen Emeramide relieve arthritis in a pet dog, cure lameness in a racehorse, and bring wild eagles and owls from near-death to flying away. Veterinary medicine and animal feed are large markets.

  • Environmental uses. There is no safe level of arsenic in drinking water, according to the US Environmental Protection Agency. Yet the EPA currently allows up to 10 parts per billion (2500 times California’s public health goal) because of the high cost and difficulty of removing arsenic from water supplies. That could change after mass production of Emeramide. The water treatment certification requirements of the National Sanitation Foundation are similar to the drug approval tests currently underway,
In short, EmeraMed's total addressable market is not as vast as Tesla’s, but it is not small.

I’m very happy to be a Tesla investor, not only for the financial potential, but also because they are helping save the world. I feel the same about EmeraMed. I am using their drug myself (with FDA permission for “compassionate use”) and I believe it is helping save my health.

Of course, anyone interested should do their own due diligence and request the company’s Private Placement Memo. Here is one of Dr Haley’s many interviews and scientific lectures on YouTube:


I'll wait for the PPM, but it seems like this company has been working on a shoestring, just based on the fact that they received an Orphan Drug Designation in 2012, only a phase IIa in 2018, and have yet to finish a phase IIb. Also, they don't show any executives, just a founder and board members. The big question with all these companies is efficacy. Without an FDA cleared phase III trial, it is only sugar water (at least in the eyes of most of the medical community).
 
Great criteria. I know another stock that fits.

I recently invested in a tiny biotech company with huge potential. This is a private placement opportunity for US Accredited Investors or non-US citizens only. The minimum investment is 50k US dollars or euros, with investor intention to hold the shares for years.

The company, EmeraMed Limited, was founded by Boyd Haley, PhD, a distinguished research scientist and former Chairman of the Chemistry Department at the University of Kentucky. Dr Haley’s team is preparing to market a new drug (Emeramide, aka NBMI) that binds tightly with mercury and other toxic metals trapped in body tissues. This binding with a metal (called chelation) stops its toxicity and allows the body to safely excrete it.

There is nothing else like Emeramide. No FDA-approved treatment exists now for mercury poisoning, and the few drugs used off-label (or on-label for lead poisoning) are not very effective and often toxic. Emeramide is extremely safe, as demonstrated since 2005 by extensive animal testing, human clinical trials, and use by thousands of people when it was briefly sold as an antioxidant (which it also is). Emeramide effectively chelates many different toxic metals, because the molecule has two arms that adjust to get a double-grip on a metal ion of any size, as shown here:


The company is currently in the final stages of seeking FDA approval to market Emeramide as a mercury chelator. Personally I believe chronic mercury poisoning is far more common than government agencies acknowledge, because:
  • No practical test exists to accurately measure mercury trapped in body organs.

  • Studies suggest mercury causes or contributes to many common diseases (heart disease, cancer, depression, Alzheimer’s, autism, ADHD, chronic fatigue, hypothyroidism, leaky gut, allergies, asthma, arthritis, autoimmunity, etc.)

  • Billions of people have been, or still are, exposed to dental amalgam fillings (which are half mercury), medical products preserved with mercury (vaccines, contact lens solutions, etc.), and mercury-contaminated fish and shellfish.
Many of EmeraMed’s investors are dentists who were mercury-poisoned by their practice, and cured themselves and their patients with Emeramide when it was available as an antioxidant supplement (then called OSR#1). Around the world, enormous health problems are also caused by arsenic in drinking water, and by lead in water pipes, paint and gasoline. So global demand should be high for an effective chelator of toxic metals in the human body.

However, EmeraMed has bigger plans. After approval for mercury, they intend to seek marketing approval for the following uses, for which clinical trials are underway or planned:
  • Iron overload. Millions of people suffer excess-iron poisoning due to Hereditary Hemochromatosis or frequent blood transfusions required for diseases such as Sickle Cell Anemia and Beta-Thalassemia Major. Emeramide binds with free iron (which is toxic) but not protein-bound iron (which is essential) and has no toxicity, unlike the leading iron chelator (Deferasirox) with annual sales over $1B. Parkinson’s Disease patients have excess iron in the brain, and many have improved rapidly from oral Emeramide.

  • Chronic Obstructive Pulmonary Disease. Toxic metals are toxic partly because they displace essential metals from body proteins, releasing free iron, copper and zinc. Free iron and copper then generate large amounts of reactive molecules (free radicals) that damage body molecules. Such damage (called oxidative stress) causes many diseases, including COPD. Emeramide reduces oxidative stress, not only by chelating toxic metals and free iron and copper, but also by binding with free radicals. COPD patients have shown impressive recoveries from using Emeramide.

  • Acetaminophen (Tylenol) toxicity. Pain medications containing Acetaminophen can damage the liver because the drug metabolizes to a free radical called NAPQI. Emeramide binds and detoxifies NAPQI and other free radicals. Thus Emeramide shows promise for treating Tylenol overdose, and for combining in a pill with Acetaminophen. Such a pain pill could be safer than Tylenol, and nonaddictive unlike opioids that are causing huge addiction problems.

  • Viral infections. Your immune system fights viruses using a self-produced antioxidant and chelator called glutathione. Emeramide boosts intracellular glutathione dramatically in people with low levels (the old or sick). It may also inhibit COVID viruses by chelating free iron that the virus releases to replicate itself.

  • Animal uses. Pets and wild animals suffer metal poisoning and oxidative stress from eating contaminated food. Dr Haley has seen Emeramide relieve arthritis in a pet dog, cure lameness in a racehorse, and bring wild eagles and owls from near-death to flying away. Veterinary medicine and animal feed are large markets.

  • Environmental uses. There is no safe level of arsenic in drinking water, according to the US Environmental Protection Agency. Yet the EPA currently allows up to 10 parts per billion (2500 times California’s public health goal) because of the high cost and difficulty of removing arsenic from water supplies. That could change after mass production of Emeramide. The water treatment certification requirements of the National Sanitation Foundation are similar to the drug approval tests currently underway,
In short, EmeraMed's total addressable market is not as vast as Tesla’s, but it is not small.

I’m very happy to be a Tesla investor, not only for the financial potential, but also because they are helping save the world. I feel the same about EmeraMed. I am using their drug myself (with FDA permission for “compassionate use”) and I believe it is helping save my health.

Of course, anyone interested should do their own due diligence and request the company’s Private Placement Memo. Here is one of Dr Haley’s many interviews and scientific lectures on YouTube:


What stage are their drug trials?

Your long lists of potential uses makes it seem more along the lines of pseudo science.

How much have you privately placed with them?
 
Whether EDTA or Emeramide or any other chelation, a decades-long pondering of mine is how can such an agent target solely that which one is trying to target, rather than binding any and all (esp. “free” ions) it encounters.
I’ve never had a cogent response.

Are you still the moderator for this forum? The reason I ask is that I'm surprised this Emeramide post has been left up. Don't get me wrong, I am fine with it. It's just that I posted something similar (actually, it was a much shorter post) and it got taken down within hours due to a non-solicitation guideline. That company (CureMatch) is in an even better position than it was a couple of months ago when I made my post since their mgmt team has been busy!

I actually think that we should create a new thread, which would be kinda of an off-shoot from this thread, for "Private Company Investments" where people could discuss all non-SpaceX investment deals, status, etc. This thread has been good for public stock market tips and the like. Or maybe we should just talk about these things in this thread.

Thoughts?
 
Whether EDTA or Emeramide or any other chelation, a decades-long pondering of mine is how can such an agent target solely that which one is trying to target, rather than binding any and all (esp. “free” ions) it encounters.
I’ve never had a cogent response.

Not sure how cogent I can be, since I'm not a biochemist. But here is what I have picked up from Dr Haley's lectures:

Experimental results with animals and humans show Emeramide does not deplete essential nutrient metals (iron, copper, zinc) in the subjects. These redox (oxidation-reduction) metals are mostly bound to proteins in a healthy body. When iron becomes unbound ("free"), such as when a virus breaks it loose from hemoglobin to replicate itself, the free iron wreaks havoc by catalytically generating large amounts of hydroxyl free radicals via the Fenton reaction. So a healthy body minimizes free iron.

How does Emeramide chelate free iron but not protein-bound iron? I don't know the mechanism, but I know that sulfur is the element the body uses to bind metals (glutathione has one sulfur atom). Maybe Emeramide, like glutathione, does not have high enough affinity for metals to tear them off other sulfur bonds in the body in significant quantity. Regardless of the mechanism, the experimental fact is it does not.
 
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I'll wait for the PPM, but it seems like this company has been working on a shoestring, just based on the fact that they received an Orphan Drug Designation in 2012, only a phase IIa in 2018, and have yet to finish a phase IIb. Also, they don't show any executives, just a founder and board members. The big question with all these companies is efficacy. Without an FDA cleared phase III trial, it is only sugar water (at least in the eyes of most of the medical community).

The executives are described in the PPM. There are a few besides Dr Haley.

As explained in the PPM, FDA has agreed to approve Emeramide based on animal studies, manufacturing and stability tests, and limited human trials, without a large Phase 3 trial. This is apparently because of the drug's extreme safety. FDA told Dr Haley in a meeting: "We know it is safe."
 
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What stage are their drug trials?

Your long lists of potential uses makes it seem more along the lines of pseudo science.

How much have you privately placed with them?

The current stage of trials is explained in the PPM.

Check Dr Haley's curriculum vitae before you accuse him of pseudoscience.

Why do you need to know my investment amount?
 
Are you still the moderator for this forum? The reason I ask is that I'm surprised this Emeramide post has been left up. Don't get me wrong, I am fine with it. It's just that I posted something similar (actually, it was a much shorter post) and it got taken down within hours due to a non-solicitation guideline. That company (CureMatch) is in an even better position than it was a couple of months ago when I made my post since their mgmt team has been busy!

I actually think that we should create a new thread, which would be kinda of an off-shoot from this thread, for "Private Company Investments" where people could discuss all non-SpaceX investment deals, status, etc. This thread has been good for public stock market tips and the like. Or maybe we should just talk about these things in this thread.

Thoughts?

What's the difference between sharing an investment idea and solicitation?
 
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I neither know nor care to look back to see if it was I or another Mod who deleted @Cosmacelf‘s post, but I absolutely acknowledge there is a significant problem in determining the line between solicitation and promotion, as follows:

”Here’s an upcoming IPO that is appealing to me because of X, Y and Z. I attest that I have no prior interest in the success of the IPO.” This post is promoting the stock but is not soliciting, unless the poster is lying.

”Here’s a stock that I think is terrific, but I’m not going to tell you that not only do I own 4.99% of it, but its CEO is my brother-in-law.” Lots of four-letter words apply to you, jack-o. Solicitation of the worst order.

“Here’s a stock I think has promise because of X, Y and Z, although I have to tell you it has done zippidy-doo-da in my portfolio since I first invested 99 years ago.” This post acknowledges the the poster Is not a disinterested party, but he’s willing to put his credit on the line by telling that he owns it and thinks you should, too.

I have been careful to acknowledge every one of the very few names I have mentioned in this thread if I already own some of it, and I think not only is that a very good idea but I am considering making it mandatory. That won’t stop a cheat, but all must remain vigilant in their own due diligence, understanding that no one here has a fiduciary obligation to any others in this thread, and so forth.
 
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Not sure how cogent I can be, since I'm not a biochemist. But here is what I have picked up from Dr Haley's lectures:

Experimental results with animals and humans show Emeramide does not deplete essential nutrient metals (iron, copper, zinc) in the subjects. These redox (oxidation-reduction) metals are mostly bound to proteins in a healthy body. When iron becomes unbound ("free"), such as when a virus breaks it loose from hemoglobin to replicate itself, the free iron wreaks havoc by catalytically generating large amounts of hydroxyl free radicals via the Fenton reaction. So a healthy body minimizes free iron.

How does Emeramide chelate free iron but not protein-bound iron? I don't know the mechanism, but I know that sulfur is the element the body uses to bind metals (glutathione has one sulfur atom). Maybe Emeramide, like glutathione, does not have high enough affinity for metals to tear them off other sulfur bonds in the body in significant quantity. Regardless of the mechanism, the experimental fact is it does not.
There's been a cure for decades.

 
I neither know nor care to look back to see if it was I or another Mod who deleted @Cosmacelf‘s post, but I absolutely acknowledge there is a significant problem in determining the line between solicitation and promotion, as follows:

”Here’s an upcoming IPO that is appealing to me because of X, Y and Z. I attest that I have no prior interest in the success of the IPO.” This post is promoting the stock but is not soliciting, unless the poster is lying.

”Here’s a stock that I think is terrific, but I’m not going to tell you that not only do I own 4.99% of it, but its CEO is my brother-in-law.” Lots of four-letter words apply to you, jack-o. Solicitation of the worst order.

“Here’s a stock I think has promise because of X, Y and Z, although I have to tell you it has done zippidy-doo-da in my portfolio since I first invested 99 years ago.” This post acknowledges the the poster Is not a disinterested party, but he’s willing to put his credit on the line by telling that he owns it and thinks you should, too.

I have been careful to acknowledge every one of the very few names I have mentioned in this thread if I already own some of it, and I think not only is that a very good idea but I am considering making it mandatory. That won’t stop a cheat, but all must remain vigilant in their own due diligence, understanding that no one here has a fiduciary obligation to any others in this thread, and so forth.

Fair enough. But since there is a dangling assumption that my post might have violated any of these red lines, I'd like to clear my name.

For CureMatch (Precision Medicine Allows Us to Rank Matched Cancer Treatment Options), I invested in it about 3 years ago in a convertible debt round - it has now been converted into series A stock and I currently own around 3.5% of the company. I went on the board a bit less than a year ago, and have received no board or other compensation. Like all board members, I help the company find other potential investors and have received zero compensation for finding the ones that I have found so far. The rest of the board may in the future throw me some options or warrants if I find a lot of investors, but I won't accept any cash payment. More likely, I'll invest more to finish off a round or something. None of my relatives work at the company or are involved in it in any way.

In a nutshell, CureMatch dramatically improves most cancer patient outcomes through genomics. The core technology was licensed from UCSD, and that older technology has been proven to dramatically improve cancer patient outcomes, typically 50% improvement (Real-world data from a molecular tumor board demonstrates improved outcomes with a precision N-of-One strategy).

CureMatch's algorithm ingests the output of a cancer patient's tumor genetic analysis, understands the genetic aberrations that are causing the tumor (there are usually several, up to eight or nine anomalies), and then uses a constantly updated expert system based AI to recommend a two or three drug cocktail that will have the best result against the unique genetic aberrations. There are over 400 FDA drugs that target various genetic aberrations, so knowing which combination is the best based on complex genetic analysis is a very hard problem, hence CureMatch.

While we are finishing up a $2M - $5M series A right now, we have been working since last November towards getting the company listed on the London AIM exchange for later this year (probably 4Q). London AIM has large group of institutional life sciences savvy investors, and is almost like a training wheels version of a public market. Reporting only happens every 6 months, there are zero shareholder strike suits, and the market is sleepy meaning no wild shareholder price swings. If the company keeps doing what it's doing, a NASDAQ IPO in a couple of years is a possibility.

Here's a quick three minute video explaining it:

And for those that are driving in a car for 45 minutes, here I am moderating a discussion/Q&A session with the company's founder, Dr. Razelle Kurzrock that I did for a local community newspaper that I also edit:

PM me with any questions if you're interested in investing.
 
The current stage of trials is explained in the PPM.

Check Dr Haley's curriculum vitae before you accuse him of pseudoscience.

Why do you need to know my investment amount?
Where is the company headquarters? I tried searching the info online but it only has a church like building that shows as an accounting firm.

name a us fda approved drug without studies?

why private placement for such a miracle? Shouldn’t spac or ipo money jump head over heals for such a thing?

im not accusing anyone of pseudoscience, just sharing my opinion of the claims.

what are there sales figures now?
 
Where is the company headquarters? I tried searching the info online but it only has a church like building that shows as an accounting firm.

name a us fda approved drug without studies?

why private placement for such a miracle? Shouldn’t spac or ipo money jump head over heals for such a thing?

im not accusing anyone of pseudoscience, just sharing my opinion of the claims.

what are there sales figures now?

1) I recommend reading the PPM.

2) Emeramide is not without studies, as I clearly said and the PPM explains.

3) Why didn't Elon start Tesla, SpaceX, Boring Co and Neurolink with a SPAC or IPO?

4) I recommend educating your opinions before sharing them.

5) There are no sales now, since the drug is not yet approved except for compassionate use, and EmeraMed is not allowed to charge for compassionate use. As explained in the PPM, when Emeramide was available as a dietary supplement (for a year and a half), it sold to roughly 1000 doctors and dentists and grossed several million dollars with gross margin over 85%. Drug pricing will likely be higher, although Dr Haley wants to keep the price reasonable so many people can benefit from the drug.

does the PPM explain why the company HQ is in Ireland and not Kentucky? Wouldn’t KY be a better place to run things from?

The PPM explains that the company "is a corporation organised under the laws of the Republic of Ireland, with subsidiaries in the United States, Ireland, and Sweden."

Why Ireland? Maybe the same reason that 1000 multinationals are based there.

 
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1) I recommend reading the PPM.

2) Emeramide is not without studies, as I clearly said and the PPM explains.

3) Why didn't Elon start Tesla, SpaceX, Boring Co and Neurolink with a SPAC or IPO?

4) I recommend educating your opinions before sharing them.

5) There are no sales now, since the drug is not yet approved except for compassionate use, and EmeraMed is not allowed to charge for compassionate use. As explained in the PPM, when Emeramide was available as a dietary supplement (for a year and a half), it sold to roughly 1000 doctors and dentists and grossed several million dollars with gross margin over 85%. Drug pricing will likely be higher, although Dr Haley wants to keep the price reasonable so many people can benefit from the drug.



The PPM explains that the company "is a corporation organised under the laws of the Republic of Ireland, with subsidiaries in the United States, Ireland, and Sweden."

Why Ireland? Maybe the same reason that 1000 multinationals are based there.


Just some friendly advice. Your tone when replying to these legitimate questions is NOT conducive to making friends and winning people over. #4 above is particularly bad.

BTW, I asked for the PPM yesterday, haven't heard anything yet.

If you can answer this question without sneering, that'd be great: Why was it a dietary supplement and then not?
 
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Just some friendly advice. Your tone when replying to these legitimate questions is NOT conducive to making friends and winning people over. #4 above is particularly bad.

BTW, I asked for the PPM yesterday, haven't heard anything yet.

If you can answer this question without sneering, that'd be great: Why was it a dietary supplement and then not?

Dietary supplements have minimal FDA regulation, so you can make a killing selling them. The major problem is that this area is filled with snake oil.

To have an "indication" for treatment of any kind you need FDA approval as a drug, and to do that requires Phases 1/2/3 clinical trials and a drug review board to give it the stamp of approval. If the owner of the medication/supplement thinks it can pass trials and is trying to move it from a supplement to a drug, I would take that as a cautiously positive indicator. But like you, I would still want to see the data.

Many MANY moons ago I obtained my undergraduate degree in Chemistry, and from that learned that biological chelation of metals has been a long-standing, thorny problem to overcome. If this medication does pan out, it would be a game-changer. But like you, I want to see that proof before dropping some coin on them.