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I hope you’re right and I’m wrong. I would love to pick up the phone and beg Rik for forgiveness. If he’ll take my call
Make no mistake, I still believe in this company and its product and to me it’s still is a long-term investment, I never looked at it as it has to yield results now.
My only gripe now is I believe Rik is making a big mistake taking this all the way to court.
I don’t think Rik is a bad person, I don’t think he’s a scoundrel or thief, or any of these other things that detractors on the board accuse him of.
I have not switched to “the dark side”, my only grape and disagreement is that they should not go all the way to court even if it means Rik stepping down. Taking it that far could mean all of us losing EVERYTHING.
Time will tail and I hope I’m wrong.
Good info there, but it never once said all the ceo had to do was resign and be barred for 5 years.
It does say the mediator pointed out how weak the sec's case was. I assume that comes as an email from the ceo or just a random poster posting his own thoughts.
And here’s the second part of his post, Rick’s response to him
https://stocktwits.com/fireman139/message/535560704;
Oh, please! Since when in all these six years have I been known to make stuff up?
I will post the screenshot of the stock twits post when I get on the computer. IHUB does not allow or at least I don’t know how to load a screenshot or photo from my phone. I can only do it from the laptop when I get home. And I will.
But basically one of the users on Stocktwits posted an email response he got back from Rik.
Here is a copy and paste of the link to that post.
https://stocktwits.com/fireman139/message/535560638;
Purchasing stock in the open market is not manipulation. Show me where the price was manipulated. Did 1000 shares move the ask. Nope. Did 100 shares move the ask. Nope. Did 10000 shares move the ask. Nope. It wouldve taken millions of shares to move the stock up. The sec is grasping at straws.
I was right about ripple. Ill be right again here.
True, but similarly anybody who says that the SEC is going to lose, is also BS, because it is an absolute guarantee that they are getting a win on the point of stock manipulation
And just that one point alone, is a win. They don’t need all the others.
What other board??? Post the board for everyone to see.
Only the sec or nphc knows what was offered in mediation as a deal to avoid trial.
So anyone that says there was a specific deal offered with terms of the deal is bs cause they dont know.
You have to read the complete thread to understand we were talking about what the sec was asking for or willing to compromise in mediation.
It turns out that only the sec and nphc knows that. So when someone else tells you what deal was offered, you know its bs unless they are the sec or nphc.
Yeah, so instead of going to court and allowing them to get everything they want, give them half of what they want now, and save the company.
The notion of the SEC losing is absolutely ridiculous when we know for a fact that Rik already admitted to stock manipulation. Does anybody really expect the jury to say “no you didn’t! We find you innocent! Despite your admission!“
If the SEC gets no conviction, but that one, then they won! They don’t need to get all the other ones.
If you read the court filing, you would see what they are asking for.
Fire up the band. BK and then the fat lady sings.
Perhaps editing it would be better.........................
Here is what's coming from Deitsch and NPHC
Here is what Deitsch the CEO has done for NPHC in 19 years:
IMHOBOTAF
I think this should be taken down. It’s embarrassing at this point! Absolutely, not true, and not happening!
I hope you’re right. Let’s see what happens.
" with a conviction against us. Never getting listed on any decent stock exchange"...
If the company meet the requirements to be listed, the conviction won't matter.
Lot's of companies loose to them and are still listed.
I believe you are correct... he will be found guilty, and the SEC will win the case.
I don’t know where you’re getting this idea that the SEC is going to lose?
It’s an absolute certainty that he’s going to be convicted of stock manipulation. How do I know? He admitted to it!
He said that he did it to push back on the shorts. Now, human to human, I totally get it. It’s screwed up what the shorts were doing at the time. But nonetheless, this is a court of law, And what he did is technically illegal. It doesn’t matter that it was $10 worth. It’s still against the law.
So although the sentence may be nothing, the fact remains, he will be convicted of it. And if all he gets convicted of is that, the SEC wins.
So after that, loss to the SEC, I ask you to please tell me where do we go from there when we are in the expert market with a conviction against us. Never getting listed on any decent stock exchange, no investors going to want to invest or buy stock. Please tell me where do we go from there?
Being that the ceo has more shares than anybody, it doesn't make sense that all he has to do is step down and bring someone else in and everything becomes fine again.
Where are you getting that info from? Is the sec lying to you? It just doesnt make sense.
Im willing to bet there is more to it. Really think about it. If everything is fine with a new ceo, then rick could walk away and do great with that outcome.
I dont believe that a replacement ceo fixes the outcome. I will look more into it.
You’d think after years and years and years of bad decision making and bad decision making and bad decision making a smart guy like Rik would wake up at one point and say “Hmmm, I make bad decisions all the time, let me for once do the opposite of what my instinct tells me. You know what, I’m going to resign and let someone else take over and save my company. I still own all my shares, and nothing gets hurt, but my ego“
Bad decision after bad decision, he lends some crook $250,000 from the company’s money, that guy doesn’t pay back, now NPHC got a judgment for 1,500,000 shares of a company that has no volume.
We have absolutely no chance of liquidating that useless company’s shares and recouping that $250,000.
We sure could have used that money now couldn’t we?
Bad decision after bad decision after bad decision, including the decision to go to court.
All these bad decisions are at our expense!
That’s why Rik needs to resign immediately and hand the reins over to somebody else!
If Rik wants to go down this reckless road, the least he should do, the least he should do is pay for his own defense and use the company money to keep us current so we don’t get kicked off the OTC.
Why is he using company money When this whole lawsuit is pretty much about his behavior?
He uses company money to defend himself, and then sends us to hell to the expert market?
I hope you’re right, and I would love to apologize to Rik if I’m wrong. And I will pick up the phone and do it because I’m a big enough man to do so.
But a massive massive risk at the expense of others is being taken, when it could be resolved right now, with a small ding to Rik’s ego
Yeah, it’s absolutely horrific to be accused of something you haven’t done, but as far as stock manipulation, even if it’s a small amount, he admitted to it.
It is absolutely horrific to be accused of something you have not done, but at the same time you look at the bigger picture and you take your partners and investors well-being into consideration.
If this was a criminal case, I would agree, 100% to fight tooth and nail, but it’s not
The worst case scenario it seems here for Rik is to be banned from holding a position in a public company for five years. That does not seem so horrific when you’re saving hundreds of peoples, and hundreds of families money.
Nphc isnt going to lose. Its going to be another stain on the crooked sec new york office. The only thing the sec has is a couple of late disclosures. It wasnt even non disclosure , it was late dosclosure.
And by the way, with regards to the count of stock manipulation, Rik is 100% guaranteed to get convicted of that. He admitted to it. I know in the past you said that it was pennies, that’s true, but you’re conflating conviction with sentencing
Yes it may be a small amount, but that won’t affect conviction, it will affect sentencing.
So he will get convicted of it, but the sentencing may be absolutely nothing because it’s a small amount. But make no mistake, 100%. He will get convicted of stock manipulation! This is guaranteed! No matter what you say to me. This is just basic 101 knowledge.
I dont know what the crooked sec is asking for. I assume you dont know either. Did the ceo tell you? But if someone accused you of something you didnt do, then you should defend yourself.
Not if we go to court and lose the case.
There are ways back from expert market. Ive seen other companies do it before.
Rik is taking a huge huge risk with the investors money by letting this go to trial. We supported him up until now, but it’s reached a point where he should just resign and turn the the company over to another CEO.
The company can still be salvage now, if it goes to trial, and he loses, that’s it! There is no coming back! We all lose our money!
Very selfish of him in my opinion.
Not maybe, it’s definitely going to the expert market! Rik stated in an email to other investors that he is saving up money for his defense.
And once in the expert market, we will never get back to OTC, you know that.
Nphc is not going to grey market. Maybe expert if they dont file financials. The non or late filings appears to be the doing of the sec which is not protecting current nphc shareholders. The sec only cares about harming the current nphc investors to collect monies from nphc to keep for themselves.
Sec lost its case. Sec employees wasted time and money to collect nothing. Ripple soared today. Same thing will happen with nphc. sour sec employees hitting the message boards will do the same when they lose to nphc.
Ripple won case against SEC....Not so fast
Ripple Labs scored a victory as Judge Analisa Torres ruled partially in favor of the company in a case brought forth by the Securities and Exchange Commission dating back to 2020.
According to documents filed on July 13, Judge Torres has granted summary judgment in favor of Ripple Labs, ruling that the XRP token is not a security, but only in regards to programmatic sales on digital asset exchanges.
However, the federal judge has ruled that XRP is a security when sold to institutional investors, as it met the conditions set in the Howey Test. (and therefore under the SEC jurisdiction).
I guess if Nutra Pharma can prove it is not a security, it can win. Might not be so difficult. If Nutra Pharma takes the position that it never was a security, and that it was a scam and always intended to be a scam and therefore SEC has no jurisdiction it might win.
(Acceptance of service, and defending not withstanding )
I see nothing in the tentative result of the Ripple case that is even remotely applicable.
Just in case I’m being negative, you obviously are more experienced than I am, and this is a sincere question, even if we win the case against the SEC, how do you envision us moving from there when we are in the gray market, and most likely OTC will not except us back?
Then, if we lose? How do you see us coming back from that? The OTC won’t take us back and we have a fraud charge against us.
This is a sincere question to you, How do we get back to over a penny or even more?
Let’s see, if that happens, I will owe Rik a big apology. But if they lose, Rik owes me $900,000! Very disproportionate I think when it could all end now with one person just bowing out
Let’s see, I would love to apologize to Rik
Sec just lost its case against Ripple. Next, the overreaching sec out of New York is going to lose the nphc case, too.
I thought Rik would be a bigger man than this. I’ve had many conversations with him, and he’s always been super smart, kind and reasonable. I even took his son out for drinks and a cigar when he came in to Los Angeles. I wanted to meet his son not just as a kind gesture, but also to see what kind of person Rik is, because you can judge the parents from their children. Rik’s son is super smart as well, but more importantly, very sweet and kind and humble and I liked him a lot. I hoped that apple didn’t fall far from the tree.
I always thought of Rik as a good guy, who, at the end of the day would do the right thing, And at this last moment, taking the fall, and not letting all of us investors lose our money is the right thing. He would still own all his shares in the company, and it wouldn’t cost him any money, just a ding to his ego for a few years.
All the pawns have been sacrificed to possibly save the King
I read on another board that the mediation yielded nothing.
Expert market here we come!
Even if the company wins the trial next year, the SEC still wins because the company is destroyed.
I hope so…
Mediation takes time.
They could go back to the table many times.
Well, good news usually trickles down to us pretty quick, since we’ve heard nothing it’s safe to say that there was no compromise. We are going to court NEXT YEAR with a stop to the expert market first.
It DOESN'T MATTER!--IT'S-A-TOTAL-FRAUD!!!
WHAT IS IT ABOUT "FRAUD" THAT THE GAMBLERS HERE DON'T UNDERSTAND!?
IT DOESN'T MATTER IF THE SEC LETS HIM OFF LIGHT OR IF THEY SAY "WE'RE PUTTING IN A NEW CEO!"
IT DOES NOT MATTER..........
BECAUSE IT'S ALL A...... F.R.A.U.D!!!!!
YOU CAN'T FIX THAT!!!
TIM COOK COULDN'T FIX THIS!!! NOBODY CAN!!
IT NEEDS TO BE SHUT DOWN!
IT'S SHOCKING TO SEE SUCH LOW INTELLIGENCE, OR SIMPLY DELUSIONAL "HOPIUM!"
... IT'S JUST RIDICULOUS!!!
HOW MANY TIMES HAVE I POSTED THE LAWSUIT, THE CROOKS RIK HIRES, THE FINANCIALS........ EVERYTHING POINTS TO FRAUD!!!
WAKE. UP!!!!!
SERIOUSLY!!!
Seems to me EVERYTHING hinges on them settling Monday
If they settle, Rik can spend money on getting us current and eventually CE remove If they don’t settle, Rik has to save every penny for the defense, he won’t get us current, and we get delisted from OTC and end up in the Gray market where stocks go to die.
Mediation on Monday decides if a reasonable compromise exists. If not, then it’s a trial next year.
Do you think that the CE might possibly be removed?
To be fair> July 10th should tell the story, I hope. As far as your congratulations goes, I say thank you. I cannot be any other way at this point but hopeful.
Only AN IDIOT-BLAMES-THE-SHORTS!!! NPHC!
THERE ARE NO SHORTS!!! (UNLESS YOU THINK THAT 5,000 REMAINING TRAPPED SHARES COUNT... ABOUT $0.50)!!!!
NO BROKERAGE WOULD EVER ALLOW YOU OR I TO SHORT A SUB PENNY STOCK!!
ONLY A COMPLETE IDIOT DOESN'T UNDERSTAND THAT YOU CAN'T MAKE ANY MONEY SHORTING A $0.0001 STOCK!! THAT'S SO STUPID!!! IT'S INFINITE RISK AND ZERO POTENTIAL FOR PROFIT!!
ONLY AN IDIOT DOESN'T KNOW HOW TO READ THE FINANCIALS AND SEE THE MASSIVE DEBT AND INEVITABLE BANKRUPTCY!!
ONLY AN IDIOT CAN'T SEE THAT THIS IS A COMPLETE AND TOTAL FRAUD!!!
THE SEC IS SUING RIK AND NPHC FOR FRAUD AND ILLEGAL STOCK MANIPULATION!!
ONLY AN IDIOT THINKS THAT THIS WILL END WELL FOR NPHC OR RIK!!!
BWAHAHAHAHAHAHAHAHAHAHAHAHA!!!
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Nutra Pharma Corp. (OTC: NPHC) is a biopharmaceutical company engaged in the acquisition, licensing and marketing of homeopathic treatments and ethical drugs for the management of pain, neurological disorders, cancer, auto-immune and infectious diseases. Nutra Pharma, through its RectoPharm subsidiary, carries out basic drug discovery research and clinical development and also seeks strategic licensing partnerships to reduce the risks associated with the drug development process ReceptoPharm is developing technologies for the production of drugs for HIV and multiple sclerosis (MS), and also offers small and start-up biotech companies a full range of contract research services.
Investment Highlights
Corporate Strategy
Nutra Pharma's over-the-counter (OTC) products allow the company to achieve profitability and fund longer-term clinical trials in the therapeutic area. The therapeutics address a market size of > $10 billion, while the OTC products segment addresses a market size of $200 million - $500 million.
Reducing Risk
Nutra Pharma's strategy aims to optimize risk and return. At present, the company has a line of OTC products that bring in cash. This revenue will not only help fund development of the company's therapeutic line but, since sales of the OTC line and therapeutic line are uncorrelated, will result in a smoother revenue stream. By having what is, essentially, two businesses under one roof, Nutra Pharma mitigates risk to shareholders.
Revenue in the Short-term from OTC products
The OTC line comprises a number of analgesics. In October 2009, Nutra Pharma launched its first, called Cobroxin®, an over-the-counter pain reliever designed to treat moderate to severe chronic pain. In May 2010, the company launched its second consumer product, called Nyloxin®, an over-the-counter pain reliever that is a stronger version of Cobroxin.® And in December 2014, it launched Pet Pain-Away, an over-the-counter pain reliever designed to treat pain in cats and dogs. Nyloxin is currently being distributed both domestically and internationally via network marketing through the nationwide distributor Lumaxa.
Maximizing Return with a High-Value Therapeutic Line
Through its wholly owned subsidiary, ReceptoPharm, Inc., Nutra Pharma conducts drug discovery research and development activities. Nutra Pharma's R&D pipeline consists of several novel therapies in various stages of development to prevent and or treat multiple sclerosis (MS), human immunodeficiency virus (HIV), adrenomyeloneuropathy (AMN), herpes, and rheumatoid arthritis (RA). And the company is pursuing, aggressively, regulatory approval for these treatments.
Nyloxin
Nyloxin is an anti-inflammatory, non-toxic, non-narcotic, non-addictive, non-steroidal analgesic designed for chronic pain relief. It was first launched as an oral spray for treating back pain, neck pain, headaches, joint pain, migraines, and neuralgia, and as a topical gel for treating joint pain, arthritis pain and pain from repetitive stress.
Since the beginning of 2014, it has been moved by the over 3,000 distributors in the Lumaxa network. Nutra Pharma is approved to distribute Nyloxin in India and is currently negotiating with large distributors throughout the region. Nutra Pharma is also working with several potential distributors in China and expects orders in India and China in the near future.
Nyloxin is clinically proven to treat Stage 2 (moderate to severe) and Stage 3 (severe) chronic pain. It is safe, non-narcotic and non-addictive, and does not impair cognitive function. Nyloxin is available in three strengths and 12 SKUs. In Regular Strength, Nyloxin is offered as an oral spray, a topical roll-on, and a topical gel. These same three preparations are offered in Extra Strength. The company also plans a 'Military Strength' Nyloxin for U.S. government buyers and military personnel.
Nyloxin Advantage
Jeff Gottfurcht is the first person in the world with rheumatoid arthritis to scale Mount Everest. Jeff reached the summit on May 14, 2011. He took Nyloxin with him as his pain reliever of choice.
Testimonials
![]() | Nyloxin Topical Gel I'm a massage therapist I have incorporated Nyloxin into my pain therapies with unbelievable results. I believe in this product so much that I became a distributor just so my clients can live pain free. - Steve Smith |
![]() | Nyloxin Extra Strength Topical Gel I have never written a testimonial before. I have to tell you I am completely amazed at how well this product has worked for me. I have been on hydrocodone for years. Four days after taking this I have not needed it. I truly am shocked at the difference this has made in my pain. I have already reordered! - Elyse Feldberg |
![]() | Nyloxin Oral Spray I am amazed at how well the Nyloxin spray has worked for me. I have had headaches for years, which sometimes turn to migrains. I have done biofeedback, been in the medical care of neurologists, and gone through testings, nothing I have tried has ever gotten rid of my headaches for any length of time, until I tried the Nyloxin spray. I even went to the mountains last weekend at 6,000 feet, for 3 days without a headache the whole time, I don't remember that ever happening. I am sold on this product. - Nancy Leamons |
*Some of the testimonials listed here may be from MyNyloxin Independent Entrepreneurs who may receive compensation which is received based on the sale of Nyloxin products."
Pet Pain-Away
Pets Owned in the U.S.: 95.6 million cats, 83.3 million dogs
The market for pain relief in dogs and cats is more than $200 million.
Millions of pets suffer from acute or chronic pain. While acute pain is a normal sensation triggered in the nervous system to alert your pet of possible injury and the need to take it easy, chronic pain is different, chronic pain persists. Pain signals keep firing in the nervous system for weeks, months, even years.
Historically, pain relief products for pets have been shown to cause other significant healthcare concerns and side effects.
Today, cobra venom is successfully being used for treating various forms of pain, autoimmune and neurological disorders. The Nutra Pharma subsidiary, ReceptoPharm, and other researchers have definitively proven that extracts from cobra venom contain constituents that control pain and inflammation in animals.
Pet Pain Away provides all-natural anti-inflammatory analgesic pain relief that is non-toxic, non-narcotic, non-steroidal and contains no aspirin or acetaminophen. Safe to use on pets, it treats conditions that cause chronic pain in animals.
Current Medical Research of the Available Remedies
Current pain relief products for pets such as NSAIDs (just for dogs) such as Carprofen (Novox or Rimadyl), Deracoxib (Deramaxx), Etodolac (Etogesic), Firocoxib (Previcox), Meloxicam (Metacam ) or Tepoxalin ( Zubrin) have been shown to cause kidney, liver, or digestive problems. Cats do not tolerate NSAIDs of any kind well. The only approved NSAID for cats in the United States is meloxicam and it is only approved for a single post-surgical injection to relieve pain. The dose must be exactly correct for the cat's weight. If it is given longer to cats, it often causes severe kidney damage.
Other medications such as Amantadine, Gabapentin and Tramadol may cause upset stomach, decreased heart rate, panting, and constipation. Veterinarians may prescribe stronger opiates only for a short periods. They usually don't prescribe steroids for pain, as they can have serious side effects. Veterinarians are usually hesitant to utilize pain therapies in companion animals because of the following: significant side effects, including nausea, vomiting, drowsiness, itching, constipation and respiratory depression; buildup of tolerance to analgesic requiring higher dosage over time to experience same effect; addictive properties that include severe withdrawal symptoms.
Therapeutic Pipeline
ReceptoPharm's research and development pipeline consists of several novel therapies in various stages of development to prevent and or treat multiple sclerosis (MS), human immunodeficiency virus (HIV), adrenomyeloneuropathy (AMN), herpes, rheumatoid arthritis (RA) and pain.
Abbreviations
Phase 1 (P-I), Phase 2 (P-II), Phase 3 (P-III)
RPI-78M
RPI-78M is derived from alpha-cobratoxin (α-CTX) by an oxidative procedure. Alpha-cobratoxin is the primary neuroactive peptide found in the venom of Asiatic cobras, and it represents the single active ingredient in the formulation under investigation. RPI-78M compares favorably with competing products. It lacks measurable toxicity, but is still capable of attaching to and affecting the target site on the cells. This means that patients cannot overdose.
Following years of investigations in humans and animals, it has displayed no serious adverse side effects. Patients experience symptomatic improvements, usually within six months of therapy. RPI-78M is extremely stable and resistant to heat, and so has a long shelf life. The drug's stability has been determined to be over four years at room temperature. It is easy to administer as a daily intramuscular injection (mcg dosing). RPI-78M has completed two trials for its use to treat adrenomyeloneuropathy (AMN). And at present, there are about 300 multiple sclerosis patients on open-label trials with RPI-78M.
RPI-MN
Nutra Pharma has received Orphan Drug Status from the FDA for RPI-78M as a candidate for the treatment of juvenile MS. Nutra Pharma is actively seeking collaborative research partners for early stage trials of RPI-78M in the treatment of juvenile multiple sclerosis (MS). The company has already been in contact with potential researchers, hospitals and sites of care for the purpose of moving forward with phase I/II clinical studies.
Nutra Pharma believes that RPI-78M provides an entirely new approach to the treatment of auto-immune diseases, including MS. As an immuno-modulating agent and not an immunosuppressive, RPI-78M could be a disruptive new drug entity in the autoimmune disease space. In previous open-label studies, RPI-78M has shown consistent symptomatic improvements within a period of less than six months in all stages of MS. The recently received Orphan Drug designation from the FDA allows the company to fast-track efforts through the clinical process. Based on existing clinical experience with RPI-78M, Nutra Pharma is confident that it can receive accelerated approval in a relatively short time-frame (expected in as little as 22-26 months).
RPI-78
Market Opportunity
According to the Centers for Disease Control and Prevention (CDC), there are currently about 1.2 million persons in the United States over the age of 13 who are human immunodeficiency virus (HIV) infected. Over the past 10 years the number of people living with HIV has increased. The incidence of new HIV infections has remained fairly stable, however, at about 50,000 new cases every year. As yet there is no cure for HIV: no compound has been isolated that kills the pathogen. But antiretroviral therapies (ART) can reduce the ability of the virus to reproduce and so keep infection at a level that does not overwhelm the immune system. The World Health Organization (WHO) estimates that, currently, there are about 37 million people worldwide living with HIV. The market size of antiretroviral therapies is estimated to be around $15 billion.
Like HIV, multiple sclerosis (MS) occurs when the immune system malfunctions. MS develops when the immune system attacks the protective sheath (myelin) that covers nerve fibers and causes communication problems between the brain and the rest of the body. The National Multiple Sclerosis Society estimates that about 2.3 million people are affected by MS worldwide. The market size of the MS drug market is about $16.7 billion. Adrenoleukodystrophy (AMN), also known as Schilder's disease and sudanophilic leukodystrophy, is another condition in which the myelin sheath is damaged. The AMN market has the potential to reach $400 million after the launch of an effective treatment. The Herpes Simplex Virus (HSV) affects thousands. According to the CDC, in 2013, some 306,000 persons visited a doctor for the first time in connection with a herpes condition. And the CDC also reports that, in 2007, about 1.5 million people in the U.S. were living with rheumatoid arthritis.
Management
Nutra Pharma is led by a management team comprised of highly experienced and educated professionals with a strong track record of excellence. This leadership is well-equipped to advance Nutra Pharma's therapeutic pipeline and increases distribution of its OTC products internationally.
Rik J. Deitsch - Chairman and Chief Executive Officer
Rik Deitsch holds both a B.S. in chemistry and an M.S. in biochemistry, and has conducted clinical and laboratory research in collaboration with scientists at Duke University Medical Center and the Cleveland Clinic. Deitsch is the author of two books and is an adjunct professor, teaching several courses for Florida Atlantic University's College of Business and Continuing Education Department.
Stewart Lonky, MD MBA - Director - Audit & Compensation Committees
Stewart Lonky is board certified in internal medicine, pulmonary and critical care medicine. He has published over a dozen articles in the peer-reviewed literature. Stewart is the former chief medical officer of a medical device company that developed diagnostic products for the early diagnosis of cervical and oral cancer. In that role, his duties included the direction of clinical research and the ultimate clearance of three new diagnostic devices by the U.S. Food and Drug Administration (FDA).
Harold H. Rump - Director
Harold Rump holds a B.S. from the United States Naval Academy. He is the former president, and director of Biogenix, Inc., a company involved with research and development of antiviral peptides from cobra venoms, including clinical trials under FDA-issued Investigational New Drug applications.
Garry R. Pottruck, CPA - Director - Chairman, Audit & Compensation Committees
Garry Pottruck is a CPA and financial expert on the NPHC's board of directors. Previously he served as chief accounting officer/controller at Scopas Technology Company, Inc., a NASDAQ-listed, development stage biotechnology research and development organization. He was, also, a principal and manager in the firm Argy, Wiltse & Robinson, PC ("Argy"), headquartered in McLean, Virginia.
Nutra Pharma Corporation | QualityStocks Investor Relations |
Please see disclaimer on the QualityStocks website: http://disclaimer.qualitystocks.net
Contact :
phone 954-509-0911
Email investor.relations@nutrapharm.com
12502 West Atlantic Bvld.
Coral Springs, FL 33071
Shares outstanding 442,185,921 as of May 23,2017.
Shares outstanding 1,233,519,298 as of July 20,2017.
http://www.otcmarkets.com/stock/NPHC/profile
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Nutra Pharma Corp. (OTCBB: NPHC) http://www.NutraPharma.com is a biopharmaceutical company specializing in the acquisition, licensing and commercialization of pharmaceutical products and technologies for the management of neurological disorders, cancer, autoimmune and infectious diseases. |
ReceptoPharm is an innovative biopharmaceutical drug discovery company developing proprietary therapeutic protein products primarily for the prevention and treatment of viral, autoimmune and neurological diseases in humans, including Adrenomyeloneuropathy (AMN), Multiple Sclerosis (MS), Rheumatoid Arthritis (RA), Pain, and Myasthenia Gravis (MG), and Human Immunodeficiency Virus (HIV). Drug Development The emphasis of ReceptoPharm's approach to drug discovery and the development of new therapeutic agents is based upon specialized receptor-binding proteins found in nature. » Learn More CRO Services ReceptoPharm offers a full range of contract services catering to start-up and small biotechnology companies. These services include pre-production studies, contract manufacturing services, US & EU regulatory support, and quality systems/GMP certification. ReceptoPharm is a wholly owned subsidiary of Nutra Pharma Corporation. |
Designer Diagnostics is a biotechnology sales and marketing company founded for the sale of diagnostics testkits for infectious diseases. Designer Diagnostics Test Kits provide a highly cost effective, highly efficient, low infrastructure solution for identifying and testing sensitivity of Nontuberculous Mycobacteria (NTM) that are capable of utilizing paraffin wax as a sole carbon source or those that are hydrophobic. Additionally Designer Diagnostics provides an efficient solution for the rapid identification and sensitivity testing of Tuberculosis (TB). Designer Diagnostics is a wholly owned subsidiary of Nutra Pharma Corporation. |
Cobroxin/Nyloxin TV Commercials and Advertising |
Here is a YouTube clip from 2013 showing the product: |
Nutra Pharma (NPHC.OB) RECENT NEWS | |||||
SOURCE: Nutra Pharma Corporation ![]()
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ADDITIONAL NUTRA PHARMA INFORMATION |
12/10/09 Webinar from Rik J Deitsch, Chairman and CEO of Nutra Pharma Corporation:http://a40.video2.blip.tv/5350002509400/Vpoole-NHPCPresentationByCEO594.wmv?bri=11.6&brs=126 |
CHECK OUT THE Nutra Pharma Blog FOR MORE INFO ON THE WORLD MONEYSHOW CONFERENCE! |
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Nutra Pharma (NPHC.OB) PATENTS |
U.S. Patent No. 5,989,857, which was granted in November 1999 with 10 claims.U.S. Patent No. 6,670,148, which was granted in December 2003, with 9 claims. The patent further describes the method for preparing a bioactive peptide (protein) found in cobra venom, in a stable, inactivated form, by treating the peptide with ozone.Buccal Delivery System, on which a patent is pending. This application describes a throat spray that permits efficient delivery of the modified peptide drugs to the body through oral mucosa.Technology contained in one pending U.S. patent application for the further development of bioactive peptides in cobra venom for use in the treatment of HIV and MS.Technology contained in two pending U.S. patent applications for Immunokine Composition and Method, which describes a method for developing modified peptides from alpha-cobratoxin.Technology contained in two patents pending for the topical delivery of our proprietary wound healing treatment, which was developed in conjunction with Bio Therapeutics. One of these products is in the form of an ointment style skin protectant and the other a foaming aerosol. |
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During our second quarter of 2015 and thereafter, the following has occurred:
On April 15, 2015 we provided an update regarding plans to market Nyloxin® through S.Zhaveri Pharmakem for distribution throughout India. The update stated that our management had been working in Mumbai throughout the week to finalize plans for the national rollout of Nyloxin®.
On April 20, 2015, our stockholders voted at a special meeting of the shareholders held in Coral Springs, Florida to approve a one-for-forty reverse stock split of our issued and outstanding shares of common stock. Under the adopted proposal, each forty shares of our presently issued and outstanding Common Stock as of the close of business on the effective date was converted automatically into one share of our post-Reverse Split Common Stock. Fractional shares and "odd lots" were rounded up to the nearest whole share. The Reverse Split did not change the number of authorized shares of our Common Stock. The principal effect of the Reverse Split was the reduction in the number of shares of Common Stock issued and outstanding, from 1,510,950,321 shares as of March 6, 2015 to 39,123,758 shares after the Reverse Split was deemed effective. The Reverse Split affected all of our shareholders uniformly and did not affect any shareholder’s percentage ownership interest in Nutra or any shareholder’s proportionate voting power. Per share and weighted average amounts have been retroactively restated in the accompanying financial statements and related notes to reflect this stock split.
On April 22, 2015 we announced that we had engaged the Vancouver Commodities Group (VCG) to begin the process of identifying and vetting potential distributors in China for Nyloxin®.
On April 30, 2015 we announced that we had received notification of the acceptance of Nyloxin® by the China International Exchange and Promotive Association for Medical and Healthcare (CPAM). This process was successfully conducted by the Vancouver Commodities Group (VCG) that had been hired by Nutra Pharma to begin the process of identifying and vetting potential distributors in China.
On May 14, 2015 we announced that we had engaged the Nature's Clinic to begin the process of regulatory approval of our Company's Over-the-Counter pain drug, Nyloxin® for marketing and distribution in Canada. The Nature’s Clinic has already begun setting up their Chatham, Ontario warehouse and expect to complete the approval process to begin distributing Nyloxin® by the end of the year.
On May 26, 2015 we announced that we had engaged Medical Strategy Consultants, LLC to aid the company in the filing of Orphan Drug applications with the U.S. Food and Drug Administration ("FDA"). The first application under development is for the treatment of Pediatric Multiple Sclerosis with the Company's lead drug candidate, RPI-78M. In order to create the application, RPI-78M needed to meet several key criteria. This included preclinical data in support of the drug that provided a reasonable rationale for the treatment of the disease based on its potential ability to treat the symptoms of multiple sclerosis. The FDA grants Orphan Drug Designation status to products that treat rare diseases, providing incentives to sponsors developing drugs or biologics. The Orphan Drug Act of 1983 is intended to assist and encourage companies to develop safe and effective therapies for the treatment of rare diseases and disorders, defined as those affecting fewer than 200,000 Americans at any given time. The designation of RPI-78M as an Orphan Drug would provide Nutra Pharma with a 7-year period of market exclusivity in the U.S. upon approval of the drug, as well as tax credits for clinical research costs, the ability to apply for grant funding, clinical trial design assistance, assistance from the FDA in the drug development process and the waiver of Prescription Drug User Fee Act (PDUFA) filing fees which could be in excess of $2.5 million. The decision to proceed with an Orphan Drug Designation submission is part of Nutra Pharma's plan to move forward with the preparation of an Investigative New Drug Application.
On June 9, 2015 we announced that we had entered into a facility and personnel sharing agreement with Nationwide Laboratory Services, Inc. (NLS): Nationwide Laboratory Services, Inc. operates as a clinical diagnostics laboratory, performing routine and specialty human diagnostics. The company also offers clinical trial services, such as specimen and special handling requirements, status of test results, turnaround time, testing, participants test results, channeling calls to technical or professional personnel, communicating specimen issues, notifying investigational site of critical calls, and telephone support with data management training services; and courier tracking services. The collaboration provides NLS with the use of our lab space and equipment and provides us with lab and clinical personnel as well as cost-savings on rent and utilities.
On June 23, 2015 we announced that we had completed a series of projects to update and expand the facilities that house the Asian cobras utilized for the production of Nyloxin®. We also announced the addition of 100 snakes to the existing milking line to increase venom production for the upcoming international orders from India and China.
On June 30, 2015 we announced that we had engaged Pickwick Capital Partners; a leading investment banking, securities and investment management firm, to provide strategic corporate planning and investment banking services. Pickwick will focus on assisting Nutra Pharma in our strategies for maximizing shareholder value through its full scope of investment banking services.
On July 10, 2015, SeeThruEquity, a leading independent equity research and corporate access firm focused on smallcap and microcap public companies, announced it has initiated coverage of Nutra Pharma Corporation with a Price Target of $0.53 per share.
On July 15, 2015 we announced that we had filed an application with the FDA for orphan drug status of the Company's RPI-78M drug candidate for the treatment of Multiple Sclerosis in children. This represents the first such filing for the company.
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