Invest in and/or try different antiviral protocol

[Stretched]

Reviewed by Barchart, Stock on NY Stock Exchange: NNVC

Ultra-Broad-Spectrum Antiviral Nanomedicines Enabled by the This Public Company’s Revolutionary Platform Would Open Up Very Large Market Opportunities

The company’s one lead drug alone, NV-387, potentially addresses a $2.5 to $4.3 billion market. We’re talking a single drug that could treat covid, RSV, the flu, and even monkey pox. And this drug has just successfully completed phase 1 clinical trials.

NV-387’s extremely broad antiviral is a host mimetic that acts as a decoy to attract and trap many diverse viruses, preventing the virus from replication and reinfection of other cells.

In laymen’s terms, NV-387 could revolutionize antiviral treatment just as antibiotics did against bacteria. Susceptible viruses CANNOT escape NV-387, even as they continue to evolve in the field into variants.

NV-387 could change medicine as we know it. Still, it is just one drug in this organization’s promising product pipeline.

Thus, this company should be at the top of your watchlist. Read more now.

 

[Florida Guy]

Antivirals have helped many people with mecfs so maybe this will too

 

[Norwegianlad]

Would this drug also help people with ME/CFS if the virus already is everywhere in the body?

 

[Norwegianlad]

As for the investment part, I would say every company in that field has ''one revolutionary drug'' that should make the company tons of money in the future. It's not investing, but gambling to buy those kind of stocks.

 

[heapsreal]

Would this drug also help people with ME/CFS if the virus already is everywhere in the body?

Possibly it should, as our cells change over at varying rates. One example is red blood cells I think die off and regenerate every 60 days or so, don't quote me on that. Other cells will take longer and it can be hard for some drugs to cross the blood brain barrier. Fingers crossed it has a broad spectrum of effects on viruses and is affordable as I think cfsme patients will have to take this type of drug for months or maybe longer to clear viruses??

 

[Norwegianlad]

Possibly it should, as our cells change over at varying rates. One example is red blood cells I think die off and regenerate every 60 days or so, don't quote me on that. Other cells will take longer and it can be hard for some drugs to cross the blood brain barrier. Fingers crossed it has a broad spectrum of effects on viruses and is affordable as I think cfsme patients will have to take this type of drug for months or maybe longer to clear viruses??

I hope it is too, but most governments / insurance companies would benefit from us being able to work again, so I am not that worried about pricing.

 

[heapsreal]

I hope it is too, but most governments / insurance companies would benefit from us being able to work again, so I am not that worried about pricing.

You would think so but there's been other antiviral treatments like valcyte that looked promising for cfs. That was 20yrs ago and it's still an expensive treatment, unfortunately. Valcyte could be a helpful treatment for certain subsets.

 

[Norwegianlad]

You would think so but there's been other antiviral treatments like valcyte that looked promising for cfs. That was 20yrs ago and it's still an expensive treatment, unfortunately. Valcyte could be a helpful treatment for certain subsets.

I didnt know that. Do you know what kind of percentage from that drug with ME/CFS get 'cured'? If it's a very low percentage I can see it. But if there is a drug that cures 50% or so, then I'm sure my government would pay for it, if it means half the people can get back to work again they save back the cost pretty quickly on the money they save on paying me every month because I cant work..

 

[heapsreal]

I didnt know that. Do you know what kind of percentage from that drug with ME/CFS get 'cured'? If it's a very low percentage I can see it. But if there is a drug that cures 50% or so, then I'm sure my government would pay for it, if it means half the people can get back to work again they save back the cost pretty quickly on the money they save on paying me every month because I cant work..

If they test the patient adequately and put them in the correct sub group, people can improve, there are a very small number cured and many that relapse. Some have been able to maintain their function from valcyte after switching to famvir or valtrex. Valcyte can be a rough treatment to tolerate and can make you feel alot worse than your usual cfsme until you finish the treatment. One needs close monitoring of liver and kidney function, initially blood work every 2 weeks and gradually don't need the testing as frequently but atleast every 3 months.

A good candidate for valcyte is someone with active cmv and or hhv6 and it is the probable cause of their cfsme.

Alot of research on valcyte and cfs 20years ago. The main Drs at the time prescribing and studying valcyte were Dr Lerner, Dr Montoya and Dr Peterson. If you google valcyte to treat cfs, you will find plenty of info. There's also many threads on here about valcyte.

I'm not confident the government would pay for this treatment, if it was the case, it would have been free and easy to get prescribed for the last 20yrs. It's not a cheap drug, Generics from India use to cost $10 a tablet and the treatment is 1-3 tablets a day from 3 months upto a couple of years in some cases.

 

[godlovesatrier]

Heaps is right.