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There has always been an I,formation leak. I have always thought it was via cdel. And that was the hold the price where it is posts come from
Boca area docs must have some inkling that B is highly effective. For a medical group or groups to start requesting multiple patients receive a compassionate use drug,indicates they have confidence that it is safe and efficacious.
B would not have been approved for use if there were major side effects. Major safety issues would have been vetted in phase 1.
Hcq was never shown to be effective. Even in later studies. Until the rules are changed government employees and former elected officials will turn into lobbyists. Our early u.s. government rules banned this practice
Merck drug will be obsolite before it hits the market. B will have a higher effectiveness rate for the full range of cases. Moderate to severe.
No intercourse. No useage
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What about the other 50% the Merck drug doesn't affect? Billions in sales
Merck drug cuts deaths in mild to moderate cases by 50% . hopefully B does better in moderate to severe cases
Review your statistics. 120 is enough to show a significant difference. FDA has a history of EAU with such sample sizes in this type of situation. Review AZT approval
Donny. What's your source? Don't say DeSantis.
You can't handle the truth. Hippa applies only if you do not want medical facts released or if you have not signed a waivery. Obviously, all involved want the facts out and the story of B told.
Loan my previous post was in reference to SOC not docs. I do not believe they would allow a study to deviate using several different standards of care. You measure your drug candidate against the 1 best treatment
Loan do you really think " several doc's were used" in the study? I believe this was strictly controlled and limited to 1 or 2 courses of treatment.
It's not how the FDA works. If you violate their rules about disclosures, your approval process will be very painful. Follow there guidance and your drug will be fast tracked thru the bureaucracy
Enough P2 outcomes must have been finalized for compassionate use to be considered. Obviously all the data has not been statistically analyzed, but the most important outcomes must have had solid results. Top line will not be released until all P2 factors are analyzed. That's just how it works
Latest p r shows Leo's strong leadership skills. Not only has he moved the cro to completion date, he has worked his magic and moved on the compassionate use issue. Quite a day. Sorry I missed p r date by 1 day.
1 million shares traded in the first 30 minutes. Manipulators are working hard to hold down the price. Only a matter of time until they are overwhelmed.
Love the volume. It has forced manipulator huge blocks of stock to Sri e the price down. Their next move will be to buy those shares back driving the stock back where it started. I'm a buyer at .220
Would love another opportunity to add at .22. Bring it on
Pete. I believe management purposely designed the study with an unusually high number of secondary endpoints. They wanted to be as comprehensive as possible. Something had to stick. Making sure they have collected all of this data has been overwhelmingly. It will be worthwhile, but it still not easy sitting in the waiting room at the maternity ward. Good luck to all longs
Studies always try to enroll extra participants to account for drop outs( for any number of reasons). Malfeasance NO. Professionalism YES
FDA would get involved in EUA because it's a worldwide PANDEMIC
Capt. You are a graphics artist. H
You were right. .27 didn't hold
Do we know how many territories ( as defined by the company)do not have a rep?
Is there a hiring freeze on at AMRN with dozens of territories not coveted? Getting ready for a sale?
Still calling for 2.50. Results have been delayed longer than I expected. I think it's because of all of the secondary endpoint analysis that needs to take place. If results are positive, you could retire from your position- if you owned stock
Marjac , is there a definitive date for the next court proceedings?
Just made my last purchase before press release. Please review what you own and confirm your plans. Press release is imminent. I believe significant information will be released between 9/14 and 9/22. Good luck
Next week we will be saying twtwtw after this week's pr
Go to your fish fry, you may not be able to attend them next year.
600,000 person study analysis. Unvaccinated 11x more likely to die from covid vs. Totally vacinnated
Minnie, the presenter is, at best, on the fringe. The theory about the petrochemical industry suffocating any non- fossil fuel engine has been around for 65 years. Musk made it happen. We have come a long way.
Donny. Please document the 5 phase 2 failures. P is 1( I'll get you started) . what are the other 4?
Vaccines like flu shots will remain blockbuster drugs. B, as a therapeutic, will supplement covid treatments and will be SOC where other viruses are concerned. One of the big pharma companies will want this therapeutic treatment.
Stock purchases in this quarter do not have to be reported on form 13 until mid November. Looking elsewhere
Looking for confirmation . trying to see when 13' s come out to see if they made any purchases. With these large blocks trading someone like them could be taking an anonymous position. That is until they have to report it
Rumor: Ipix is on the Baker Bros. Watch list
The science is extremely promising. This compound and the company are not exactly a household name, e.g.. Penicillin. If P2 is successful Dr Grado may be as well known as Fleming. It's going to take a good result and a good communications campaign to get this stock ready for a buyout
Minnie, isn't P2 designed so that B is compared to the FDA designated SOC?