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Depends on the perception of the majority of the share holders and buyers today. Will this afterhours CC reveal something major that will affect the PPS THURSDAY or not. Meaning for those that do believe , then TSNP is a HOLD , for those that don't today is when one gets out. Whatever close TSNP has today before the CC should represent majority view IMO
Would imagine that is how most shareholders here view TSNP's CC. With a heavy prejudice to a optimistic positive side.
My guess would be THURSDAY so to piggyback whatever news comes out of the TSNP CC for an intended double boost on FORW.
A lot will depend on WHAT comes out of that TSNP CC and WHAT the FORW people could say in their ties to TSNP and what they can state in their own right
Consolidation today ? After the nice UP moves in the past week a little pullback is normal. Current PPS still holding some of yesterdays gains so far today. That is to be considered positive IMO. Some traders buy on the RUMER and SELL on the news are a day or two ahead on their trading maybe. SHORTERS are always out there but many will hold through the CC as it may reveal more positive news that we don't know currently. That will make this coming THURSDAY an interesting day of trading here.
Close above 30 cents BODS well for tomorrow's continued upward move. AIMO
Well WE (I) knew that FORW was going to move up in tandem with TSNP. Am a bit surprised that the % gain today on FORW was so much HIGHER than TSNP
That tells me nothing as a search for "free stock group" brings up squat. So what is his IHUB handle ? again TIA
DGB (DGBUSD) is no BITCOIN (BTCUSD) that's for sure. How it relates to TSNP am not fully understanding just yet.
SHOW ME THE MONEY and a reduction in the mammoth O/S is what shareholders would like to see next week IMO
In that we don't know what news might be released we don't know if these shares are cheapies. PPS already way up recently.
Sorry BUT with a close below 20 cents TODAY see a RED CLOSE TOMORROW. All just IMO of course , nothing fixed in concreate.
One FACT for sure remains , " WE ARE GOING TO NEED MORE COOPER OVER THE NEXT FEW DECADES ". That is based on the expected move into EVs alone. Current suppliers can not produce to that level even with increased mining activity as their grade levels are dropping. SO WHERE WILL THE NEEDED COOPER COME FROM ??? If little to no new cooper deposits are found and mined elsewhere PEBBLES remains an option.
If you had a gain at 55 you did good IMO . There was no way we could have known or even reasonably guessed that it would make it to 70 short term .
In time see it going back above 70 but short term could drop back below 30.
NRGU has and remains a trading stock. Timing IN and OUT is as much luck as it is strategy. GLTU
Guess so as NRGU has been coming DOWN steadily in the last few trading days . Currently 57.45 , down from that 70 6 days ago
Agree , looking like a POP and DROP setup currently to me. Average volume 157M/day and has yet to hit a million volume. Many current shareholders will be more than happy to take a 300% gain today IMO.
The days close and volume will be more telling if TSNP will continue this week to advance more or pullback.
Nice of you to be doing that BUT the BIG CAHONA here that they will listen to is the ACoE. If they say its a "NO GO" then its a NO GO.
BIGGEST LOSSERS here are the NATIVE PEOPLES of BRISTOL BAY. Their lives will stay at no improvement should they chose to stay in the Bristol Bay Area.
Going to be interesting what kind of article SANDY SZWARC / FOR MUST READ ALASKA writes after this release from the ACoE.
NRGU touched over 70 now. More than doubled in the past month. Overall markets are stronger too. Is a recovery coming sooner than most would think , or are we seeing a hopeful market bubble ?
Most investors in NAK DO NOT LIVE IN ALASKA but WHEN in time the PEBBLES MINE PROJECT is permitted and dramatically changes the lives of the locals in the BRISTOL BAY AREA for the BETTER , then they (we) can take some pride in having been an investor here.
That page does not exist , so my computer states , TRY AGAIN to post a link
The way COVID is spreading WORLD WIDE , that ANNOUNCEMENT based on preliminary test results so far of BRILACIDIN was to be expected.
GO IPIX GO BRILACIDIN , be an instrument of help to mankind
What trial ? ARE YOU KIDDING ME ???
Company finalizing Brilacidin protocol; clinical study anticipated to commence in 4Q2020
WAKEFIELD, MA – November 2, 2020 (GLOBE NEWSWIRE) Innovation Pharmaceuticals (OTCQB:IPIX) (“the Company”), a clinical stage biopharmaceutical company, announced today receipt of written feedback from the U.S. Food and Drug Administration (FDA) that is in general agreement with the Company’s planned clinical trial for Brilacidin, a defensin-mimetic drug candidate, for the treatment of COVID-19. The FDA response completes the Pre-Investigational New Drug (Pre-IND) process.
The FDA provided feedback on clinical development plans for the evaluation of Brilacidin as a treatment for COVID-19. The Company is now incorporating this feedback and finalizing the trial protocol for its planned Phase 2, randomized, double-blind, placebo-controlled, multi-national study to evaluate the efficacy and safety of Brilacidin in hospitalized patients with COVID-19. Target enrollment for the trial is 120 patients. Contract Research Organizations have been secured to expedite trial enrollment with many clinical sites expressing interest in participating in the study. The Company anticipates commencing the Brilacidin for COVID-19 clinical trial in 4Q2020.
“Getting to the point of being able to advance Brilacidin as a potential treatment for COVID-19 required an enormous amount of time, resources, and team effort,” commented Leo Ehrlich, Chief Executive Officer at Innovation Pharmaceuticals. “From the manufacturing of drug supply, to researching Brilacidin’s mechanisms of action in vitro against SARS-CoV-2 in infected cells, to now preparing and planning for the COVID-19 clinical study—was an extraordinary effort.”
Ehrlich added: “We are extremely grateful for the hard work of our employees, consultants and affiliated researchers. While no one can predict with certainty how Brilacidin will perform in clinical testing against COVID-19, we are optimistic based on the compelling preclinical antiviral data we have released and Brilacidin’s consistently successful results in other clinical trials. Our hope is Brilacidin for COVID-19 can be an important part of the solution to help rid the world of this deadly coronavirus.”
Brilacidin COVID-19 Preprint
The Company, based on pre-clinical research conducted in collaboration with George Mason University, has released a preprint, prior to formal peer review submission, demonstrating Brilacidin’s COVID-19 treatment potential. The preprint can now be downloaded on bioRxiv.org at the link below.
· Brilacidin, a COVID-19 Drug Candidate, Exhibits Potent In Vitro Antiviral Activity Against SARS-CoV-2
https://www.biorxiv.org/content/10.1101/2020.10.29.352450v1
Global COVID-19 Cases and Mortality
An online tool tracking COVID-19 cases and mortality, both in the U.S. and globally, can be found on the Company’s website (http://www.ipharminc.com), and at the following link:
https://ipixcovid19tracker.com/
Brilacidin and COVID-19
Brilacidin is one of the few drugs targeting COVID-19 that has been tested in human trials (a total of 8) for other clinical indications, providing established safety and efficacy data on over 460 subjects, thereby potentially enabling it to rapidly help address the novel coronavirus crisis. Laboratory testing at independent laboratories supports Brilacidin’s antiviral ability to safely and potently inhibit SARS-CoV-2. In a human lung cell line, Brilacidin achieved a Selectivity Index of 426. A molecular screening study of 11,552 compounds also supports Brilacidin as a promising novel coronavirus treatment. Additional pre-clinical and clinical data support Brilacidin’s inhibition of IL-6, IL-1ß, TNF-a and other pro-inflammatory cytokines and chemokines, which have been identified as central drivers in the worsening prognoses of hospitalized COVID-19 patients. Brilacidin’s robust antimicrobial properties might also help to fight secondary bacterial infections, which can co-present in up to 20 percent of COVID-19 patients. Collectively, these data support Brilacidin as a unique 3 in 1 combination—antiviral, immuno/anti-inflammatory, and antimicrobial—COVID-19 therapeutic candidate.
http://www.ipharminc.com/press-release/2020/11/2/innovation-pharmaceuticals-receives-pre-ind-response-from-fda-on-covid-19-trial
YET AGAIN TOTAL MISDIRECTION of FOCUS. None of us knows what may or may not be transpiring with a BP. At this TIME it's not important. The results of the upcoming TRIAL WILL BE , PERIOD
What is to be HIGHLY FOCUS on here is the effectiveness of the IPIX's BRILACIDIN in the upcoming COVID TRIAL , not the stock PPS , not the management , not who wins the election. The ENTIRE WORLD is in the grip of this COVID EPODEMIC . What we NEED is a working cure for those INFECTED like maybe IPIX's BRILACIDIN and a VACCINE. ALL ELSE IS BS
AGAIN that is a TOTAL MISDIRECTION of where ones focus needs to be on current situation. FOCUS - Does BRILACIDIN work as an acceptable medical treatment against COVID or NOT. We will soon officially find out. ALL ELSE IS PURE BS NOISE.
That's a total MISDIRECTION of the focus one should have on this company. Currently we are waiting on the START of an INDEPENDANT GOVERNMENT COVID TRIAL STUDY using IPIX's BRILACIDIN. Depending on the results the FDA could approve it's usage. PICKING on Leo , who has no direct involvement , has NO VALUE IMO
Chinese vaccine causes serious adverse effects, clinical trial in Brazil suspended for safety concerns.
https://www.cnn.com/2020/11/10/health/brazil-suspends-china-vaccine-trials-intl-hnk/index.html
Quote:
n China, drug makers have been administering experimental vaccines on tens of thousands of people since July under a government-approved emergency uses program, which allows vaccine candidates to be used on a limited scale before their safety and efficacy have been fully proven by clinical trials.
The move is controversial as some experts worry that fast-tracking the normal approval process could potentially expose participants to unknown side effects, and Chinese drug makers are taking risks that contravene international ethical and safety norms.
TREATMENTS are the answer, until we know whether and which vaccines might be safe and effective, after they have been tested over time as vaccines have been tested in the past -- and even then, there are cases of vaccines being approved that DID cause bad side effects and had to be withdrawn. (First shingles vaccine, for instance)
The "90% efficacy" claim is troubling. Based on what? This is a misleading claim. Because they are not releasing details, what seems to be able to be gleaned from what they are saying is that 90% of the cases of COVID-19 were in members of the control group. However, there are only 94 cases of COVID out of the 44,000 volunteers, and this, after only two months after vaccination.
Also, Pfizer's vaccine requires two doses, and the vaccine has to be stored and transported at extremely low temperatures. What are the chances that the vaccine will always be handled properly so that it is effective?
And, what are the chances that this vaccine is indeed safe and does not have longer-term side effects? Just as a recent example, the initial shingles vaccine was widely hailed as a safe and effective vaccine. Then, after a lot of people got dosed -- whoops, guess what, it is NOT safe and in some people TRIGGERED cases of shingles. (Please note: that vaccine has been withdrawn and the current one is safer -- supposedly.)
There have been many other cases of vaccines that appeared to be safe which turned out to have bad side effects over the longer term, when given to a very large population. Swine flu vaccine, anyone?
Also, they are saying that they will have enough vaccine to dose 15-20 million people in the next year. Even if this vaccine is safe and effective, and does not cause long-term side effects -- 15-20 million people vaccinated with even an optimistic 90% efficacy will NOT get the pandemic under control.
TREATMENTS will. And if you or a family member are among those who get COVID in the next year, you're going to be mighty grateful if there are good treatments available -- like, for instance, Brilacidin.
AGREE , See ZM as a great company that will still grow BUT BUT BUT because so many people ( investors ) see or have seen that the PPS went to a WAY WAY WAY OVERBOUGHT position. Even with today's drop still see more downside coming. Have NO PREDICTIONS of my own as to a fair PPS yet BUT see the COMPANY as having a great future ahead of it. COVID has created a proven workable and acceptable WORK-AT-HOME situation for employers that would otherwise not have likely existed without it.
So much for a predicted BIG CRASH in the PPS of NAK today. LOL
Progress here still being made DISPITE who gets ELECTED
Think you just got BURNED a bit , mainly for bad timing.
The PEBBLES MINE PROJECT is mainly a " COPPER " play SO has only a very small RARE EARTH FACTOR in its makeup. CHINA will not be able to supply the FUTURE DEMAND for copper to itself much less the U.S. down the road. So NAK is FAR FAR FAR from even being close to toast.
BTW - the GOLD and SILVER deposits alone makes it a future HUGE PLAY
TOTAL POLITICAL BS - It has been NO SECREAT even YEARS AGO that the PEBBLES MINE PROJECT was DOWNSIZED to make it less of a threat to wildlife and the Salmon in BRISTAL BAY and therefore more acceptable and more likely to get APPROVED in a smaller version. Once operating at a smaller version and PROVING IN AN OPERATIONAL setting that it was not HARMING ANYTHING , farther expansion could THEN BE approved. The Senator from Washington State has always been AGAINST the project so no surprise her calling for an investigation as the Project gets closer to OFFICIAL APPROVAL. The TRUE VALID investigation findings which most all will accept comes from the ACOE and science not POLITICAL BS. NOTICE she is NOT CHALLEGING the ACOE. She would LOSE
There is also GUSH and DRIP too
But all are to be used as SHORT TERM trading platforms . Holding is not the best of ideas usually. QUICK TRADES in and out for now
All major indexes hit hard this morning in the PM. Going to be a rough day for a lot of investors. NAK will be most likely no exception but it is going to be SHORT TERM IMO. ROD release still coming and other news of progress too is coming. Uncertainty over the election outcome may be playing a roll in here too.
With the increase in COVID cases and an EXPECTED farter RISE in COVID cases over the Holiday season causing a high probability of increased SHUT DOWNS, oil usage will drop IMO. Not good for oil companies profitability , oil prices , or NRGU. Easy to SEE a down trend continue here for awhile
Think most monitors like me are for now waiting till AFTER the ELECTION BS gets out of the way. Seems NAK is in a quite period anyway as we wait on the next bit of news hopefully getting through the next successful milestone event. Then more NAK REAL chatter can start up again. Like seeing more new posters here even if off topic a lot lately as it shows that they have an interest in NAK and their posting here supports that.
What ever works for you I say go for it. May not agree with your comments but rather read what anyone HONESTLY thinks rather than BS to manipulate a stock UP or DOWN.
BRILACIDIN is not out of the running yet. Still in for another government trial study that I remember when funds are available. Earlier trials showed BRILACIDIN outperformed Remdesivir by a huge factor. A lot of attention and money is going for a (maybe questionable) VACCINE and slowing down progress for TREATMENT DRUGS but TREATMENT DRUGS are just as important. maybe more so
IMO the price of the metals known to be present in the PEBBLES MINE PROJECT will come into play when it is CLEAR to all the project is a GO. Meaning sometime after the release of the ROD , the Federal license , and permits are successfully being acquired. That will de-risk any negotiations an interested MAJOR would have in getting involved with PEBBLES and talks can then be made with confidence going forward.