Cabot is pitching its Stock of the Week service, which chooses a favorite stock from among all of Cabot’s newsletters each week, and in order to entice subscribers they’re dangling the promise of huge gains… including this promise: “If you’ll give me just 10 minutes a week, I promise our Cabot Stock of the Week […]
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So if you’re reading this one first, you missed out on the explanation … if you want the full story (and another lovely Gumshoe read) start with my other writeup that feeds from this same email ad, for Bill Mann’s Global Gains service over at the Motley Fool. This is the second teased stock from […]
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Please don’t spew your ignorant comments on here. Your negativity on medical imaging is harmful to the community. Fact...
JAMA...another highly tainted and untrustworthy entity, along with the FDA and CDC, designed to assist Big Pharma in mai...
Hello, hitman, I'm just getting started, only own 7 stocks. Was looking over your list, looking for validation I guess....
Fluorine is a known neurotoxin as well as a bone toxin and is linked to osteosarcoma. Teeth are made of hydroxyapatite,...
Your proposed actions are a violation the Nurenburg Code of 1948 to which the USA is signatory. Since no vaccine has e...
There was an interesting show on ABC 20/20 Friday 3/16/2019 about Elizabeth Holmes and her company, Theranos. She suppos...
Not quite, but it’s usually an easier path than the typical drug approval process. Diagnostic tests have to be FDA ap...
I'd like to point out that since they are not developing a treatment or therapy, they are immune to the lengthy and trap...
This is what I have found about their latest Phase 3 trial: "The BETonMACE trial is currently expected to be completed w...
Travis, hi! Excellent work and i appreciate Gumshoe intellectual efforts. in the background, some fake news edited by b...
Big Pharma will squash any cure for cancer. They depend on people getting cancer to keep the money flowing. Big Pharma...
Does your brain require stimulating? FDA Events Can Send Stocks Soaring: https://finance.yahoo.com/news/fda-events-sen...
As a grower and processor of hemp for CBD in Colorado, I can attest to the efficacy of high quality full spectrum CBD f...
I’ve always found the expression “Clinical stage” confusing for the description of biotech companies performing R&...
An orphan drug is defined as one with fewer than 200,000 people with the "disease". If this imaging agent will "treat" 8...
Hello Travis, I too was curious about the FDA approval drug, so I dug into it also. You have verified the same info that...
Well then Matthew McCall its pitching the same company with his Blockbuster FDA Approval Summit 2019 something that it's...
agree, this stock has been ho-hum at best. Was expecting a lot more bounce once FDA approval....quite disappointed actua...
What you need to realize is that they have raised money twice in the last year and a half - or whatever the timeline is....
Ok! FDA has now approved AC5 so where is the jump in stock price? Am I being impatient? What should realistic expectatio...
Keep the faith. The process has taken a lot longer then the initial excitement by some were hoping for. But the fact AC5...
$ARTH Long and OW - not to toot my own horn, but I believe I predicted a 14 or 17 Dec decision from that wonderful gover...
$ARTH FDA clearance - https://ir.archtherapeutics.com/all-sec-filings/content/0001144204-18-064761/tv509257_8k.htm...
$ZFGN long And if you're wondering why the share price plummeted today. https://www.fool.com/investing/2018/11/26/why-...
2018 Turkey. I agree that APRI was probably a 20 pound Bird in the roasting pan. When FDA didn't sign off, it HIT THE ...
#CRMD no position, but interested. Their trial for their medical device was stopped by the FDA back in the summer for...
$ARTH - Arch Therapeutics to Provide Corporate Update at the 11th Annual LD Micro Main Event on Tuesday, December 4,...
You gave a strange date range, "Let’s take a look at the remarkably large number of new cancer therapeutics that obtai...
Great Article! Thanks Doc Gumshoe. The problems of big pharma did not arise overnight anymore than somebodies arteri...
If something really works, the FDA will either find a way to make it illegal or just not available unless it comes from ...
$ARTH atlas long possibly approx 60 more days to go, right? and probably even longer since apparently FDA hasn't been...
$ARTH - also long. Interesting question. I don't think we will know till it happens. And it will happen. But the stock ...
Long term holder - what is everyone's expectations on stock price once Arth gets FDA approval? What about on announcem...
Did you actually read this report? Take an anatomy & physiology class, and / or a cell biology class, and get a gli...
Travis ,isn't it amazing how people get away with "stealing" other peoples' researched ideas and passing it off as their...
Another "cover-up" of natural cures? After sitting through most of their video presentation, I opted for their book and ...
I just saw that there is a class action lawsuit filed today against Namaste. It says the company made false and mislead...
I bought my shares through Interactive Brokers. I do not recommend IB their software is the product of programmers gone ...
You are correct the FDA has up to 90 days to respond. Arch Therapeutics now has a person on board to deal with submissio...
I believe that the FDA has 90 calendar days from the submission date of the 510K to respond. So that means we should he...
I think we need to listen to his presentation tomorrow for an updated to that. We have been here already what more does ...
$ARTH - Arch Therapeutics Announces 510(k) Submission to the U.S. FDA for AC5™ Topical Gel https://ir.archthera...
Joined the service when it was launched. I spend a lot of time with the FDA trader recommendations. But it has payed ...
Hi Cleveland, Do you think 510k will be (hopefully) approved closer to 90 days as application was already submitted onc...
If 510K is submitted soon, hopefully already has been. Does the 90 day FDA clock start again or should it be quicker? Re...
$ARTH - Arch Therapeutics to Provide Corporate Update at the Ladenburg Thalmann 2018 Healthcare Conference on Tuesda...
I read the results of the Phase 3 trials and they failed to meet expectations by a sizeable margin, so the stock, Proge...
I am always pleased and entertained to see the variety of comments in reponse to my contributions to Gumshoe World. At...
Agreed. Team A brings the solution to FDA approval, TeamB comes in 'after' approval to minimize cash burn... e.g. after...
I wish I had your patience BnG. I understand mistakes can and will be made, but the ones ARTH has been guilty of, seem t...
Cleveland: Assuming $ARTH gets thru 3rd trial and FDA approval, can you share your thoughts on their go-to-market strat...
Thank you Cleveland the numbers bespeak your experience. Considering what has transpired with this stock with this si...
So the Big Parma influenced FDA is going to cut the throat of the medical mafia, which is almost 20% of our GDP, by sanc...
I too am interested in what Ray Blanco, FDA Trader, is talking about. A big announcement on Wed., Sept. 5 about how a D...
And the diseases they are targeting are much more able to have a conclusion in a clinical trial. If it doesn't cure the ...
nicotinamide adenine dinucleotide(NAD) $CDXC$ ChromaDex Corporation thought to combat age related diseases using Nico...
Why would it appear that way? We're just going by the promises in the ad, which builds this "you'll make a fortune" pr...
It makes one wonder if there isn't more to it, in the current administration, than proving the drug works using the guid...
So much EMF we will soon be exposed to in terms of the broad rollout of G5 that a major health crisis may be in order. ...
As far as lsdyf they got a little bump in revenue about 200k from the canna strips which are flavored strips for breath...
Right. that's why, I think, one has to look at the current valuation of clinical-stage biotechs with a very critical eye...
I've been rethinking the underlying thesis of investing in clinical stage biotechs. The overarching idea is that the sci...
Hi backoffice, Let me give you my best guess on the 5 companies touted by Tremblay's Bio Insider Alert. I am quoting br...
FDA to end Orphan designation for pediatric subpopulations...will close loopholes that allow drug companies to avoid con...
$AKAO Hey folks. Today Achaogen announced a major restructuring, laying off 28% of employees, as well as the coming d...
In 1988 the first report showing that ham radio operators had a much higher incidence of leukemia than the public was pu...
It just refering to mostly the well established bio tech marijuana stocks now that gw phar has a cannabis based product ...
In its May press release announcing its phase 3 trial result of its cholesterol-lowering drug, Esperion had to admit tha...
into phase 2 soon after clearance from hc and fda. patient 5 totally cancer free after 180 days. trial one only needed...
the above comment is dead wrong. TLT patient #5 no cancer after 180 days. got clearance HC and FDA for phase 2 after s...
$MBRX Moleculin Expects to Meet FDA IND Filing Requirements for its Pancreatic Cancer Drug Candidate with Development Wo...
Thank you. That was the most comprehensive and clearest description on osteoporosis I've seen. A couple of questions...
What $1 pot Stock is Jimmy Mengel referring to that is being evaluated by the FDA for approval. Why are these guys so ...
7/2/18 $APTO (FP) -- SEC FILING giving more details about FDA lifting the clinical hold on APTO-253: "....a root...
6/29/18 $APTO Press release "FDA Lifts Clinical Hold so MYC Inhibitor APTO-253 Can Return to Phase 1b Trial In Pat...
If the current raise is enough to carry them through until their next FDA submission....
aahhhh, maybe that is where I first saw GWPH, from Hillary Kramer; thanks StockMidas. Today June 25 the US FDA approved...
Opioid FDA approval is granted to a private company called US world Med. Their product is going to be available this ye...
Asking for evidence that a potential new treatment cures (or at least causes remission) is laughable. It is only the FD...
Glad to, billy. Norchi lined up all the people needed for the sensitivity test, got them enrolled, and started the test ...
I'd like to discuss $CLRB, but perhaps we could take it to a different thread? regarding $ARTH, to be honest, I don't...
$CYDY np Does anyone still follow a story of CytoDyn? They have reached a primary endpoint in their phase2b/3 study on ...
$ARTH (fp) - Thanks for the update Cleveland, I appreciate your technical and financial analysis you provide. I believ...
$ARTH long. In addition to the two-week turnaround to get the 510(k) filed by the end of September, Norchi committed to ...
$PTN Hi Allison-- I don't know how valuable my insight might be; I'm not nearly an expert on this stuff, and while...
$MBRX wow Moleculin Targets accelerated FDA approval of WP1732; Pursues Development for Ocular Tumors Click here to ...
$APTO Re my earlier post I see (hear) from the audio of Aptose' webcast of 1oth May that the necessary data had by that ...
Even if "Broadcast Power" (synonymous term for Nanoelectricity) were to be approved by all the agencies in the US - the ...
$APTO hello, is anyone keeping tabs on the position re the clinical hold? Over the last couple of days I've seen various...
Has anyone looked at BICX. They claim to have a novel way of providing medication for an extended time period 1 1/2 mont...
$CLRB FDA Grants Rare Pediatric Disease Designation to Cellectar Biosciences’ CLR 131 for the Treatment of Rhabdomyosa...
$CLRB and CLRBZ wow! > FDA Grants Rare Pediatric Disease Designation to Cellectar Biosciences’ CLR 131 for the Treatme...
$CLRB FDA Grants Rare Pediatric Disease Designation to CLR 131 for the Treatment of Rhabdomyosarcoma THX ODI! https://t...
You are right. As soon as Norchi realized the CE Mark would be delayed, he split the planned FDA filing into two parts, ...
" I don’t know why it has taken the manufacturer so long to complete the right paperwork, but my guess is that it requ...
No, the CE Mark is a safety approval that is much easier to get - you don't even have to do a clinical trial. (But you h...
That's a great point John, I didn't take that into account. One would hope if all aspects of the application are the sam...
The trial is 90 days long. I am talking about the length of time the FDA will review the refiled 510(k) application befo...
Because this was the only issue the FDA had and because they have approved the study design, I expect a positive outcome...