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There is something more than meets the eye with this stock.
With the current pipeline and OS. This should be much much higher...
Something isn't right...
No reason for this to be at these levels, but we know nothing about the workings of this company.
Somone with much more information is keeping this down at these levels.
My opinion
There is something more than meets the eye with this stock.
With the current pipeline and OS. This should be much much higher...
Something isn't right...
No reason for this to be at these levels, but we know nothing about the workings of this company.
Somone with much more information is keeping this down at these levels.
My opinion
Buy more please, I'm depending on it. -J
If you are looking for "probable", then that money needs to seek mutual funds and bonds.
The "possible" is where speculative funds play and it is how OTC stocks generate those 50x, 100x, 200x type returns...
IMO, what we are looking for are signs that the IP is increasing in value and progressing to the next step. Moving from "possible" to "probable" and generating massive ROI.
Agree completely. The market cap is ridiculous here and there are plenty of OTC stocks trading 5-10 million valuation with no IP, no significant assets; let alone an extremely promising drug candidate that has progressed to final preclinical stages within the NIH program to mitigate the opioid crisis! amongst other promising drug candidates!
Couple that with new VP and institutional debt getting shares at .0015 and some preclinical acquisitions and deals in the pharma business netting 100s of millions, this truly becomes a no brainer!
Good luck, my average is just over .0009 so now just holding unless it drops in the .0005 range but I hope and don't see it happening.
I guess i have some catching up to do
Thanks I have ten million even , I am good
Jack you are on the wrong board.
The runs is the jaguar health board.
I got 9.89 million shares i would like to sell for 10 cents per share if you want them
Undervalued MC 774,682 👍
No brainer. We could easily be waiting at 10 million versus sub 1 million for updates.
The move can happen at anytime imho!
I also continue to accumulate.
Easily with partnership/funding to further their pain/epilepsy drug candidate post-NIH final preclinical trials. That would only be a 40 mil market cap now. Even if OS doubles, 80 mil market cap would seem very cheap considering the implications of success in mitigating opioid crisis as well as the size of that market…
There is just not clear visibility of timing of “possible” success there, nor timeline status of other programs like OSA. Could be 6 days or 6 months or longer? I am content accumulating.
It is possible.. but not probable
why was this at 0007 few weeks ago
It would be nice to see .05+ in the next few months
Hard to put a timeline/price on any speculative investment. Note the wording investment and not trade.
My perspective is there are two possibily extremely valuable and lucrative paths they are on in the near term. OSA drug program and Epilepsy/Pain drug program.
The OSA program has some funding set-up and pieces in place it appears. Their approach is logical and hopefully the new technology can overcome past hinderances. It makes sense that it very well could and will, however needs proven. Maybe they are waiting on further patent news, or FDA or additional funding or ??? or maybe we will hear something soon too.
The Epilepsy/Pain progress is substantial, IMO. Google search the candidate, review the reports and listen to the interviews. Something more than a peanut farm is brewing with this. Odds of success are always low in drug development, but their current positive progress certainly has increased their chances significantly. Success on this path, IMO, will make this one of the most valuable OTC pharma historically. How long to wrap up the NIH final trials? Months, Quarters? How much dilution is left? Are there big pharmas now, "purse strings" in the mix?
Success is surely not guaranteed. Timing is unknown. But I am in the camp you do just accumulate for the long haul. Whether days or months or quarters down the road. Steps taken and noted in the filings appear to be positioning for success, although such is never guaranteed. GLTA.
Ok. I will pick up a few at .0006 this time
This was and will always be 3+ by end of 2014. Guranteed!
As a newbie, do any of you experienced investors think it likely this stock sp will reach a penny by end of 2014?
True. However...
There is evidence in the filings of increasing confidence hence the fixed price salary for new exec and debt settlement and good terms eliminating some debt, 0% with .0015 fixed price for both. Minimal expectations of trading many multiples of that higher to make those decisions wise, IMO. Also the moves towards payable events, etc. Curious if the 10-K due soon will highlight additional clean-up in this regard.
Couple that with all the volume being absorbed... roughly 500 million shares maybe since right before bringing in their dealmaker? Why the sudden increase for previously/past boring turtle level progress?
Clearly recognize the risk, as with all OTC's especially, but hard not to be excited about the potential considering confirmed progress. Good as any place for speculative dollars, IMO.
The history looms heavy. Much investment was sunk in the past, and it made the ticker radioactive. But there was a reason why this happened, the promise and the science is extremely compelling. It still is, since the company has been “artificially” kept alive a long, long time. I’d make an analogy to the AI winter. AI was a radioactive term for a long, long time too.
A simple fact is always you need to see: they keep diluting the crap out of this and it won't stop. Why is that? Don't see the great potential here? Why is no one buying this out? Come on man... we are not all Trumpers to believe that theory
Agree. Anyone can look at the success probability of any drug development and see that the average is extremely low. Always massive risk vs massive reward in pharma space, especially OTC.
It is valuable to hear input from a historical perspective, so any tidbits to consider positive or negative should always be welcome. From a cursory look, it appears they have been working on addressing these unmet pharma needs for a decade. Lack of funding and failure is expected and looks to be experienced historically.
IMO, I see two very plausible and positive paths they are currently on.
In regards to OSA, I think newer technology related to nanotech and controlled release is logically more likely to help overcome the past trials where it appears the path was correct, but ability to get to finish line more than uncertain to unlock the investment risk. It appears the new approach makes more sense and is much more possible for success. Couple it with some improved financing options in place, I think they are on to something. I think everyone would be curious as to a status update of that program.
In regards to Epilepsy/Pain candidate drug. All the DD, whether interviews, independent publications or commentary appears extremely enthusiastic and optimistic. Clearing the NIH hurdles in presumably robust preclinicals is more than promising. Considering the opioid crisis and national headlines, and the current progress in the NIH program, one can imagine the possibilities here far exceed historical comparable OTC pharmas.
IMO, the speculative value is much much higher than current reflections in the market so I will accumulate over time.
Jeff would like people keep buying. This is more important than setting and forgetting it. He will let you know when we are near the set/forget phase.
Right with You!!!
Patience all that's needed! Shares getting soaked up.
I would imagine anything is possible considering the maturing advancement in NIH pre-clinicals for a high profile national pharma need to mitigate the opioid crisis.
Exactly the point.
Savvy investors accumualting
Traders are typical ignorant to the DD, rather watching the ticks and hoping they can scalp tickets to the rocket ride vs. purchasing them at early bird prices.
Setting it and forgetting it. Potential is great, and so is price IMO
$RSPI
Jeff not liking what you are saying. We need these postes and posters. -J
While I appreciate the news. Continued publishing of the info on big stages and contact with BP will drive this company into the clouds!
Update on the website: RespireRx Pharmaceuticals Inc. Reports Publication of Preclinical Research Results Demonstrating the Ability of CX1739, its Lead Clinical AMPAkine, to Improve Bladder Function After Spinal Cord Injury March 26, 2024
https://respirerx.com/wp-content/uploads/2024/03/RespireRx-SCI-Bladder-paper-final-approved-for-distribution.pdf
Rspi message board has a ton of ignorant posters.
You can tell by the language used..
Definitely not savvy...
Specifically terms, goes to show that, if you posters cannot even get terms correct, I question all the supposedly DD.
Terms are important..
Scary that those are the people buying this stock.
Wow, hahaha
Agree with that. If some debt holders want to convert at giveaway prices, there is going to be plenty of saavy folks happy to absorb them. Been happening for months here.
The one month chart shows RSPI coming up off a double bottom bounce
lol..ulness we get a complete clusterfuk of selling it aint happening.
Hit the ask.
I got a few more milly to go to catch up with you!!
Want to get there before the run starts.
Yes it would be nice , I would gather up atleast 5m GLTA
That's my target number. Anything more is golden.
I'll take trips. I'd love it for a couple of days of downward trend into about 0005. That would be fine.
Just slapped the ask for a million , just goal my goal of 10M so now a wait game . GLTA
Very little interest here it seems for so much potential! Peeps selling into .001 today … trips again?
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Moderators DTGoody crazy horse 0 Lime Time archilles jacksonjohn |
RespireRx Pharmaceuticals Inc. and its subsidiaries and business units are discovering and developing medicines for the treatment of psychiatric and neurological disorders, with a focus on treatments that address conditions affecting millions of people, but for which there are few or poor treatment options, including epilepsy, pain, attention deficit hyperactivity disorder (“ADHD”), recovery from spinal cord injury (“SCI”), certain neurological orphan diseases and obstructive sleep apnea (“OSA”). The RespireRx Group is developing a pipeline of new and repurposed drug products based on our broad patent portfolios for two drug platforms: (i) neuromodulators, which include GABAkines and AMPAkines, proprietary chemical entities that positively modulate (positive allosteric modulators or “PAMs”) GABAA receptors and AMPA-type glutamate receptors, respectively, and (ii) pharmaceutical cannabinoids, which include dronabinol, a synthetic compound that acts upon the nervous system’s endogenous cannabinoid receptors and
The RespireRx Group holds exclusive licenses and owns patents and patent applications or rights thereto for certain families of chemical compounds that claim the chemical structures and their uses in the treatment of a variety of disorders, as well as claims for novel uses of known drugs.
EndeavourRx: Neuromodulators
GABAkines. Under a License Agreement with the University of Wisconsin-Milwaukee Research Foundation, Inc. (“UWMRF”) and on behalf of its EndeavourRx business unit, RespireRx has licensed rights to certain selectively acting GABAkines because of their ability to selectively amplify inhibitory neurotransmission at a highly specific subset of GABAA receptors, thus producing a unique efficacy profile with reduced side effects. Preclinical studies have documented their efficacy in a broad array of animal models of interrelated neurological and psychiatric disorders including epilepsy, pain, anxiety, and depression in the absence of or with greatly reduced propensity to produce sedation, motor-impairment, tolerance, dependence and abuse. EndeavourRx currently is focusing on developing KRM-II-81 for the treatment of epilepsy and pain.
KRM-II-81 has displayed a high degree of anti-convulsant activity in a broad range of preclinical studies, including in treatment resistant and pharmaco-resistant models. Not only was KRM-II-81 highly effective in these models, but pharmaco-resistance or tolerance did not develop to its anti-convulsant properties. These latter results are particularly important because pharmaco-resistance occurs when medications that once controlled seizures lose efficacy as a result of chronic use and it is a principal reason some epileptic patients require brain surgery to control their seizures. In support of its potential clinical efficacy, translational studies have demonstrated the ability of KRM-II-81 to dramatically reduce epileptiform electrical activity when administered in situ to brain slices excised from treatment resistant epileptic patients undergoing surgery.
In addition, KRM-II-81 has displayed a high degree of analgesic activity in a broad range of preclinical studies. In intact animal models of pain, the analgesic efficacy of KRM-II-81 was comparable to or greater than commonly used analgesics. At the same time, KRM-II-81 did not display side effects such as sedation and motor impairment, but even more importantly, it did not produce tolerance, dependence, respiratory depression or behavioral changes indicative of abuse liability, which are produced by opioid narcotics and are at the heart of the opioid epidemic.
AMPAkines. Through an extensive translational research effort from the cellular level through Phase 2 clinical trials, RespireRx has developed a family of novel, low impact AMPAkines, including CX717, CX1739 and CX1942 that may have clinical application in the treatment of CNS-driven neurobehavioral and cognitive disorders, spinal cord injury, neurological diseases, and certain orphan indications. Our lead clinical compounds, CX717 and CX1739, have successfully completed multiple Phase 1 safety trials. Both compounds have also completed Phase 2 proof of concept trials demonstrating target engagement, by antagonizing the ability of opioids to induce respiratory depression.
AMPAkines have demonstrated positive activity in animal models of ADHD, results that have been extended translationally into statistically significant improvement of symptoms observed in a Phase 2 human clinical trial of CX717 in adult patients with ADHD. Statistically significant therapeutic effects were observed within one week. We believe AMPAkines may represent a novel, non-stimulant treatment for ADHD with a more rapid onset of action than alternative non-stimulants, such as Straterra® (atomoxetine), and without the drawbacks of amphetamine-type stimulants.
In a series of important studies funded by grants from the National Institutes of Health and published in a number of peer reviewed articles, Dr. David Fuller (University of Florida), a long-time RespireRx collaborator, has demonstrated the ability of CX1739 and CX717, RespireRx’s lead AMPAkines, to improve motor nerve activity and muscle function in a number of animal models of spinal cord injury (SCI).
Form Type | Received | Period End Date | Report |
---|---|---|---|
8-K | 09/06/2024 | 08/30/2024 | PDFRTFHTMLXLS |
8-K | 08/02/2024 | 07/29/2024 | PDFRTFHTMLXLS |
8-K | 07/08/2024 | 07/02/2024 | PDFRTFHTMLXLS |
8-K | 05/29/2024 | 05/29/2024 | PDFRTFHTMLXLS |
8-K | 04/16/2024 | 04/10/2024 | PDFRTFHTMLXLS |
NT 10-K | 04/01/2024 | 12/31/2023 | PDFRTFHTMLXLS |
8-K | 02/02/2024 | 01/30/2024 | PDFRTFHTMLXLS |
8-K | 01/22/2024 | 01/18/2024 | PDFRTFHTMLXLS |
8-K | 12/11/2023 | 12/06/2023 | PDFRTFHTMLXLS |
10-Q | 11/17/2023 | 09/30/2023 | PDFRTFHTMLXLS |
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Nothing in the contents transmitted on this board should be construed as an investment advisory, nor should it be used to make investment decisions.
There is no express or implied solicitation to buy or sell securities.
The author(s) may have positions in the stocks or financial relationships with the company or companies discussed and may trade in the stocks mentioned.
Readers are advised to conduct their own due diligence prior to considering buying or selling any stock.
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