Register for free to join our community of investors and share your ideas. You will also get access to streaming quotes, interactive charts, trades, portfolio, live options flow and more tools.
Register for free to join our community of investors and share your ideas. You will also get access to streaming quotes, interactive charts, trades, portfolio, live options flow and more tools.
$ODYY Making its move!!
We hit ..42 today!! Nobody concerned about that garbage. lol yesterday's news! $ODYY
$ODYY HIT .42 today Just getting started!!!!
$ODYY Nice day today. See ya Monday-;)
Lol. Odyssey NEVER received it. You can’t just ask someone to repay someone else’s debt. Good luck with them getting that. I’ll place my bet that ODYY will be all set
Cabo that was more that 2 months ago. Obviously the Company website is up to date. Let's keep it real please
Not from what I can see, unless you have some inside info?
https://www.odysseyhealthinc.com/board-of-directors
The story says the funds went to Prevacus, at the time Prevacus was private. Again this has nothing to do with ODYY as they were not the recipients of this funds! Looks like the only one with an issue is Jake? So there's no need to drag ODYY through their mud
Cabo how much more do you know? Jake is still your wife's cousin?
os_tacos
Member Level
Re: None
Wednesday, February 10, 2021 7:19:15 AM
Post# of 210 Go
Jake is my wife’s cousin .. His concoction works . He’s been talking it up at Xmas parties
for years . It’s never been about the money for him . He really wants to help people . He just needed a company that had the wherewith-all to take it further ....Folks don’t come any better than Jake
It’s safe and effective .
Enjoy the ride
Who is they? I know ODYY doesn't owe the $$$!!
$ODYY More great news!!
Odyssey Health, Inc. Forms Pharmaceutical Subsidiary Focused on Treating Neurological Diseases
Las Vegas, Nevada, Oct. 11, 2022 (GLOBE NEWSWIRE) -- Odyssey Health, Inc. (OTC: ODYY), f/k/a Odyssey Group International, Inc., a company focused on developing unique, life-enhancing medical products, announces the formation of Odyssey Neuropharma, Inc., a wholly owned subsidiary, focused on developing drugs to treat neurological disorders. The blood-brain barrier (BBB) represents a significant obstacle for drug delivery to the brain. Many drugs have failed in neuroscience research due to the inability to jump the hurdle that is the BBB. The Company will utilize its unique intranasal delivery device coupled with its powdered formulations to allow drugs to be delivered more directly to the brain, providing for efficient and quick delivery. This targeted approach requires less drug to accomplish neuroprotection further reducing drug levels in the plasma which minimizes side effects.
Odyssey has a portfolio of products planned for development including drugs for mild traumatic brain injury aka concussion, Niemann-Pick type C Disease, and an Organophosphate Nerve Agent antidote. Odyssey’s unique breath propelled intranasal device is lightweight and easy to use. The drug device combination has been developed to increase brain drug exposure in minutes. The olfactory nerve used for the detection of smell provides a direct highway into the brain. Previous work in humans completed by Odyssey has shown that intranasal administration of spray-dried powders leads to very low plasma concentrations compared to an intravenous route. This finding is highly suggestive that most of the drug of interest is entering the brain and does not go systemic throughout the body.
Odyssey’s spray-dried powder formulation technology allows for drugs to be designed for ease of delivery with minimal force of breath, painless interaction with the nasal mucosa, targeting to the superior portion of the nasal cavity for direct flow to the brain and particle sizes that can not be inhaled and interrupt lung function. Odyssey’s unique breath-propelled route of administration closes the soft palate and traps the drug of interest in the nasal cavity for longer periods of absorption. Safe, efficient, and targeted approaches for neurological disorders provide a much greater chance of regulatory and patient success.
About Odyssey Health Inc. (formerly Odyssey Group International, Inc.)
Odyssey Health Inc. (OTC: ODYY) is a medical company with a focus in the area of life-saving medical solutions. Odyssey's corporate mission is to create, acquire and develop distinct assets, intellectual property, and exceptional technologies that provide meaningful medical solutions. The company is focused on areas that have an identified technological advantage, provide superior clinical utility, and have a substantial market opportunity. For more information, visit the company’s website at www.odysseyhealthinc.com
We encourage our shareholders to visit our corporate social media accounts for updates:
https://twitter.com/OdysseyHealth1
https://www.facebook.com/odysseyhealthinc
https://www.linkedin.com/company/odysseyhealthinc
https://www.youtube.com/channel/UCsS--v0od_fYIBu2tvqmj9Q
About Our Drug Candidates
PRV-001 is a fully synthetic non-naturally occurring neurosteroid being developed for Niemann-Pick type C disease. An orphan disorder with a high mortality rate in a pediatric population which has no available treatment. In pre-clinical studies PRV-001 has been shown to improve neuromotor function and reduce brain inflammation leading to better cognitive performance. Toxicology studies suggest that PRV-001 will be well-tolerated in clinical trials. Odyssey owns fifty percent of this drug candidate.
PRV-002 is a fully synthetic non-naturally occurring neurosteroid being developed for the treatment of concussion. A frequent occurrence in athletes and military personnel there is currently no treatment for concussion. In preclinical studies, PRV-002 has demonstrated equivalent, if not superior, neuroprotective effects compared to related neurosteroids. Odyssey’s Phase I clinical trial showed that PRV-002 was well-tolerated with minimal systemic exposure when delivered intranasally.
Intranasal Powdered Oximes is a novel delivery method of an inhibitor to organophosphates, the pathological ingredient of nerve gas agents. Currently, Oximes are delivered with an autoinjector and must be used multiple times for efficacy. Intranasal delivery provides for a painless, non-infective means of delivery that is fast and targeted to the Central Nervous System. Time is of the essence when combating a nerve gas agent where central respiratory failure can lead to death. Odyssey’s lightweight drug device combination can be carried in the pocket of civilians around the world at risk as a means of biodefense.
Forward-Looking Statements
This news release may contain forward-looking statements within the meaning of the "safe harbor" provisions of the Private Securities Litigation Reform Act of 1995. Such statements are based upon our current expectations and speak only as of the date hereof. Our actual results may differ materially and adversely from those expressed in any forward-looking statements as a result of various factors and uncertainties, including our ability to successfully develop products, successful pre-clinical trials and human clinical trials with our drugs, regulatory, competitive developments and our ability to continue to raise needed funds.
Inquiries:
Odyssey Health
info@odysseyhealthinc.com
https://www.globenewswire.com/newsroom/ti?nf=ODY2MjQxNiM1MTk3MTQxIzUwMDA4NjI2NA==
https://ml.globenewswire.com/media/ZTBkY2Q5ZTctYzkxNC00ZTRkLWEwOGUtOTJhNWM2MTQ5NDM1LTUwMDA4NjI2NA==/tiny/Odyssey-Health-Inc.png
Source: Odyssey Health, Inc
Cabo i get it. But that's NOT stock in ODYY!! There definitely was some nefarious crap with Prevacus back then, but that has no effect on ODYY!JMHO
$ODYY More great news!!
Odyssey Health, Inc. Forms Pharmaceutical Subsidiary Focused on Treating Neurological Diseases
Las Vegas, Nevada, Oct. 11, 2022 (GLOBE NEWSWIRE) -- Odyssey Health, Inc. (OTC: ODYY), f/k/a Odyssey Group International, Inc., a company focused on developing unique, life-enhancing medical products, announces the formation of Odyssey Neuropharma, Inc., a wholly owned subsidiary, focused on developing drugs to treat neurological disorders. The blood-brain barrier (BBB) represents a significant obstacle for drug delivery to the brain. Many drugs have failed in neuroscience research due to the inability to jump the hurdle that is the BBB. The Company will utilize its unique intranasal delivery device coupled with its powdered formulations to allow drugs to be delivered more directly to the brain, providing for efficient and quick delivery. This targeted approach requires less drug to accomplish neuroprotection further reducing drug levels in the plasma which minimizes side effects.
Odyssey has a portfolio of products planned for development including drugs for mild traumatic brain injury aka concussion, Niemann-Pick type C Disease, and an Organophosphate Nerve Agent antidote. Odyssey’s unique breath propelled intranasal device is lightweight and easy to use. The drug device combination has been developed to increase brain drug exposure in minutes. The olfactory nerve used for the detection of smell provides a direct highway into the brain. Previous work in humans completed by Odyssey has shown that intranasal administration of spray-dried powders leads to very low plasma concentrations compared to an intravenous route. This finding is highly suggestive that most of the drug of interest is entering the brain and does not go systemic throughout the body.
Odyssey’s spray-dried powder formulation technology allows for drugs to be designed for ease of delivery with minimal force of breath, painless interaction with the nasal mucosa, targeting to the superior portion of the nasal cavity for direct flow to the brain and particle sizes that can not be inhaled and interrupt lung function. Odyssey’s unique breath-propelled route of administration closes the soft palate and traps the drug of interest in the nasal cavity for longer periods of absorption. Safe, efficient, and targeted approaches for neurological disorders provide a much greater chance of regulatory and patient success.
About Odyssey Health Inc. (formerly Odyssey Group International, Inc.)
Odyssey Health Inc. (OTC: ODYY) is a medical company with a focus in the area of life-saving medical solutions. Odyssey's corporate mission is to create, acquire and develop distinct assets, intellectual property, and exceptional technologies that provide meaningful medical solutions. The company is focused on areas that have an identified technological advantage, provide superior clinical utility, and have a substantial market opportunity. For more information, visit the company’s website at www.odysseyhealthinc.com
We encourage our shareholders to visit our corporate social media accounts for updates:
https://twitter.com/OdysseyHealth1
https://www.facebook.com/odysseyhealthinc
https://www.linkedin.com/company/odysseyhealthinc
https://www.youtube.com/channel/UCsS--v0od_fYIBu2tvqmj9Q
About Our Drug Candidates
PRV-001 is a fully synthetic non-naturally occurring neurosteroid being developed for Niemann-Pick type C disease. An orphan disorder with a high mortality rate in a pediatric population which has no available treatment. In pre-clinical studies PRV-001 has been shown to improve neuromotor function and reduce brain inflammation leading to better cognitive performance. Toxicology studies suggest that PRV-001 will be well-tolerated in clinical trials. Odyssey owns fifty percent of this drug candidate.
PRV-002 is a fully synthetic non-naturally occurring neurosteroid being developed for the treatment of concussion. A frequent occurrence in athletes and military personnel there is currently no treatment for concussion. In preclinical studies, PRV-002 has demonstrated equivalent, if not superior, neuroprotective effects compared to related neurosteroids. Odyssey’s Phase I clinical trial showed that PRV-002 was well-tolerated with minimal systemic exposure when delivered intranasally.
Intranasal Powdered Oximes is a novel delivery method of an inhibitor to organophosphates, the pathological ingredient of nerve gas agents. Currently, Oximes are delivered with an autoinjector and must be used multiple times for efficacy. Intranasal delivery provides for a painless, non-infective means of delivery that is fast and targeted to the Central Nervous System. Time is of the essence when combating a nerve gas agent where central respiratory failure can lead to death. Odyssey’s lightweight drug device combination can be carried in the pocket of civilians around the world at risk as a means of biodefense.
Forward-Looking Statements
This news release may contain forward-looking statements within the meaning of the "safe harbor" provisions of the Private Securities Litigation Reform Act of 1995. Such statements are based upon our current expectations and speak only as of the date hereof. Our actual results may differ materially and adversely from those expressed in any forward-looking statements as a result of various factors and uncertainties, including our ability to successfully develop products, successful pre-clinical trials and human clinical trials with our drugs, regulatory, competitive developments and our ability to continue to raise needed funds.
Inquiries:
Odyssey Health
info@odysseyhealthinc.com
https://www.globenewswire.com/newsroom/ti?nf=ODY2MjQxNiM1MTk3MTQxIzUwMDA4NjI2NA==
https://ml.globenewswire.com/media/ZTBkY2Q5ZTctYzkxNC00ZTRkLWEwOGUtOTJhNWM2MTQ5NDM1LTUwMDA4NjI2NA==/tiny/Odyssey-Health-Inc.png
Source: Odyssey Health, Inc
$ODYY More great news!!!
Odyssey Health, Inc. Forms Pharmaceutical Subsidiary Focused on Treating Neurological Diseases
Las Vegas, Nevada, Oct. 11, 2022 (GLOBE NEWSWIRE) -- Odyssey Health, Inc. (OTC: ODYY), f/k/a Odyssey Group International, Inc., a company focused on developing unique, life-enhancing medical products, announces the formation of Odyssey Neuropharma, Inc., a wholly owned subsidiary, focused on developing drugs to treat neurological disorders. The blood-brain barrier (BBB) represents a significant obstacle for drug delivery to the brain. Many drugs have failed in neuroscience research due to the inability to jump the hurdle that is the BBB. The Company will utilize its unique intranasal delivery device coupled with its powdered formulations to allow drugs to be delivered more directly to the brain, providing for efficient and quick delivery. This targeted approach requires less drug to accomplish neuroprotection further reducing drug levels in the plasma which minimizes side effects.
Odyssey has a portfolio of products planned for development including drugs for mild traumatic brain injury aka concussion, Niemann-Pick type C Disease, and an Organophosphate Nerve Agent antidote. Odyssey’s unique breath propelled intranasal device is lightweight and easy to use. The drug device combination has been developed to increase brain drug exposure in minutes. The olfactory nerve used for the detection of smell provides a direct highway into the brain. Previous work in humans completed by Odyssey has shown that intranasal administration of spray-dried powders leads to very low plasma concentrations compared to an intravenous route. This finding is highly suggestive that most of the drug of interest is entering the brain and does not go systemic throughout the body.
Odyssey’s spray-dried powder formulation technology allows for drugs to be designed for ease of delivery with minimal force of breath, painless interaction with the nasal mucosa, targeting to the superior portion of the nasal cavity for direct flow to the brain and particle sizes that can not be inhaled and interrupt lung function. Odyssey’s unique breath-propelled route of administration closes the soft palate and traps the drug of interest in the nasal cavity for longer periods of absorption. Safe, efficient, and targeted approaches for neurological disorders provide a much greater chance of regulatory and patient success.
About Odyssey Health Inc. (formerly Odyssey Group International, Inc.)
Odyssey Health Inc. (OTC: ODYY) is a medical company with a focus in the area of life-saving medical solutions. Odyssey's corporate mission is to create, acquire and develop distinct assets, intellectual property, and exceptional technologies that provide meaningful medical solutions. The company is focused on areas that have an identified technological advantage, provide superior clinical utility, and have a substantial market opportunity. For more information, visit the company’s website at www.odysseyhealthinc.com
We encourage our shareholders to visit our corporate social media accounts for updates:
https://twitter.com/OdysseyHealth1
https://www.facebook.com/odysseyhealthinc
https://www.linkedin.com/company/odysseyhealthinc
https://www.youtube.com/channel/UCsS--v0od_fYIBu2tvqmj9Q
About Our Drug Candidates
PRV-001 is a fully synthetic non-naturally occurring neurosteroid being developed for Niemann-Pick type C disease. An orphan disorder with a high mortality rate in a pediatric population which has no available treatment. In pre-clinical studies PRV-001 has been shown to improve neuromotor function and reduce brain inflammation leading to better cognitive performance. Toxicology studies suggest that PRV-001 will be well-tolerated in clinical trials. Odyssey owns fifty percent of this drug candidate.
PRV-002 is a fully synthetic non-naturally occurring neurosteroid being developed for the treatment of concussion. A frequent occurrence in athletes and military personnel there is currently no treatment for concussion. In preclinical studies, PRV-002 has demonstrated equivalent, if not superior, neuroprotective effects compared to related neurosteroids. Odyssey’s Phase I clinical trial showed that PRV-002 was well-tolerated with minimal systemic exposure when delivered intranasally.
Intranasal Powdered Oximes is a novel delivery method of an inhibitor to organophosphates, the pathological ingredient of nerve gas agents. Currently, Oximes are delivered with an autoinjector and must be used multiple times for efficacy. Intranasal delivery provides for a painless, non-infective means of delivery that is fast and targeted to the Central Nervous System. Time is of the essence when combating a nerve gas agent where central respiratory failure can lead to death. Odyssey’s lightweight drug device combination can be carried in the pocket of civilians around the world at risk as a means of biodefense.
Forward-Looking Statements
This news release may contain forward-looking statements within the meaning of the "safe harbor" provisions of the Private Securities Litigation Reform Act of 1995. Such statements are based upon our current expectations and speak only as of the date hereof. Our actual results may differ materially and adversely from those expressed in any forward-looking statements as a result of various factors and uncertainties, including our ability to successfully develop products, successful pre-clinical trials and human clinical trials with our drugs, regulatory, competitive developments and our ability to continue to raise needed funds.
Inquiries:
Odyssey Health
info@odysseyhealthinc.com
https://www.globenewswire.com/newsroom/ti?nf=ODY2MjQxNiM1MTk3MTQxIzUwMDA4NjI2NA==
https://ml.globenewswire.com/media/ZTBkY2Q5ZTctYzkxNC00ZTRkLWEwOGUtOTJhNWM2MTQ5NDM1LTUwMDA4NjI2NA==/tiny/Odyssey-Health-Inc.png
Source: Odyssey Health, Inc
Exactly all that BEFORE ODYY acquired Prevacus!! This has NOTHING to do with ODYY!! Onward and upward!!
Text promo in full gear this morning! Already received 2 of them. Someone has to pay for these failed promos...
What about ? The fact that he was removed? Keep in mind $ODYY is fully reporting, ESPN published an inaccurate story stating that Favre is a "major" investor, and Odyssey received the misguided funds, that's false as well. Read the filings!!
Although Odyssey was mentioned, the Company had zero involvement with those individuals. That was the prior shell insiders. But thanks for sharing
thanks Blaz got $MYNZ locked in!!!
I love the space. $TORVF just might be the one!!!
$ODYY expecting next move today!!!
$ODYY making next move today!!!
Zar thanks for the heads up on $TORVF
$ODYY UP 50% TODAY!!!
$ODYY UP 50% TODAY
I'm also excited the $ODYY is up 49% today))
$ODYY Mentioned in this article very interesting!!!
ABVIE, the venture capital arm of Abbott Labs is very active in the Concussion space and the comment belows mentions ODYY in context and ABVIE already has FDA approval of their own TBI Plasma Test:
September 24, 2022 | Tim Tapp | Print Article
Op-ed views and opinions expressed are solely those of the author.
Millions of Americans suffer concussions every single year, which can be life-altering. But up to now, there is no cure for the often serious brain injury. For the first time in history, medical science is on track to not only diagnose but also treat concussions, with the combination of an FDA-approved test, new research that reveals its effectiveness, and a new treatment that is currently in human trials.
A new study published in The Lancet Neurology revealed that doctors can now identify biomarkers that predict how someone will recover from a traumatic brain injury. By tracking those biomarkers in the immediate aftermath of any head trauma, doctors will be able to tell if someone has suffered a concussion or something more serious.
The researchers made use of the FDA-approved i-STAT™ TBI Plasma test from Abbott Laboratories (NYSE: ABT), a global healthcare company that has a portfolio of technologies spanning the spectrum of healthcare, with businesses and products in diagnostics, medical devices, nutritional, and branded generic medicines. The markers were measured using the company’s ARCHITECT core laboratory instrument using research prototype assays, both of which helped predict recovery.
Researchers measured levels of Glial Fibrillary Acidic Protein (GFAP) and Ubiquitin carboxy-terminal Hydrolase L1 (UCH-L1) present in blood plasma within 24 hours of injury. After testing biomarker levels on the day of injury, researchers evaluated patients six months later, tracking how individuals fared and how biomarker levels corresponded to their recovery.
“Brain injury biomarkers will one day be the standard of care to evaluate and treat patients,” said Dr. Fred Korley, an associate professor of emergency medicine at the University of Michigan and the first author of the study in a press release from Abbott. “Objective biomarker data can be profoundly helpful in determining prognosis for a patient, helping to gauge how severe a brain injury is, and can ultimately inform how best to counsel family members about care for their loved ones with brain injury.”
Abbott is pursuing FDA clearance under Breakthrough Designation for the TBI test on its Alinity i and ARCHITECT core laboratory instruments, which will broaden access and ensure that tests are available both in the lab and in other settings where people need immediate answers and care. Abbott’s TBI test on Alinity i is CE Marked and available outside the U.S.
Abbott’s TBI blood test was developed in collaboration with the U.S. Department of Defense (DoD) – which has been dedicated to creating a solution for the objective detection and evaluation of TBI for more than a decade. The DoD, through the U.S. Army Medical Research and Development Command‘s (USAMRDC) U.S. Army Medical Materiel Development Activity (USAMMDA), played a critical role in developing the test run on Abbott’s i-STAT TBI platform.
This test and research bookends well with the potentially first-ever concussion treatment currently in human trials. Odyssey Health, Inc. (OTC: ODYY), a company focused on developing unique, life-enhancing medical products, recently announced the successful completion of safety measures for their Phase I Multi-Day Ascending Dosing (MAD) clinical trial for a new potential concussion treatment. Odyssey’s trial involves administering the company’s novel drug to treat concussions, PRV-002, to healthy human subjects. For MAD Cohort I, the drug was safe and well tolerated.
The global market for concussion treatment was valued at $6.9 billion in 2020 and is forecasted to reach $8.9 billion by 2027, according to Grandview Research. Common settings for suffering concussion include contact sports, military training and operations, motor vehicle accidents, children at play, and falls in elderly assisted-living facilities.
“After reviewing the data from MAD Cohort I, I have strong confidence that PRV-002 will continue to show safety during the final, high-dose MAD portion of the Phase I clinical trial. We have unanimously approved the start of MAD Cohort II. The overall low levels of PRV-002 in the blood support the hypothesis that more of the drug is getting to the brain itself when administered with the intranasal device. If this turns out to be the case, not only can the targeted effects of the drug be more efficacious, but the drug will also likely have fewer potential side effects,” commented Dallas Hack, MD, member of the Safety Review Committee, in an Odyssey press release.
Odyssey Health has been built at the intersection of vast unmet medical needs and multiple market opportunities. The company’s development of novel drug compounds that could provide treatment for the damage from concussions could ultimately create the first FDA-approved treatment for concussions. In the U.S., there are more than five million concussions reported each year, with more than 69 million worldwide, representing a potential $400 billion market opportunity.
$ODYY PHASE 1 RESULTS !!!!!!
Odyssey Health, Inc. Announces Successful Completion of Phase I Clinical Trial for Concussion Drug
Las Vegas, Nevada, Sept. 28, 2022 (GLOBE NEWSWIRE) -- Odyssey Health, Inc. (OTC: ODYY), f/k/a Odyssey Group International, Inc., a company focused on developing unique, life-enhancing medical products, today announces the completion of all cohorts for its Phase I Single Ascending Dosing (SAD) and Multiple Ascending Dosing (MAD) clinical trial. Odyssey’s trial involved administering PRV-002, the Company’s novel drug to treat concussion, to healthy human subjects. Throughout the trial, the drug was safe and well tolerated.
The Phase I trial was conducted at Avance Clinical and Nucleus Network, two leading clinical research organizations. The trial consisted of a total of forty (40) healthy human volunteers. The trial was double-blinded, randomized and placebo controlled. For the SAD component twenty-four (24) subjects were separated into three (3) different groups and received drug at a ratio of 3:1 with placebo. The treatment groups were given either a low, medium, or high-single dose of PRV-002. For the MAD portion there were sixteen (16) subjects separated into two groups of eight and each subject received a single low or high dose for five (5) consecutive days. Following each cohort, the subjects were monitored by the Safety Review Committee (SRC). No severe adverse events were noted as PRV-002 was well-tolerated for all cohorts. No delays were instituted between cohorts. Vital signs, EKG readings, sleep patterns and breathing function were all normal through the entirety of the study. Blood labs showed no alterations associated with the PRV-002 treatment. Pharmacokinetic analysis showed a direct linear relationship between drug dosing concentration and blood plasma levels across all cohorts. Blood levels of PRV-002 were significantly lower with intranasal administration to what would be expected with other routes, suggesting a greater delivery to the brain.
“After reviewing the data from each of the cohorts, I have strong confidence that it is safe to proceed to the next clinical trial phase where PRV-002 will be administered for 10 consecutive days to subjects following concussion. Of particular note, the overall low levels of PRV-002 in the blood supports the hypothesis that more drug is getting to the brain itself when administered with the intranasal device. Less systemic exposure with this targeted approach promotes patient safety,” commented Dallas Hack, M.D., member of the Safety Review Committee.
Philip Ryan, M.D., Principal Investigator for Nucleus Network, commented, “PRV-002 was well-tolerated throughout the Phase I trial. The SRC has confidence about the safety of the intranasal delivery of PRV-002. We look forward to following the development process of Odyssey’s drug, PRV-002, during Clinical Phase II/III as they determine the efficacy of PRV-002 for concussed patients.”
Concussions in the armed forces are a serious issue. Odyssey is working with the United States military to identify sites for the Phase II trials.
“I’m excited to see that Odyssey’s drug was considered safe throughout the Phase I study. Safety always comes first for our soldiers. Now we can start the important work to determine the efficacy of PRV-002 a much-needed brain injury solution for the military and beyond. We need a treatment to prevent the deleterious sequelae of concussion as too many of our military men and women are retiring from the service with mental health disorders that lessen their quality of life,” remarked, Francis Beaudette, retired Commanding General of the U.S. Army Special Operations Command.
Odyssey is currently communicating with the Food and Drug Administration (FDA) to present the findings from the Phase I Trial. Phase II trial sites are being identified and study design is being created with the site’s medical leadership and Odyssey Medical Advisors. Concussions represent an “unmet” medical need and affects millions worldwide. Repetitive concussions can increase the risk of developing Chronic Traumatic Encephalopathy (CTE) and other neuropsychiatric disorders.
The global market for concussion treatment was valued at $6.9 billion in 2020 and is forecasted to reach $8.9 billion by 2027, according to Grandview Research. Common settings for concussion include contact sports, military training and operations, motor vehicle accidents, children at play and elderly assistive-living facilities due to falls.
About Odyssey Health Inc. (formerly Odyssey Group International, Inc.)
Odyssey Health Inc. (OTC: ODYY) is a medical company with a focus in the area of life-saving medical solutions. Odyssey’s corporate mission is to create, acquire and develop distinct assets, intellectual property, and exceptional technologies that provide meaningful medical solutions. The company is focused on areas that have an identified technological advantage, provide superior clinical utility, and have a substantial market opportunity. For more information, visit the company’s website at www.odysseyhealthinc.com.
We encourage our shareholders to visit our corporate social media accounts for updates:
https://twitter.com/OdysseyHealth1
https://www.facebook.com/odysseyhealthinc
https://www.linkedin.com/company/odysseyhealthinc
https://www.youtube.com/channel/UCsS--v0od_fYIBu2tvqmj9Q
$ODYY PHASE 1 RESULTS !!!!!!
Odyssey Health, Inc. Announces Successful Completion of Phase I Clinical Trial for Concussion Drug
Las Vegas, Nevada, Sept. 28, 2022 (GLOBE NEWSWIRE) -- Odyssey Health, Inc. (OTC: ODYY), f/k/a Odyssey Group International, Inc., a company focused on developing unique, life-enhancing medical products, today announces the completion of all cohorts for its Phase I Single Ascending Dosing (SAD) and Multiple Ascending Dosing (MAD) clinical trial. Odyssey’s trial involved administering PRV-002, the Company’s novel drug to treat concussion, to healthy human subjects. Throughout the trial, the drug was safe and well tolerated.
The Phase I trial was conducted at Avance Clinical and Nucleus Network, two leading clinical research organizations. The trial consisted of a total of forty (40) healthy human volunteers. The trial was double-blinded, randomized and placebo controlled. For the SAD component twenty-four (24) subjects were separated into three (3) different groups and received drug at a ratio of 3:1 with placebo. The treatment groups were given either a low, medium, or high-single dose of PRV-002. For the MAD portion there were sixteen (16) subjects separated into two groups of eight and each subject received a single low or high dose for five (5) consecutive days. Following each cohort, the subjects were monitored by the Safety Review Committee (SRC). No severe adverse events were noted as PRV-002 was well-tolerated for all cohorts. No delays were instituted between cohorts. Vital signs, EKG readings, sleep patterns and breathing function were all normal through the entirety of the study. Blood labs showed no alterations associated with the PRV-002 treatment. Pharmacokinetic analysis showed a direct linear relationship between drug dosing concentration and blood plasma levels across all cohorts. Blood levels of PRV-002 were significantly lower with intranasal administration to what would be expected with other routes, suggesting a greater delivery to the brain.
“After reviewing the data from each of the cohorts, I have strong confidence that it is safe to proceed to the next clinical trial phase where PRV-002 will be administered for 10 consecutive days to subjects following concussion. Of particular note, the overall low levels of PRV-002 in the blood supports the hypothesis that more drug is getting to the brain itself when administered with the intranasal device. Less systemic exposure with this targeted approach promotes patient safety,” commented Dallas Hack, M.D., member of the Safety Review Committee.
Philip Ryan, M.D., Principal Investigator for Nucleus Network, commented, “PRV-002 was well-tolerated throughout the Phase I trial. The SRC has confidence about the safety of the intranasal delivery of PRV-002. We look forward to following the development process of Odyssey’s drug, PRV-002, during Clinical Phase II/III as they determine the efficacy of PRV-002 for concussed patients.”
Concussions in the armed forces are a serious issue. Odyssey is working with the United States military to identify sites for the Phase II trials.
“I’m excited to see that Odyssey’s drug was considered safe throughout the Phase I study. Safety always comes first for our soldiers. Now we can start the important work to determine the efficacy of PRV-002 a much-needed brain injury solution for the military and beyond. We need a treatment to prevent the deleterious sequelae of concussion as too many of our military men and women are retiring from the service with mental health disorders that lessen their quality of life,” remarked, Francis Beaudette, retired Commanding General of the U.S. Army Special Operations Command.
Odyssey is currently communicating with the Food and Drug Administration (FDA) to present the findings from the Phase I Trial. Phase II trial sites are being identified and study design is being created with the site’s medical leadership and Odyssey Medical Advisors. Concussions represent an “unmet” medical need and affects millions worldwide. Repetitive concussions can increase the risk of developing Chronic Traumatic Encephalopathy (CTE) and other neuropsychiatric disorders.
The global market for concussion treatment was valued at $6.9 billion in 2020 and is forecasted to reach $8.9 billion by 2027, according to Grandview Research. Common settings for concussion include contact sports, military training and operations, motor vehicle accidents, children at play and elderly assistive-living facilities due to falls.
About Odyssey Health Inc. (formerly Odyssey Group International, Inc.)
Odyssey Health Inc. (OTC: ODYY) is a medical company with a focus in the area of life-saving medical solutions. Odyssey’s corporate mission is to create, acquire and develop distinct assets, intellectual property, and exceptional technologies that provide meaningful medical solutions. The company is focused on areas that have an identified technological advantage, provide superior clinical utility, and have a substantial market opportunity. For more information, visit the company’s website at www.odysseyhealthinc.com.
We encourage our shareholders to visit our corporate social media accounts for updates:
https://twitter.com/OdysseyHealth1
https://www.facebook.com/odysseyhealthinc
https://www.linkedin.com/company/odysseyhealthinc
https://www.youtube.com/channel/UCsS--v0od_fYIBu2tvqmj9Q
$ODYY PHASE 1 RESULTS !!!!!!
Odyssey Health, Inc. Announces Successful Completion of Phase I Clinical Trial for Concussion Drug
Las Vegas, Nevada, Sept. 28, 2022 (GLOBE NEWSWIRE) -- Odyssey Health, Inc. (OTC: ODYY), f/k/a Odyssey Group International, Inc., a company focused on developing unique, life-enhancing medical products, today announces the completion of all cohorts for its Phase I Single Ascending Dosing (SAD) and Multiple Ascending Dosing (MAD) clinical trial. Odyssey’s trial involved administering PRV-002, the Company’s novel drug to treat concussion, to healthy human subjects. Throughout the trial, the drug was safe and well tolerated.
The Phase I trial was conducted at Avance Clinical and Nucleus Network, two leading clinical research organizations. The trial consisted of a total of forty (40) healthy human volunteers. The trial was double-blinded, randomized and placebo controlled. For the SAD component twenty-four (24) subjects were separated into three (3) different groups and received drug at a ratio of 3:1 with placebo. The treatment groups were given either a low, medium, or high-single dose of PRV-002. For the MAD portion there were sixteen (16) subjects separated into two groups of eight and each subject received a single low or high dose for five (5) consecutive days. Following each cohort, the subjects were monitored by the Safety Review Committee (SRC). No severe adverse events were noted as PRV-002 was well-tolerated for all cohorts. No delays were instituted between cohorts. Vital signs, EKG readings, sleep patterns and breathing function were all normal through the entirety of the study. Blood labs showed no alterations associated with the PRV-002 treatment. Pharmacokinetic analysis showed a direct linear relationship between drug dosing concentration and blood plasma levels across all cohorts. Blood levels of PRV-002 were significantly lower with intranasal administration to what would be expected with other routes, suggesting a greater delivery to the brain.
“After reviewing the data from each of the cohorts, I have strong confidence that it is safe to proceed to the next clinical trial phase where PRV-002 will be administered for 10 consecutive days to subjects following concussion. Of particular note, the overall low levels of PRV-002 in the blood supports the hypothesis that more drug is getting to the brain itself when administered with the intranasal device. Less systemic exposure with this targeted approach promotes patient safety,” commented Dallas Hack, M.D., member of the Safety Review Committee.
Philip Ryan, M.D., Principal Investigator for Nucleus Network, commented, “PRV-002 was well-tolerated throughout the Phase I trial. The SRC has confidence about the safety of the intranasal delivery of PRV-002. We look forward to following the development process of Odyssey’s drug, PRV-002, during Clinical Phase II/III as they determine the efficacy of PRV-002 for concussed patients.”
Concussions in the armed forces are a serious issue. Odyssey is working with the United States military to identify sites for the Phase II trials.
“I’m excited to see that Odyssey’s drug was considered safe throughout the Phase I study. Safety always comes first for our soldiers. Now we can start the important work to determine the efficacy of PRV-002 a much-needed brain injury solution for the military and beyond. We need a treatment to prevent the deleterious sequelae of concussion as too many of our military men and women are retiring from the service with mental health disorders that lessen their quality of life,” remarked, Francis Beaudette, retired Commanding General of the U.S. Army Special Operations Command.
Odyssey is currently communicating with the Food and Drug Administration (FDA) to present the findings from the Phase I Trial. Phase II trial sites are being identified and study design is being created with the site’s medical leadership and Odyssey Medical Advisors. Concussions represent an “unmet” medical need and affects millions worldwide. Repetitive concussions can increase the risk of developing Chronic Traumatic Encephalopathy (CTE) and other neuropsychiatric disorders.
The global market for concussion treatment was valued at $6.9 billion in 2020 and is forecasted to reach $8.9 billion by 2027, according to Grandview Research. Common settings for concussion include contact sports, military training and operations, motor vehicle accidents, children at play and elderly assistive-living facilities due to falls.
About Odyssey Health Inc. (formerly Odyssey Group International, Inc.)
Odyssey Health Inc. (OTC: ODYY) is a medical company with a focus in the area of life-saving medical solutions. Odyssey’s corporate mission is to create, acquire and develop distinct assets, intellectual property, and exceptional technologies that provide meaningful medical solutions. The company is focused on areas that have an identified technological advantage, provide superior clinical utility, and have a substantial market opportunity. For more information, visit the company’s website at www.odysseyhealthinc.com.
We encourage our shareholders to visit our corporate social media accounts for updates:
https://twitter.com/OdysseyHealth1
https://www.facebook.com/odysseyhealthinc
https://www.linkedin.com/company/odysseyhealthinc
https://www.youtube.com/channel/UCsS--v0od_fYIBu2tvqmj9Q
$ODYY PHASE 1 RESULTS !!!!!!
Odyssey Health, Inc. Announces Successful Completion of Phase I Clinical Trial for Concussion Drug
Las Vegas, Nevada, Sept. 28, 2022 (GLOBE NEWSWIRE) -- Odyssey Health, Inc. (OTC: ODYY), f/k/a Odyssey Group International, Inc., a company focused on developing unique, life-enhancing medical products, today announces the completion of all cohorts for its Phase I Single Ascending Dosing (SAD) and Multiple Ascending Dosing (MAD) clinical trial. Odyssey’s trial involved administering PRV-002, the Company’s novel drug to treat concussion, to healthy human subjects. Throughout the trial, the drug was safe and well tolerated.
The Phase I trial was conducted at Avance Clinical and Nucleus Network, two leading clinical research organizations. The trial consisted of a total of forty (40) healthy human volunteers. The trial was double-blinded, randomized and placebo controlled. For the SAD component twenty-four (24) subjects were separated into three (3) different groups and received drug at a ratio of 3:1 with placebo. The treatment groups were given either a low, medium, or high-single dose of PRV-002. For the MAD portion there were sixteen (16) subjects separated into two groups of eight and each subject received a single low or high dose for five (5) consecutive days. Following each cohort, the subjects were monitored by the Safety Review Committee (SRC). No severe adverse events were noted as PRV-002 was well-tolerated for all cohorts. No delays were instituted between cohorts. Vital signs, EKG readings, sleep patterns and breathing function were all normal through the entirety of the study. Blood labs showed no alterations associated with the PRV-002 treatment. Pharmacokinetic analysis showed a direct linear relationship between drug dosing concentration and blood plasma levels across all cohorts. Blood levels of PRV-002 were significantly lower with intranasal administration to what would be expected with other routes, suggesting a greater delivery to the brain.
“After reviewing the data from each of the cohorts, I have strong confidence that it is safe to proceed to the next clinical trial phase where PRV-002 will be administered for 10 consecutive days to subjects following concussion. Of particular note, the overall low levels of PRV-002 in the blood supports the hypothesis that more drug is getting to the brain itself when administered with the intranasal device. Less systemic exposure with this targeted approach promotes patient safety,” commented Dallas Hack, M.D., member of the Safety Review Committee.
Philip Ryan, M.D., Principal Investigator for Nucleus Network, commented, “PRV-002 was well-tolerated throughout the Phase I trial. The SRC has confidence about the safety of the intranasal delivery of PRV-002. We look forward to following the development process of Odyssey’s drug, PRV-002, during Clinical Phase II/III as they determine the efficacy of PRV-002 for concussed patients.”
Concussions in the armed forces are a serious issue. Odyssey is working with the United States military to identify sites for the Phase II trials.
“I’m excited to see that Odyssey’s drug was considered safe throughout the Phase I study. Safety always comes first for our soldiers. Now we can start the important work to determine the efficacy of PRV-002 a much-needed brain injury solution for the military and beyond. We need a treatment to prevent the deleterious sequelae of concussion as too many of our military men and women are retiring from the service with mental health disorders that lessen their quality of life,” remarked, Francis Beaudette, retired Commanding General of the U.S. Army Special Operations Command.
Odyssey is currently communicating with the Food and Drug Administration (FDA) to present the findings from the Phase I Trial. Phase II trial sites are being identified and study design is being created with the site’s medical leadership and Odyssey Medical Advisors. Concussions represent an “unmet” medical need and affects millions worldwide. Repetitive concussions can increase the risk of developing Chronic Traumatic Encephalopathy (CTE) and other neuropsychiatric disorders.
The global market for concussion treatment was valued at $6.9 billion in 2020 and is forecasted to reach $8.9 billion by 2027, according to Grandview Research. Common settings for concussion include contact sports, military training and operations, motor vehicle accidents, children at play and elderly assistive-living facilities due to falls.
About Odyssey Health Inc. (formerly Odyssey Group International, Inc.)
Odyssey Health Inc. (OTC: ODYY) is a medical company with a focus in the area of life-saving medical solutions. Odyssey’s corporate mission is to create, acquire and develop distinct assets, intellectual property, and exceptional technologies that provide meaningful medical solutions. The company is focused on areas that have an identified technological advantage, provide superior clinical utility, and have a substantial market opportunity. For more information, visit the company’s website at www.odysseyhealthinc.com.
We encourage our shareholders to visit our corporate social media accounts for updates:
https://twitter.com/OdysseyHealth1
https://www.facebook.com/odysseyhealthinc
https://www.linkedin.com/company/odysseyhealthinc
https://www.youtube.com/channel/UCsS--v0od_fYIBu2tvqmj9Q
Shorters?? It’s only traded $300.00. Lol.
They’re not. The 9;30 buy on the offer didn’t fool anyone. Let’s see if they can beat the $1500.00 that traded yesterday …
They tried that last week with a failed promotion. Try again!!!
iv'e been doing this way too long!! There's NO RETAIL!! 6 Trades so far today. What does that tell you??
Date/Time Price Shares Exch/Mkt
09/13/2022 13:57:07 EDT 0.03355 2786 OTCBB
09/13/2022 13:57:07 EDT 0.034 16858 OTCBB
09/13/2022 12:48:34 EDT 0.035 10000 OTCBB
09/13/2022 10:05:17 EDT 0.035 10000 OTCBB
09/13/2022 9:46:01 EDT 0.0379 2000 OTCBB
09/13/2022 9:30:19 EDT 0.03545 2790 OTCBB
There’s no retail market. Insiders calling buddies to buy some or else it wouldn’t trade at all.
Trading by appointment now. Another bad sign...
$ODYY CONCUSSION DRUG NEWS OUT!!!
Odyssey Health Achieves Positive Safety Outcomes for Concussion Drug in Multiple Ascending Dosing Trial, Cohort II
Las Vegas, NV, Sept. 13, 2022 (GLOBE NEWSWIRE) -- Odyssey Health, Inc. (OTC: ODYY), f/k/a Odyssey Group International, Inc., a company focused on developing unique, life-enhancing medical products, today announced the successful completion of safety measures for the second cohort of their Phase I Multi-Day Ascending Dosing (MAD) clinical trial. Odyssey’s trial involves administering PRV-002, the Company’s novel drug to treat concussion, to healthy human subjects to determine drug safety. For all cohorts of the trial, the drug was found to be safe and well tolerated.
The Phase I MAD clinical trial consists of a total of 16 healthy subjects. In Cohort I, eight patients received a low dose of drug and in Cohort II, patients received a high dose of drug. In both cohorts the drug was well tolerated and safe with no severe adverse events reported.
Michael Redmond, CEO of Odyssey Health, Inc. commented, “At double the dose of the previous cohort we saw no serious adverse events. As we come close to completing the Phase I trial, I am very pleased with the safety profile of our concussion pharmaceutical treatment, PRV-002. I’m equally pleased that the intranasal drug/device combination has functioned nicely and has been easy to operate in the clinical setting.”
Odyssey is currently selecting clinical sites and developing the Investigator’s Brochure for the Phase II trial. Concussions represent an ‘unmet’ medical need and affect millions worldwide. Repetitive concussions can lead to rapid cognitive decline and emotional lability.
The global market for concussion treatment was valued at $6.9 billion in 2020 and is forecasted to reach $8.9 billion by 2027, according to Grandview Research.
About Odyssey Health Inc. (formerly Odyssey Group International, Inc.)
Odyssey Health Inc. (OTC: ODYY) is a medical company with a focus in the area of life-saving medical solutions. Odyssey's corporate mission is to create, acquire and develop distinct assets, intellectual property, and exceptional technologies that provide meaningful medical solutions. The company is focused on areas that have an identified technological advantage, provide superior clinical utility, and have a substantial market opportunity. For more information, visit the company’s website at www.odysseyhealthinc.com
We encourage our shareholders to visit our corporate social media accounts for updates:
https://twitter.com/OdysseyHealth1
https://www.facebook.com/odysseyhealthinc
https://www.linkedin.com/company/odysseyhealthinc
https://www.youtube.com/channel/UCsS--v0od_fYIBu2tvqmj9Q
About PRV-002
PRV-002 is a fully synthetic non-naturally occurring neurosteroid being developed for the treatment of mTBI (concussion). In preclinical studies, PRV-002 has demonstrated equivalent, if not superior, neuroprotective effects compared to related neurosteroids. Animal models of concussion demonstrated that PRV-002 reduces the behavioral pathology associated with brain injury symptoms such as memory impairment, anxiety, and motor/sensory performance. Additionally, PRV-002 is lipophilic and can easily cross the blood-brain barrier to rapidly eliminate swelling, oxidative stress and inflammation in the brain while restoring proper blood flow.
About Nucleus Network
Nucleus Network is the only multi-site Phase 1 clinical trials provider located in Australia and the USA. Nucleus Network provides high-quality, first-in-human and early-phase trials for biotechnology and pharmaceutical companies across the USA, Europe and Asia. Located within cutting-edge health precincts, their cost-effective, accelerated clinical development solutions are supported by advanced technology, clinical excellence, and research expertise.
Forward-Looking Statements
This news release may contain forward-looking statements within the meaning of the "safe harbor" provisions of the Private Securities Litigation Reform Act of 1995. Such statements are based upon our current expectations and speak only as of the date hereof. Our actual results may differ materially and adversely from those expressed in any forward-looking statements as a result of various factors and uncertainties, including our ability to continue to raise needed funds, successfully complete the Phase I trial, our ability to successfully develop products, rapid changes in our markets, changes in demand for our future products, and legislative, regulatory, competitive developments and general economic conditions.
Inquiries:
Odyssey Health
info@odysseyhealthinc.com
https://www.globenewswire.com/newsroom/ti?nf=ODY0NTUxNiM1MTQ5Nzc3IzUwMDA4NjI2NA==
https://ml.globenewswire.com/media/ZDViZjA1YWYtNjJlMy00NjNlLTgyMmYtZmZkZWFjYTg5ODQ3LTUwMDA4NjI2NA==/tiny/Odyssey-Health-Inc.png
Source: Odyssey Health, Inc
© 2022 GlobeNewswire, Inc.
Back to News Headlines
Other Financial Information
Recent News & Disclosure Filings
Recent SEC Filings
Pink Open Market Logo
Pink Current Information
Transfer Agent Verified IconTransfer Agent Verified
Shell Risk IconShell Risk
Independent Directors IconIndependent Directors
$ODYY MORE POSITIVE NEWS!!!!
Odyssey Health Achieves Positive Safety Outcomes for Concussion Drug in Multiple Ascending Dosing Trial, Cohort II
Las Vegas, NV, Sept. 13, 2022 (GLOBE NEWSWIRE) -- Odyssey Health, Inc. (OTC: ODYY), f/k/a Odyssey Group International, Inc., a company focused on developing unique, life-enhancing medical products, today announced the successful completion of safety measures for the second cohort of their Phase I Multi-Day Ascending Dosing (MAD) clinical trial. Odyssey’s trial involves administering PRV-002, the Company’s novel drug to treat concussion, to healthy human subjects to determine drug safety. For all cohorts of the trial, the drug was found to be safe and well tolerated.
The Phase I MAD clinical trial consists of a total of 16 healthy subjects. In Cohort I, eight patients received a low dose of drug and in Cohort II, patients received a high dose of drug. In both cohorts the drug was well tolerated and safe with no severe adverse events reported.
Michael Redmond, CEO of Odyssey Health, Inc. commented, “At double the dose of the previous cohort we saw no serious adverse events. As we come close to completing the Phase I trial, I am very pleased with the safety profile of our concussion pharmaceutical treatment, PRV-002. I’m equally pleased that the intranasal drug/device combination has functioned nicely and has been easy to operate in the clinical setting.”
Odyssey is currently selecting clinical sites and developing the Investigator’s Brochure for the Phase II trial. Concussions represent an ‘unmet’ medical need and affect millions worldwide. Repetitive concussions can lead to rapid cognitive decline and emotional lability.
The global market for concussion treatment was valued at $6.9 billion in 2020 and is forecasted to reach $8.9 billion by 2027, according to Grandview Research.
About Odyssey Health Inc. (formerly Odyssey Group International, Inc.)
Odyssey Health Inc. (OTC: ODYY) is a medical company with a focus in the area of life-saving medical solutions. Odyssey's corporate mission is to create, acquire and develop distinct assets, intellectual property, and exceptional technologies that provide meaningful medical solutions. The company is focused on areas that have an identified technological advantage, provide superior clinical utility, and have a substantial market opportunity. For more information, visit the company’s website at www.odysseyhealthinc.com
We encourage our shareholders to visit our corporate social media accounts for updates:
https://twitter.com/OdysseyHealth1
https://www.facebook.com/odysseyhealthinc
https://www.linkedin.com/company/odysseyhealthinc
https://www.youtube.com/channel/UCsS--v0od_fYIBu2tvqmj9Q
About PRV-002
PRV-002 is a fully synthetic non-naturally occurring neurosteroid being developed for the treatment of mTBI (concussion). In preclinical studies, PRV-002 has demonstrated equivalent, if not superior, neuroprotective effects compared to related neurosteroids. Animal models of concussion demonstrated that PRV-002 reduces the behavioral pathology associated with brain injury symptoms such as memory impairment, anxiety, and motor/sensory performance. Additionally, PRV-002 is lipophilic and can easily cross the blood-brain barrier to rapidly eliminate swelling, oxidative stress and inflammation in the brain while restoring proper blood flow.
About Nucleus Network
Nucleus Network is the only multi-site Phase 1 clinical trials provider located in Australia and the USA. Nucleus Network provides high-quality, first-in-human and early-phase trials for biotechnology and pharmaceutical companies across the USA, Europe and Asia. Located within cutting-edge health precincts, their cost-effective, accelerated clinical development solutions are supported by advanced technology, clinical excellence, and research expertise.
Forward-Looking Statements
This news release may contain forward-looking statements within the meaning of the "safe harbor" provisions of the Private Securities Litigation Reform Act of 1995. Such statements are based upon our current expectations and speak only as of the date hereof. Our actual results may differ materially and adversely from those expressed in any forward-looking statements as a result of various factors and uncertainties, including our ability to continue to raise needed funds, successfully complete the Phase I trial, our ability to successfully develop products, rapid changes in our markets, changes in demand for our future products, and legislative, regulatory, competitive developments and general economic conditions.
Inquiries:
Odyssey Health
info@odysseyhealthinc.com
https://www.globenewswire.com/newsroom/ti?nf=ODY0NTUxNiM1MTQ5Nzc3IzUwMDA4NjI2NA==
https://ml.globenewswire.com/media/ZDViZjA1YWYtNjJlMy00NjNlLTgyMmYtZmZkZWFjYTg5ODQ3LTUwMDA4NjI2NA==/tiny/Odyssey-Health-Inc.png
Source: Odyssey Health, Inc
© 2022 GlobeNewswire, Inc.
Back to News Headlines
Other Financial Information
Recent News & Disclosure Filings
Recent SEC Filings
Pink Open Market Logo
Pink Current Information
Transfer Agent Verified IconTransfer Agent Verified
Shell Risk IconShell Risk
Independent Directors IconIndependent Directors
$ODYY MORE POSITIVE NEWS!!!!
Odyssey Health Achieves Positive Safety Outcomes for Concussion Drug in Multiple Ascending Dosing Trial, Cohort II
Las Vegas, NV, Sept. 13, 2022 (GLOBE NEWSWIRE) -- Odyssey Health, Inc. (OTC: ODYY), f/k/a Odyssey Group International, Inc., a company focused on developing unique, life-enhancing medical products, today announced the successful completion of safety measures for the second cohort of their Phase I Multi-Day Ascending Dosing (MAD) clinical trial. Odyssey’s trial involves administering PRV-002, the Company’s novel drug to treat concussion, to healthy human subjects to determine drug safety. For all cohorts of the trial, the drug was found to be safe and well tolerated.
The Phase I MAD clinical trial consists of a total of 16 healthy subjects. In Cohort I, eight patients received a low dose of drug and in Cohort II, patients received a high dose of drug. In both cohorts the drug was well tolerated and safe with no severe adverse events reported.
Michael Redmond, CEO of Odyssey Health, Inc. commented, “At double the dose of the previous cohort we saw no serious adverse events. As we come close to completing the Phase I trial, I am very pleased with the safety profile of our concussion pharmaceutical treatment, PRV-002. I’m equally pleased that the intranasal drug/device combination has functioned nicely and has been easy to operate in the clinical setting.”
Odyssey is currently selecting clinical sites and developing the Investigator’s Brochure for the Phase II trial. Concussions represent an ‘unmet’ medical need and affect millions worldwide. Repetitive concussions can lead to rapid cognitive decline and emotional lability.
The global market for concussion treatment was valued at $6.9 billion in 2020 and is forecasted to reach $8.9 billion by 2027, according to Grandview Research.
About Odyssey Health Inc. (formerly Odyssey Group International, Inc.)
Odyssey Health Inc. (OTC: ODYY) is a medical company with a focus in the area of life-saving medical solutions. Odyssey's corporate mission is to create, acquire and develop distinct assets, intellectual property, and exceptional technologies that provide meaningful medical solutions. The company is focused on areas that have an identified technological advantage, provide superior clinical utility, and have a substantial market opportunity. For more information, visit the company’s website at www.odysseyhealthinc.com
We encourage our shareholders to visit our corporate social media accounts for updates:
https://twitter.com/OdysseyHealth1
https://www.facebook.com/odysseyhealthinc
https://www.linkedin.com/company/odysseyhealthinc
https://www.youtube.com/channel/UCsS--v0od_fYIBu2tvqmj9Q
About PRV-002
PRV-002 is a fully synthetic non-naturally occurring neurosteroid being developed for the treatment of mTBI (concussion). In preclinical studies, PRV-002 has demonstrated equivalent, if not superior, neuroprotective effects compared to related neurosteroids. Animal models of concussion demonstrated that PRV-002 reduces the behavioral pathology associated with brain injury symptoms such as memory impairment, anxiety, and motor/sensory performance. Additionally, PRV-002 is lipophilic and can easily cross the blood-brain barrier to rapidly eliminate swelling, oxidative stress and inflammation in the brain while restoring proper blood flow.
About Nucleus Network
Nucleus Network is the only multi-site Phase 1 clinical trials provider located in Australia and the USA. Nucleus Network provides high-quality, first-in-human and early-phase trials for biotechnology and pharmaceutical companies across the USA, Europe and Asia. Located within cutting-edge health precincts, their cost-effective, accelerated clinical development solutions are supported by advanced technology, clinical excellence, and research expertise.
Forward-Looking Statements
This news release may contain forward-looking statements within the meaning of the "safe harbor" provisions of the Private Securities Litigation Reform Act of 1995. Such statements are based upon our current expectations and speak only as of the date hereof. Our actual results may differ materially and adversely from those expressed in any forward-looking statements as a result of various factors and uncertainties, including our ability to continue to raise needed funds, successfully complete the Phase I trial, our ability to successfully develop products, rapid changes in our markets, changes in demand for our future products, and legislative, regulatory, competitive developments and general economic conditions.
Inquiries:
Odyssey Health
info@odysseyhealthinc.com
https://www.globenewswire.com/newsroom/ti?nf=ODY0NTUxNiM1MTQ5Nzc3IzUwMDA4NjI2NA==
https://ml.globenewswire.com/media/ZDViZjA1YWYtNjJlMy00NjNlLTgyMmYtZmZkZWFjYTg5ODQ3LTUwMDA4NjI2NA==/tiny/Odyssey-Health-Inc.png
Source: Odyssey Health, Inc
© 2022 GlobeNewswire, Inc.
Back to News Headlines
Other Financial Information
Recent News & Disclosure Filings
Recent SEC Filings
Pink Open Market Logo
Pink Current Information
Transfer Agent Verified IconTransfer Agent Verified
Shell Risk IconShell Risk
Independent Directors IconIndependent Directors