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We can cross our fingers and think positive thoughts. My glass is always half full…even when it’s not!
Wow is all that can be said….pathetic!
Confirmed with company NASDAQ up listing still in the works
Nice news lately
Who has 125 block trade after trade hitting the screen?
What's going on? No volume what so ever today....is it halted?
TIA
What does trading 1 share or 13 shares signal?
I read 25k per quarter
Very nice interview
Good morning! Where do we go from here?
Cuba….cash stream…..? What’s the story 2 years later after feb 2020 rebirth article?
.0037 to .0053 …. What’s going on?
What an interesting story, recapture of history. So many people shy away from the sun and the gifts from earth…..natural foods, natural environments, etc. The higher powers gave all of us earthly beings everything we need to survive and thrive. I’m going to forward your information to my 21 year son. He appreciates such insight! Thank you for your research, your honest perception, etc…..it’s very much appreciated.
Thanks
What’s current RSI?
Some not so flattering investment articles being posted on fsr, nikola and one other ev company.
Excellent information. Understanding importance of the value of D3 on our overall health and ability to fight off infection is so important. We need to all start taking it more seriously. Thanks for sharing Gio.
You make a solid point….he points fault at others and owns none of it.
Lol….I’m from Texas…lol. We’re a bit basic. Seriously though JJ’s arrogance will be of detriment to him unless he can self reflect and make a change. Imho
Share price indicates JJ is getting his “come up-in’s”
2022 could be the year for Covid therapeutics. Therapeutics of all sorts have been held back deliberately.
Do you know if something happened between March 29th, when the developer announced that the drug met its primary endpoint and November 12th, when IPIX said that it hadn't? ….. no I do not. I wish I did have better insight.
Complete analysis of trial results already has begun, with the aim to potentially identify positive trends in the data that could support Brilacidin for inclusion in larger COVID-19 platform trials, such as the U.K.’s CTAP program and the NIH’s ACTIV program. The purpose of these programs is to prioritize development of promising COVID-19 therapeutics. Some COVID-19 drug candidates that did not meet their trial’s primary endpoint, for example Relief Therapeutics’ aviptadil, or those that showed inconclusive results in early clinical testing
From Tuesday’s update from ipix.
Collaborative work with NIH and other researchers on Brilacidin’s broad-spectrum antiviral properties is ongoing and generating promising data, with future updates planned.
Has anyone talk to or corresponded with Leo?
Thanks Mike…How many iu’s of each
Nice piece….thank you for finding and sharing.
Detailed Description:
This is a Phase 3, multi-center, randomized, double blind, placebo controlled, clinical study of bucillamine (2 dosage levels) in patients with mild-moderate COVID-19. Patients will be randomized 1:1:1 to receive bucillamine 100 mg 3 times a day (TID), bucillamine 200 mg TID or placebo TID for up to 14 days. After the first interim analysis when a single dose is selected, patients will then be randomized 2:1 to the selected bucillamine dose or placebo The study will be overseen by an independent Data and Safety Monitoring Board (DSMB). Up to 10 centers in the United States will conduct this study.
Patients qualifying for study enrollment will initiate therapy as outpatients, under home quarantine. Patients will receive continued standard care of therapy (per study site written policies or guidelines) together with bucillamine and/ or matching placebo for up to 14 days. Dosing should continue until the treatment course is completed or as medically indicated (e.g., deterioration of clinical status and alternative therapy required). If the patient requires hospitalization during the study period, treatment will be discontinued.
Following completion of the treatment course, follow up assessments will be performed by a study nurse 14, 28, 42, and 60 days following the end of treatment.
Up to 1000 patients will be enrolled in this study. Patients will participate in the study approximately 45 days.
Study Description
Go to sections
Brief Summary:
This is a Phase 3, multi-center, randomized, double blind, placebo controlled, clinical study of bucillamine (2 dosage levels) in patients with mild-moderate COVID-19. Patients will be randomized 1:1:1 to receive bucillamine 100 mg 3 times a day (TID), bucillamine 200 mg TID or placebo TID for up to 14 days. After the first interim analysis when a single dose is selected, patients will then be randomized 2:1 to the selected bucillamine dose or placebo The study will be overseen by an independent Data and Safety Monitoring Board (DSMB). Up to 10 centers in the United States will conduct this study. Up to 1000 patients will be enrolled in this study. Patients will participate in the study approximately 45 days.
Revive Therapeutics Clarifies Status of Its Phase 3 Clinical Trial for Bucillamine in COVID-19
Source: InvestorsHub NewsWire
Revive Therapeutics Clarifies Status of Its Phase 3 Clinical Trial for Bucillamine in COVID-19
Approximately 700 subjects participated in the enrollment period
Expected to begin subject enrollment in Turkey by mid-February
Expected to complete enrollment in Q1-2022
TORONTO, January 6th, 2022 -- InvestorsHub NewsWire -- Revive Therapeutics Ltd. ("Revive" or the "Company") (OTCQB: RVVTF) (CSE: RVV) (FRANKFURT:31R), a specialty life sciences company focused on the research and development of therapeutics for medical needs and rare disorders, wishes to clarify certain disclosures in its press release titled "Revive Therapeutics Provides Update on Phase 3 Clinical Trial for Bucillamine in COVID-19," issued on December 29, 2021 that provided an update on the Company's U.S. Food & Drug Administration ("FDA") Phase 3 clinical trial (the "Study") (NCT04504734) to evaluate the safety and efficacy of Bucillamine, an oral drug with anti-inflammatory and antiviral properties, in patients with mild to moderate COVID-19.
As of December 29, 2021, there were approximately 700 subjects that participated in the enrollment period of the Study. In addition, the Company has begun the process to expand the Study's patient population in Turkey in collaboration with Delta Health, which will add research sites from the largest hospital group in Turkey, MLP Care and Istinye University.
The Company expects patient enrollment in Turkey to occur by mid-February and completion of the Study's enrollment in Q1-2022.
The Company is not making any express or implied claims that its product has the ability to eliminate or cure COVID-19 (SARS-2 Coronavirus) at this time.
About Revive Therapeutics Ltd.
Revive is a life sciences company focused on the research and development of therapeutics for infectious diseases and rare disorders, and it is prioritizing drug development efforts to take advantage of several regulatory incentives awarded by the FDA such as Orphan Drug, Fast Track, Breakthrough Therapy and Rare Pediatric Disease designations. Currently, the Company is exploring the use of Bucillamine for the potential treatment of infectious diseases, with an initial focus on severe influenza and COVID-19. With its acquisition of Psilocin Pharma Corp., Revive is advancing the development of Psilocybin-based therapeutics in various diseases and disorders. Revive's cannabinoid pharmaceutical portfolio focuses on rare inflammatory diseases and the company was granted FDA orphan drug status designation for the use of Cannabidiol (CBD) to treat autoimmune hepatitis (liver disease) and to treat ischemia and reperfusion injury from organ transplantation. For more information, visit www.ReviveThera.com.
For more information, please contact:
Michael Frank
Chief Executive Officer
Revive Therapeutics Ltd.
Tel: 1 888 901 0036
Email: mfrank@revivethera.com
Website: www.revivethera.com
Neither the Canadian Securities Exchange nor its Regulation Services Provider has reviewed or accepts responsibility for the adequacy or accuracy of this release.
Cautionary Statement
This press release contains 'forward-looking information' within the meaning of applicable Canadian securities legislation. These statements relate to future events or future performance. The use of any of the words "could", "intend", "expect", "believe", "will", "projected", "estimated" and similar expressions and statements relating to matters that are not historical facts are intended to identify forward-looking information and are based on Revive's current belief or assumptions as to the outcome and timing of such future events. Forward looking information in this press release includes information with respect to the the Company's cannabinoids, psychedelics and infectious diseases programs. Forward-looking information is based on reasonable assumptions that have been made by Revive at the date of the information and is subject to known and unknown risks, uncertainties, and other factors that may cause actual results or events to differ materially from those anticipated in the forward-looking information. Given these risks, uncertainties and assumptions, you should not unduly rely on these forward-looking statements. The forward-looking information contained in this press release is made as of the date hereof, and Revive is not obligated to update or revise any forward-looking information, whether as a result of new information, future events or otherwise, except as required by applicable securities laws. The foregoing statements expressly qualify any forward-looking information contained herein. Reference is made to the risk factors disclosed under the heading "Risk Factors" in the Company's annual MD&A for the fiscal year ended June 30, 2021, which has been filed on SEDAR and is available under the Company's profile at www.sedar.com.
Similar to….what is the meaning of “why?”
Answer…..”Because”
Agree.
Love it!! You make this board “worthy” to hang out on!
What you state is absolutely true and worthy of living life by.
Definitely!