Revive Therapeutics Provides Update on Phase 3 Clinical Trial for Bucillamine in COVID-19
14 Febrero 2022 - 5:53AM
InvestorsHub NewsWire
Revive
Therapeutics Provides Update on Phase 3 Clinical Trial for
Bucillamine in COVID-19
- Ethics Committee approval to proceed with Phase 3 clinical
trial in Turkey
- 13 clinical sites selected to date in Turkey
TORONTO, Feb. 14, 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, is pleased to provide 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.
The Company, in collaboration with Delta Health,
has recently received approval for the Study by the Ethics
Committee of Istinye University in Turkey where the study
activities are ongoing. The Company is working with MLP Care, the
largest hospital group in Turkey, and Istinye University with
access to 30 clinical research sites and over 6000 in-patient
hospital beds.
The Company has initially selected the following
13 clinical research sites in Turkey:
- Istinye University Faculty of Medicine
- Liv Hospital Vadi Istanbul
- VM Medical Park Samsun Hospital
- Liv Hospital Samsun
- Medical Park Ankara Hospital
- VM Medical Park Maltepe Hospital
- Istinye University Research Hospital
- Medical Park Göztepe Hospital Complex
- Aydin University Research Hospital
- VM Medical Park Pendik Hospital
- Medical Park Bahçelievler Hospital
- VM Medical Park Mersin Hospital
- Medical Park Antalya Hospital Complex
Covid-19 infections in Turkey continues to grow.
Turkey has recorded 12.8 million Covid-19 infections and about
90,000 deaths. The seven-day average of daily Covid-19 infections
and Covid-19 deaths is approximately 98,000 and 250,
respectively.
Michael Frank, CEO of the Company commented, "Our expansion to
Turkey is important to our enrollment goals and commercialization
initiatives in the U.S. and international markets."
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.
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