Talis Biomedical to Announce First Quarter 2021 Financial Results on May 11, 2021

MENLO PARK, Calif., May 04, 2021 (GLOBE NEWSWIRE) — Talis Biomedical Corporation (“TLIS”), a company dedicated to developing innovative molecular diagnostic tests for infectious diseases at the point-of-care, today announced that it will release financial results for the first quarter after market close on Tuesday, May 11, 2021. Talis will host a conference call, beginning at 1:30 p.m. Pacific Time (4:30 p.m. Eastern Time) to discuss financial and operational results.

Interested parties may access the live call via telephone by dialing 833-715-1329 for participants in the U.S. or Canada and 430-775-1933 for international callers, using conference ID 7657867. A live and archived webcast of the event can be accessed via the News & Events page of the investor section of Talis Biomedical’s website at www.talis.bio.

About Talis Biomedical

Talis is dedicated to transforming diagnostic testing by developing and commercializing innovative products that are designed to enable accurate, low cost and rapid molecular testing for infectious diseases at the point-of-care, beginning with COVID-19. The company is developing Talis One, a compact, sample-to-answer, cloud-enabled, molecular diagnostic platform. Talis is headquartered in Menlo Park, California. For more information, please visit talis.bio.

Contact

Media & Investors
Emily Faucette
[email protected]
415-595-9407



Investors Who Have Lost Money in Their Ubiquiti Investment Should Contact Block & Leviton, Who Is Investigating Securities Fraud Claims Against Ubiquiti

BOSTON, May 04, 2021 (GLOBE NEWSWIRE) — Block & Leviton is investigating whether Ubiquiti Inc. (NYSE: UI) committed violations of securities fraud, and investors who have lost money should contact the firm to learn more about how they might recover those losses. For more details, visit https://www.blockleviton.com/cases/ui.

What is this all about?

On March 30, 2021, Krebs on Security reported that a whistleblower has claimed that Ubiquiti’s January 11, 2021 data breach was “catastrophic,” and much more serious than the company previously let on. The report claims Ubiquiti hid a “massive” breach that put customer data and device security at risk. We are investigating whether Ubiquiti lied or misrepresented to investors the severity of the data breach when the Company announced it in January.

Who is eligible?

On this news, the Ubiquiti share price dropped from its March 30, 2021 open of $375.30 to an April 1, 2021 close of just $289.15 per share, representing a two day drop of approximately 23%. Investors who have lost money on their Ubiquiti investment – – whether or not they have sold that investment – – are potentially eligible and should contact Block & Leviton to learn more.

What is Block & Leviton doing?

Block & Leviton is considering filing a securities class action lawsuit to attempt to recover losses on behalf of investors who have lost money.

What should I do next?

If you’ve lost money on your investment, you should contact Block & Leviton to learn more via our case website, by email at [email protected], or by phone at (617) 398-5600.

Why should I contact Block & Leviton?

Many law firms have issued releases about this matter; many of those firms do not actually litigate securities class actions. Block & Leviton is a law firm that actually litigates cases. We are dedicated to obtaining significant recoveries on behalf of defrauded investors through active litigation in the federal courts across the country. Many of the nation’s top institutional investors hire us to represent their interests. You can learn more about us at our website, www.blockleviton.com, or call (617) 398-5600 or email [email protected] with any questions.

This notice may constitute attorney advertising.

CONTACT:
BLOCK & LEVITON LLP
260 Franklin St., Suite 1860
Boston, MA 02110
Phone: (617) 398-5600
Email: [email protected]
SOURCE: Block & Leviton LLP
www.blockleviton.com



Strategic Alternatives Process: Boulder Energy Ltd.

CALGARY, Alberta, May 04, 2021 (GLOBE NEWSWIRE) — Boulder Energy Ltd. (“Boulder” or the “Company”) has engaged National Bank Financial Inc. (“NBF”) as Financial Advisor and Raymond James Ltd. (“Raymond James”) as Co-Financial Advisor to initiate a process (the “Strategic Review”) to identify, examine and consider all strategic and financial alternatives available to the Company, including a sale of the Company’s assets, with the ultimate view of enhancing stakeholder value.

Strategic Review

The Strategic Review is intended to explore a comprehensive range of strategic and transaction alternatives, including, but not limited to, a sale of the Company, investment in, merger or other business combination, a recapitalization or refinancing, a sale of all or a portion of the Company’s assets, or any combination thereof, among all other alternatives to improve the Company’s financial position and maximize value.

Overview of Boulder

Boulder Energy Ltd. is a private oil and natural gas producer with high-working-interest operations in the multi-zone Belly River play at Brazeau in the Alberta Deep Basin. Key highlights include:

  • 44 degree API light sweet oil with top tier operating netbacks;
  • ~100% owned and operated infrastructure;
  • More than 165,000 net acres of land controlled;
  • Inventory of high-quality prospective drilling locations for oil; and
  • Successful enhanced oil recovery (EOR) schemes with minimal capital required to increase and expand gas injection programs.

The Company provides a stable, low-decline production base, with average daily production net to Boulder in March 2021 of approximately 2,860 boe/d, consisting of approximately 1,928 bbls/d of oil and natural gas liquids and 5,594 mcf/d of natural gas.

Net operating income for calendar 2020 totaled approximately $16.7 million. The Company estimates Q1 2021 net operating income to be approximately $7.0 million, or $28.0 million annualized.

A downloadable, non-confidential summary of opportunity will be posted to Boulder’s website when available – see www.boulderenergy.ca.

Advisor Contacts

For access to marketing materials and a Confidentiality Agreement (“CA”) please contact NBF or Raymond James. More detailed confidential information and process timeline will be provided to any party executing a CA.

Offers relating to this transaction will be accepted until 12:00pm MST on May 27, 2021.

National Bank Financial Inc.

Chris Muldoon
Managing Director, Investment Banking
Phone: (403) 290-5105
Email: [email protected]

Raymond James Ltd.

Dion Degrand
Managing Director, Head of Canadian Oil & Gas Investment Banking
Phone: (403) 509-0517
Email: [email protected]



BlueCat launches Integrity 9.3 with improved DNS, DHCP, and IP Address Management (DDI) capabilities to enable business transformation and enterprise cloud adoption

BlueCat Integrity 9.3 provides customers with greater observability, comprehensive automation, and accelerates cloud adoption while enhancing overall system performance.

TORONTO, May 04, 2021 (GLOBE NEWSWIRE) — BlueCat, the Adaptive DNS Company™, today announced the latest release of its flagship product, BlueCat Integrity. Integrity 9.3, which allows enterprises to better manage their DNS, DHCP, and IP Address Management (DDI), now includes new functionality that allows customers to better leverage these critical services to optimize their increasingly complex networks, more quickly adopt automation and deliver on hybrid cloud initiatives.

“We continue to provide our global customers, who rely on DNS as a critical service, the ability to support network resilience, cybersecurity, and automation requirements, as well as the ability to better meet their current goals around cloud adoption and business transformation,” said Martin McNealis, BlueCat’s Chief Product Officer.

BlueCat’s Integrity 9.3 release enables the enterprise to:

  • Better manage complex networks. Two thirds (66%) of network teams struggle to support strategic business initiatives using decentralized, legacy DNS infrastructures. Network complexity is compounded by private and overlapping address space, distributed deployment environments, M&A activity, and more. Using Integrity 9.3, customers can now centrally document and navigate these complex relationships across their cloud, on-prem and virtualized networks.
  • Ramp up automation. More than half (56%) of IT managers admit their teams are overwhelmed by DNS tickets and service requests, stalling innovation across the organization. BlueCat customers can now use Integrity 9.3 to ramp up their automation efforts and provision at scale that ensures consistency and reduce human error.
  • Improve visibility and compliance. Nearly two-thirds (63%) of network teams do not have central visibility or control over their DDI audit data. This visibility gap introduces security risks and data compliance challenges. With Integrity 9.3, customers gain even more control with improvements in capturing, maintaining, and exporting system and DNS data. Not only can Integrity 9.3 customers capture both query and response for all DNS resolution, the system level data can all be tracked as well. This data can be integrated with an external security instance and event management platform (SIEM) or data lake, enabling compliance with all audit and retention policies.

“With the incredible pace of innovation in our networking environment today, Integrity 9.3’s tracking of overlapping space gives us the visibility and control we need to meet our ever-more demanding SLAs,” said a BlueCat customer, who manages IT at a medical services provider. Another BlueCat customer, a global telecommunications company, praised the release, saying, “in our dynamic network today, we need the ability to zero-touch provision new services anywhere. Integrity 9.3 provides us the capability to do so with the core tools we use today.”

For a complete list of new features included in the Integrity 9.3 release, please visit this information page.

About BlueCat

BlueCat is the Adaptive DNS™ company. The company’s mission is to help the world’s largest organizations thrive on network complexity, from the edge to the core. To do this, BlueCat re-imagined DNS. The result – Adaptive DNS™ – is a dynamic, open, secure, scalable, and automated resource that supports the most challenging digital transformation initiatives, like adoption of hybrid cloud and rapid application development. Learn more at www.bluecatnetworks.com.



Contact:
[email protected]
#: 416 966 3428

Treatment’s healthcare AI developed by over 40 doctors

VANCOUVER, British Columbia, May 04, 2021 (GLOBE NEWSWIRE) — Treatment.com International Inc. (CSE: TRUE), a disruptive healthcare technology company that is harnessing the power of AI to help Canadians improve their health has developed the most sophisticated medical AI engine to “think like a doctor”.

The Company enlisted a team of leading doctors and engineers around the world to train its AI to process information and provide insights in the same way a doctor would. Its exclusive technology was developed from the ground up by doctors, and as a result, its ability to absorb unique and complex health information and reason like a doctor to provide an accurate assessment is unparalleled.

Treatment.com, led by its Chief Medical Officer, Dr. Kevin Peterson, assembled a team of 40 doctors to build a global library of medical knowledge specifically designed to train the AI. The AI was tested by a top 10 North American medical school, and it was so effective that the university is using it to test and train future doctors.

“I have been practicing and teaching medicine for over 35 years, and I am particularly excited by the ability of our AI to perform complex medical reasoning. The software can support and empower all of us in making better health decisions,” said Dr. Peterson.

“The applications of the technology are boundless. By understanding disease in the same way that a doctor was taught, the AI provides a medical perspective that can improve consumer health decisions or support doctors in their everyday clinical decisions. By improving everyone’s access to medical knowledge, we can promote prevention, provide earlier identification of medical problems, enhance access to medical care, and support treatments that can improve the lives of billions of people.”

The first product to use this ground-breaking resource will be Treatment.com’s Cara mobile application. Providing a symptom-based assessment for consumers, Cara is designed to assess the context of a medical problem, and to collect and track personalized information that can help a consumer make better health decisions. Cara is scheduled to be released summer 2021.

About Treatment.com

Treatment.com is a disruptive healthcare technology company that is harnessing the power of AI to help Canadians improve their health through personalized recommendations and insights. Based in Vancouver, the company spent the last five years working with a team of world-class doctors, engineers, mathematicians, and AI specialists to develop a complex AI engine that leverages the most robust, personalized data to generate highly predictive and accurate insights. Treatment.com is the parent company of Cara. This summer, Cara will be empowering Canadians to take control of their health with the launch of an innovative mobile app powered by this exclusive AI engine.

For more investor information on Treatment.com please visithttps://treatment.com/investors/.

Forward Looking Statement

This news release contains forward-looking statements relating to the future operations of Treatment.com, International, Inc. (Treatment) and other statements that are not historical facts. Forward-looking statements are often identified by terms such as “will”, “may”, “should”, “anticipate”, “expects” and similar expressions. All statements other than statements of historical fact, included in this release, including, without limitation, statements regarding the future plans and objectives of Treatment, are forward-looking statements that involve risks and uncertainties. There can be no assurance that such statements will prove to be accurate and actual results and future events could differ materially from those anticipated in such statements. Important factors that could cause actual results to differ materially from Treatment’s expectations include other risks detailed from time to time in the filings made by Treatment with securities regulators.

The reader is cautioned that assumptions used in the preparation of any forward-looking information may prove to be incorrect. Events or circumstances may cause actual results to differ materially from those predicted, as a result of numerous known and unknown risks, uncertainties, and other factors, many of which are beyond the control of Treatment. The reader is cautioned not to place undue reliance on any forward-looking information. Such information, although considered reasonable by management at the time of preparation, may prove to be incorrect and actual results may differ materially from those anticipated. Forward-looking statements contained in this news release are expressly qualified by this cautionary statement. The forward-looking statements contained in this news release are made as of the date of this news release and Treatment will only update or revise publicly the included forward-looking statements as expressly required by Canadian securities law.

For more information:

Investor Contact: [email protected]



Recce Pharmaceuticals Announces Positive Data on Bactericidal Activity of RECCE® 327 Against All Six ESKAPE Pathogens


Highlights:

  • More than 99.9% effective against full suite of ESKAPE pathogens, within hours of exposure to RECCE

    ®

    327 (R327) in independent bacterial efficacy studies
  • R327 remains effective against hypermutated ESKAPE superbugs, including multi-drug resistant (MDR) forms, a current market challenge of all existing antibiotics
  • On-track to be the only company developing an efficacious anti-infective against ESKAPE pathogens globally

SYDNEY, Australia, May 04, 2021 (GLOBE NEWSWIRE) — Recce Pharmaceuticals Ltd (ASX:RCE) (FSE:R9Q) (Company), the Company developing new classes of synthetic anti-infectives, is pleased to announce RECCE® 327 (R327) has demonstrated bactericidal activity against all six antibiotic resistant ESKAPE pathogens, including drug resistant mutations (superbugs) as well as two additional World Health Organization (WHO) priority pathogens list.

“We are encouraged by the data from this study and will continue to explore the potential of RECCE® 327 to treat hospital-acquired infections,” said Recce Pharmaceuticals CEO James Graham. “Antimicrobial resistance is one of the most urgent threats to global public health with the suite of ESKAPE pathogens posing a significant threat due to their virulence and rapid development of drug-resistance. Additionally, with R327 effective against two more priority pathogens listed by the WHO, we believe this reinforces the potential of R327 to treat some of the greatest threats to human health.”

These antibiotic resistant bacteria acronymically dubbed ‘ESKAPE’ due to their propensity of ‘escaping’ the biocidal action of antibiotics, are collectively responsible for over 720,000 hospital acquired (nosocomial) infections in the United States alone each year.1 The ESKAPE pathogens include both Gram-positive and Gram-negative bacteria; Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, and Enterobacter species.

The study was conducted by an independent contract research organization to assess the in-vitro efficacy of R327 against all ESKAPE pathogen bacterial strains. R327 is a broad-spectrum synthetic anti-infective that has potential to address the urgent global health threat posed by antibiotic resistant superbugs and emerging viral pathogens.

Graphics accompanying this announcement are available at
https://www.globenewswire.com/NewsRoom/AttachmentNg/a3b15bb1-79c7-44fd-b457-734d4e2fa7d0

https://www.globenewswire.com/NewsRoom/AttachmentNg/a695f826-f4e3-4061-bea3-d0ae89a8d31f

ESKAPE pathogens are responsible for 42.2% of blood infections,2 around 50 million infections each year, resulting in one in five deaths in the community or one in three deaths in hospitals3 and are associated with higher lengths of stay, cost of care, and mortality compared with non-ESKAPE pathogens.2

The dilution method of R327 used in these studies slightly increased the minimum inhibitory concentration (MIC) across the wide range of Gram-positive, Gram-negative and superbug forms of bacteria. The slight variation (+/-) between one experiment to the next is likely due to small variance in the sensitivity of the instruments used in detection. The dilution of R327 that showed efficacy against K. pneumonia (CRE) is higher than previous findings though still well within the therapeutic window dosing range.

Additionally, R327 was shown to be effective against the WHO global priority pathogens carbapenem-resistant Escherichia coli (E. coli CRE) and multi-drug resistant Neisseria gonorrhoeae4 (N. gonorrhea MDR). These bacteria are listed on the WHO’s list of priority pathogens as those for which new antibiotics are urgently needed in addition to ESKAPE pathogens.

A graphic accompanying this announcement is available at
https://www.globenewswire.com/NewsRoom/AttachmentNg/08edf798-57a0-4634-8bb3-593db59a0b48

The minimum inhibitory concentration (MIC), or the lowest concentration of a drug that prevents visible growth of a bacterium or bacteria, was first determined to define the test concentrations for the time-kill study. The time-kill study was performed to determine the bacterial killing effect of R327 at a total of five concentrations, ranging from 0.5X to 8X the MIC and to measure killing kinetics of treatment with R327 against each strain.

Time-kill curves of R327 at various concentrations against strains of ESKAPE pathogens. In the time kill assay, each R327 dilution was tested in duplicate with the average plot shown.

The bactericidal activity of R327 demonstrated a three-log or 99.9% reduction in the number of colony forming units (CFUs) over 24 hours against all six strains at various concentrations and times.

Additional time kill concentration studies are underway with drug-resistant bacterial and are expected to be in-line with existing MIC/Time Kill. Data is expected in around a month and as pivotal inclusion in a Whitepaper/Abstract for presentation at the World Microbe Forum (20-24 June 2021) 5.

About Recce Pharmaceuticals Ltd

Recce Pharmaceuticals Ltd (ASX: RCE) is pioneering the development and commercialisation of New Classes of Synthetic Anti-Infectives designed to address the urgent global health problems of antibiotic resistant superbugs and emerging viral pathogens.

Recce’s anti-infective pipeline is unique and comprised of broad-spectrum synthetic polymer antibiotics RECCE® 327, RECCE® 435, and RECCE® 529 for viral infections with unique mechanisms of action against hyper-mutation on bacteria and viruses, respectively.

Patented lead candidate RECCE® 327 has been developed for the treatment of blood infections and sepsis derived from E. coli and S. aureus bacteria – including their superbug forms. Recce’s new antibiotic compound, RECCE® 435, has been formulated for oral use.

The FDA has awarded RECCE® 327 Qualified Infectious Disease Product designation under the Generating Antibiotic Initiatives Now (GAIN) Act – labelling it for Fast Track Designation, plus 10 years of market exclusivity post approval. Further to this designation, RECCE® 327 has been included on The Pew Charitable Trusts Global New Antibiotics in Development Pipeline as the only synthetic polymer and sepsis drug candidate in development.

Recce wholly owns its automated manufacturing, ready to support first-in-human clinical trials. Recce’s anti-infective pipeline seeks to exploit the unique capabilities of RECCE® technologies targeting synergistic, unmet medical needs.

Chief Executive Officer


James Graham
Recce Pharmaceuticals Ltd
+61 (02) 9256 2571
[email protected]

Media and Investor Relations (AU)


Andrew Geddes
CityPR
+61 (02) 9267 4511
[email protected]

Media and Investor Relations (USA)


Meredith Sosulski, PhD
LifeSci Communications
+1 929 469 3851
[email protected]


https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4871955/#:~:text=The%20ESKAPE%20pathogens%20(Enterococcus%20faecium,nosocomial%20infections%20throughout%20the%20world.
2https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6902016/
3https://www.sensium.co.uk/news/lancet-publication-finds-one-in-five-deaths-due-to-sepsis/
4https://www.pharmacologydiscoveryservices.com/catalogmanagement/viewitem/Neisseria-gonorrhoeae-MDR-WHO-L-CCUG-57598-MIC/612505
5https://www.worldmicrobeforum.org/ 



The RMR Group Inc. Releases Annual Sustainability Report

The RMR Group Inc. Releases Annual Sustainability Report

Report Highlights ESG Strategies and Notable Achievements

NEWTON, Mass.–(BUSINESS WIRE)–The RMR Group Inc. (Nasdaq: RMR) today announced the publication of its annual Sustainability Report, which outlines the Environmental, Social and Governance (ESG) strategies, practices and industry recognitions of RMR and its clients, including Service Properties Trust (Nasdaq: SVC), Diversified Healthcare Trust (Nasdaq: DHC), Office Properties Income Trust (Nasdaq: OPI), Industrial Logistics Properties Trust (Nasdaq: ILPT), Five Star Senior Living Inc. (Nasdaq: FVE) and Sonesta International Hotels Corporation (Private).

Adam Portnoy, President and Chief Executive Officer of RMR made the following statement:

“In our annual sustainability report, we are proud to continue sharing our ESG strategies and showcasing our successes. Over our more than three decades in operation, sustainability has been integral to our business and our clients. Our sustainability practices — minimizing our impact on the environment, embracing the communities where we operate and attracting and supporting top professionals — are critical components of our long-term success.”

The most notable ESG-related achievements over the past year, summarized in the 2020 Sustainability Report, include the following:

  • For the third consecutive year, RMR was named a 2021 ENERGY STAR® Partner of the Year by the Environmental Protection Agency (EPA) and for the first time was recognized in the program’s Sustained Excellence category. Additionally, OPI was honored as an ENERGY STAR® Partner of the Year for the fourth consecutive year and recognized in the Sustained Excellence category for the second consecutive year.
  • As of December 31, 2020, RMR’s managed portfolio included 53 buildings that were designated as BOMA 360 properties, 63 buildings that are ENERGY STAR® Certified and 35 buildings that hold LEED certifications. RMR ranked second for the number of buildings that were designated by the Building Owners and Managers Association (BOMA) as BOMA 360 properties.
  • RMR, OPI and ILPT were named as three of the Fastest Growing Middle Market Companies in Massachusetts by the Boston Business Journal in 2021. Both RMR and OPI were recognized for the second consecutive year as part of this program.
  • RMR was named one of The Boston Globe’s Top Places to Work in Massachusetts in the Large Employers category.
  • RMR was ranked ninth in Commercial Property Executive’s 2020 list of Top 30 Commercial Property Management Companies.

The RMR Group provides property management services nationwide for nearly 1,300 properties with approximately 92 million square feet of office, industrial, medical office, life science and retail space. RMR exclusively provides property management services to its managed clients and does not offer stand-alone property management services to third-parties.

RMR’s full 2020 Sustainability Report is available on the Corporate Sustainability section of its website and can be downloaded here.

About The RMR Group Inc.

The RMR Group Inc. (Nasdaq: RMR) is a holding company and substantially all of its business is conducted by its majority owned subsidiary, The RMR Group LLC, or RMR. RMR is a leading U.S. alternative asset management company, unique for its focus on commercial real estate (CRE) and related businesses. RMR’s vertical integration is supported by its more than 600 real estate professionals in over 30 offices nationwide who manage $32 billion in assets under management and leverage 35 years of institutional experience in buying, selling, financing and operating CRE. RMR is headquartered in Newton, MA and was founded in 1986. For more information, please visit www.rmrgroup.com.

Christopher Ranjitkar

Senior Director, Marketing & Corporate Communications

(617) 219-1473

KEYWORDS: Massachusetts United States North America

INDUSTRY KEYWORDS: Finance Environment Professional Services Commercial Building & Real Estate Construction & Property

MEDIA:

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GBT and Sickle Cell Disease Association of America Kick Off “Lift Every Voice to Shine the Light on Sickle Cell” Spoken Word Contest in Honor of World Sickle Cell Day 2021

SOUTH SAN FRANCISCO, Calif. and HANOVER, Md., May 04, 2021 (GLOBE NEWSWIRE) — In recognition of World Sickle Cell Day, which falls on June 19, 2021, Global Blood Therapeutics, Inc. (GBT) (NASDAQ: GBT) and the Sickle Cell Disease Association of America, Inc. (SCDAA) today launched “Lift Every Voice to Shine the Light on Sickle Cell” – a contest that will feature original spoken word pieces to raise awareness of sickle cell disease (SCD). The contest, which aims to elevate the voices and experiences of people living with SCD and their caregivers, is presented by Sickle Cell Speaks, GBT’s SCD education campaign that highlights authentic stories of those living with SCD to dispel misconceptions about the disease.

“People with sickle cell disease possess an incredibly rich and diverse array of creative abilities, often used to express the physical and emotional burden of living with this complex and devastating disease,” said Beverley Francis-Gibson, M.A., president and CEO of the SCDAA. “Celebrating these voices is critical as we work to overcome the legacy of stigma and misinformation that have a direct impact on health outcomes. We are proud to partner with GBT to shine the light on the challenges that SCD warriors face with strength and resilience.”

Spoken word poetry is an art form rooted in traditions of storytelling to convey compelling messages and personal experiences. People living with SCD and their caregivers are invited to sign up to submit videos of themselves performing original spoken word pieces about their experience with SCD. To learn more about the contest details and how to submit a video, please email [email protected] or visit www.facebook.com/SickleCellSpeaks. Participants must sign up by May 24, 2021, and be U.S. residents. For each eligible submission received, GBT will donate $100 to the SCDAA, up to a total donation of $5,000. The contest winner will be featured in a GBT event at the SCDAA Annual Convention in October 2021. “Shine the Light on Sickle Cell” is a collaboration between SiNERGe and SCDAA.

“GBT is proud to partner with SCDAA to recognize the many inspiring voices within the sickle cell community who have rallied for progress in the face of tremendous health and societal challenges over the last year,” said Jung E. Choi, chief business and strategy officer, and head of patient advocacy and government affairs at GBT. “People with SCD suffer from a terrible, life-threatening disease that is made worse by being subjected to racial bias. We reiterate our commitment to shining a brighter light on the inequities these patients encounter and will continue working with all our partners to ensure access to the high-quality care patients deserve.”

Performances by the spoken word contest winner and finalists will be featured in a virtual event on Friday, June 18, 2021, at 4:00 p.m. PT and Saturday, June 19, 2021, at 12:00 p.m. PT on the Sickle Cell Speaks Facebook and Instagram pages. The event will be hosted and feature performances by three SCD advocates who are passionate about using spoken word to educate and inspire change:

  • Charly Richard, musician and writer
  • DeMitrious Wyant, musician and entrepreneur
  • Candis St. John, nurse and poet

About Sickle Cell Disease

Sickle cell disease (SCD) affects an estimated 100,000 people in the United States,1 an estimated 52,000 people in Europe,2 and millions of people throughout the world, particularly among those whose ancestors are from sub-Saharan Africa.1 It also affects people of Hispanic, South Asian, Southern European, and Middle Eastern ancestry.1 SCD is a lifelong inherited blood disorder that impacts hemoglobin, a protein carried by red blood cells that delivers oxygen to tissues and organs throughout the body.3 Due to a genetic mutation, people with SCD form abnormal hemoglobin known as sickle hemoglobin. Through a process called hemoglobin polymerization, red blood cells become sickled – deoxygenated, crescent-shaped, and rigid.3-5 The sickling process causes hemolytic anemia (low hemoglobin due to red blood cell destruction) and blockages in capillaries and small blood vessels, which impede the flow of blood and oxygen throughout the body. The diminished oxygen delivery to tissues and organs can lead to life-threatening complications, including stroke and irreversible organ damage.4-7

About SCDAA

Sickle Cell Disease Association of America (SCDAA) advocates for people affected by sickle cell conditions and empowers community-based organizations to maximize quality of life and raise public consciousness while advancing the search for a universal cure. The association and more than 50 member organizations support sickle cell research, public and professional health education and patient and community services. Visit www.sicklecelldisease.org.

About Global Blood Therapeutics

Global Blood Therapeutics (GBT) is a biopharmaceutical company dedicated to the discovery, development, and delivery of life-changing treatments that provide hope to underserved patient communities. Founded in 2011, GBT is delivering on its goal to transform the treatment and care of sickle cell disease (SCD), a lifelong, devastating inherited blood disorder. The company has introduced Oxbryta® (voxelotor), the first FDA-approved treatment that directly inhibits sickle hemoglobin polymerization, the root cause of red blood cell sickling in SCD. GBT is also advancing its pipeline program in SCD with inclacumab, a P-selectin inhibitor in development to address pain crises associated with the disease, and GBT021601 (GBT601), the company’s next-generation hemoglobin S polymerization inhibitor. In addition, GBT’s drug discovery teams are working on new targets to develop the next wave of treatments for SCD. To learn more, please visit www.gbt.com and follow the company on Twitter @GBT_news.

References

  1. Centers for Disease Control and Prevention website. Sickle Cell Disease (SCD). https://www.cdc.gov/ncbddd/sicklecell/data.html. Accessed June 3, 2019.
  2. European Medicines Agency. https://www.ema.europa.eu/en/medicines/human/orphan-designations/eu3182125. Accessed June 12, 2020.
  3. National Heart, Lung, and Blood Institute website. Sickle Cell Disease. https://www.nhlbi.nih.gov/health-topics/sickle-cell-disease. Accessed August 5, 2019.
  4. Rees DC, et al. Lancet. 2010;376(9757):2018-2031.
  5. Kato GJ, et al. Nat Rev Dis Primers. 2018;4:18010.
  6. Kato GJ, et al. J Clin Invest. 2017;127(3):750-760. 
  7. Caboot JB, et al. Paediatr Respir Rev. 2014;15(1):17-23.

GBT Contact Information:

Steven Immergut
650-410-3258
[email protected]

SCDAA Contact Information:

Emma Day
[email protected]

Kyri Jacobs
[email protected]



Cortexyme to Present at the BofA Securities 2021 Healthcare Conference on May 11, 2021

Cortexyme to Present at the BofA Securities 2021 Healthcare Conference on May 11, 2021

SOUTH SAN FRANCISCO, Calif.–(BUSINESS WIRE)–
Cortexyme, Inc. (Nasdaq: CRTX), a company advancing a pivotal trial in Alzheimer’s disease with topline data expected in the fourth quarter of 2021 and a growing pipeline of therapeutics for degenerative diseases, today announced Chris Lowe, the company’s chief operating officer and chief financial officer, will participate in a fireside chat at the BofA Securities 2021 Healthcare Conference, a virtual event, on Tuesday, May 11, 2021, at 3:30 p.m. EDT (12:30 p.m. PDT).

A live webcast of the fireside chat will be accessible on the Investor Calendar page under the News & Events heading of Cortexyme’s investor website at ir.cortexyme.com. The webcast will be archived at that location for 90 days.

About Cortexyme

Cortexyme, Inc. (Nasdaq: CRTX) is a clinical stage biopharmaceutical company pioneering upstream therapeutic approaches designed to improve the lives of patients diagnosed with Alzheimer’s and other degenerative diseases. Based upon the evidence generated to date, Cortexyme is currently advancing its lead therapeutic candidate, atuzaginstat (COR388), in the GAIN Trial, an ongoing Phase 2/3 clinical trial in patients with mild to moderate Alzheimer’s disease. Cortexyme is targeting a specific, infectious pathogen found in the brain and other organs and tied to degeneration and inflammation in humans and animal models. To learn more about Cortexyme, visit www.cortexyme.com or follow @Cortexyme on Twitter.

Corporate Contact:

Stacy Roughan

Vice President, Corporate Communications & Investor Relations

Cortexyme, Inc.

[email protected]

KEYWORDS: United States North America California

INDUSTRY KEYWORDS: Research Seniors Dental Clinical Trials Biotechnology General Health Pharmaceutical Consumer Health Science

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Medolife Rx Announces Historic Product Registration in Dominican Republic Enabling Escozine to Be Sold Throughout Latin America as Natural Alternative Cancer Medicine

BURBANK, Calif., May 04, 2021 (GLOBE NEWSWIRE) — via NewMediaWire — Medolife Rx, Inc. (“Medolife”), a global integrated biopharmaceutical company with R&D, manufacturing, and consumer product distribution, which is a majority owned subsidiary of Quanta, Inc. (OTC PINK: QNTA), announced today the Company has renewed a product registration certificate for its lead drug candidate Escozine® from the Ministry of Health in the Dominican Republic (DR). The registration enables Escozine® to be prescribed as a natural bioactive alternative medicine to be used in cancer treatments as well as a treatment for the SARS-CoV-2 (COVID-19) virus, after Medolife performed a safety and efficacy study on COVID-19. This registration in the DR through in-place trade agreements opens the door for distribution and sales in most of Latin America.

The registration was renewed after the Company provided study data on the efficacy of Escozine® in assisting cancer treatments of various kinds including common types of cancer such as breast, prostate, lung, and some uncommon forms of cancer such as bladder and ovarian. The registration allows for Escozine® to be marketed as a bioactive alternative cancer medicine across the DR and most other countries in Latin America, where the burden of cancer and mortality rates are among the highest in the world. Latin America has a combined population of over 400 million people with over one million diagnosed with cancer annually, let alone those being treated for ongoing cancer-related issues. With this registration, the Company is able to negotiate distribution agreements with pharmaceutical chains and distributors throughout Latin America to bring Escozine® to this in-need population. The Company also plans to negotiate with the government in the DR for the purchase of Escozine® for use as a treatment for COVID-19.

The Company has compiled large amounts of clinical data validating Escozine’s ability to not only improve quality of life in cancer patients, but also its potential ability to kill cancer cells, as shown in numerous pre-clinical and clinical studies on various forms of cancer that led to this historic registration. Medical professionals in the DR have embraced the use of Escozine® in cancer treatment regimens for some time now, including one providing a full recommendation on the drug’s cancer-fighting and quality-of-life improving attributes.

“This registration not only validates Escozine® as a cancer therapeutic but creates an unbelievable revenue generation opportunity for our company in that the product can be off-label prescribed for treatment of COVID-19 patients as a supportive therapy where vaccination progression has been slow,” said Medolife CEO Dr. Arthur Mikaelian. “Through free trade agreements, we will be able to market Escozine to one of the largest populations in the world. Cancer remains one of the leading causes of death worldwide and estimates have shown between four and five percent of humans will develop cancer in their lifetime. It is our mission to reach these patients with our polarized drug Escozine and improve their quality of life while helping to fight the cancer itself, and we are now registered to do so.”

Medolife has been researching Escozine®, a proprietary formulation consisting of small molecule peptides derived from Rhopalurus princeps scorpions, which is amplified by the Company’s polarization technology, as a potential treatment for cancer as well as COVID-19 in parallel clinical research programs in both the United States and the DR. The Company has completed numerous safety and efficacy studies on the drug and recently announced that it has filed its final data set with the US Food and Drug Administration (FDA) as it relates to an Investigational New Drug (IND) filing on Escozine®. The Company is in the process of registration for medical ethics committee approval to conduct double-blind placebo human studies on Escozine®, which would mark a substantial step forward in Escozine’s path toward worldwide registration and adoption.

“Beyond the massive opportunity this registration creates, when working with regulatory bodies in both the United States and abroad, having an approved product that is being administrated to large populations such as what we are doing with Escozine in Latin America, can provide an expedited path to approval in other countries. This was an important and momentous step for us and only positions Escozine and Medolife for further success,” Mikaelian added.

The DR is home to Medolife’s “first-of-its-kind” scorpion reservation, where the Company is able to safely and humanely cultivate the scorpions needed to produce the peptides that are used in the manufacturing of Escozine®. Recently, the Company has been expanding the reservation and preparing to increase capacity in order to meet the demand driven by this registration and others in the future.

About Medolife Rx

Medolife Rx, Inc. is a global biotechnology company with operations in clinical research, manufacturing, and consumer products. Medolife Rx was created through the merger of Medolife, a private company founded by Dr. Arthur Mikaelian who pioneered the unlaying polarization technology that makes the Company’s portfolio of pharmaceutical and nutraceutical products so effective, and Quanta, Inc., a direct-to-consumer wellness product portfolio company. The Company’s lead clinical development programs include Escozine®, a proprietary formulation consisting of small molecule peptides derived from Rhopalurus princeps scorpions, which is amplified by the Company’s polarization technology and is being researched as a treatment of various indications, including COVID-19 and cancer. The Company has completed preclinical safety and efficacy research on Escozine® and is pursuing product registration and drug approval in various countries, including the United States and throughout Latin America. 

Through its subsidiary QuantRx, Medolife manufactures and distributes consumer wellness products in high-impact consumer areas such as pain relief, beauty, and general wellness. QuantRx products are designed using Dr. Mikaelian’s polarization technology, which applies advances in quantum biology to increase the potency of active ingredients. Ultimately, Quanta’s mission is to deliver better, more effective ingredients to elevate product efficacy, reduce waste, and facilitate healthier, more sustainable consumption.

Beyond its own clinical and consumer applications, the polarization technology used by Medolife and its subsidiaries has many potential applications. From potentiating bio-ingredients, to producing more-effective carbon-trapping plants, to transformative anti-aging solutions, Medolife has the opportunity to upend how commercial and pharmaceutical products are made and increase their benefits, while decreasing their chemical concentration.

Forward-Looking Statements

Safe Harbor Statement under the U.S. Private Securities Litigation Reform Act of 1995: This release contains statements that are forward-looking in nature which express the beliefs and expectations of management including statements regarding the Company’s expected results of operations or liquidity; statements concerning projections, predictions, expectations, estimates or forecasts as to our business, financial and operational results and future economic performance; and statements of management’s goals and objectives and other similar expressions concerning matters that are not historical facts. In some cases, you can identify forward-looking statements by terminology such as “anticipate,” “estimate,” “plan,” “project,” “continuing,” “ongoing,” “expect,” “we believe,” “we intend,” “may,” “will,” “should,” “could,” and similar expressions. Such statements are based on current plans, estimates and expectations and involve a number of known and unknown risks, uncertainties and other factors that could cause the Company’s future results, performance or achievements to differ significantly from the results, performance or achievements expressed or implied by such forward-looking statements. These factors and additional information are discussed in the Company’s filings with the Securities and Exchange Commission and statements in this release should be evaluated in light of these important factors. Although we believe that these statements are based upon reasonable assumptions, we cannot guarantee future results. Forward-looking statements speak only as of the date on which they are made, and the Company undertakes no obligation to update publicly or revise any forward-looking statement, whether as a result of new information, future developments or otherwise.

Kyle Porter
[email protected]
858-264-6600