Assembly Biosciences Presents Data from HBV Core Inhibitor Programs in Poster Sessions at the 2020 AASLD The Liver Meeting Digital Experience™

– Data show longer-term, differentiated safety profile
of
vebicorvir
and
the
importance of HBV
preg
e
n
o
mic
(
pg
) RNA as a key biomarker
,
as well as
highlight Assembly Bio’s core inhibitor
clinical
pipeline

SOUTH SAN FRANCISCO, Calif., Nov. 13, 2020 (GLOBE NEWSWIRE) — Assembly Biosciences, Inc. (Nasdaq: ASMB), a clinical-stage biotechnology company developing innovative therapeutics targeting hepatitis B virus (HBV) and diseases associated with the microbiome, today announced that data from its HBV core inhibitor programs and related research will be highlighted during four poster sessions – including two late-breakers – at the 2020 American Association for the Study of Liver Diseases (AASLD) The Liver MeetingDigital ExperienceTM. The posters include data from the company’s HBV core inhibitor research and development programs, as well as a collaborative translational study using Assembly Bio’s sensitive HBV nucleic acid assays.

“Findings from these studies are adding to a growing body of clinical data that supports the differentiated safety profile of vebicorvir in combination with nucleos(t)ide therapy,” said Ira M. Jacobson, MD, Director of Hepatology at New York University Langone Medical Center. “New treatment options for HBV patients are long overdue and the addition of a core inhibitor to the standard-of-care regimen may offer better chronic suppressive therapy to a significant patient population. These longer-term safety data, along with the demonstrated association of HBV pgRNA and changes in HBV viral antigens presented at this conference, are very encouraging and support the continued advancement of the company’s core inhibitor programs.”  

“Chronic hepatitis B virus infection is incredibly complex. Through this research, we are proud to continue to contribute to the scientific community’s understanding of hepatitis B and the importance of deepening virologic suppression as it relates to both improving chronic suppressive therapy and reducing downstream clinically important liver-related events,” said John McHutchison, AO, MD, Chief Executive Officer and President at Assembly Biosciences. “Further, these data highlight the potential of our more potent core inhibitor candidates, ABI-H2158 and ABI-H3733. We believe that core inhibitors represent a significant advancement in the HBV field and we remain focused on upcoming milestones, including planned Phase 3 registrational trials of vebicorvir in China and globally in the first half of 2021.”   

The Liver Meeting Digital Experience 2020 Presentations:

The posters will be made available on the “Events and Presentations” page in the Investors section of assemblybio.com.

Vebicorvir (VBR,
or
ABI-H0731)
, Assembly Bio’s Lead HBV Core Inhibitor


Poster Presentation 820

:
Analysis of the longer-term safety profile of the hepatitis B virus core inhibitor
VBR
in an open-label extension study

Presenter: Ira M. Jacobson, MD, Director, Hepatology, NYU Langone Health

This poster includes data from a controlled comparison of 24 patients receiving placebo + nucleos(t)ide analogs (NrtI) for 24 weeks versus 95 patients receiving Assembly Bio’s lead core inhibitor product VBR + NrtI for up to 1.5 years. Data support the differentiated safety profile and continued development of VBR combination therapy.

Key
R
esults:

  • The safety profile of combination treatment with VBR+NrtI was similar to placebo+NrtI over a 24-week controlled-comparison and was stable with longer-term treatment of VBR+NrtI up to 1.5 years.
  • Rashes without systemic involvement observed with VBR+NrtI treatment were predominantly Grade 1 resolving without VBR+NrtI interruption.
  • There was no pattern of increased alamine aminotransferase (ALT) and/or aspartate aminotransferase (AST), indicative of hepatoxicity.


Late





Breaking


Poster


LP37


:

Changes in viral antigens are more strongly associated with HBV pgRNA than HBV DNA in studies of vebicorvir and NrtI in treatment-naive patients with chronic HBV infection

Presenter: Mark Sulkowski, MD, Medical Director, Viral Hepatitis Center, Johns Hopkins University School of Medicine

This poster details the results of post hoc analyses of data from studies of VBR in treatment naïve patients with HBeAg positive chronic HBV infection to better understand the correlations between changes in HBV DNA and pgRNA with those of other HBV antigens. Two approaches were used: correlation analyses with a Pearson’s coefficient and a Mixed-Effects Model for Repeated Measures. These results demonstrate the importance of pgRNA as a meaningful biomarker for chronic HBV.

Key
R
esults:

  • Changes in other HBV antigens are more strongly associated with the change in pgRNA compared with the change in HBV DNA.
  • Correlations between pgRNA and HBeAg and HBcrAg were greater relative to the correlations with HBsAg, likely due to the substantial contribution of HBV integrants to HBsAg levels.
  • A >2 log10 decline in pgRNA in patients receiving VBR + entecavir (ETV) more significantly predicted the decline in the HBeAg and HBcrAg consistent with the second phase decline with core inhibitor treatment reflecting reduction in cccDNA pools.

Assembly Bio’s
Next-Generation of
Core Inhibitors


Late





Breaking


Poster


LP45

:
Amino acid substitutions in the inhibitor binding pocket of HBV core protein confer differential changes in susceptibility to three generations of HBV core inhibitors

Presenter: Dawei Cai, PhD, Senior Scientist, Assembly Bio

This poster describes the in vitro resistance profiles of Assembly Bio’s first-generation core inhibitor, VBR, and next-generation core inhibitor candidates ABI-H2158 (2158) and ABI-H3733 (3733). Researchers evaluated the antiviral activity of these candidates against known substitutions to the core inhibitor binding pocket. They also assessed whether these substitutions affect the ability of core inhibitors to block cccDNA formation as well as HBV replication through inhibition of pgRNA encapsidation.

Key
Results:

  • 2158 and 3733 showed greater potency in terms of preventing cccDNA formation compared with VBR and had more favorable resistance profiles against a panel of substitutions.
  • ETV retains activity against all tested core protein substitutions suggesting that combination therapy with NrtIs will prevent viral breakthrough due to pre-existence or potential emergence of core protein substitutions, consistent with the current clinical data.

Use of
Assembly Bio’s Highly Sensitive HBV Assays
to Characterize
the
A
ssociation of HBV with HCC


Poster 738

:
Persistently detectable serum HBV pgRNA is associated with subsequent HCC development in chronic hepatitis B patients receiving chronic NrtI treatment

Presenter:
 Lung-Yi Mak, MBBS, MRCP, PDipID, FHKCP, FHKAM Department of Medicine, Queen Mary Hospital, The University of Hong Kong, Hong Kong

In this poster, researchers detail findings from a case control study to assess whether residual HBV viraemia is associated with the development of hepatocellular carcinoma (HCC), the most common type of primary liver cancer. The study evaluated 104 chronic HBV patients, 39% of whom had cirrhosis, on ≥ 3 years ETV with unquantifiable HBV DNA by standard assays. Findings highlight the need for more potent viral suppression to further reduce the risk of HCC.

Key
Results:

  • More sensitive assays revealed that patients still had ongoing replication as evidenced by detection of HBV DNA and pgRNA.
  • More than 50% of chronic HBV patients on ETV with HBV DNA<LLOQ (lower limit of quantification) by standard assay had persistent viraemia as determined by a more sensitive HBV DNA assay.
  • Detectable viral nucleic acids (HBV DNA and/or pgRNA) were associated with a higher 2-year risk of HCC development.

About HBV

Chronic hepatitis B virus (HBV) infection is a debilitating disease of the liver that afflicts over 250 million people worldwide with up to 90 million people in China, as estimated by the World Health Organization. HBV is a global epidemic that affects more people than hepatitis C virus (HCV) and HIV infection combined—with a higher morbidity and mortality rate. HBV is a leading cause of chronic liver disease and need for liver transplantation, and up to one million people worldwide die every year from HBV-related causes.

The current standard of care for patients with chronic HBV infection is life-long suppressive treatment with medications that reduce, but do not eliminate, the virus, resulting in very low cure rates. There is a significant unmet need for new therapies to treat HBV.

About Assembly Biosciences

Assembly Biosciences, Inc. is a clinical-stage biotechnology company developing innovative therapeutics targeting hepatitis B virus (HBV) and diseases associated with the microbiome. The HBV program is focused on advancing a new class of potent, oral core inhibitors that have the potential to improve the treatment options available to chronically infected patients. The microbiome program is developing novel oral live microbial biotherapeutic candidates with Assembly’s fully integrated platform, including a robust process for strain identification and selection, GMP manufacturing expertise and targeted delivery to the lower gastrointestinal tract with the GEMICEL® technology. For more information, visit assemblybio.com.

Forward-Looking Statements

The information in this press release contains forward-looking statements that are subject to certain risks and uncertainties that could cause actual results to materially differ. These risks and uncertainties include: Assembly Bio’s ability to initiate and complete clinical trials involving its HBV therapeutic product candidates in the currently anticipated timeframes; safety and efficacy data from clinical studies may not warrant further development of Assembly Bio’s product candidates; clinical and nonclinical data presented at conferences may not differentiate Assembly Bio’s product candidates from other companies’ candidates; Assembly Bio may not observe sustained virologic response in patients who stop therapy in Study 211; Assembly Bio’s ability to maintain financial resources necessary to continue its clinical trials and fund business operations; any impact that the spread of the coronavirus and resulting COVID-19 pandemic may have on Assembly Bio’s business and operations, including initiation and continuation of its clinical trials or timing of discussions with regulatory authorities; and other risks identified from time to time in Assembly Bio’s reports filed with the U.S. Securities and Exchange Commission (the SEC). You are urged to consider statements that include the words may, will, would, could, should, might, believes, hopes, estimates, projects, potential, expects, plans, anticipates, intends, continues, forecast, designed, goal or the negative of those words or other comparable words to be uncertain and forward-looking. Assembly Bio intends such forward-looking statements to be covered by the safe harbor provisions contained in Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. More information about Assembly Bio’s risks and uncertainties are more fully detailed under the heading “Risk Factors” in Assembly Bio’s filings with the SEC, including its most recent Annual Report on Form 10-K, Quarterly Reports on Form 10-Q and Current Reports on Form 8-K. Except as required by law, Assembly Bio assumes no obligation to update publicly any forward-looking statements, whether as a result of new information, future events or otherwise.

Investor
Contact

Assembly Biosciences, Inc.
Lauren Glaser
Senior Vice President, Investor Relations and Corporate Affairs
(415) 521-3828
[email protected]

Media Contact

Sam Brown Inc.
Audra Friis
(917) 519-9577
[email protected]

MiMedx To Host Virtual 2020 Annual Meeting of Shareholders on Friday, November 20

MARIETTA, Ga., Nov. 13, 2020 (GLOBE NEWSWIRE) — MiMedx Group, Inc. (NASDAQ: MDXG) (“MiMedx” or the “Company”), an industry leader in advanced wound care and a therapeutic biologics company, today provided additional information about its upcoming virtual 2020 Annual Meeting of Shareholders (“Annual Meeting”). Timothy R. Wright, Chief Executive Officer, is scheduled to present an overview of the Company, and Rohit Kashyap, Ph.D., Executive Vice President and Chief Commercial Officer, and Robert B. Stein, M.D., Ph.D., Executive Vice President, Research and Development, are scheduled to present an overview of the Company’s commercial and R&D initiatives. Additional members of senior management also plan to be available for a question and answer session from shareholders as of the record date of 5:00 p.m. Eastern Time on October 7, 2020. Guests may join the virtual 2020 Annual Meeting, including the shareholder question and answer session, in a listen-only mode without a control number.

The meeting is scheduled to be held on Friday, November 20, 2020 at 10:00 a.m. Eastern Time and will be conducted in a virtual format only in light of public health concerns regarding the coronavirus (COVID-19) outbreak.

To participate in the virtual Annual Meeting, shareholders must visit www.virtualshareholdermeeting.com/MDXG2020 on Friday, November 20, 2020 and enter the 16-digit control number found on their proxy materials or voting instruction form. Please log in at least 15 minutes before the Annual Meeting begins to ensure ample time to complete the check-in procedures and test your computer audio system. Presentation materials will be posted on the Webcasts & Presentations section of the Company’s website immediately prior to the start of the meeting.

The Company has filed its definitive proxy statement with the U.S. Securities and Exchange Commission (“SEC”) and has mailed it with an accompanying proxy card for the virtual 2020 Annual Meeting to its shareholders. A free copy of the Proxy Statement and other relevant documents that the Company files with the SEC may be obtained through the SEC’s website at www.sec.gov or on the Company’s website at www.mimedx.com.

About
MiMedx

MiMedx® is an industry leader in advanced wound care and a therapeutic biologics company developing and distributing human placental tissue allografts with patent-protected processes for multiple sectors of healthcare. The Company processes the human placental tissue utilizing its proprietary PURION® process methodology, among other processes, to produce allografts by employing aseptic processing techniques in addition to terminal sterilization. MiMedx has supplied more than two million allografts, through both direct and consignment shipments. For additional information, please visit www.mimedx.com.

Contact

Hilary Dixon
Investor Relations & Corporate Communications
770.651.9066
[email protected]

 



Exchange Listing, LLC to Open NEO Stock Exchange

Exchange Listing, LLC to join in the opening bell ceremony at the NEO Exchange on Monday, Nov. 16 to celebrate Exchange Listing’s acceptance into NEO’s Trusted Service Provider Program

NEW YORK, Nov. 13, 2020 (GLOBE NEWSWIRE) — via InvestorWire — Exchange Listing, LLC and its chairman, Peter Goldstein, will be joined by Erik Sloane, chief revenue officer of NEO, on Monday, Nov. 16, to celebrate Exchange Listing’s acceptance into NEO’s Trusted Service Provider Program.

The NEO Exchange is Canada’s next-generation senior stock exchange, bringing much-needed competition and disruption to the Canadian market. Focused on doing what is right for investors and capital-raising companies, NEO offers a Trusted Service Provider Program, which enables a better public listing experience for issuers.

Members of the NEO Exchange Trusted Service Provider Program are leading experts in their fields, across all verticals, who are carefully vetted; committed to meeting the needs of capital-raising companies; and aligned with NEO’s vision, values and commitment to exceptional client service.

Exchange Listing LLC was founded to provide growth companies with a cost-effective one-stop strategic planning and implementation service to list on senior exchanges.

“We are currently working with two issuer clients on their application processes to list to the NEO Exchange,” Goldstein said. “One issuer is a European specialty pharmaceutical company and the other is a U.S.-based global provider of award-winning e-commerce and fintech solutions. Both companies are looking to benefit from the NEO platform technology for trading, to broaden investor confidence, to improve liquidity and to gain global exposure.”

About NEO Exchange

NEO Exchange is a progressive stock exchange that brings together investors and capital raisers within a fair, efficient and service-oriented environment. Fully operational since June 2015, NEO puts investors first and provides access to trading all Canadian-listed securities on a level playing field. The NEO Exchange lists senior companies and investment products seeking a stock exchange that enables investor trust, quality liquidity and broad awareness, including unfettered access to market data.

Connect with NEO: Website | LinkedIn | Twitter 

About Exchange Listing LLC

The objective to list on a publicly traded exchange has become increasingly complex. Exchange Listing was launched to provide a myriad of services, including capital markets advisory services to private companies looking to access the public capital markets as well as public companies looking to grow to the next level. Our role is to actively work hand in hand with our clients, senior exchanges, investment bankers, lawyers, auditors, etc., and to add shareholder value with a focus on structure, timing, managing the exchange listing application process and to make introductions to outside resources, as needed. For more information, please visit: http://exchangelistingllc.com or contact [email protected].

Wire Service Contact

InvestorWire (IW)
Los Angeles, California
www.InvestorWire.com
212.418.1217 Office
[email protected]

Cardinal Renewables, A Strategic Partnership Between The Carlyle Group and Alchemy Renewable Energy, Secures PPA with Direct Energy Business

Developer, Holocene Clean Energy, commences construction of Twittys Creek Solar, LLC, a 14-megawatt-AC solar installation located in Charlotte County, Virginia

SPRINGFIELD, Nov. 13, 2020 (GLOBE NEWSWIRE) — Cardinal Renewables, a strategic partnership between the global investment firm, The Carlyle Group, and Alchemy Renewable Energy, an industry leader in renewable energy projects and tax equity financing, has secured a power purchase agreement (PPA) with Direct Energy Business, one of North America’s largest retail providers of electricity, natural gas, and home business energy-related services, through Twittys Creek Solar, LLC, supporting construction of its a 14 MWAC solar power installation located in Charlotte County, Virginia.

Providing a lasting clean energy alternative to traditional fossil fuels, Twittys Creek reduces the amount of harmful carbon emissions released into the atmosphere. The new solar installation, developed by Holocene Clean Energy, is expected to be operational in December 2020.

“We are excited to expand our operations with Twittys Creek, allowing us to broaden our coverage into Virginia and launching us one step closer to the clean energy transition,” said Lacie Clark, CEO of Alchemy Renewable Energy. “The project would not have been possible without our joint venture with Carlyle, and collaboration with Direct Energy Business and Holocene Clean Energy.”

The new installation spans approximately 75-acres and will generate nearly 14 MWAC of clean power, which is estimated to offset over 700,000 Mt CO2e over 40 years of operation. This emissions reduction is equivalent to powering about 2,250 homes, removing nearly 4,125 passenger cars from the road, or reducing gasoline consumption by 2.1 million gallons every year the project generates electricity. By adding a new, renewable energy generation source to the grid, Twittys Creek Solar, LLC, fosters a cleaner future for power supply.

“Each of our renewable energy projects creates new power generation assets for the United States,” said Pooja Goyal, Co-Head of the Infrastructure Group at The Carlyle Group. “Twittys Creek Solar, LLC, is expected to have a positive impact on the community of Charlotte County and the region by providing a clean energy source that is intended to provide efficient power delivery, improve the environment, and reduce dependency on fossil fuels.”

“We appreciate our collaboration with Cardinal Renewables and Direct Energy Business, who ultimately helped give life to the project. After working so closely with our partners and Charlotte County, seeing the stakes put into the ground was a truly joyful moment for our team,” said Laura Tillett, Business Development at Holocene Clean Energy.

“Direct Energy is proud to have partnered with Holocene and Cardinal Renewables to commence construction on Twittys Creek. It is important for us to have sustainable assets as part of our supply portfolio to assist our customers in achieving their carbon reduction goals,” said Ray Polakowski, Manager of Wholesale Origination for Direct Energy Business. 

“Competitive markets drive cost-effective renewable energy adoption and create associated localized economic development benefits. This 14 MWAC solar project located in Charlotte County, Virginia will benefit the community and consumers,” said Ron Cerniglia, Direct Energy’s Director of Corporate & Regulatory Affairs.  

 

About Cardinal Renewables

Cardinal Renewables, a strategic partnership between The Carlyle Group and Alchemy Renewable Energy, is focused on creating long-term value for investors, companies, and communities through the development, acquisition, financing, and operation of solar power generation projects throughout the United States, with a focus on projects ranging from 5-80 MWAC. The Carlyle Group, through the Carlyle Renewable and Sustainable Energy Fund, has made a $100 million commitment to this partnership.

 

About The Carlyle Group

The Carlyle Group (NASDAQ: CG) is a global investment firm with deep industry expertise that deploys private capital across four business segments: Corporate Private Equity, Real Assets, Global Credit and Investment Solutions. With $230 billion of assets under management as of September 30, 2020, Carlyle’s purpose is to invest wisely and create value on behalf of its investors, portfolio companies and the communities in which we live and invest. Carlyle employs more than 1,800 people in 30 offices across six continents. Further information is available at www.carlyle.com. Follow Carlyle on Twitter @OneCarlyle.

 

About Alchemy Renewable Energy

Alchemy Renewable Energy is an industry leader in renewable energy projects as well as comprehensive long-term debt and tax equity financing. The firm utilizes a credentialed team, a strong network of joint ventures, and parent company Monarch Private Capital to support premium mid-size utility-scale renewable energy projects, including solar and biomass power generation. The Company leverages Monarch Private Capital’s tax equity placement services as the final element of its projects’ capital structure. In addition, Alchemy reduces overall project costs and produce higher overall investor returns by eliminating the need to source third-party development and financing support.

 

About Holocene Clean Energy

Holocene Clean Energy is building the foundation for the future of solar power supply, battery storage, and delivery. As a leading innovator, they create scalable distributed solar generation and storage project portfolios to reduce dependency on traditional fuels, increase grid reliability, and improve the efficiency of power delivery. The Company’s distributed generation strategy allows power consumers to procure renewable energy at competitive prices while providing meaningful benefits to local communities hosting their generation facilities.

 

About Direct Energy

Direct Energy is one of North America’s largest retail providers of electricity, natural gas, and home and business energy-related services with nearly four million customers. Direct Energy gives customers choice, simplicity, and innovation where energy, data, and technology meet. A subsidiary of Centrica plc (LSE: CNA), an international energy and services company, Direct Energy, its subsidiaries and/or affiliates, operate in 50 U.S. states plus the District of Columbia and 8 provinces in Canada. To learn more about Direct Energy, please visit www.directenergy.com.

Jane Rafeedie
Monarch Private Capital
4702838431
[email protected]

Sir Kenny Dalglish MBE Appointed Global Sporting Ambassador to British Cyber Technology Company

    V-Health Passport

Test Agnostic & Secure Digital COVID Health Passport

to Get Sports Fans Back Into Stadiums 



Liverpool Legend Takes COVID 19 Orient Gene / Healgen


Rapid Antigen & Antibody Test 

To view the
video
click here

https://youtu.be/jF3iibf4dhY

MANCHESTER, United Kingdom, Nov. 13, 2020 (GLOBE NEWSWIRE) — One of the most iconic and celebrated figures in British football history Sir Kenny Dalglish MBE is the latest high-profile name from the world of sport to join British cyber technology company VST Enterprises (VSTE) as its Global Sporting Ambassador for football. The role is established through VSTE’s American partner company VR Sports Group, which is also giving VSTE a powerful presence in the USA with further intention of a global rollout of their cutting-edge platform V-Health Passport.

The celebrated Scottish football player and former Liverpool Manager has joined forces with former England Rugby Captain and 2003 World Cup Winner Mike Tindall MBE, equestrian World Champion and Olympic Silver Medalist Zara Tindall MBE to pioneer a UK wide campaign to get sports fans back into stadiums.

The Manchester based cyber technology company which was founded by tech entrepreneur Louis-James Davis has developed a secure digital health passport – V-Health Passport as the key to unlocking the return of fans back to football stadiums. The TEST AGNOSTIC health passport app – which works alongside all Covid 19 testing kits including PCR lab tests and new emerging 15 minute rapid ‘antigen’ and 10 minute ‘antibody’ test kits – also has its own unique contact tracing technology which is specifically designed for sports and football stadiums, music and theatre venues.

As VSTE’s global football ambassador, Sir Kenny will highlight the importance of using the secure VCode® digital technology behind V-Health Passport™ and the importance of using the ‘best in class’ technology alongside rapid Covid testing for sports fans and players. Sir Kenny will also raise the important issue of all football players being subject to rapid Covid testing, in addition to existing PCR based lab tests as an early warning indicator.

Sir Kenny undertook a Covid 19 rapid ‘antigen’ and rapid antibody test in Liverpool recently which was administered by CHB Medical. The nasal swab Orient Gene /Healgen rapid ‘antigen’ test was administered first taking 15 minutes, followed by the finger prick Orient Gene rapid ‘antibody’ test which also took ten minutes to administer. Both results showed Sir Kenny was negative on both tests and the results were then uploaded to his ‘test agnostic’ V-Health Passport in under 30 seconds.

Commenting on the Orient Gene/Healgen rapid ‘antigen’ and rapid ‘antibody’ tests Dr Robert Hutchins MB BS MS FRCS (Eng) FRCS (Gen Surg) a London NHS Consultant said;

“Rapid point of care Covid-19 testing is the most promising way to ensure a return to normal activity and an assurance that we capture infections and prevent further re
infection. Rapid antigen’ testing on a regular basis, alongside rapid antibody’ screening and then authenticated in a secure digital health passport technology such as VHealth Passport would give much greater mobility and confidence to the public.

In d
oing so it would allow the public to return to their workplace environments, airline passengers being ‘fit to flyand more confident with the health status of their fellow passengers. It would also allow sports to return safely and allow team selection with confidence. Fans would be able to potentially return to the stadiums having taken a test and uploaded their results into the secure VHealth Passport verifying their identity and test status.”

Sir Kenny, along with Mike Tindall MBE and Zara Tindall MBE will champion the Manchester cyber technology’s ‘FANS ARE BACK™’ pilot scheme for football fans which has been submitted to the UK Government, The Department For Digital, Culture, Media and Sport (DCMS), Sports Minister Nigel Huddlestone and the Sports Technology Innovation Group (STIG).

The ‘FANS ARE BACK™’ pilot is an end-to-end solution for sports fans with Covid rapid testing using 15minute rapid ‘antigen’ and 10 minute rapid ‘antibody’ test kits, a secure digital V-Health Passport™ and V-Health Passports ‘True Contact™’ contact tracing solution to get fans back into stadiums safely and watching their beloved teams. The technology can also be integrated with smart stadium devices for security gates and multi-functional safe zone cams for high flow body heat monitoring and social distancing crowd control.

The scheme was devised by VSTE and a consortium of British companies including leading public safety and event /venue management company Halo Solutions, occupational health company Latus Health, football and sports marketing/ rights agency holder REDSTRIKE. The pilot campaign has also been submitted to the Sports Ground Safety Authority (SGSA) and the Premier League. It has also received the backing and support of former Sports Minister Rt. Hon. Richard Caborn. Caborn was one of the longest serving Sports Ministers under Tony Blair and was responsible for successfully bringing the 2012 Olympics to London.

Commenting on his new appointment Sir Kenny Dalglish MBE said;


I was impressed to learn about what Louis-James and his team at
VST
Enterprises are trying to
achieve with their


FANS ARE BACK


™’

campaign and the V-Health Passport

technology. Getting fans back into football stadiums safely is the number one priority for all football clubs across the UK and globally right now and for the future of the game.
Without the fans there is no beautiful game, it

s a way of life to so many people, it

s tribal, it’s about a group of like-minded people who have a passion and who are proud of what they’re team represents.

Football is part of our DNA, it

s our culture,
we have been through two world wars and many national tragedies along the way, but football has always been a unifying force. The Corona virus outbreak has impacted many people across the country, families have lost loved ones. I too myself tested positiv
e for
Covid
earlier this year and the support and care I received from the NHS was outstanding, so I understand firsthand. Football and sport in the UK contribute massively to positive mental health and any technology that can ensure that fans safely retur
n to the game is a winner.

Commenting on the appointment VSTE Founder & CEO Louis-James Davis said;


We are truly
honoured
and delighted to have such an iconic football player and manager as Sir Kenny joining us as a global sporting ambassador for
VST
Enterprises and the V-Health Passport

project. Sir Kenny

s achievements in football both as a player and manager are unsurpassed. But his relationship with the fans, in particular Liverpool FC is what makes him stand out as a truly iconic figure in foot
ball alongside the greats of the game like Bill Shankly, Bob Paisley, and Sir Matt Busby.

The VCode® and VPlatform® technology which powers the V-Health Passport™ has being hailed as the cyber security’s version of ‘human DNA’. The technology has a number of applications and uses from secure health passports to ticketing, payments, identity provisioning and authentication across all spectator sports. The technology’s innovative capabilities across football, rugby, golf and motorsport is vast. It can be used for secure paperless ticketing to stamping out counterfeit tickets, security and access, health passports for players and fans, content delivery and sponsor /brand activation.

The ultra secure V-Health Passport™ also uses the VCode® security coding which has been referred to as the cyber world’s equivalent of human DNA. Bar codes and QR codes represent 1st and 2nd generation code scanning technology which is unsecure. QR codes in particular can be cloned and hacked under a process called “Attagging”. In India alone there are over 1 BILLION fraudulent financial transactions every day using QR codes. The use of any form of a QR code in a health passport could potentially lead to a persons data being hacked and compromised.

Commenting on the appointment VR Sports Group CEO Jonny Tungen said;

At VR Sports Group we are proud to partner with both Sir Kenny Dalglish MBE and VST Enterprises. Sir Kenny is not only revered as a distinguished player and one of the greatest football managers of all time, but also for his charitable work in society and the community. We are delighted to have strengthened our partnership by bringing together Sir Kenny with a leading tech entrepreneur like Louis-James Davis and his team. Together it creates infinite possibilities, leveraging future oriented technology to design a better, safer and more convenient life for sports fans and the public.

VSTE™ is currently using its VCode® cyber security technology to work with the UNITED NATIONS as part of their SDG Collaboratory (Sustainable Development Goals) program – to provide a wide range of unique identifiers and technology services to 9 Billion people by 2030. It is also using its V-Health Passport™ across a number of sectors including the airline and aviation industry – with its FIT TO FLY campaign, as well as other major transport infrastructure including rail and maritime assets.


For more information on VCode® and VPlatform® technology please visit

https://
www.vstenterprises.com

For more information on V-HEALTH PASSPORT™.
https://www.v-healthpassport.co.uk


For all media enquiries
Please contact Gerard Franklin – Head Of Communications & External Relations
M: 07885 388398  e: [email protected]
VST Enterprises Ltd | The Lexicon | Mount Street | Manchester | M2 5NT

NOTES TO EDITORS

Sir Kenny Dalglish MBE undertook the Orient Gene/ Healgen Covid 19 testing using the rapid ‘antigen’ and rapid ‘antibody’ test cassettes. The test was administered by CHB Medical.

The ten minute Orient Gene/ Healgen antibody test has been validated by multiple organisations and bodies including Imperial College London details of which can be provided on request. It is manufactured in an FDA approved facility and CE marked. The 15 minute Orient Gene/Healgen antigen test kit has been Public Health England assessed and passed and is manufactured in an FDA approved facility and CE marked.

Antigen Test Cassette – Relative Sensitivity: 97% Relative Specificity: 99% Accuracy: 99%

Antibody Test Cassette – Relative Sensitivity: 100% Relative Specificity: 100% Accuracy: 100%

Photos accompanying this announcement are available at
https://www.globenewswire.com/NewsRoom/AttachmentNg/cffeb53b-cbb9-4208-9595-27b5e6508e81
https://www.globenewswire.com/NewsRoom/AttachmentNg/9e501635-2fdc-41e6-9825-ee379ba3a15f
https://www.globenewswire.com/NewsRoom/AttachmentNg/64d2bb4c-1214-420a-8c46-5c695742ac66

Call of Duty: Black Ops Cold War Available Now Worldwide

Call of Duty: Black Ops Cold War Available Now Worldwide

#1 Selling Call of Duty Series Continues Franchise Momentum and Releases to the Largest, Most Engaged Community at the time of Launch in Call of Duty History

SANTA MONICA, Calif.–(BUSINESS WIRE)–
Activision today announced the worldwide launch of the highly-anticipated Call of Duty®: Black Ops Cold War, an all-new entry in the #1 selling series in Call of Duty and a direct sequel to the fan favorite Call of Duty: Black Ops.

The new title infuses 1980s pop culture into a gripping conspiracy set at the height of the Cold War. In the fictional story campaign players must stop a plot decades in the making that could destabilize the global balance of power and change the course of history. The game delivers the next generation of online multiplayer combat with an arsenal of Cold War weapons and equipment across a wide variety of new maps and modes. Black Ops Cold War also provides an all-new co-operative Zombies survival mode experience.

The title supports cross-play across next generation and current generation systems with cross progression across all modes. Players can look forward to the biggest series of free, post-launch content in Black Ops history across Multiplayer and Zombies, as well as a robust schedule of in-game community events.

“Today’s launch starts the next great Black Ops experience across story, multiplayer and zombies in a direct sequel to one of the most iconic titles in Call of Duty,” said Byron Beede, Executive Vice President and General Manager, Call of Duty, Activision. “This is just the beginning. Our players can look forward to the biggest series of post-launch free content, community events and ongoing support ever in Black Ops plus tight integration across the ecosystem with Warzone. It’s a great time to play Call of Duty.”

The release of a new Black Ops title, the top selling Call of Duty series, adds to the ongoing momentum across Call of Duty following the recent releases of Warzone™ and Modern Warfare®, which, along with Call of Duty: Mobile, have driven Call of Duty to more than 100 million monthly active users. Call of Duty: Mobile has now surpassed more than 300 million downloads* worldwide.

The free-to-play, free-for-everyone Call of Duty: Warzone will take on a new dimension as it integrates with both Black Ops Cold War and Modern Warfare. Player progression will be synchronized across all three titles, and weapon progression from Black Ops Cold War or Modern Warfare both will be shared with Warzone. Starting now, Black Ops Cold War Operators will be available for play in Warzone, and beginning December 10 at the launch of Season One, Black Ops Cold War weapons will become available in Warzone, allowing Warzone players to access either their Black Ops Cold War or Modern Warfare loadouts, respectively, for play.

The battle pass system continues beginning Season One in December with brand new content for Black Ops Cold War and Warzone. Players can progress through the battle pass system by playing any of the three Call of Duty games.

Call of Duty: Black Ops Cold War is available now worldwide on PlayStation® 5 (Australia, Japan, New Zealand, North America, Singapore, South Korea; rest of world availability Nov. 19th), PlayStation® 4, the Xbox Series X|S and Xbox One, and on PC, in a fully optimized experience for Battle.net, Blizzard Entertainment’s online gaming service. The title is published by Activision, a wholly-owned subsidiary of Activision Blizzard (NASDAQ: ATVI), and developed by award-winning studios Treyarch and Raven Software with additional development support from Beenox, Demonware, High Moon Studios, Activision Shanghai and Sledgehammer Games. For more information visit: www.callofduty.com, or follow @CallofDuty on Twitter, Instagram and Facebook.

About Activision

Headquartered in Santa Monica, California, Activision is a leading global producer and publisher of interactive entertainment. Activision maintains operations throughout the world and is a division of Activision Blizzard (NASDAQ: ATVI), an S&P 500 company. More information about Activision and its products can be found on the company’s website, www.activision.com or by following @Activision.

Cautionary Note Regarding Forward-looking Statements: Information in this press release that involves Activision Publishing’s expectations, plans, intentions or strategies regarding the future, including statements about the expected availability, features, and content for Call of Duty: Black Ops Cold War and Warzone, including about Season One, the battle pass system and community events, are forward-looking statements that are not facts and involve a number of risks and uncertainties. Factors that could cause Activision Publishing’s actual future results to differ materially from those expressed in the forward-looking statements set forth in this release include unanticipated product delays and other factors identified in the risk factors sections of Activision Blizzard’s most recent annual report on Form 10K and any subsequent quarterly reports on Form 10-Q. The forward-looking statements in this release are based upon information available to Activision Publishing and Activision Blizzard as of the date of this release, and neither Activision Publishing nor Activision Blizzard assumes any obligation to update any such forward-looking statements. Forward-looking statements believed to be true when made may ultimately prove to be incorrect. These statements are not guarantees of the future performance of Activision Publishing or Activision Blizzard and are subject to risks, uncertainties and other factors, some of which are beyond its control and may cause actual results to differ materially from current expectations.

*Based on Activision internal estimates

ACTIVISION, CALL OF DUTY, CALL OF DUTY BLACK OPS, CALL OF DUTY WARZONE, MODERN WARFARE, and WARZONE are trademarks of Activision Publishing, Inc. All other trademarks and trade names are the properties of their respective owners.

“PlayStation” is a registered trademark and “PS4” is a trademark of Sony Computer Entertainment Inc.

PR Contact:

Activision

Kyle Walker

[email protected]

KEYWORDS: United States North America California

INDUSTRY KEYWORDS: Technology Electronic Games Teens Women Entertainment Men Software Audio/Video Consumer Consumer Electronics

MEDIA:

Akero Presents Additional Positive Data from Phase 2a BALANCED Study Demonstrating Potential of Efruxifermin as a Foundational NASH Monotherapy

Akero Presents Additional Positive Data from Phase 2a BALANCED Study Demonstrating Potential of Efruxifermin as a Foundational NASH Monotherapy

Data to be presented at the Presidential Plenary Talk at The Liver Meeting®

100% of patients in 50mg group demonstrated more than 50% relative reduction in liver fat

50% of patients with F2/F3 fibrosis at baseline achieved two stage improvement in fibrosis score

Type 2 diabetic patients showed improved glycemic control with HbA1c reduced by up to 0.9%

SOUTH SAN FRANCISCO, Calif.–(BUSINESS WIRE)–
Akero Therapeutics, Inc. (Nasdaq: AKRO) today announced the presentation of additional data analysis from the Phase 2a BALANCED study at the Presidential Oral Plenary Session at The Liver Meeting®. The data continue to demonstrate the potential of efruxifermin (EFX) as a foundational monotherapy for patients with non-alcoholic steatohepatitis (NASH).

Overall, the data show large magnitudes of reduction in liver fat across all EFX dose groups with 100% of participants in the 50mg EFX dose group achieving more than 50% relative reduction in liver fat and 53% of patients in the same dose group achieving more than 70% relative reduction in liver fat.

Among all EFX-treated patients who were fibrosis stage F2 or F3 at baseline (n=22), 50% experienced a two-stage improvement in fibrosis (n=11), while 68% experienced at least a one-stage improvement in fibrosis (n=15).

Additional analysis of the BALANCED data showed substantial improvement in glycemic control for patients with both NASH and Type 2 diabetes, a group that comprises about half of all NASH patients. The company previously reported mean absolute reductions in HbA1c among all study participants of 0.1% for the 28mg dose, 0.4% (p<0.05) for the 50mg dose and 0.5% (p<0.01) for the 70mg dose. In patients with both NASH and Type 2 diabetes, researchers observed decreases of 0.6% in the 50mg dose and 0.9% (p<0.01) in the 70mg dose. Among EFX patients with NASH and Type 2 diabetes, the relative decreases in mean C-peptide levels ranged from 27 to 33% across EFX dose groups, compared to 22 to 29% for all EFX patients.

“Additional analyses from the BALANCED study, including the proportion of subjects with at least 50 and 70% reductions in liver fat and the high proportion of subjects with F2/F3 fibrosis at baseline with fibrosis improvement, strengthens the potential of EFX to be truly transformative for people living with NASH, with improvements across multiple parameters for NASH and cardio-metabolic conditions,” said Andrew Cheng, M.D., Ph.D., president and CEO of Akero. “With some of the strongest results reported to date in NASH, we eagerly anticipate the initiation of our adaptive Phase 2b/3 study of efruxifermin with hopes of improving lives of the more than 17 million Americans who are living with this disease.”

EFX has received European Medicines Agency Priority Medicines (PRIME) designation as a treatment for NASH. Akero plans to begin a Phase 2b/3 adaptive clinical trial in biopsy confirmed NASH patients in the first half of 2021. The company will be using 28mg and 50mg doses for that trial.

Akero previously reported data from the BALANCED study demonstrating that each of the 28, 50 and 70mg EFX dose groups met the primary endpoint compared to placebo, with absolute reductions of 12%, 13% and 14% of liver fat, respectively, compared with 0.3% for placebo, and relative reductions of 63%, 71% and 72% percent, compared to 0% for placebo. All of these results were highly statistically significant at p<0.001.

Prior Reporting of secondary and exploratory endpoints revealed that of the 40 EFX treatment responders who had end-of-treatment biopsies, 48% achieved at least a one-stage improvement in fibrosis without worsening of NAFLD activity score (NAS) and 28% achieved at least a two-stage improvement in fibrosis. Additionally, 48% of responders achieved NASH resolution with no worsening of fibrosis. Improvements in glycemic control and dyslipidemia, as well as weight loss, were also observed across all dose groups. Treatment with EFX was generally reported to be well tolerated.

About NASH

NASH (non-alcoholic steatohepatitis) is a serious form of NAFLD (non-alcoholic fatty liver disease) and is estimated to affect 17 million Americans. NASH is closely linked to the obesity and diabetes epidemics seen around the world. NASH is characterized by an excessive accumulation of fat in the liver that causes stress and injury to liver cells, leading to inflammation and fibrosis, which can progress to cirrhosis, liver failure, cancer and eventually death. NASH is a leading cause of liver transplants in the US and Europe.

About the BALANCED Study

The Phase 2a BALANCED study is a multicenter, randomized, double-blind, placebo-controlled, dose-ranging trial in biopsy-confirmed adult patients with NASH. The main study enrolled a total of 80 patients. Participants were randomized to receive weekly subcutaneous doses of efruxifermin (EFX), formerly known as AKR-001, or placebo for up to 16 weeks, with safety and tolerability followed through week 20. The primary efficacy endpoint for the study is absolute change from baseline in hepatic fat fraction measured by magnetic resonance imaging – proton density fat fraction (MRI-PDFF) at week 12. Secondary measures include change from baseline in ALT at 12 weeks, the number of patients who had a decrease of ≥2 points in the NAFLD activity score (NAS) at 24 weeks and safety and tolerability measures.

About Efruxifermin

Efruxifermin (EFX), formerly known as AKR-001, is Akero’s lead product candidate for NASH, currently being evaluated in the ongoing Phase 2a BALANCED study. EFX is designed to reduce liver fat and inflammation, reverse fibrosis, increase insulin sensitivity and improve lipoproteins. This holistic approach offers the potential to address the complex, multi-system disease state of NASH, including improvements in lipoprotein risk factors linked to cardiovascular disease – the leading cause of death in NASH patients. Engineered to mimic the biological activity profile of native FGF21, EFX offers convenient once-weekly dosing and has been generally well-tolerated in clinical trials to date.

About Akero Therapeutics

Akero is a cardio-metabolic NASH company dedicated to reversing the escalating NASH epidemic by developing pioneering medicines designed to restore metabolic balance to improve overall health. The company’s lead product candidate, Efruxifermin (EFX), formerly known as AKR-001, is currently being evaluated in an ongoing Phase 2a clinical trial. Akero Therapeutics is headquartered in South San Francisco, CA. For more information, please visit www.akerotx.com.

Forward Looking Statements

Statements contained in this press release regarding matters that are not historical facts are “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995. Because such statements are subject to risks and uncertainties, actual results may differ materially from those expressed or implied by such forward-looking statements. Such statements include, but are not limited to, statements regarding: Akero’s guidance regarding its business plans and objectives for EFX, including the therapeutic potential and clinical benefits thereof, as well as the safety and tolerability of EFX and future clinical development plans; Akero’s Phase 2a BALANCED clinical trial, including its results and Akero’s analysis of such results; Akero’s design, implementation and expected timing of the Phase 2b/3 trial; the potential benefits conferred by the EMA on Akero’s PRIME designation; and the potential impact of COVID-19 on patient retention, strategy, future operations and clinical trials.

Any forward-looking statements in this statement are based on management’s current expectations of future events and are subject to a number of risks and uncertainties that could cause actual results to differ materially and adversely from those set forth in or implied by such forward-looking statements. Risks that contribute to the uncertain nature of the forward-looking statements include: risks related to the impact of public health epidemics affecting countries or regions in which we have operations or do business, such as COVID-19, including potential negative impacts on Akero’s employees, manufacturers, supply chain and production as well as on global economies and financial markets; the company’s ability to execute on its strategy; positive results from a clinical study may not necessarily be predictive of the results of future or ongoing clinical studies; regulatory developments in the United States; and risks related to the competitive landscape. For a discussion of these and other risks and uncertainties, and other important factors, any of which could cause Akero’s actual results to differ from those contained in the forward-looking statements, see the section entitled “Risk Factors” in the company’s 2019 Annual Report on Form 10-K filed with the United States Securities and Exchange Commission (SEC) and quarterly reports on Form 10-Q filed with the SEC, as well as discussions of potential risks, uncertainties, and other important factors in Akero’s other filings with the SEC. All forward-looking statements contained in this press release speak only as of the date on which they were made. Akero undertakes no obligation to update such statements to reflect events that occur or circumstances that exist after the date on which they were made.

Media Contact:

Carolyn Hawley

Canale Communications

[email protected]

619-849-5382

Investor Contact:

Christina Tartaglia

Stern Investor Relations

[email protected]

212-362-1200

KEYWORDS: California United States North America

INDUSTRY KEYWORDS: Health Diabetes Research Pharmaceutical Science Biotechnology

MEDIA:

Logo
Logo

Emerald Appoints Hervé Sedky as President and Chief Executive Officer

Emerald Appoints Hervé Sedky as President and Chief Executive Officer

Sedky Brings a Distinguished Track Record in Events and Business Travel

NEW YORK–(BUSINESS WIRE)–
Emerald Holding, Inc. (NYSE:EEX) (“Emerald” or the “Company”) today announced that the Company’s Board of Directors has appointed Hervé Sedky to the position of President and Chief Executive Officer of Emerald. Mr. Sedky will assume his new role on January 5, 2021. Brian Field, Emerald’s Interim President and Chief Executive Officer, will continue to serve as the Company’s Chief Operating Officer.

“We are thrilled to have Hervé join the Emerald team. His long and successful career in leadership roles serving the business travel and events markets, along with his strategic acumen, transformative approach, and results-orientation are an ideal fit for Emerald’s next phase of growth,” said Kosty Gilis, Chairman of Emerald’s Board of Directors.

Mr. Sedky brings three decades of experience including, most recently, six years as President of Reed Exhibitions Americas, where he led a business of over 100 annual sector-leading events in North and South America. This highly-relevant role is complemented by a distinguished 20-year executive career at the American Express Company, where he held the title of Senior Vice President and General Manager of American Express Business Travel, guiding the growth of a $1 billion revenue business and serving on American Express’ senior management team.

“I am excited to join the world-class Emerald team and can’t think of a better place to reinforce what people and businesses need most: human connections. If there is one thing we have learned personally and professionally from the ongoing pandemic, it is that nothing can replace the high value of the live, in-person experience. Emerald has already begun to demonstrate that face-to-face events can once again be staged safely. We will continue to enhance our customer experience with the extraordinary learning we have acquired this year and apply the kind of creativity we didn’t think possible—the kind of innovation that will drive better results, better customer experience and value,” said Mr. Sedky.

“Hervé is a tremendous leader whom I have known as an industry colleague for some time; he demonstrates a fantastic blend of personal leadership, industry insight, and a keen customer focus. I am excited to work closely with him, as we together continue to accelerate Emerald’s pathways for growth, and build upon the many remarkable foundations we have put in place over this year,” said Mr. Field.

Mr. Gilis added, “On behalf of the entire Board, I would like to sincerely thank Brian for assuming the role of Interim President and CEO for the last year. He has very capably led the organization during what has been an unexpectedly turbulent time for the industry against the backdrop of the coronavirus pandemic, all while driving forward many important transformational initiatives for the business which have positioned Emerald to emerge stronger on the other side of the pandemic. The Board looks forward to continuing to work with Brian in his capacity as Chief Operating Officer.”

About Emerald

Emerald is a leader in building dynamic, market-driven business-to-business platforms that integrate live events with a broad array of industry insights, digital tools, and data-focused solutions to create uniquely rich experiences. As true partners, we at Emerald strive to build our customers’ businesses by creating opportunities that inspire, amaze, and deliver breakthrough results. With over 140 events each year, our teams are creators and connectors who are thoroughly immersed in the industries we serve and committed to supporting the communities in which we operate.

Emerald Holding, Inc.

David Doft

Chief Financial Officer

1-866-339-4688 (866EEXINVT)

[email protected]

KEYWORDS: New York United States North America

INDUSTRY KEYWORDS: Software Technology Networks Data Management

MEDIA:

Ondas Holdings Inc. Announces Reverse Stock Split of Common Stock

Ondas Holdings Inc. Announces Reverse Stock Split of Common Stock

SUNNYVALE, Calif.–(BUSINESS WIRE)–
Ondas Holdings Inc. (OTCQB: ONDS), through its wholly owned subsidiary, Ondas Networks Inc., a developer of private licensed wireless data networks for mission-critical industrial markets (the “Company”), today announced it will effect a one-for-three reverse stock split of its issued and outstanding Common Stock. Pursuant to the Certificate of Change filed with the Secretary of State of the State of Nevada, the reverse stock split will be effective at 5:31 p.m., Eastern Time, on November 13, 2020. The Company expects that upon the opening of trading on November 16, 2020, its Common Stock will trade on the OTCQB on a split-adjusted basis under the current trading symbol “ONDS” and the new CUSIP number 68236H 204.

No fractional shares will be issued as a result of the reverse stock split. Any fractional shares that would result from the reverse stock split will be rounded up to the nearest whole share. Following the reverse stock split, the Company will have 116,666,667 shares of Common Stock authorized and approximately 19,796,029 shares of Common Stock outstanding.

Shareholders of record are not required to send in their current stock certificates or evidence of book-entry or other electronic positions for exchange. Following the effectiveness of the reverse stock split, each stock certificate and book-entry or other electronic position representing issued and outstanding shares of the Company’s common stock will be automatically adjusted. Those shareholders holding common stock in “street name” will receive instructions from their brokers if they need to take any action in connection with the reverse stock split.

About Ondas Holdings Inc.

Ondas Holdings Inc., through its wholly owned subsidiary, Ondas Networks Inc., is a developer of private licensed wireless data networks for mission-critical industrial markets. The Company designs and manufactures its multi-patented, Software Defined Radio (SDR) platform for Mission Critical IoT (MC- IoT) applications. Ondas Networks’ customer end markets include utilities, oil and gas, transportation, and government entities whose demands span a wide range of mission critical applications that require secure communications over large and diverse geographical areas, many of which are within challenging radio frequency environments. Customers use the Company’s SDR technology to deploy their own private licensed broadband wireless networks. The Company also offers mission-critical entities the option of a managed network service. Ondas Networks’ SDR technology supports IEEE 802.16s, the new worldwide standard for private licensed wide area industrial networks. For additional information, visit www.ondas.com, www.otcmarkets.com or follow Ondas Networks on Twitter and LinkedIn.

Forward Looking Statements

Statements made in this release that are not statements of historical or current facts are “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995. We caution readers that forward-looking statements are predictions based on our current expectations about future events.

These forward-looking statements are not guarantees of future performance and are subject to risks, uncertainties and assumptions that are difficult to predict. Our actual results, performance, or achievements could differ materially from those expressed or implied by the forward-looking statements as a result of a number of factors, including, the risks discussed under the heading “Risk Factors” in our Annual Report on Form 10-K filed with the Securities and Exchange Commission (SEC) on March 13, 2020, and in our other filings with the SEC. We undertake no obligation to publicly update or revise any forward- looking statements, whether as a result of new information, future events or otherwise that occur after that date, except as required by law.

Stewart Kantor, CFO

Ondas Holdings Inc.

888.350.9994 Ext. 1009

KEYWORDS: United States North America California

INDUSTRY KEYWORDS: Technology Networks Data Management

MEDIA:

Logo
Logo

KB Home Announces the Grand Opening of Central Park – Villa Collection

KB Home Announces the Grand Opening of Central Park – Villa Collection

Homebuilder offers personalized, new paired homes in a premier Denver master-planned community priced from the $450,000s

DENVER–(BUSINESS WIRE)–
KB Home (NYSE: KBH) today announced the grand opening of its Central Park – Villa Collection, a new enclave of paired homes situated in the final phase of Central Park, one of Denver’s most popular master-planned communities. The newly developed North End will serve as the final chapter for this highly desirable neighborhood. Homebuyers will enjoy the community’s proximity to Interstate 70, Denver International Airport and the area’s major job centers. Additionally, the new community hosts 80 acres of amenities, including pools, athletic fields, sports courts, jogging and biking paths, barbecue and picnic areas, a play fountain and a large playground with climbing boulders as well as a sledding hill, remote control boating lake and amphitheater.

This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20201113005131/en/

KB Home announces the grand opening of Central Park – Villa Collection. (Photo: Business Wire)

KB Home announces the grand opening of Central Park – Villa Collection. (Photo: Business Wire)

The low-maintenance, two-story, paired homes at KB Home’s Central Park – Villa Collection showcase desirable design characteristics like gourmet kitchens overlooking expansive great rooms, lofts, large master suites with walk-in closets, and optional basements. The community’s floor plans feature up to five bedrooms and three-and-a-half baths, and range in size from approximately 1,200 to 1,500 square feet. The community also offers the KB Home Office, a dedicated room that homebuyers can personalize for the way they work.

“We are excited to offer our popular Villa Collection at one of Denver’s premier master-planned communities. In addition to featuring world-class amenities, Central Park is also close to a variety of shopping, dining and entertainment as well as Denver International Airport and the area’s major employment centers,” said Randy Carpenter, President of KB Home’s Colorado division. “As with other KB Home communities, Central Park – Villa Collection provides home shoppers the opportunity to purchase a new KB home that can be personalized to reflect their lifestyle and needs.”

KB Home stands out from other homebuilders as the company gives homebuyers exceptional choice and control. KB Home starts by offering a wide variety of homes at an affordable price. From there, the builder gives buyers the ability to personalize their homes from homesites and floor plans to design features. The KB Home team works hand in hand with homeowners every step of the way so they have a real partner in the process.

Every KB home is designed to be ENERGY STAR® certified thanks to the quality construction techniques and materials utilized that ultimately deliver significant savings on utility bills compared to used homes. Additionally, all new KB homes are designed to deliver an enhanced indoor environment and include high performance ventilation systems, low- or zero-VOC products and other features guided by the Environmental Protection Agency’s (EPA) Indoor airPLUS standards.

The Central Park – Villa Collection sales office and model homes are open for private in-person tours by appointment, and walk-in visits are welcome. Homebuyers also have the flexibility to arrange a live video tour with a sales counselor. Pricing begins from the $450,000s.

For more information on KB Home, call 888-KB-HOMES or visit kbhome.com.

About KB Home

KB Home is one of the largest and most recognized homebuilders in the United States and has been building quality homes for over 60 years. Today, KB Home operates in 42 markets across eight states, serving a wide array of buyer groups. What sets us apart is how we give our customers the ability to personalize their homes from homesites and floor plans to cabinets and countertops, at a price that fits their budget. We are the first builder to make every home we build ENERGY STAR® certified. In fact, we go beyond the EPA requirements by ensuring every ENERGY STAR certified KB home has been tested and verified by a third-party inspector to meet the EPA’s strict certification standards, which help to lower the cost of ownership and to make our new homes healthier and more comfortable than new ones without certification. We also work with our customers every step of the way, building strong personal relationships so they have a real partner in the homebuying process, and the experience is as simple and easy as possible. Learn more about how we build homes built on relationships by visiting kbhome.com.

Craig LeMessurier, KB Home

925-580-1583

[email protected]

KEYWORDS: Colorado United States North America

INDUSTRY KEYWORDS: Architecture Construction & Property Environment Family Urban Planning Consumer Interior Design Residential Building & Real Estate

MEDIA:

Logo
Logo
Photo
Photo
KB Home announces the grand opening of Central Park – Villa Collection. (Photo: Business Wire)