LGI Homes Opens a New Community North of Houston, Pinewood Trails

CLEVELAND, Texas, Nov. 19, 2020 (GLOBE NEWSWIRE) — LGI Homes, Inc. (Nasdaq:LGIH) today announced the opening of a new home community in the greater Houston area, Pinewood Trails, where the builder plans to construct 974 single-family homes. Located in eastern Montgomery County near I-69, Pinewood Trails offers a collection of homes equipped with LGI’s CompleteHome™ package, competitively priced from the $190s.

“Pinewood Trails presents the opportunity for our customers to purchase a new home in an appealing location at an incredible value,” said Brian Batten, division president of LGI Homes. “In addition to easy access to the businesses and attractions located along the Eastex Freeway, homeowners at Pinewood Trails will enjoy quality-built new homes and family-friendly amenities at a price that suits their budget.”

LGI Homes at Pinewood Trails is offering five distinct floor plans with three to five bedrooms, up to two and a half baths, and ranging in size from approximately 1,400 to 2,600 square feet. The exceptionally designed homes feature open-concept entertaining areas, flex rooms, private owner retreats and large closets. Move-in-ready, the new homes at Pinewood Trails include an impressive selection of interior upgrades at no additional cost, including a full suite of kitchen appliances by Whirlpool®, 36-inch upper cabinets topped with crown molding, Moen® faucets in the kitchen and bathrooms, programmable thermostats and Wi-Fi-enabled garage door openers.

Homeowners at Pinewood Trails will enjoy the community’s numerous planned amenities including a 4-acre park featuring children’s playgrounds, a party pavilion, picnic areas and open lawn space. The wooded neighborhood includes lush landscaping, multiple water features and paved walking paths throughout. Every home site includes a privately fenced back yard and front yard landscaping.  

Pinewood Trails is close to I-69, Hwy 105 and TX-99/Grand Parkway, offering convenient access to a multitude of employers, schools, retailers and activities. Several grocers and retailers are located minutes from the community, including a Walmart Supercenter and H-E-B in Cleveland, Archie’s Food Basket in Splendora, and Valley Ranch Town Center in New Caney. Students living in Pinewood Trails attend schools within the Splendora Independent School District.

New homes for sale within this community start in the $190s. To accommodate homebuyers during this time, the Pinewood Trails information center is open for tours by appointment only and is in compliance with Centers for Disease Control and Prevention and local safety guidelines. To schedule a tour or learn more, interested homebuyers are encouraged to call (866) 341-9849 ext. 936 or visit LGIHomes.com/PinewoodTrails.

About LGI Homes, Inc.

Headquartered in The Woodlands, Texas, LGI Homes, Inc. engages in the design, construction and sale of homes in Texas, Arizona, Florida, Georgia, New Mexico, Colorado, North Carolina, South Carolina, Washington, Tennessee, Minnesota, Oklahoma, Alabama, California, Oregon, Nevada, West Virginia and Virginia. Recently recognized as the 10th largest residential builder in America, based on units closed, the Company has a notable legacy of more than 17 years of homebuilding operations, over which time it has closed more than 40,000 homes. For more information about the Company and its new home developments, please visit the Company’s website at www.LGIHomes.com.

MEDIA CONTACT:
Rachel Eaton
(281) 362-8998 ext. 2560

A photo accompanying this announcement is available at https://www.globenewswire.com/NewsRoom/AttachmentNg/dfcf0e33-5c77-4447-9477-c9c1841479b3



Canadians are playing more video games to stay connected and entertained during COVID-19

From: 


Entertainment Software Association of Canada


TORONTO, Nov. 19, 2020 (GLOBE NEWSWIRE) — The COVID-19 pandemic continues to have a significant impact on the lives of Canadians. In its most recent study – conducted by The NPD Group – the Entertainment Software Association of Canada (ESAC), found that Canadians are increasing their levels of video game play as a way to stay connected and entertained during these difficult times.

Every two years ESAC, national trade association for Canada’s video game industry, conducts a study on video game consumers to identify how, what, where and why Canadians are playing video games.

Today, ESAC released its latest study entitled Real Canadian Gamer – Essential Facts 2020.

This study provides an in-depth look at the video game player community and consumers in Canada; which is already one of the world’s largest video game hubs with 61% of our population reporting regularly playing video games.

Key Findings

Although the pandemic has not resulted in substantial new video game consumers – with less than 2% of Adult Canadians (18 to 64) deciding to take up a controller for the first time during the pandemic – it has significantly boosted the amount that existing video game consumers played in Canada.


  • 58% of


    A


    dult


    Gamer


    s and 80% of


    T


    een


    Gamer


    s


    reported


    playing more video games during the pandemic.

Not only are Canadians playing more video games, but a majority of them say it is helping them feel better emotionally and mentally while following stay-at-home measures. Games are also helping parents find common ground with their kids while helping them spend time connecting.


  • 65% of


    A


    dult


    Gamer


    s and 78


    %


    of


    T


    een


    Gamer


    s find that gaming while supporting stay-at-home health measures makes them feel better.

  • 70% of Teen gamers reported using online video games to stay connected while isolating at home.

  • 6


    5


    % of


    Adult


    G


    amers


    with children ages 6 to 17


    reported playing video games with their children and 44% reported playing more often during COVID-19.

Many also identified video games as a means of helping family and friends stay bonded and connected throughout the pandemic.

Quotes

“COVID-19 is not going away anytime soon. Canadians are finding ways to stay connected and engage their minds in positive ways; they are looking for joy and entertainment in what can only be characterized as one of the most difficult times in modern human history. We have found that Canadian gamers recognize the power of play and they are engaging more and more in the immersive and connected experiences that our industry creates. We will get through this period together and video games will continue to be both an outlet for people but also an important way to keep them connected to their families and friends.”

Jayson Hilchie, President & CEO, Entertainment Software Association of Canada

Quick facts

  • 61% of Canadians reported playing video games in the past four weeks.
  • The gender split between Adult Gamers in Canada was 50/50 male to female, which is the same as 2018.
  • The average age of Adult Gamers in Canada is 38.
  • Mobile devices continue to be the primary way Adult Gamers access and play video games, with consoles overtaking mobile devices as the most popular among Kids and Teens.
  • Saskatchewan has the most video game players per capita in Canada with 68% reporting regular game play with an average of 10 hours per week spent among those who play.
  • Digital downloads of full games continue to grow with retail purchases continuing to decline in both Adults and Teens.
  • The most popular genres of video games in Canada are puzzle and word games.
  • More Canadians are participating in esports as viewers (spectators) than ever before. 40% of Canadian gamers view game streaming content; specifically, 41% of Adults and 46% of kids and Teens.
  • 40% of Canadian Adult Gamers play games online solo, 40% play with others online, 20% play online with other players in the room, and 30% of Canadian Adult Gamers play online with players.

Associated links

Contacts

Media Relations

Corinne Crichlow
Director, Public Relations & Communications
[email protected]

About

ESAC represents major video game console makers, publishers, large and small independent developers as well as national distributors. ESAC is the national voice of the video game industry in Canada. We work for our members – Activision Blizzard, Glu, EA, Gameloft, Ubisoft, Kabam, Other Ocean Interactive, Ludia, Microsoft, Nintendo, Sony Interactive Entertainment, Relic Entertainment, Solutions 2 Go, WB Games, Square Enix, Take-Two Interactive, Codename Entertainment, Certain Affinity and NetEase games – to ensure regulatory and public affairs environments are favourable to long-term industry development. For more information, visit theESA.Ca.



Breakfast Club of Canada Thanks Canadians for Their Generosity During Its 2020 Back-to-School Campaign

MONTRÉAL, Nov. 19, 2020 (GLOBE NEWSWIRE) — Breakfast Club of Canada (BCC) wishes to thank all its generous donors and partners. While the pandemic is having a major impact on the economy and business activities, the support shown to BCC has not diminished. This support is needed more than ever as food insecurity continues to rise, motivating the Club to set the most ambitious campaign goal in its 25-year history: $10 million. Thanks to its loyal donors and partners, Breakfast Club of Canada succeeded in raising a record $11.7 million to fight food insecurity that affects more than 2 million children in the country every day.

“We are honoured to have the support of Canadians as more and more families, businesses and organizations face problems in the current situation,” acknowledged BCC General Manager Tommy Kulczyk. “We want to take this opportunity to thank our generous donors who, like us, make children’s health, nutrition and education a priority.”

The funds raised will go to support the 250,000 children who use breakfast programs across the country and help meet ever-growing demand, which translates to one in three children arriving hungry at school every morning. Complying with the measures set forth by public health authorities has resulted in a significant increase in costs, especially costs related to food. Despite the record amount collected, these funds will not be enough to meet the need, given the huge impact of the pandemic on the household finances of Canadians, families in particular.

To ensure that the nutritional needs of children are met, the Club works to raise awareness among the country’s policy-makers, advocating for them to make children’s nutrition a priority. Asserting the needs and rights of children is especially important, given that Canada is the only G7 country not to have a national school food program. BCC represented Canada this week at the Global Child Nutrition Forum, stressing the urgency of implementing such a program.

To help establish solid foundations on which to build a national school food program, the Club is rallying financial allies from all spheres of activity. BCC is thankful for all of the financial donations and commitments received to support our mission and would like to acknowledge the following major donors for their generosity during this back-to-school campaign:

Lending their voices and influence, six businesswomen dedicated to children’s academic success and nutrition were part of a newly created campaign cabinet. The Club thanks them for their invaluable contributions to the campaign:

  • Joan Kelley Walker, Chair of the Breakfast Club of Canada Back-to-School Campaign Cabinet; Journalist, Philanthropist and Host
  • Shelley Mayer, Founder and President, Ramp Communications
  • Gail Nyberg, former Executive Director, Daily Bread Food Bank
  • Anne Fortin, Senior Vice President of Direct Distribution and Chief Marketing Officer, Intact Financial Corporation
  • Isabelle Rayle-Doiron, Vice-President, Public Affairs, and General Counsel, Danone
  • Brett Clapperton, Director, Community Investment and LBG Canada, SiMPACT Strategy Group

About
Breakfast Club of Canada

Accredited by Imagine Canada for its effective governance, the Club provides much more than breakfast: its approach is based on commitment, self-esteem and capacity development using an optimal formula adapted to local needs. Breakfast Club of Canada helps feed more than 257,000 children and youth in 1,887 schools across the country. To learn more, visit breakfastclubcanada.org or follow on Facebook, Instagram, Twitter and LinkedIn. #FeedKidsNow #EndChildHunger #StopChildHunger #BacktoSchool2020

Media
enquiries

For more information and to schedule interviews with Breakfast Club of Canada spokespeople, please contact:

Justine Plourde |1

888

442-1217,
ext
.
 
3369 |

[email protected]

Nathalie Rochette | 514

404-5660 |

[email protected]



Baudax Bio Announces an additional Orange Book listed patent for ANJESO®

MALVERN, Pa., Nov. 19, 2020 (GLOBE NEWSWIRE) — Baudax Bio, Inc. (NASDAQ:BXRX), a pharmaceutical company focused on therapeutics for acute care settings, recently announced the issuance of United States Patent No.10,709,713 (the ‘713 Patent) on July 14, 2020. The ‘713 Patent covers the use of ANJESO® to treat moderate to severe pain, and has been listed in the United States Food and Drug Administration’s (FDA) Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations as it relates to ANJESO®.

The ‘713 Patent is an additional ANJESO® patent to be listed in the Orange Book with an expiry date of May of 2030. The ‘713 Patent joins four other patents listed in the Orange Book, amongst others owned or licensed by Baudax that currently provide exclusivity to the ANJESO® franchise.

“We are pleased by the progress we have made in the United States Patent and Trademark Office and the recognition of the inventive nature of our ANJESO® franchise,” said Gerri Henwood, Baudax Bio’s President and Chief Executive Officer. “The ‘713 Patent is expected to provide a significant barrier for generic entry and will likely be joined by other patents currently pending in the USPTO.”

About ANJESO
®

ANJESO (meloxicam) injection is a proprietary, long-acting, preferential COX-2 inhibitor that possesses analgesic, anti-inflammatory and antipyretic activities, which are believed to be related to the inhibition of cyclooxygenase type 2 pathway (COX-2) and subsequent reduction in prostaglandin biosynthesis. ANJESO was launched in the U.S. in June 2020 following its approval by the Food and Drug Administration in February 2020. ANJESO is indicated for the management of moderate to severe pain, alone or in combination with other non-NSAID analgesics. Because of the delayed onset of analgesia, ANJESO alone is not recommended for use when rapid onset of analgesia is required. ANJESO is supported by two pivotal Phase III clinical efficacy trials, a large double-blind, placebo-controlled Phase III safety trial and four Phase II clinical efficacy trials, as well as other safety studies. As a non-opioid, Baudax Bio believes ANJESO has the potential to overcome many of the issues associated with commonly prescribed opioid therapeutics, including respiratory depression, constipation, excessive nausea and vomiting, as well as having no addictive potential, while maintaining meaningful analgesic effects for relief of pain. ANJESO was designed using the NanoCrystal® platform, a technology that enables enhanced bioavailability of poorly water-soluble drug compounds. NanoCrystal® is a registered trademark of Alkermes Pharma Ireland Limited (APIL).

About Baudax Bio

Baudax Bio is a pharmaceutical company focused on therapeutics for acute care settings. The launch of Baudax Bio’s first commercial product ANJESO® began in June 2020 following its approval by the U.S. Food and Drug Administration in February 2020. ANJESO is a once daily IV NSAID with preferential Cox-2 activity, which has successfully completed three Phase III clinical trials, including two pivotal efficacy trials, a large double-blind Phase III safety trial and other studies for the management of moderate to severe pain. In addition to ANJESO, Baudax has a pipeline of other pharmaceutical assets including two novel neuromuscular blocking agents (NMBAs) and a proprietary chemical reversal agent specific to these NMBAs which is currently in preclinical studies, and intranasal dexmedetomidine which is being developed for possible uses in pain or sedation. For more information please visit www.baudaxbio.com.

Cautionary Statement Regarding Forward Looking Statements

This press release contains forward-looking statements that involve risks and uncertainties. Such forward-looking statements reflect Baudax Bio’s expectations about its future performance and opportunities that involve substantial risks and uncertainties. When used herein, the words “anticipate,” “believe,” “estimate,” “may,” “upcoming,” “plan,” “target,” “goal,” “intend,” and “expect,” and similar expressions, as they relate to Baudax Bio or its management, are intended to identify such forward-looking statements. These forward-looking statements are based on information available to Baudax Bio as of the date of publication on this internet site and are subject to a number of risks, uncertainties, and other factors that could cause Baudax Bio’s performance to differ materially from those expressed in, or implied by, these forward-looking statements. These forward-looking statements are subject to risks and uncertainties including, among other things, the ongoing economic and social consequences of the COVID-19 pandemic, including any adverse impact on the commercial launch of ANJESO® or disruption in supply chain, Baudax Bio’s ability to maintain regulatory approval for ANJESO, Baudax Bio’s ability to successfully commercialize ANJESO; the acceptance of ANJESO by the medical community, including physicians, patients, health care providers and hospital formularies; Baudax Bio’s ability and that of Baudax Bio’s third party manufacturers to successfully scale-up our commercial manufacturing process for ANJESO, Baudax Bio’s ability to produce commercial supply in quantities and quality sufficient to satisfy market demand for ANJESO, Baudax Bio’s ability to raise future financing for continued product development, payment of milestones and ANJESO commercialization, Baudax Bio’s ability to pay its debt and satisfy conditions necessary to access future tranches of debt, Baudax Bio’s ability to comply with the financial and other covenants under its credit facility, Baudax Bio’s ability to manage costs and execute on our operational and budget plans, the accuracy of Baudax Bio’s estimates of the potential market for ANJESO, Baudax Bio’s ability to achieve its financial goals; and Baudax Bio’s ability to obtain, maintain and successfully enforce adequate patent and other intellectual property protection. These forward-looking statements should be considered together with the risks and uncertainties that may affect our business and future results included in our filings with the Securities and Exchange Commission at www.sec.gov. These forward-looking statements are based on information currently available to us, and we assume no obligation to update any forward-looking statements except as required by applicable law.

CONTACT:

Investor Relations Contact:

Argot Partners
Sam Martin / Claudia Styslinger
(212) 600-1902
[email protected]
[email protected]

Baudax Bio, Inc.

Ryan D. Lake
(484) 395-2436
[email protected]

Media Contact:

Argot Partners
David Rosen
(212) 600-1902
[email protected]



AAON Receives Sustainable Tulsa’s Bellmon Award

TULSA, Okla., Nov. 19, 2020 (GLOBE NEWSWIRE) — AAON, Inc. (NASDAQ: AAON), a leading manufacturer of heating and cooling products, announced that it received the 2020 Henry Bellmon Award in the Large Business category, from Sustainable Tulsa. The Bellmon nominees were selected from the top-ranking Scor3card® verified organizations during the 2019-2020 year. Winners were then chosen from the nomination list by the Henry Bellmon family and members of the Henry Bellmon Judges Panel based on the number of verified items and quality of answers within the Scor3card sustainability assessment and a tracking tool. AAON achieved Platinum level, the highest attainment level, in the 2020 Sustainable Tulsa Scor3card verification program.

“AAON is honored to receive a 2020 Henry Bellmon Award in recognition of our sustainability efforts. AAON designs and manufactures HVAC equipment with energy efficiency in mind, with premium features and options available for sustainable building applications. In addition to our high standard of product performance, is a commitment to sustainability for our employees, our shareholders and our customers,” said Gary Fields, President and CEO of AAON.

About Sustainable Tulsa:
Sustainable Tulsa provides education, tools, and resources to inform and engage businesses and individuals in the three areas of sustainability: social responsibility, economic vitality, and environmental stewardship — people, profit, planet. Sustainable Tulsa launched Scor3card in 2016 as an online sustainability tracking and assessment tool for organizations to track and improve their sustainability efforts. This holistic approach to sustainability allows organizations to engage their employees, bolster their economic growth, and become better environmental stewards. In 2010, Sustainable Tulsa and Southside Rotary of Tulsa collaborated to form the Henry Bellmon Awards, named after one of Oklahoma’s most respected statesmen and an early champion of sustainability in Oklahoma. In 2018, Southside Rotary of Tulsa graciously passed the baton in order for Sustainable Tulsa to continue the awards through their Scor3card program.

About AAON

AAON is engaged in the engineering, manufacturing, marketing, and sale of air conditioning and heating equipment consisting of standard, semi-custom, and custom rooftop units, chillers, packaged outdoor mechanical rooms, air handling units, condensing units, makeup air units, energy recovery units, geothermal/water-source heat pumps, coils, and controls. Since the founding of AAON in 1988, AAON has maintained a commitment to design, develop, manufacture and deliver heating and cooling products to perform beyond all expectations and demonstrate the value of AAON to our customers. For more information, please visit www.AAON.com.

Contact:
Stephanie Cameron
AAON, Inc.
918-688-9796
[email protected]



MeiraGTx Announces Pricing of Public Offering of Ordinary Shares

LONDON and NEW YORK, Nov. 19, 2020 (GLOBE NEWSWIRE) — MeiraGTx Holdings plc (Nasdaq:MGTX), a vertically integrated, clinical stage gene therapy company, today announced the pricing of an underwritten public offering of 5,000,000 of its ordinary shares at a public offering price of $12.85 per share. In addition, MeiraGTx has granted the underwriters a 30-day option to purchase up to an additional 750,000 of its ordinary shares at the public offering price, less underwriting discounts and commissions. Gross proceeds to MeiraGTx from the offering are expected to be approximately $64.3 million, before deducting underwriting discounts and commissions and offering expenses, but excluding any exercise of the underwriters’ option. All of the ordinary shares in the offering are being sold by MeiraGTx.

BofA Securities, Piper Sandler, Evercore ISI, Barclays and Chardan are acting as joint book-running managers for the offering. The offering is expected to close on or about November 23, 2020, subject to customary closing conditions.

The ordinary shares are being offered by MeiraGTx pursuant to an effective shelf registration statement on Form S-3 that was previously filed with the Securities and Exchange Commission (SEC) on July 17, 2019 and declared effective by the SEC on July 19, 2019. This offering is being made only by means of a written prospectus and prospectus supplement that form a part of the registration statement. A preliminary prospectus supplement relating to and describing the terms of the offering was filed with the SEC and is available on the SEC’s website at www.sec.gov. The final terms of the offering will be disclosed in a final prospectus supplement to be filed with the SEC. When available, copies of the final prospectus supplement and the accompanying prospectus relating to these securities may also be obtained by contacting: BofA Securities, Attention: Prospectus Department, NC1-004-03-43, 200 North College Street, 3rd Floor, Charlotte, NC 28255, or by email at [email protected]; Piper Sandler & Co., 800 Nicollet Mall, J12S03, Minneapolis, Minnesota, 55402, Attention: Prospectus Department, by telephone at (800) 747-3924 or by email at [email protected]; Evercore Group L.L.C., Attention: Equity Capital Markets, 55 East 52nd Street, 35th Floor, New York, NY 10055, by telephone at (888) 474-0200 or by e-mail at [email protected]; Barclays Capital Inc., Attention: Broadridge Financial Solutions, 1155 Long Island Avenue, Edgewood, New York 11717, telephone: +1 888 603 5847, or email: [email protected]; or Chardan Capital Markets, LLC, 17 State Street, 21st floor, New York, New York 10004.

This press release does not constitute an offer to sell or the solicitation of an offer to buy the securities, nor shall there be any sale of the securities in any jurisdiction in which such offer, solicitation or sale would be unlawful prior to the registration or qualification under the securities laws of such jurisdiction.

Forward Looking Statement

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. All statements contained in this press release that do not relate to matters of historical fact should be considered forward-looking statements, including, without limitation, statements regarding the public offering, including statements related to anticipated gross proceeds and anticipated closing date, as well as statements that include the words “expect,” “intend,” “plan,” “believe,” “project,” “forecast,” “estimate,” “may,” “should,” “anticipate” and similar statements of a future or forward-looking nature. These forward-looking statements are based on management’s current expectations. These statements are neither promises nor guarantees, but involve known and unknown risks, uncertainties and other important factors that may cause actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements, including, but not limited to, the Company’s incurrence of significant losses; any inability to achieve or maintain profitability, raise additional capital, identify additional and develop existing product candidates, successfully execute strategic priorities, bring product candidates to market, expansion of the Company’s manufacturing facilities and processes, successfully enroll patients in and complete clinical trials, accurately predict growth assumptions, recognize benefits of any orphan drug designations, retain key personnel or attract qualified employees, or incur expected levels of operating expenses; the impact of the COVID-19 pandemic on the status, enrollment, timing and results of the Company’s clinical trials and on its business, results of operations and financial condition; failure of early data to predict eventual outcomes; failure to obtain FDA or other regulatory approval for product candidates within expected time frames or at all; the novel nature and impact of negative public opinion of gene therapy; failure to comply with ongoing regulatory obligations; contamination or shortage of raw materials or other manufacturing issues; changes in healthcare laws; risks associated with the Company’s international operations; significant competition in the pharmaceutical and biotechnology industries; dependence on third parties; risks related to intellectual property; changes in tax policy or treatment; the Company’s ability to utilize its loss and tax credit carryforwards; litigation risks; and the other important factors discussed under the caption “Risk Factors” in the Company’s Quarterly Report on Form 10-Q for the quarter ended September 30, 2020, as such factors may be updated from time to time in its other filings with the SEC, which are accessible on the SEC’s website at www.sec.gov. These and other important factors could cause actual results to differ materially from those indicated by the forward-looking statements made in this press release. Any such forward-looking statements represent management’s estimates as of the date of this press release. While the Company may elect to update such forward-looking statements at some point in the future, unless required by law, the Company disclaims any obligation to do so, even if subsequent events cause its views to change. Thus, one should not assume that the Company’s silence over time means that actual events are bearing out as expressed or implied in such forward-looking statements. These forward-looking statements should not be relied upon as representing the Company’s views as of any date subsequent to the date of this press release.

Contacts

Investors:

MeiraGTx
Elizabeth (Broder) Anderson
(646) 860-7983
[email protected]

or

Media:

W2O pure
Christiana Pascale
(212) 257-6722
[email protected]



Opera Limited announces third quarter 2020 financial results

  • Opera’s total user base grew to over 380 million monthly active users in the third quarter
  • Third quarter revenue of $42.4 million, excluding both microlending and retail that are classified as discontinued operations
  • Strong revenue trends for search and advertising — back to YoY growth in the quarter, and up 33% QoQ driven by increased users, monetization of Opera News, and recovery from COVID-19 impacts
  • Third quarter adjusted EBITDA(1) of $10.7 million; representing a 25% margin
  • Net income of $154.4 million, including a gain of $148.1 million from discontinued operations following the Nanobank transaction
  • European fintech nearing official launch in Spain; additional markets planned in 2021

OSLO, Norway, Nov. 19, 2020 (GLOBE NEWSWIRE) — Opera Limited (NASDAQ: OPRA), one of the world’s largest internet consumer brands with over 380 million monthly active users, today announced its unaudited consolidated financial results for the quarter ended September 30, 2020.


Third quarter 2020 financial highlights

    Three Months Ended
September 30,
    Year-over-     Nine Months Ended
September 30,
    Year-over-  
[US$ thousands, except for margins and per ADS amounts]   2019     2020     year %

change
    2019     2020     year %

change
 
Revenue   47,820     42,416     -11.3 %   128,315     114,827     -10.5 %
                                     
Net income (loss)   28,120     154,367     449.0 %   35,923     150,648     319.4 %
Margin   58.8 %   363.9 %         28.0 %   131.2 %      
                                     
Adjusted EBITDA (1)   8,140     10,658     30.9 %   17,484     10,917     -37.6 %
Margin   17.0 %   25.1 %         13.6 %   9.5 %      
                                     
Adjusted net income (1)   26,977     9,553     -64.6 %   37,791     16,680     -55.9 %
Margin   56.4 %   22.5 %         29.5 %   14.5 %      
                                     
Diluted net income per ADS, US$   0.25     1.31     426.3 %   0.32     1.26     294.4 %
                                     
Diluted adjusted net income per ADS, US$ (1)   0.24     0.08     -66.1 %   0.34     0.15     -55.4 %

_______________________________________

(1) Please see the separate section “About non-IFRS financial measures” for the definitions of adjusted EBITDA and adjusted net income.

Song Lin, Opera’s Co-CEO, said, “This quarter, we really showed the strength of Opera’s core business with both our browsers and Opera News having very nice growth in users and engagement. This in turn led to combined search and advertising revenue returning to year-over-year growth and recovering faster from COVID-19 than initially expected. Specifically, search and advertising revenues grew by 20% and 50%, respectively, versus the second quarter. Finally, we were able to drive significant adjusted EBITDA margin expansion, while investing in several initiatives we believe could meaningfully accelerate growth rates beyond the solid growth from our core business.”


Third quarter 2020 user base and product highlights


(All comparisons are relative to the third quarter of 2019 unless otherwise stated)

  • Opera News average Monthly Active Users (“MAUs”) grew 35% to 219 million
  • Total smartphone average MAUs grew to 242 million, up 5%
  • PC average MAUs were 75 million, up 10%

Mr. Song Lin commented, “I am very pleased with our execution. We continued to grow users, invest in future products and make strides in monetization despite a challenging environment from COVID-19.

“Our user base in the third quarter exceeded 380 million monthly active users, an increase of 18 million users compared to the second quarter. This was driven by growth across our core regions and platforms. Specifically, Opera News continued its strong trajectory, growing approximately 30% year-over-year. Browsers grew nicely as well and this was highlighted by PC users growing 10% year-over-year, driven by Opera GX, and record smartphone users.

“We continue to push forward aggressively on our new initiatives. Highlighting one of our bigger initiatives, European Fintech, we are making significant progress. We’ve been testing our first product in Spain, a buy-now-pay-later offering, and the next step will be to formally launch and introduce new branding. This is planned to be followed by expansion into several other markets, and efforts to broaden our offering next year. We believe European fintech and several of our other new initiatives have the potential to significantly benefit our growth rates.

“To sum it up, we are executing against our growth strategy, recovering more quickly from COVID-19 than anticipated, and think we’ve built a strong foundation to outperform next year and beyond.”


Business outlook

Mr. Frode Jacobsen, Opera’s CFO, said, “Our growth trends accelerated throughout the third quarter and this has continued so far into the fourth quarter. Further, the strong recovery of search and advertising revenue has led to significant margin expansion. While some impacts from the pandemic remain, we are once again in a position to provide forward looking guidance.”

For the fourth quarter, we expect revenues of $45 million to $47 million, excluding revenue from retail and microlending which are both classified as discontinued operations. The expected results will be driven by continued improvement in year-over-year growth rates for search and advertising, resulting in an expected larger increase from the third to fourth quarter compared to last year. Tech revenue is expected to decline slightly compared to this past quarter.

Adjusted EBITDA is expected to be between $10 million and $12 million, representing an adjusted EBITDA margin of 24% at the midpoint. We anticipate search and advertising margin contribution to increase relative to the third quarter, while we continue to invest in new growth initiatives.

As we look to 2021, we expect to benefit from multiple factors — the strong user gains we made throughout 2020, the acceleration from offline to online, and more normalized monetization. As such, we indicate a baseline revenue expectation around $200 million for 2021, representing approximately 25% growth over 2020. This indication is primarily driven by search and advertising growth and only includes small revenue contributions from new initiatives. We intend to provide a more detailed 2021 guidance with our fourth quarter results.


Nanobank and other investments

On a pro forma basis in the third quarter, Nanobank posted revenue of $34.9 million, up 87% compared to the second quarter, and disbursed 2.5 million loans representing $155 million in total value. Adjusted EBITDA was $8.8 million and post tax profits were $6.0 million. Further, Nanobank continues to recover from COVID-19 impacts with metrics improving in all geographies during the third quarter. Indonesia is now close to pre-COVID levels, with India and Kenya recovering more gradually, and Mexico, while still early, is scaling.

Nanobank continues to prioritize profitable lending versus a faster scaling with more credit risk. In the fourth quarter, we expect Nanobank revenues to continue to scale rapidly with profit margin expansion. We believe this puts Nanobank on a trajectory to reach pre-COVID levels in 2021 for revenue as well as profitability.

In terms of other investments, OPay continues to grow and scale its payment offerings. In October, OPay processed a gross transaction value of $1.4 billion on its platform, more than three-times the level in January. Starmaker is also experiencing strong growth. Daily active users are up approximately 80% year-to-date and revenues have more than doubled year-to-date, to an annual run rate of over $100 million.

Opera owns 42% of Nanobank, 13.1% of OPay and 19.35% of Starmaker.


Third quarter 2020 consolidated financial results

All comparisons in this section are relative to the third quarter of 2019 unless otherwise stated. Fintech and retail revenue are not included in comparisons as they are classified as discontinued operations.

Revenue decreased 11% to $42.4 million

  • Search revenue declined 1% to $21.2 million due to the impact of COVID-19 on monetization, despite strong underlying user growth. Search grew 20% compared to the second quarter
  • Advertising revenue increased 4% to $19.0 million, subject to the same effects as search revenue. Advertising revenue grew 50% compared to the second quarter.
  • Technology licensing and other revenue was $2.2 million. This declined $5.8 million compared to the previous year as Opera has been phasing out low-margin professional services for an investee.

Operating expenses decreased 15% to $39.0 million.

  • Cost of revenue was $2.9 million, a decrease of 47% year-over-year. Within this total, $2.1 million related to the browser and news business area and $0.7 million related to other revenue.
  • Personnel expenses, including share-based remuneration, were $15.3 million, a 17% increase year-over-year. This expense consists of cash-based compensation expense of $13.6 million, and $1.7 million of share-based remuneration expense. The increase was driven by increased resources relating to new growth initiatives.
  • Marketing and distribution expenses were $11.0 million, a decrease of 34% year-over-year. The sequential decrease was primarily related to lower marketing activity following strong organic user growth, and reduced unit costs.
  • Depreciation and amortization expenses were $4.9 million, a 10% increase year-over-year primarily related to capitalized development and other intangible assets.
  • Other operating expenses were $4.3 million, a 35% decrease year-over-year driven by general reductions across many areas.

Operating profit was $3.0 million, representing an operating margin of 7%, compared to operating profit of $2.2 million and a 5% margin during the third quarter of 2019. The increase was primarily due to lower operating expenses, particularly marketing and distribution expenses in response to strong organic user growth in the quarter.

Other items include share of net profit of associates and joint ventures of $0.2 million. This includes Nanobank, which had profits of $3.3 million in the partial period after the transaction closed, of which Opera recognized 42% less $0.9 million in PPA amortization cost. Further, net finance gains were $4.4 million.

Income tax expense was $1.3 million in the quarter.

Net income was $154.4 million, comprising $6.3 million in profits from continued operations and $148.1 million in profits relating to discontinued operations, fueled by the gain from the creation of Nanobank. This compared to a net income of $28.1 million in the third quarter of 2019.

Net income per ADS was $1.33 in the quarter. Each ADS represents two shares in Opera Limited. In the quarter, the average number of shares outstanding was 235.6 million, corresponding to 117.8 million ADSs.

Adjusted EBITDA was $10.7 million, representing a 25% adjusted EBITDA margin, compared to adjusted EBITDA of $8.1 million in the third quarter 2019. Adjusted EBITDA excludes share-based remuneration and non-recurring expenses, as well as other income and discontinued operations.

Adjusted Net Income was $9.6 million in the quarter, compared to adjusted net income of $27.0 million in third quarter 2019. Adjusted net income excludes share-based remuneration, non-recurring expenses, discontinued operations and amortization of intangible assets related to acquisitions.

Adjusted net income per ADS was $0.08 in the quarter.

Share repurchases were 2.5 million ADSs in the quarter for a total spend of $22.4 million. Year-to-date, 5.0 million ADSs have been repurchased for a total spend of $40.9 million. $9.1 million remained available under the current repurchase authorization as of September 30, 2020.

Discontinued operations include Opera’s retail business, which was discontinued following a strategic assessment as it had not been profit generating, and Opera’s fintech business, which was contributed to Nanonbank on August 19, 2020. Opera owns 42% of Nanobank as of September 30, 2020. Retail would have added $4.4 million to third quarter revenue had it not been classified as discontinued operations.

We have posted unaudited supplemental information at https://investor.opera.com, including: 1) Opera’s financial historical results by quarter over 2019 and YTD 2020, reflecting microlending and retail as discontinued operations; and 2) Nanobank pro-forma financial results by quarter over 2019 and YTD 2020.


Conference call

Opera’s management will host a conference call to discuss the third quarter 2020 financial results on Thursday, November 19th at 8:00 am Eastern Time (EST) (2:00 PM Central European Time, 9:00 PM Beijing/Hong Kong time). Listeners may access the call by dialing the following numbers:

United States: +1 833 570-1161
China: +86 400 682 8609
Hong Kong: +852 5819 4851
Norway: +47 2396 4173
United Kingdom: +44 (0)203 107 0289
International: +1 918 922-6511
Confirmation Code: 3159725

A live webcast of the conference call will be posted at https://investor.opera.com.


About non-IFRS financial measures

To supplement our consolidated financial statements, which are prepared and presented based on IFRS, we use adjusted EBITDA and adjusted net income, both non-IFRS financial measures, to understand and evaluate our core operating performance. These non-IFRS financial measures, which may differ from similarly titled measures used by other companies, are presented to enhance investors’ overall understanding of our financial performance and should not be considered a substitute for, or superior to, the financial information prepared and presented in accordance with IFRS.

We define adjusted EBITDA as net income (loss) excluding income tax expense (benefit), net finance expense (income), share of net loss (income) of associates and joint ventures, restructuring costs, depreciation and amortization, share-based remuneration, other income, non-recurring expenses and discontinued operations.

We define adjusted net income as net income excluding share-based remuneration, amortization of acquired intangible assets, non-recurring expenses and discontinued operations, net of associated income tax adjustments.

We believe that adjusted EBITDA and adjusted net income provide useful information to investors and others in understanding and evaluating our operating results. These non-IFRS financial measures adjust for the impact of items that we do not consider indicative of the operational performance of our business. While we believe that these non-IFRS financial measures are useful in evaluating our business, this information should be considered as supplemental in nature and is not meant as a substitute for the related financial information prepared and presented in accordance with IFRS. Please refer to our financial statements at the end of this announcement for a table reconciling our non-IFRS financial measures to net income (loss), the most directly comparable IFRS financial measure.


Safe harbor statement

This press release contains statements of a forward-looking nature. These statements, including statements relating to the Company and its investees’ future financial and operating results, are made under the “safe harbor” provisions of the U.S. Private Securities Litigation Reform Act of 1995. You can identify these forward-looking statements by terminology such as “will,” “expects,” “believes,” “anticipates,” “intends,” “estimates” and similar statements. Among other things, management’s quotations and the Business outlook section contain forward-looking statements. These forward-looking statements involve known and unknown risks and uncertainties and are based on current expectations, assumptions, estimates and projections about the Company, its investees, the industry in which they operate, and the duration and effects of the COVID-19 pandemic. Potential risks and uncertainties include, but are not limited to, those relating to the development of the COVID-19 situation, those relating to the Company and its goals and strategies; expected development and launch, and market acceptance, of products and services; Company and its investees’ expectations regarding demand for and market acceptance of their brands, platforms and services; Company’s expectations regarding growth in its user base and level of engagement; Company’s ability to attract, retain and monetize users; Company’s ability to continue to develop new technologies and/or upgrade its existing technologies and quarterly variations in Company’s operating results caused by factors beyond its control and global macroeconomic conditions and their potential impact in the markets in which Company or its investees have businesses. All information provided in this press release is as of the date hereof, and the Company undertakes no obligation to update any forward-looking statements to reflect subsequent occurring events or circumstances, or changes in its expectations, except as may be required by law. Although the Company believes that the expectations expressed in these forward-looking statements are reasonable, it cannot assure you that its expectations will turn out to be correct, and investors are cautioned that actual results may differ materially from the anticipated results. Further information regarding risks and uncertainties faced by Opera is included in the Company’s filings with the U.S. Securities and Exchange Commission, including its annual reports on Form 20-F.


About Opera

Opera is a global web innovator. Opera’s browsers, news products and fintech solutions are the trusted choice of more than 380 million people worldwide. Opera is headquartered in Oslo, Norway and listed on the NASDAQ stock exchange (OPRA).

Investor Relations Contact:

Derrick Nueman
[email protected] or (408) 596-3055

For media enquiries, please contact: [email protected]

 
UNAUDITED CONSOLIDATED STATEMENT OF OPERATIONS
 
    Three Months Ended
September 30,
    Nine Months Ended
September 30,
 
[US$ thousands, except per share and ADS amounts]   2019     2020     2019     2020  
                         
Revenue   47,820     42,416     128,315     114,827  
Other income       (426 )       5,568  
Operating expenses                        
Cost of revenue   (5,372 )   (2,856 )   (9,855 )   (9,401 )
Personnel expenses including share-based remuneration   (12,670 )   (15,260 )   (34,285 )   (44,330 )
Marketing and distribution expenses   (16,831 )   (11,038 )   (51,735 )   (35,542 )
Credit loss expense   345     34     (200 )   (1,242 )
Depreciation and amortization   (4,480 )   (4,920 )   (12,874 )   (14,357 )
Non-recurring expenses       (648 )       (3,222 )
Other expenses   (6,636 )   (4,302 )   (19,210 )   (17,108 )
Total operating expenses   (45,644 )   (38,989 )   (128,159 )   (125,204 )
                         
Operating profit (loss)   2,176     3,001     156     (4,808 )
                         
Share of net income (loss) of associates and joint ventures   23,295     155     26,252     (1,322 )
Change in fair value of preferred shares in associates               6,000  
                         
Net finance income (expense)                        
Finance income   613     4,668     3,971     8,467  
Finance expense   (154 )   (123 )   (471 )   (486 )
Net foreign exchange gain (loss)   (516 )   (158 )   (492 )   (588 )
Net finance income (expense)   (58 )   4,387     3,007     7,393  
                         
Profit before income taxes   25,414     7,543     29,415     7,262  
Income tax (expense) benefit   (895 )   (1,290 )   1,112     (632 )
Profit from continuing operations   24,519     6,254     30,527     6,631  
                         
Profit from discontinued operations   3,601     148,113     5,396     144,017  
                         
Net income   28,120     154,367     35,923     150,648  
                         
Net income attributable to:                        
Equity holders of the parent   28,120     154,367     35,923     150,648  
Non-controlling interests                
Total net income attributed   28,120     154,367     35,923     150,648  
                         
Weighted average number of ordinary shares outstanding                        
Basic, millions(1)   221.55     232.71     220.31     236.37  
Diluted, millions(2)   225.89     235.62     224.83     239.06  
                         
Profit per ordinary share from continuing operations                        
Basic, US$   0.11     0.03     0.14     0.03  
Diluted, US$   0.11     0.03     0.14     0.03  
                         
Profit per ADS from continuing operations                        
Basic, US$   0.22     0.05     0.28     0.06  
Diluted, US$   0.22     0.05     0.27     0.06  
                         
Net income per ordinary share                        
Basic, US$   0.13     0.66     0.16     0.64  
Diluted, US$   0.12     0.66     0.16     0.63  
                         
Net income per ADS                        
Basic, US$   0.25     1.33     0.33     1.27  
Diluted, US$   0.25     1.31     0.32     1.26  

(1) As of September 30, 2020, the total number of shares outstanding for Opera Limited was 230,136,862, equivalent to 115,068,431 ADSs.
 
(2) Includes the net dilutive impact of employee equity awards, all of which are dilutive.

 
UNAUDITED CONSOLIDATED STATEMENT OF COMPREHENSIVE INCOME (LOSS)
 
    Three Months Ended
September 30,
  Nine Months Ended
September 30,
 
[US$ thousands]   2019     2020   2019     2020  
                       
Net income   28,120     154,367   35,923     150,648  
                       
Other comprehensive income (loss) that may be reclassified to the Statement of Operations in subsequent periods (net of tax)                      
Exchange differences on translation of foreign operations   (1,982 )   451   (2,092 )   (902 )
Reclassification of exchange differences on loss of control       3,098   7     3,087  
Share of other comprehensive income (loss) of associates and joint ventures         (41 )    
Net other comprehensive income (loss) that may be reclassified to the Statement of Operations in subsequent periods   (1,982 )   3,549   (2,126 )   2,185  
Total comprehensive income   26,139     157,917   33,797     152,834  
                       
                       
Total comprehensive income attributable to:                      
Equity holders of the parent   26,139     157,917   33,797     152,834  
Non-controlling interests              
Total comprehensive income attributed   26,139     157,917   33,797     152,834  
                       

 
UNAUDITED CONSOLIDATED STATEMENT OF FINANCIAL POSITION
 
    As of December 31,     As of September 30,  
[US$ thousands]   2019     2020  
ASSETS            
Non-current assets            
Furniture, fixtures and equipment   26,053     19,556  
Intangible assets   110,807     113,960  
Goodwill   421,578     425,582  
Investments in associates and joint ventures   76,300     346,848  
Non-current financial assets   1,351     2,497  
Deferred tax assets   6,204     3,945  
Total non-current assets   642,293     912,389  
             
Current assets            
Trade receivables   49,371     32,608  
Loans to customers   93,115      
Other receivables   59,112     10,204  
Prepayments   25,809     13,705  
Inventories   7,752     178  
Other current financial assets   1,535      
Marketable securities   42,146     55,220  
Cash and cash equivalents   139,487     64,416  
Total cash, cash equivalents, and marketable securities   181,633     119,636  
Total current assets   418,327     176,332  
TOTAL ASSETS   1,060,620     1,088,721  
             
             
EQUITY AND LIABILITIES            
Equity            
Share capital   24     24  
Other paid in capital   814,177     773,323  
Retained earnings   99,513     253,796  
Foreign currency translation reserve   (1,508 )   677  
Equity attributed to equity holders of the parent   912,206     1,027,820  
Non-controlling interests        
Total equity   912,206     1,027,820  
             
Non-current liabilities            
Non-current lease liabilities and other loans   9,181     3,908  
Deferred tax liabilities   10,526     13,022  
Other non-current liabilities   137     97  
Total non-current liabilities   19,844     17,027  
             
Current liabilities            
Trade and other payables   57,125     26,058  
Current lease liabilities and other loans   47,793     5,185  
Income tax payable   7,803     908  
Deferred revenue   708     2,749  
Other current liabilities   15,142     8,974  
Total current liabilities   128,570     43,875  
             
Total liabilities   148,414     60,902  
TOTAL EQUITY AND LIABILITIES   1,060,620     1,088,721  
             

 
UNAUDITED CONSOLIDATED STATEMENT OF CHANGES IN EQUITY
 
[US$ thousands]   Share
capital
    Other paid
in

capital
    Retained

earnings
    Foreign

currency

translation

reserve
    Total equity  
As of December 31, 2018, as previously reported   22     738,690     36,432     316     775,460  
Impact of implementing IFRS 16 Leases           64         64  
As of January 1, 2019, restated   22     738,690     36,496     316     775,524  
Net income           35,923         35,923  
Other comprehensive income (loss)               (2,126 )   (2,126 )
Total comprehensive income (loss)           35,923     (2,126 )   33,797  
Contribution of equity, net of transaction costs   2     70,986             70,986  
Acquisition of treasury shares       (5,780 )           (5,780 )
Share-based remuneration expense           3,624         3,624  
As of September 30, 2019   24     803,896     76,044     (1,810 )   878,154  
                               

[US$ thousands]   Share
capital
    Other paid
in

capital
    Retained

earnings
    Foreign

currency

translation

reserve
    Total equity  
As of December 31, 2019   24     814,177     99,513     (1,508 )   912,206  
Net income           150,648         150,648  
Other comprehensive income               2,185     2,185  
Total comprehensive income           150,648     2,185     152,833  
Acquisition of treasury shares       (40,854 )           (40,854 )
Share-based remuneration expense           3,635         3,635  
As of September 30, 2020   24     773,323     253,796     677     1,027,820  
                               

 
UNAUDITED CONSOLIDATED STATEMENT OF CASH FLOWS
 
    Three Months Ended
September 30,
    Nine Months Ended
September 30,
 
[US$ thousands]   2019     2020     2019     2020  
Cash flow from operating activities                        
Net income (loss) before income taxes from continuing operations   25,414     7,546     29,415     8,511  
Net income (loss) before income taxes from discontinued operations   4,383     147,943     7,482     139,277  
Income taxes paid   (173 )   (899 )   2,966     (8,001 )
Depreciation and amortization   4,511     4,955     12,934     14,511  
Share of net loss (income) of associates and joint ventures   (23,295 )   (155 )   (26,252 )   1,322  
Change in fair value of preferred shares in associates and joint ventures               (6,000 )
Equity component of share-based payment expense   1,377     1,401     3,640     3,635  
Gain on disposal of fintech segment       (152,048 )       (152,048 )
Net finance expense (income)   151     (4,387 )   (2,728 )   (7,393 )
Change in inventories   (1,933 )   6     (1,932 )   7,573  
Change in trade and other receivables   (7,107 )   14,555     (10,515 )   20,116  
Change in loans to customers   (33,253 )   (5,689 )   (52,416 )   73,433  
Change in trade and other payables   9,325     3,779     23,585     (24,530 )
Change in deferred revenue   (59 )   (1,279 )   (773 )   2,058  
Change in prepayments   (2,823 )   9,739     (12,485 )   7,387  
Change in other liabilities   7,468     (4,901 )   5,333     (5,519 )
Other   (1,525 )   (3,199 )   (2,715 )   1,505  
Net cash flow from (used in) operating activities   (17,539 )   17,370     (24,460 )   75,838  
                         
Cash flow from investment activities                        
Purchase of intangibles assets       (789 )       (2,278 )
Purchase of equipment   (2,588 )   (86 )   (7,154 )   (2,319 )
Investment in, and loans to associates and joint ventures           (6,758 )    
Acquisition of subsidiary, net of cash acquired               (4,882 )
Disbursement of short-term loans               (4,497 )
Cash transferred with Okash Group       (39,260 )       (39,260 )
Release of escrow account               1,000  
Repayment of short-term loans               4,497  
Deposit of collateral for loan facility               (1,000 )
Net sale (purchase) of listed equity instruments   (31,625 )   6,313     (45,673 )   (3,089 )
Development expenditure   (1,098 )   (2,132 )   (3,209 )   (5,938 )
Interest income received       105         531  
Net cash flow from (used in) investing activities   (35,311 )   (35,849 )   (62,794 )   (57,235 )
                         
Cash flow from financing activities                        
Acquisition of treasury shares       (22,384 )   (4,983 )   (40,854 )
Proceeds from loans and borrowings   20,335         19,515     6,905  
Interests on loans and borrowings   (106 )   29     (387 )   (1,676 )
Proceeds from issues of equity instruments   71,852         71,852      
Repayment of loans and borrowings   (437 )       (1,337 )   (53,180 )
Transaction costs on issue of equity instruments   (864 )       (864 )    
Payment of lease liabilities   (574 )   (1,525 )   (2,755 )   (3,777 )
Net cash flow from (used in) financing activities   90,206     (23,880 )   81,041     (92,582 )
                         
Net change in cash and cash equivalents   37,356     (42,359 )   (6,213 )   (73,979 )
                         
Cash and cash equivalents at beginning of period   134,155     105,453     177,873     139,487  
Net foreign exchange difference   (813 )   1,322     (962 )   (1,092 )
Cash and cash equivalents at end of period   170,697     64,416     170,697     64,416  
                         

 
Financial details by business area
 
The tables below specify the contribution by each business area:
 
[US$ thousands]   Three Months Ended September 30, 2019  
Business area   Browser and
News
    Other     Total  
Revenue categories                  
Search   21,527         21,527  
Advertising   18,349         18,349  
Technology licensing and other revenue       7,944     7,944  
Total revenue   39,876     7,944     47,820  
                   
Cost of revenue   (207 )   (5,165 )   (5,372 )
Marketing and distribution expenses   (16,831 )       (16,831 )
Credit loss expense   345         345  
Direct expenses   (16,693 )   (5,165 )   (21,858 )
                   
Contribution by business area   23,183     2,779     25,963  
                   

[US$ thousands]   Three Months Ended September 30, 2020  
Business area   Browser and
News
    Other     Total  
Revenue categories                  
Search   21,237         21,237  
Advertising   18,968     36     19,004  
Technology licensing and other revenue       2,175     2,175  
Total revenue   40,205     2,211     42,416  
                   
Cost of revenue   (2,131 )   (725 )   (2,856 )
Marketing and distribution expenses   (10,879 )   (159 )   (11,038 )
Credit loss expense   34         34  
Direct expenses   (12,976 )   (884 )   (13,860 )
                   
Contribution by business area   27,229     1,327     28,556  
                   

[US$ thousands]   Nine Months Ended September 30, 2019  
Business area   Browser and
News
    Other     Total  
Revenue categories                  
Search   63,514         63,514  
Advertising   48,649         48,649  
Technology licensing and other revenue       16,152     16,152  
Total revenue   112,163     16,152     128,315  
                   
Cost of revenue   (1,420 )   (8,435 )   (9,855 )
Marketing and distribution expenses   (51,730 )   (5 )   (51,735 )
Credit loss expense   (200 )       (200 )
Direct expenses   (53,350 )   (8,440 )   (61,790 )
                   
Contribution by business area   58,813     7,712     66,525  
                   

[US$ thousands]   Nine Months Ended September 30, 2020  
Business area   Browser and
News
    Other     Total  
Revenue categories                  
Search   58,527         58,527  
Advertising   48,389     36     48,425  
Technology licensing and other revenue       7,875     7,875  
Total revenue   106,916     7,911     114,827  
                   
Cost of revenue   (5,614 )   (3,787 )   (9,401 )
Marketing and distribution expenses   (34,974 )   (568 )   (35,542 )
Credit loss expense   (534 )   (708 )   (1,242 )
Direct expenses   (41,122 )   (5,063 )   (46,185 )
                   
Contribution by business area   65,794     2,848     68,642  
                   

Personnel expenses including share-based remuneration
 
The table below specifies the amounts of personnel expenses including share-based remuneration:
 
[US$ thousands]   Three Months Ended
September 30,
    Nine Months Ended
September 30,
 
Personnel expenses including share-based remuneration   2019     2020     2019     2020  
Personnel expenses excluding share-based remuneration   11,187     13,596     29,831     40,616  
Share-based remuneration, including related social security costs   1,483     1,663     4,454     3,714  
Total   12,670     15,260     34,285     44,330  
                         

Other expenses
 
The table below specifies the nature of other expenses:
 
[US$ thousands]   Three Months Ended
September 30,
    Nine Months Ended
September 30,
 
Other expenses   2019     2020     2019     2020  
Hosting   1,879     1,790     5,277     5,942  
Audit, legal and other advisory services   1,473     1,119     5,145     4,308  
Software license fees   745     467     1,784     1,450  
Rent and other office expense   1,074     793     3,227     2,302  
Travel   1,007     114     2,353     1,094  
Other   459     19     1,423     2,013  
Total   6,636     4,302     19,210     17,108  
                         

 
Non-IFRS financial measures
 
    Three Months Ended
September 30,
    Nine Months Ended
September 30,
 
[US$ thousands, except per share and ADS amounts]   2019     2020     2019     2020  
Reconciliation of net income (loss) to adjusted EBITDA                        
Net income   28,120     154,367     35,923     150,648  
Add: Income tax expense (benefit)   895     1,290     (1,112 )   632  
Add: Net finance expense (income)   58     (4,387 )   (3,007 )   (7,393 )
Add: Share of net loss (income) of associates and joint ventures   (23,295 )   (155 )   (26,252 )   1,322  
Add: Change in fair value of preferred shares in associates               (6,000 )
Add: Depreciation and amortization   4,480     4,920     12,874     14,357  
Add: Share-based remuneration   1,483     1,663     4,454     3,714  
Add: Non-recurring expenses       648         3,222  
Less: Other income       426         (5,568 )
Less: Profit from discontinued operations   (3,601 )   (148,113 )   (5,396 )   (144,017 )
Adjusted EBITDA   8,140     10,658     17,484     10,917  
                         
Reconciliation of net income (loss) to adjusted net income                        
Net Income   28,120     154,367     35,923     150,648  
Add: Share-based remuneration   1,483     1,663     4,454     3,714  
Add: Amortization of acquired intangible assets   1,280     1,340     3,840     4,013  
Add: Non-recurring expenses       648         3,222  
Income tax adjustment (1)   (305 )   (352 )   (1,030 )   (900 )
Less: Profit from discontinued operations   (3,601 )   (148,113 )   (5,396 )   (144,017 )
Adjusted net income   26,977     9,553     37,791     16,680  
                         
Weighted average number of ordinary shares outstanding                        
Basic, millions   221.55     232.71     220.31     236.37  
Diluted, millions   225.89     235.62     224.83     239.06  
                         
Adjusted net income (loss) per ordinary share                        
Basic, US$   0.12     0.04     0.17     0.08  
Diluted, US$   0.12     0.04     0.17     0.07  
                         
Adjusted net income (loss) per ADS                        
Basic, US$   0.24     0.08     0.34     0.15  
Diluted, US$   0.24     0.08     0.34     0.15  

(1) Reversal of tax benefit related to the social security cost component of share-based remuneration and deferred taxes on the amortization of acquired intangible assets.



Alnylam Receives Approval for OXLUMO™ (lumasiran) in the European Union for the Treatment of Primary Hyperoxaluria Type 1 in All Age Groups

Alnylam Receives Approval for OXLUMO™ (lumasiran) in the European Union for the Treatment of Primary Hyperoxaluria Type 1 in All Age Groups

– OXLUMO is the First Therapeutic Approved for the Treatment of PH1, and the Only Therapy Proven to Lower Harmful Oxalate Levels that Drive the Progression of PH1 Disease –

CAMBRIDGE, Mass.–(BUSINESS WIRE)–
Alnylam Pharmaceuticals, Inc. (Nasdaq: ALNY), the leading RNAi therapeutics company, today announced that the European Commission (EC) has granted marketing authorization for OXLUMO™ (lumasiran), an RNAi therapeutic, for the treatment of primary hyperoxaluria type 1 (PH1) in all age groups.

PH1 is an ultra-rare orphan disease characterized by excessive oxalate production, which can lead to life threatening end-stage renal disease (ESRD) and other systemic complications. Heterogeneity in disease manifestation often contributes to delays in diagnosis – particularly in adult PH1 patients, with a median time from symptoms onset to diagnosis of approximately six years. Untreated PH1 leads to progressive kidney damage; patients with advanced kidney disease require intensive dialysis to help filter waste products, including oxalate, from their blood until they are able and eligible to receive a dual or sequential liver/kidney transplant, an invasive procedure associated with a high risk of morbidity and mortality, and life-long immunosuppression.

“Prior to now there have been no approved treatment options for PH1 in Europe, so this is a potentially life-changing milestone for people diagnosed with this ultra-rare, debilitating disease – many of whom are infants and children – and their families. Lumasiran will address the urgent unmet need that exists for patients with PH1 and its approval today marks our continued commitment to rare disease communities,” said John Maraganore, Ph.D., Chief Executive Officer, Alnylam Pharmaceuticals. “Alnylam has taken lumasiran from identification of compound to regulatory approval in just six years and we will progress with the same sense of urgency as we work with national reimbursement bodies across Europe to bring lumasiran to patients.”

Lumasiran is an RNAi therapeutic targeting the hydroxyacid oxidase 1 (HAO1) mRNA that encodes glycolate oxidase (GO) – an enzyme upstream of the disease-causing defect in PH1. By degrading the HAO1mRNA and reducing the synthesis of GO, lumasiran stops the production of oxalate – the toxic metabolite that directly contributes to the clinical manifestations of PH1.

“PH1 affects patients of all ages. It is particularly devastating when infants are born with the condition and develop kidney failure within the first few months of life. PH1 patients develop kidney stones from the overproduction of oxalate, and in many we see a progressive decline in kidney function, which can ultimately lead to life-threatening end-stage kidney disease. Until recently the only treatment options available have been combined liver and kidney transplantation, with vitamin B6 slowing down kidney failure in a limited number of sensitive patients,” said Sally-Anne Hulton, M.D., Consultant Paediatric Nephrologist, Birmingham Women’s and Children’s Hospital NHS Trust, UK. “For the first time, lumasiran provides those of us treating PH1 children and adults with a new therapeutic option to tackle the root cause of this disease and prevent the production of oxalate. The data show meaningful and sustained reductions in urinary and plasma oxalate with an encouraging safety and tolerability profile, providing us with hope for improving care for these patients.”

“In line with our Patient Access Philosophy, Alnylam is committed to being as innovative commercially as we have been scientifically,” said Brendan Martin, Acting Head of CEMEA, Alnylam. “While the ability to enter into innovative agreements varies by country and local regulations, we intend to work with health authorities across Europe to achieve responsible and sustainable access arrangements for lumasiran that address the diverse patient population affected by PH1, which ranges from infants to adults, and we will adapt to the local context. Our goal is to ensure that all patients in need have access to lumasiran while minimizing budget uncertainty for health services.”

The approval in the European Union is based on efficacy and safety findings from both the ILLUMINATE-A and ILLUMINATE-B Phase 3 studies of lumasiran. In the ILLUMINATE-A study conducted in adults and children six years or older, lumasiran achieved the primary endpoint with a 53 percent mean reduction in urinary oxalate relative to placebo and showed a 65 percent mean reduction in urinary oxalate relative to baseline. Eighty-four percent of patients achieved normal1 or near-normal2 levels of urinary oxalate and more than half of patients (52 percent) reached normalization, compared to zero percent in the placebo group. Findings from the ILLUMINATE-A pivotal study were presented in June 2020 at the virtual European Renal Association-European Dialysis and Transplant Association (ERA-EDTA) International Congress. In the ILLUMINATE-B Phase 3 study, the efficacy results and safety profile of lumasiran in infants and children under the age of six years were found to be similar to those observed in ILLUMINATE-A. Results from the ILLUMINATE-B pediatric study were presented on October 22 at the virtual American Society of Nephrology (ASN) Annual Congress.

Lumasiran was granted Priority Medicines (PRIME) designation by the EMA as well as Orphan Designation in the European Union. Lumasiran was also granted an Accelerated Assessment by the EMA, which is awarded to medicines deemed to be of major public health interest and therapeutic innovation and is designed to bring new treatments to patients more quickly. This approval in the European Union follows the positive opinion from the Committee for Medicinal Products for Human Use (CHMP) in October 2020. Alnylam has filed a New Drug Application (NDA) with the U.S. Food and Drug Administration (FDA). The FDA has granted a Priority Review for the NDA and has set an action date of December 3, 2020 under the Prescription Drug User Fee Act (PDUFA).

Footnotes:

1Normal is defined as urinary oxalate levels at or below the upper limit of normal (ULN; ≤ 0.514 mmol/24 hr/1.73 m2).

2Near-normal is defined as urinary oxalate levels at or below 1.5 x ULN (≤ 0.771 mmol/24 hr/1.73 m2).

About OXLUMO™ (lumasiran)

OXLUMO (lumasiran) is an RNAi therapeutic targeting hydroxyacid oxidase 1 (HAO1) for the treatment of primary hyperoxaluria type 1 (PH1) to lower urinary oxalate levels in pediatric and adult patients. HAO1 encodes glycolate oxidase (GO), an enzyme upstream of the disease-causing defect in PH1 and lumasiran works by degrading HAO1 messenger RNA and reducing the synthesis of GO, which inhibits hepatic production of oxalate – the toxic metabolite responsible for the clinical manifestations of PH1. Lumasiran utilizes Alnylam’s Enhanced Stabilization Chemistry (ESC)-GalNAc conjugate technology designed to increase potency and durability. In the pivotal ILLUMINATE-A study, lumasiran was shown to significantly reduce levels of urinary oxalate relative to placebo, with the majority of patients reaching normal or near-normal levels. Injection site reactions (ISRs) were the most common drug-related adverse reaction. In the ILLUMINATE-B pediatric Phase 3 study, lumasiran demonstrated an efficacy and safety profile consistent to that observed in ILLUMINATE-A. Lumasiran is administered via subcutaneous injection once monthly for three months, then once quarterly thereafter at a dose based on actual body weight. For patients who weigh less than 10 kg, ongoing dosing remains monthly. OXLUMO should be administered by a healthcare professional.

About Primary Hyperoxaluria Type 1 (PH1)

PH1 is an ultra-rare disease in which excessive oxalate production results in the deposition of calcium oxalate crystals in the kidneys and urinary tract and can lead to the formation of painful and recurrent kidney stones and nephrocalcinosis. Renal damage is caused by a combination of tubular toxicity from oxalate, calcium oxalate deposition in the kidneys, and urinary obstruction by calcium oxalate stones. Compromised kidney function exacerbates the disease as the excess oxalate can no longer be effectively excreted, resulting in subsequent accumulation and crystallization in bones, eyes, skin, and heart, leading to severe illness and death. Current treatment options are very limited and include frequent renal dialysis or combined organ transplantation of liver and kidney, a procedure with high morbidity that is limited due to organ availability. Although a small minority of patients respond to vitamin B6 therapy, there are no approved pharmaceutical therapies for PH1.

About RNAi

RNAi (RNA interference) is a natural cellular process of gene silencing that represents one of the most promising and rapidly advancing frontiers in biology and drug development today. Its discovery has been heralded as “a major scientific breakthrough that happens once every decade or so,” and was recognized with the award of the 2006 Nobel Prize for Physiology or Medicine. By harnessing the natural biological process of RNAi occurring in our cells, a new class of medicines, known as RNAi therapeutics, is now a reality. Small interfering RNA (siRNA), the molecules that mediate RNAi and comprise Alnylam’s RNAi therapeutic platform, function upstream of today’s medicines by potently silencing messenger RNA (mRNA) – the genetic precursors – that encode for disease-causing or disease pathway proteins, thus preventing them from being made. This is a revolutionary approach with the potential to transform the care of patients with genetic and other diseases.

Important Safety Information

Contraindications

Severe hypersensitivity to lumasiran or any of the excipients.

Severe or end-stage renal impairment

Treatment with lumasiran increases plasma glycolate levels, which may increase the risk of metabolic acidosis or worsening of pre-existing metabolic acidosis in patients with severe or end‑stage renal disease. These patients should therefore be monitored for signs and symptoms of metabolic acidosis.

Moderate or severe hepatic impairment

In patients with moderate or severe hepatic impairment there is a potential for decreased efficacy. Therefore, efficacy should be monitored in these patients.

Adverse Reactions

The most common adverse reaction reported was injection site reaction (32%) and abdominal pain (21%).

About AlnylamPharmaceuticals

Alnylam (Nasdaq: ALNY) is leading the translation of RNA interference (RNAi) into a whole new class of innovative medicines with the potential to transform the lives of people afflicted with rare genetic, cardio-metabolic, hepatic infectious, and central nervous system (CNS)/ocular diseases. Based on Nobel Prize-winning science, RNAi therapeutics represent a powerful, clinically validated approach for the treatment of a wide range of severe and debilitating diseases. Founded in 2002, Alnylam is delivering on a bold vision to turn scientific possibility into reality, with a robust RNAi therapeutics platform. Alnylam’s commercial RNAi therapeutic products are ONPATTRO® (patisiran), approved in the U.S., EU, Canada, Japan, Brazil, and Switzerland, GIVLAARI® (givosiran), approved in the U.S., EU, Brazil, and Canada, and OXLUMO™ (lumasiran) approved in the EU. Alnylam has a deep pipeline of investigational medicines, including six product candidates that are in late-stage development. Alnylam is headquartered in Cambridge, MA.

Alnylam Forward Looking Statements

Various statements in this release concerning Alnylam’s future expectations, plans and prospects, including, without limitation, Alnylam’s views with respect to the safety and efficacy of lumasiran as demonstrated in the ILLUMINATE-A and ILLUMINATE-B Phase 3 studies and the potential for lumasiran to prevent or inhibit oxalate over-production in PH1 patients, meet urgent unmet needs of PH1 patients across all age groups, and have a favorable impact on PH1 disease manifestations, Alnylam’s plans to progress with discussions and negotiations with national reimbursement bodies across Europe and intention to work with health authorities across Europe to achieve responsible and sustainable access arrangements for lumasiran that address the diverse patient population affected by PH1, and to adapt to local requirements, its goal to ensure that all patients in need have access to lumasiran while minimizing budget uncertainty for health services, Alnylam’s expectations with respect to the review timeline for the lumasiran NDA by the FDA, Alnylam’s plans, assuming regulatory approvals, to bring lumasiran to patients with PH1 around the world, and expectations regarding the continued execution on its “Alnylam 2020” guidance for the advancement and commercialization of RNAi therapeutics, constitute forward-looking statements for the purposes of the safe harbor provisions under The Private Securities Litigation Reform Act of 1995. Actual results and future plans may differ materially from those indicated by these forward-looking statements as a result of various important risks, uncertainties and other factors, including, without limitation: the direct or indirect impact of the COVID-19 global pandemic or any future pandemic, such as the scope and duration of the outbreak, government actions and restrictive measures implemented in response, material delays in diagnoses of rare diseases, initiation or continuation of treatment for diseases addressed by Alnylam products, or in patient enrollment in clinical trials, potential supply chain disruptions, and other potential impacts to Alnylam’s business, the effectiveness or timeliness of steps taken by Alnylam to mitigate the impact of the pandemic, and Alnylam’s ability to execute business continuity plans to address disruptions caused by the COVID-19 or any future pandemic; Alnylam’s ability to discover and develop novel drug candidates and delivery approaches and successfully demonstrate the efficacy and safety of its product candidates; the pre-clinical and clinical results for its product candidates, which may not be replicated or continue to occur in other subjects or in additional studies or otherwise support further development of product candidates for a specified indication or at all; actions or advice of regulatory agencies, which may affect the design, initiation, timing, continuation and/or progress of clinical trials or result in the need for additional pre-clinical and/or clinical testing; delays, interruptions or failures in the manufacture and supply of its product candidates or its marketed products; obtaining, maintaining and protecting intellectual property; intellectual property matters including potential patent litigation relating to its platform, products or product candidates; obtaining regulatory approval for its product candidates, including lumasiran in other countries, and maintaining regulatory approval and obtaining pricing and reimbursement for its products, including ONPATTRO, GIVLAARI and OXLUMO; progress in continuing to establish an ex-United States infrastructure; successfully launching, marketing and selling its approved products globally, including ONPATTRO, GIVLAARI and OXLUMO, and achieving net product revenues for ONPATTRO within its revised expected range during 2020; Alnylam’s ability to successfully expand the indication for ONPATTRO in the future; competition from others using technology similar to Alnylam’s and others developing products for similar uses; Alnylam’s ability to manage its growth and operating expenses within the ranges of guidance provided by Alnylam through the implementation of further discipline in operations to moderate spend and its ability to achieve a self-sustainable financial profile in the future without the need for future equity financing; Alnylam’s ability to establish and maintain strategic business alliances and new business initiatives; Alnylam’s dependence on third parties, including Regeneron, for development, manufacture and distribution of certain product candidates, including eye and CNS product candidates, and Vir for the development of ALN-COV and other potential RNAi therapeutics targeting SARS-CoV-2 and host factors for SARS-CoV-2; the outcome of litigation; the risk of government investigations; and unexpected expenditures; as well as those risks more fully discussed in the “Risk Factors” filed with Alnylam’s most recent Quarterly Report on Form 10-Q filed with the Securities and Exchange Commission (SEC) and in other filings that Alnylam makes with the SEC. In addition, any forward-looking statements represent Alnylam’s views only as of today and should not be relied upon as representing its views as of any subsequent date. Alnylam explicitly disclaims any obligation, except to the extent required by law, to update any forward-looking statements.

Alnylam Pharmaceuticals, Inc.

Fiona McMillan

(EU & Canada Head of Communications)

+44 7741655570

Christine Regan Lindenboom

(Investors and Media)

+1-617-682-4340

Josh Brodsky

(Investors)

+1-617-551-8276

KEYWORDS: Massachusetts Europe United States North America

INDUSTRY KEYWORDS: FDA Health Genetics Clinical Trials Pharmaceutical Biotechnology

MEDIA:

Logo
Logo

Rockwell Automation Combats Industrial Cyber Threats With New Security Certifications and Products

Rockwell Automation Combats Industrial Cyber Threats With New Security Certifications and Products

The company’s new certifications and expanded product line can help protect industrial operations and customer information

MILWAUKEE–(BUSINESS WIRE)–
Companies continue to need help securing their industrial operations as they connect production and IT systems and contend with cyberthreats targeting industrial control systems. To meet this need, Rockwell Automation continues expanding its cybersecurity certifications and incorporating advanced security capabilities into more of its products.

This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20201119005490/en/

(Graphic: Business Wire)

(Graphic: Business Wire)

Rockwell Automation recently received certification to the IEC (International Electrotechnical Commission) 62443-3-3 cybersecurity standard. The certification, performed by third party TÜV Rheinland, means Rockwell Automation has demonstrated the ability to install and configure production systems to meet security requirements to level 1 as defined in the world’s leading global standard.

Rockwell Automation offers reference architectures for implementing a certified production system, such as PlantPAx 5.0, the modern distributed control system (DCS) for plantwide process control. The architectures were developed to help customers certify production systems while minimizing the need to buy new technologies as part of the process. To date, Rockwell Automation has received several certifications for the IEC 62443 series of standards.

Rockwell Automation also recently received certification for the ISO (International Organization for Standardization) 27001 standard, confirming that the company’s information security management system used to protect data meets the standard’s requirements. This can give peace of mind to customers that Rockwell Automation is using best practices to protect their intellectual property, such as when customers use services like remote support and monitoring.

“Companies are facing the dual challenge of digital transformation to stay competitive, while also keeping their people, operations and intellectual property secure,” said Sujeet Chand, senior vice president and chief technology officer, Rockwell Automation. “We continue to aggressively expand our cybersecurity skills, certifications, product capabilities and services in ways that help our customers stay ahead of new threats and focus on realizing new possibilities with digital transformation.”

In addition to earning the new certifications, Rockwell Automation is also releasing new products with CIP Security to help companies secure their communications. Developed by the global trade and standard development organization ODVA, CIP Security is the only standard designed to secure communications between industrial control systems and other devices on an EtherNet/IP network.

New industrial control products offering CIP Security include:

  • Allen-Bradley PowerFlex 755T AC drives
  • Kinetix 5300 servo drives

Other Rockwell Automation products that already support CIP Security include:

  • ControlLogix 5580 controllers
  • Kinetix 5700 servo drives
  • 1756-EN4TR communication module

To help protect the many devices in use today that don’t support CIP Security, Rockwell Automation is also introducing the new CIP Security Proxy device. When used in a physically secured location, the device provides CIP Security for a wide range of industrial control devices and create more secure industrial networks.

About Rockwell Automation

Rockwell Automation, Inc. (NYSE: ROK), is a global leader in industrial automation and digital transformation. We connect the imaginations of people with the potential of technology to expand what is humanly possible, making the world more productive and more sustainable. Headquartered in Milwaukee, Wisconsin, Rockwell Automation employs approximately 23,000 problem solvers dedicated to our customers in more than 100 countries. To learn more about how we are bringing The Connected Enterprise to life across industrial enterprises, visit www.rockwellautomation.com.

Allen-Bradley, ControlLogix, Kinetix, PlantPAx and PowerFlex are trademarks of Rockwell Automation Inc.

Steve Ludwig

Rockwell Automation

440.646.4013

[email protected]

Leanne Lindseth

Padilla

612.455.1776

[email protected]

KEYWORDS: Wisconsin United States North America

INDUSTRY KEYWORDS: Engineering Data Management Security Technology Manufacturing Software

MEDIA:

Logo
Logo
Photo
Photo
(Graphic: Business Wire)

GCI Liberty Announces Certain Privately Negotiated Repurchases of Existing Debentures and Update to Sale of LendingTree Stake

GCI Liberty Announces Certain Privately Negotiated Repurchases of Existing Debentures and Update to Sale of LendingTree Stake

ENGLEWOOD, Colo.–(BUSINESS WIRE)–
GCI Liberty, Inc. (“GCI Liberty”) (Nasdaq: GLIBA, GLIBP) today announced that it has agreed to repurchase approximately $458.988 million aggregate original principal amount, of the $477.25 million aggregate original principal amount outstanding, of its 1.75% Exchangeable Senior Debentures due 2046 (the “Debentures”), exchangeable for Charter Communications, Inc. Class A common stock (“Charter Common Stock”), in separate and privately negotiated transactions with certain holders of Debentures. Based on the closing price of shares of Charter Common Stock on November 18, 2020, thetotal cost of the repurchases is estimated to be approximately $819 million in cash.

GCI Liberty also announced the closing of the sale of its stake of LendingTree, Inc. (“LendingTree”). Gross proceeds of the sale were $1,007 million. Net proceeds after estimated taxes and the settlement of its forward sale contract on LendingTree shares are expected to be approximately $900 million. The tax liability on the sale is expected to be partially offset by tax loss carryforwards and the tax loss incurred upon the repurchase of the Debentures. After the repurchase of the Debentures, GCI Liberty intends to use the remaining proceeds of the sale for general corporate purposes, which could include share repurchases post-closing of the planned merger (the “Combination”) with Liberty Broadband Corporation (“Liberty Broadband”).

Forward-Looking Statements

This press release includes certain forward-looking statements including without limitation, statements about the separate and privately negotiated repurchase transactions and the sale of LendingTree shares, including the use of proceeds therefrom and related tax matters. These forward-looking statements involve many risks and uncertainties that could cause actual results to differ materially from those expressed or implied by such statements, including, without limitation, general market conditions. These forward-looking statements speak only as of the date of this press release, and GCI Liberty expressly disclaims any obligation or undertaking to disseminate any updates or revisions to any forward-looking statement contained herein to reflect any change in GCI Liberty’s expectations with regard thereto or any change in events, conditions or circumstances on which any such statement is based. Please refer to the publicly filed documents of GCI Liberty, including its most recent Annual Report on Form 10-K and Quarterly Reports on Form 10-Q, for additional information about the risks and uncertainties related to GCI Liberty which may affect the statements made in this press release.

About GCI Liberty, Inc.

GCI Liberty, Inc. (Nasdaq: GLIBA, GLIBP) operates and owns interests in a broad range of communications businesses. GCI Liberty’s assets consist of its subsidiary GCI Holdings, LLC (“GCI”) and interests in Charter Communications and Liberty Broadband. GCI is Alaska’s largest communications provider, providing data, wireless, video, voice and managed services to consumer and business customers throughout Alaska and nationwide. GCI has delivered services for nearly 40 years to some of the most remote communities and in some of the most challenging conditions in North America.

Additional Information

Nothing in this communication shall constitute a solicitation to buy or an offer to sell any securities of Liberty Broadband or GCI Liberty, nor shall it constitute an offer, solicitation, or any sale in any jurisdiction in which such offer, solicitation, or sale is unlawful. The offer and sale of shares in the Combination will only be made pursuant to Liberty Broadband’s effective registration statement. Liberty Broadband’s stockholders, GCI Liberty’s stockholders and other investors are urged to read the joint proxy statement/prospectus included in the registration statement on Form S-4 filed regarding the Combination and any other relevant documents filed with the SEC, as well as any amendments or supplements to those documents, because they will contain important information about the Combination. Copies of these SEC filings are available free of charge at the SEC’s website (http://www.sec.gov). Copies of the filings together with the materials incorporated by reference therein are also available, without charge, by directing a request to Liberty Broadband, 12300 Liberty Boulevard, Englewood, Colorado 80112, Attention: Investor Relations, Telephone: (720) 875-5700 or to GCI Liberty, Inc., 12300 Liberty Boulevard, Englewood, Colorado 80112, Attention: Investor Relations, Telephone: (720) 875-5900.

Participants in the Solicitation

Liberty Broadband and GCI Liberty and their respective directors and executive officers and other persons may be deemed to be participants in the solicitation of proxies in respect of the Combination. Information about Liberty Broadband’s directors and executive officers is available in Liberty Broadband’s definitive proxy statement for its 2020 annual meeting of stockholders, which was filed with the SEC on April 10, 2020. Information about GCI Liberty’s directors and executive officers is available in GCI Liberty’s definitive proxy statement for its 2020 annual meeting of stockholders, which was filed with the SEC on April 10, 2020. Other information regarding the participants in the proxy solicitation and a description of their direct and indirect interests, by security holdings or otherwise, are contained in the joint proxy statement/prospectus included in the registration statement on Form S-4 filed with the SEC and other relevant materials to be filed with the SEC, as well as any amendments or supplements to those documents, regarding the Combination when they become available. Investors should read the joint proxy statement/prospectus included in the registration statement on Form S-4 carefully before making any voting or investment decisions. You may obtain free copies of these documents from Liberty Broadband and GCI Liberty as indicated above.

GCI Liberty, Inc.

Courtnee Chun, 720-875-5420

KEYWORDS: Colorado United States North America

INDUSTRY KEYWORDS: Technology Mobile/Wireless Internet Telecommunications

MEDIA:

Logo
Logo