Lydall to Host Virtual Investor Day on December 9, 2020

MANCHESTER, Conn., Dec. 01, 2020 (GLOBE NEWSWIRE) — Lydall, Inc. (NYSE: LDL) announced today that it will host its Lydall Investor Day 2020 event virtually on Wednesday, December 9, 2020.

Lydall’s leadership team will unveil the Company’s strategic roadmap to deliver long-term shareholder value, including capital allocation strategy and financial targets. A video invitation from President and Chief Executive Officer Sara Greenstein can be viewed here: https://www.youtube.com/watch?v=9nRImRYLIDI&feature=youtu.be

The presentation will begin at 10:00am Eastern Time, to be immediately followed by a question and answer session. The Company’s statements may contain or constitute material information that has not been previously disclosed. The event will be hosted by:

  • Sara A. Greenstein, President and Chief Executive Officer;
  • Randall B. Gonzales, Executive Vice President and Chief Financial Officer; and
  • Ashish Diwanji, President, Lydall Performance Materials.

To access and register for this event, please go to Lydall’s Investor Relations page (https://ir.lydall.com), or click on the following link: https://primetime.bluejeans.com/a2m/register/xffprpvc

A live webcast and audio archive of the presentation will be available via the Investor Relations section of the company’s Web site at https://ir.lydall.com. Participants should allow approximately five to ten minutes prior to the presentation’s start time to visit the site and download any streaming media software needed to listen to the Internet webcast. A replay of the webcast will also be available on the company’s website for 90 days.

Headquartered in Manchester, Connecticut with global manufacturing operations, Lydall delivers value-added engineered materials and specialty filtration solutions that promote a cleaner, safer and quieter world. We partner with our customers to develop bespoke, high-performing and efficient solutions that are adaptable and scalable to meet their needs. Lydall is a New York Stock Exchange-listed company. For more information, visit http://www.lydall.com. Lydall is a registered trademark of Lydall, Inc. in the U.S. and other countries.  

For further information contact:
Media:
Danielle Orsino
Telephone 949-365-6609
[email protected]

Investors

Brendan Moynihan
Vice President, Investor Relations
Telephone 860-646-1233
Facsimile 860-646-8847
www.lydall.com
[email protected]



Special Accreditation Offering for Small-to-Medium Health Plans

URAC, one of the nation’s oldest and most prestigious accrediting organizations announced today that they have developed a special accreditation offering for small-to-medium sized health plans.

Washington, DC, Dec. 01, 2020 (GLOBE NEWSWIRE) — URAC, one of the nation’s oldest and most prestigious accrediting organizations announced today that they have developed a special accreditation offering for small-to-medium sized health plans, with a focus on affordability while still adhering to the highest standards in health care quality. These smaller health plans face particular challenges, especially in the current health care landscape and URAC aims to address some of these challenges with its new accreditation offering. URAC aims to reduce the financial barrier to entry so that smaller health plans earn recognition for their quality improvement activities, position themselves and demonstrate their value in caring for their membership, delivering the highest outcomes. URAC accreditation helps to improve the quality of health care delivered by health plans of all sizes. URAC knows that accreditation can help improve health care quality. Because health plans, like much of the health care ecosystem, have faced challenges throughout the pandemic, URAC made the decision to reduce the price of their accreditation to ensure that cost is not a barrier to improving health outcomes for health plan members. Recognizing that health plans of all sizes can benefit from a URAC Accreditation and that purchasing this accreditation has been challenging for smaller plans, URAC has established a new pricing structure for small health plans seeking accreditation that offers greater affordability than they have offered in the past. “These times are particularly difficult and health care is an especially challenging industry to work through,” said Shawn Griffin, MD, URAC’s President and CEO. “Health plans are facing some fundamental unknowns that can make it difficult to make longer-term plans.” URAC aims to be part of the solution for health care quality in this uncertain time and beyond. “We want to help health plans make decisions to improve quality, and knowing that we can make the accreditation decision easier for smaller health plans by offering this new lower pricing, we are happy to do so,” added Griffin. URAC stands with its clients and other health care organizations during the pandemic and its aftermath. —————————————– About URAC Celebrating its 30th anniversary in 2020, URAC is the independent leader in promoting health care quality through leadership, accreditation, measurement and innovation. URAC is a non-profit organization that uses evidence-based measures and develops standards through inclusive engagement with a range of stakeholders who are committed to improving the quality of health care. Its portfolio of accreditation and certification programs span the health care industry, addressing health care management and operations, health plans, pharmacies, telehealth providers, physician practices, and more. URAC accreditation is a symbol of excellence for organizations to showcase their validated commitment to quality.

Attachment



Laura Wood, Director
URAC
202-326-3968
[email protected]

Sensus Healthcare Announces Study Showing Single Low Dose of Superficial Radiation Therapy Prevents Keloid Recurrence Following Surgical Excision

Prospective study published in Journal of the American Academy of Dermatology

BOCA RATON, Dec. 01, 2020 (GLOBE NEWSWIRE) — Sensus Healthcare, Inc. (Nasdaq: SRTS), a medical device company specializing in highly effective, non-invasive, minimally-invasive and cost-effective treatments for oncological and non-oncological conditions, announces the publication of a prospective clinical study showing that a single low dose of superficial radiation therapy (SRT) following excision of 14 keloids had an approximate 6.25% recurrence rate at six months, and for the 10 patients available for follow-up at 24 months none of the keloids had recurred.

The study was published in the Journal of the American Academy of Dermatology and can be found here. Lead authors were Yuna Son, M.S., Ernest Owen Nicandro Phillips B.S. and Kristin Magrini Price, M.D., all of the Department of Biomedical Sciences and Division of Dermatology, Florida State University College of Medicine.

A total of 15 black patients with 20 untreated keloids in various anatomic locations were recruited for the study to undergo surgical excision followed by a single dose of superficial radiation. The authors concluded that a single 8 Gy dose of superficial 50 kV radiation delivered an average of 34 days after keloid excision may be sufficient to minimize recurrence, including in individuals who are resistant to steroids. The authors noted that higher radiation energies, doses or fractions may be unnecessary for keloid therapy.

“Although this was a small study, the outcome is important,” said Joe Sardano, chief executive officer of Sensus Healthcare. “The investigators noted that there are few prospective studies with SRT following keloidectomy, and that the doses of SRT studied have not been standardized. This study shows that just one low dose of SRT can be impactful.  Not only does this minimize radiation exposure to the patient, but it also is cost effective. 

“We are delighted that the dermatology community is becoming increasingly aware of the role of SRT in treating disfiguring keloids. The publication of this study comes on the heels of a retrospective study published in the Journal of Clinical and Aesthetic Dermatology showing keloidectomy followed by SRT had an approximate 10% recurrence rate, compared with an expected recurrence rate of more than 80% following surgical excision alone,” Mr. Sardano added.

About Sensus Healthcare

Sensus Healthcare, Inc. is a medical device company specializing in highly effective, non-invasive, minimally-invasive and cost-effective treatments for both oncological and non-oncological conditions. The Sculptura™ modulated robotic brachytherapy radiation oncology system provides targeted directional anisotropic radiation therapy (ART) and brachytherapy utilizing our proprietary, state-of-the-art 3D Beam Sculpting™ to treat patients undergoing cancer treatment during surgery, or at the tumor site, fast and efficiently. Sensus also offers its proprietary low-energy X-ray technology known as superficial radiation therapy (SRT), which is the culmination of more than a decade of research and development, to treat non-melanoma skin cancers and keloids with its SRT-100™, SRT-100+™ and SRT-100 Vision™ systems. With its portfolio of innovative medical device products, Sensus provides revolutionary treatment options to enhance the quality of life of patients around the world.

For more information, visit www.sensushealthcare.com.

Forward-Looking Statements

This press release includes statements that are, or may be deemed, ”forward-looking statements.” In some cases these forward-looking statements can be identified by the use of forward-looking terminology including “believes,” “estimates,” “anticipates,” “expects,” “plans,” “intends,” “may,” “could,” “might,” “will,” “should,” “approximately,” “potential” or, in each case, their negative or other variations thereon or comparable terminology, although not all forward-looking statements contain these words.

By their nature, forward-looking statements involve risks and uncertainties because they relate to events, competitive dynamics and healthcare, regulatory and scientific developments, and depend on the economic circumstances that may or may not occur in the future or may occur on longer or shorter timelines than anticipated. Although we believe that we have a reasonable basis for each forward-looking statement contained in this press release, we caution you that forward-looking statements are not guarantees of future performance and that our actual results of operations, financial condition and liquidity, and the development of the industry in which we operate may differ materially from the forward looking statements contained in this press release, as a result of, among other factors: the continuation and severity of the COVID-19 pandemic, including its impact on sales and marketing; our ability to achieve and sustain profitability; market acceptance of our product lines; our ability to successfully commercialize our products; our ability to compete effectively in selling our products and services, including responding to technological change and cost containment efforts of our customers; our need and ability to obtain additional financing in the future; our ability to expand, manage and maintain our direct sales and marketing organizations; our ability to obtain and maintain intellectual property of sufficient scope to adequately protect our products, and our ability to avoid infringing or otherwise violating the intellectual property rights of third parties; the willingness of healthcare providers to purchase our products if coverage, reimbursement and pricing from third party payors for procedures using our products declines; the level and availability of government and third party payor reimbursement for clinical procedures using our products; our ability to effectively manage our anticipated growth, including hiring and retaining qualified personnel; the regulatory requirements applicable to us and our competitors; our ability to manufacture our products to meet demand; our current reliance on third party manufacturers and sole- or single-source suppliers, as well as our ability to successfully transition manufacturing of our products in-house; our ability to reduce the per unit manufacturing costs; our ability to efficiently manage our manufacturing processes; the regulatory and legal risks, and certain operating risks, that our international operations subject us to; the fact that product quality issues or product defects may harm our business; the accuracy of our financial statements and accounting estimates, including allowances for accounts receivable and inventory obsolescence; any product liability claims; new legislation, administrative rules, or executive orders, including those that impact taxes and international trade regulation; concentration of our customers in the U.S. and China, including the concentration of sales to one particular customer in the U.S.; and other risks described from time to time in Sensus Healthcare’s filings with the Securities and Exchange Commission, including our Annual Report on Form 10-K.

In addition, even if our results of operations, financial condition and liquidity, and the development of the industry in which we operate are consistent with the forward-looking statements contained in this press release, they may not be predictive of results or developments in future periods. Any forward-looking statements that we make in this press release speak only as of the date of such statement, and we undertake no obligation to update such statements to reflect events or circumstances after the date of this press release. You should read carefully our “Cautionary Note Regarding Forward-Looking Information” and the factors described in the “Risk Factors” section of our periodic reports filed with the Securities and Exchange Commission to better understand the risks and uncertainties inherent in our business.

Contact:


LHA Investor Relations
Kim Sutton Golodetz
212-838-3777
[email protected]



SSE Enterprise Telecoms Expands High-capacity Fiber Network with Infinera, Enabling 5G Across the UK

SUNNYVALE, Calif., Dec. 01, 2020 (GLOBE NEWSWIRE) — Infinera (NASDAQ: INFN) announced today that SSE Enterprise Telecoms, one of the UK’s leading connectivity providers, has selected Infinera’s XTM Series for the second phase of its UK-wide network expansion. The expanded network will bring high-capacity services to more businesses across the UK, further facilitating 5G rollouts, and aiding in the deployment of next-generation connectivity technologies such as the Industrial Internet of Things (IIoT).

With Infinera’s XTM Series, SSE Enterprise Telecoms leverages an industry-leading optical solution optimized for 5G transport with high-performance synchronization capabilities and low latency. The network’s Layer 2 packet optical aggregation features also provide enterprise customers with high-bandwidth connectivity services over the same network. These benefits extend across SSE Enterprise Telecoms’ network, which upon completion will span over 30,000 km, delivering the high-speed, performance, and reach required to support the growing digital needs of UK organizations.

“This network expansion with Infinera’s XTM Series is key to our UK initiative as it enables new technologies including the IIoT and autonomous vehicles, as well as opening the door to new business technologies such as seamless, instant video streaming and immersive virtual and augmented reality,” said Dave Eddy, COO, SSE Enterprise Telecoms. “Infinera’s XTM solution provided the high performance, scalability, and flexibility required to meet our network needs.”

“The UK market’s bandwidth is growing exponentially, and SSE Enterprise Telecoms is poised to meet this growing demand as it more than doubles its number of connected exchanges,” said Nick Walden, Senior Vice President, Sales at Infinera. “We are proud to be a part of SSE Enterprise Telecoms’ network expansion as it ushers the era of 5G with the unique capabilities of Infinera’s XTM.”

Infinera Contacts:

Media:

Anna Vue
Tel. +1 (916) 595-8157
[email protected]

Investors:

Amitabh Passi
Head of Investor Relations
[email protected]

About SSE Enterprise Telecoms

SSE Enterprise Telecoms provides class-leading connectivity and data centre services that deliver very high performance, cost efficiency and a competitive edge. The company operates a 20,000+km private telecoms network and an estate of 90 commercial data centres that span the UK. With its extensive telecoms and data centre operational expertise it offers commercial security with unrivalled in-house engineering resource.

About Infinera

Infinera is a global supplier of innovative networking solutions that enable carriers, cloud operators, governments, and enterprises to scale network bandwidth, accelerate service innovation, and automate network operations. The Infinera end-to-end packet optical portfolio delivers industry-leading economics and performance in long-haul, submarine, data center interconnect, and metro transport applications. To learn more about Infinera, visit www.infinera.com, follow us on Twitter @Infinera, and read our latest blog posts at www.infinera.com/blog.

Infinera and the Infinera logo are registered trademarks of Infinera Corporation.

This press release contains forward-looking statements. These statements are not guarantees of results and should not be considered as an indication of future activity or future performance. Actual results may vary materially from these expectations as a result of various risks and uncertainties. Information about these risks and uncertainties, and other risks and uncertainties that affect Infinera’s business, is contained in the risk factors section and other sections of Infinera’s Quarterly Report on Form 10-Q for the Fiscal Quarter ended September 26, 2020 as filed with the SEC on November 5, 2020, as well as any subsequent reports filed with or furnished to the SEC. These reports are available on Infinera’s website at www.infinera.com and the SEC’s website at www.sec.gov. Infinera assumes no obligation to, and does not currently intend to, update any such forward-looking statements.



Safe and Efficacious Treatment of Spondylolisthesis via MIS TLIF Approach with the FlareHawk® Expandable Cage

IJSS-published review finds that the novel biplanar expandable cage provides effective vertebral body slip or spondylolisthesis reduction and improvement in radiographic and clinical parameters with no reported subsidence, migration, or endplate violation

PALM BEACH GARDENS, Fla., Dec. 01, 2020 (GLOBE NEWSWIRE) — Integrity Implants Inc., a privately held medical device company dedicated to delivering innovative solutions for spine surgery, today announced the publication of another in a series of recent clinical articles in the International Journal of Spine Surgery (www.ijssurgery.com) highlighting its FlareHawk® expandable interbody cage. In their paper, Clinical and Radiographic Outcomes After Minimally Invasive Transforaminal Lumbar Interbody Fusion (MIS TLIF) – Early Experience Using a Biplanar Expandable Cage for Lumbar Spondylolisthesis (International Journal of Spine Surgery October 2020, 7125; DOI: https://doi.org/10.14444/7125), Lee A. Tan, Joshua Rivera, Xiao A. Tan, Vivian P. Le, Larry T. Khoo, and Sigurd H. Berven demonstrate favorable vertebral body slip or spondylolisthesis reduction accompanied by an increase in segmental lordosis and positive patient-reported outcomes.

The retrospective review of 13 patients treated during a one-year period found a mean slippage reduction of 6.0mm along with an improvement in segmental lordosis, increases in foraminal and posterior disc height, as well as improvement in all radiographic parameters postoperatively. Patient-reported outcome measures including VAS back, VAS leg, and EQ5D also improved across the board. There were no findings of endplate violation, cage subsidence, or cage migration, and there were no reoperations or implant-related complications.

Lee Tan, M.D., Assistant Professor of Neurological Surgery at UCSF Medical Center in San Francisco, California, shares, “My early experience shows good short-term radiographic and clinical outcomes, with almost complete reduction of spondylolisthesis postoperatively in all cases. The absence of nerve root injury is suggestive that the biplanar expandable cage is safe and obviates the need for excessive nerve root retraction during cage insertion.”

As discussed in the article, one possible explanation for the clinical success is that the expansion of the cage in the horizontal plane increases surface area contact with the endplates to better distribute the load and reduce stress, while the multi-material cage design consisting of a titanium shim inserted into a PEEK shell allows the cage to contour to the patient’s endplates, further reducing the risk of endplate violation.

Sigurd Berven, M.D., Professor in Residence, Department of Orthopaedic Surgery at the University of California at San Francisco, adds, “A challenging aspect of the MIS TLIF procedure is inserting the cage through a relatively small surgical corridor with protection of the neural elements. Additionally, in a lordotic disc space, the posterior disc height is typically shorter than the anterior disc height, thus limiting the size of cage that can be inserted posteriorly, potentially limiting the amount of lordosis restoration. In these cases that often present with a collapsed disc space and bone-on-bone pathology, the low-profile, biplanar, and lordotically expanding FlareHawk cage is ideal for reducing risk to the neural elements on insertion of the implant, and for improving the surface area of the implant with the endplate and the restoration of segmental lordosis. After insertion, the cage and prepared disc space can be filled with allograft or autograft to optimize fusion. The results of the study are encouraging regarding the efficacy of MIS fusion using the technique.”

Dr. Tan concludes, “Remarkably, we had no cases of endplate violation or cage subsidence in this cohort. This is significantly lower than the rates reported in the current literature, which range from 6% up to 33%. I believe that the biplanar expansion is key to decreasing the likelihood of subsidence.”

The FlareHawk spinal implant is the flagship product for Integrity Implants and represents the first of its kind in the expandable cage market. Much like coronary stents that offer patients a less-invasive alternative to open-heart procedures, the FlareHawk expandable cage features a PEEK shell that is inserted in a compressed form that can be effectively passed through small neural pathways, and, once within the intervertebral disc space, expanded to a larger footprint and height. An open-architecture titanium shim inserted within the PEEK shell produces the expansion and creates a solid-state construct that is resistant to collapse yet has shown the ability to conform to endplate anatomy to increase surface contact area and lower stresses. The Adaptive Geometry™ and advanced multi-material composition embodied in the FlareHawk device respect patient anatomy both during insertion and for long-term stability. To date, over 8,500 FlareHawk cages have been implanted in more than 6,000 patients.

Chris Walsh, Integrity Implants CEO, adds, “Last month, we shared the encouraging results of a multi-center study highlighting the favorable fusion efficacy and endplate conforming geometry of the FlareHawk cage. This work by surgeons Lee Tan, Sig Berven, and Larry Khoo represents the third peer-reviewed study of the FlareHawk cage this year. Beyond intrinsic cage design and performance, the study addresses a specific pathology solution that resonates with surgeons. It is encouraging to see published literature echo surgeon confidence in the FlareHawk cage, and documenting the application of Adaptive Geometry to the important and increasingly popular MIS TLIF approach is yet another step in confirming our technology as a compelling clinical choice for surgeons.”

About FlareHawk Expandable Lumbar Interbody Fusion System

The FlareHawk Interbody Fusion System is indicated for spinal intervertebral body fusion with autogenous bone graft and/or allogeneic bone graft composed of cancellous and/or corticocancellous bone in skeletally mature individuals with degenerative disc disease (DDD) at one or two contiguous levels from L2 to S1, following discectomy. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have at least six (6) months of non-operative treatment. Additionally, these patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). FlareHawk system spacers are intended to be used with supplemental fixation instrumentation, which has been cleared for use in the lumbar spine.

About Integrity Implants Inc.

Integrity Implants, founded in 2016 by seasoned business partners and spine leaders Chris Walsh and Wyatt Geist, is a privately held medical device company headquartered in Palm Beach Gardens, Florida. The Company is dedicated to delivering innovative spine products and solutions to surgeons and their patients around the globe. Its proprietary Adaptive Geometry™ technology fundamentally respects a patient’s neural, vascular, bony, and soft tissue anatomy, both during and after implantation.

For more information, please visit the Company’s website at www.integrityimplants.com.

Media Contact:

Mark Richards
512-913-9572
[email protected]



Conn’s, Inc. Schedules Conference Call to Discuss Third Quarter Fiscal Year 2021 Results

THE WOODLANDS, Texas, Dec. 01, 2020 (GLOBE NEWSWIRE) — Conn’s, Inc. (NASDAQ: CONN), a specialty retailer of furniture and mattresses, home appliances, consumer electronics, home office products and provider of consumer credit, today announced it will host a conference call on December 8, 2020 to discuss its third quarter fiscal year 2021 financial results. The conference call will begin at 10:00 A.M. CT (11:00 A.M. ET). A press release regarding the operating results will be released the same day before the market opens.

Participants can join the call by dialing 877-451-6152 or 201-389-0879. The conference call will also be broadcast simultaneously via webcast on a listen-only basis. A link to the earnings release and webcast will be available at ir.conns.com.

About Conn’s, Inc.

Conn’s HomePlus is a specialty retailer currently operating 140+ retail locations in Alabama, Arizona, Colorado, Florida, Georgia, Louisiana, Mississippi, Nevada, New Mexico, North Carolina, Oklahoma, South Carolina, Tennessee, Texas, and Virginia.

The Company’s primary product categories include:

  • Furniture and mattress, including furniture and related accessories for the living room, dining room and bedroom, as well as traditional and specialty mattresses;
  • Home appliance, including refrigerators, freezers, washers, dryers, dishwashers and ranges;
  • Consumer electronics, including LED, OLED, QLED, Ultra HD, and internet-ready televisions, gaming consoles, home theater and portable audio equipment; and
  • Home office, including computers, printers and accessories.

Additionally, Conn’s HomePlus offers a variety of products on a seasonal basis. Unlike many of its competitors, Conn’s HomePlus provides flexible in-house credit options for its customers in addition to third-party financing programs and third-party lease-to-own payment plans.

CONN-G
Investor Contact:
S.M. Berger & Company
Andrew Berger, (216) 464-6400

 



The GIANT Company Celebrates Giving Tuesday by Thanking Community Partners Working to Connect Families for a Better Future

Company Marks Global Day of Giving by Surprising Six Nonprofit Partners with Donations

CARLISLE, Pa., Dec. 01, 2020 (GLOBE NEWSWIRE) — Joining the global movement designed to celebrate philanthropy and encourage social good, this Giving Tuesday, The GIANT Company will recognize and thank six community partners in Pennsylvania that share its purpose of connecting families for a better future. GIANT Company will award product and financial donations totaling $25,000 to six local nonprofit organizations across Pennsylvania.

“Of the many lessons we’ve learned this year, one is the lasting impact an act of kindness can have and how we can change the world by giving back,” said Emily Steinkamp, social impact manager at The GIANT Company. “While The GIANT Company works 365 days a year to help make our neighborhoods and families stronger, surprising some of our incredible nonprofit partners on Giving Tuesday is a way for us to say thanks for the care and support they’ve provided to their community in a year unlike any other.”

This year, The GIANT Company is thanking the following nonprofit organizations with donations:

  • Autism Wings – Located in Plymouth Meeting, Pa., the nonprofit works to lift up the needs of individuals with autism, as well as their families and caregivers. Autism Wings has been raising funds for the Autismobile, an RV that will be converted to a mobile service delivery unit to meet clients at their homes. This donation will provide funds for the purchase and upgrades of this vehicle.

  • Big Heart Harvest – Based in Douglasville, Pa., the organization feeds the hungry by distributing goods to local soup kitchens and rescue missions, as well as personal delivery to families in need. Big Heart Harvest will use the donation to care for and provide food for chickens, whose eggs are given freely to rescue missions, soup kitchens and individuals in need.

  • Capital Area Head Start – Serving families across Harrisburg, Pa., the nonprofit prepares children and families for success in school and life while supporting children’s health and well-being. A program of Keystone Human Services, The GIANT Company’s donation will allow the organization to continue to provide nutritious and hot meals for families in need.

  • Carlisle Area Family Life Center – Headquartered in The GIANT Company’s hometown, the Carlisle Area Family Life Center aims to provide support, education, and practical assistance in a loving way to women and families. The GIANT Company will provide pallets of diapers, formula, wipes and baby supplies to families in need.

  • Power Packs Project – Located in Lancaster, Pa., the nonprofit empowers families with education and ingredients to create nutritious weekend meals, so their children return to school fed and ready to learn. Funds from The GIANT Company will help provide holiday dinners to the over 1,000 families served.

  • Shiremanstown Fire Department – The volunteer fire department serves the borough of Shiremanstown, Pa., and provides mutual aid response to neighboring townships. The fire department will use this donation to purchase training aids for members.

“Thanks to this generous gift from The GIANT Company, Autism Wings is now one step closer to soaring into our community,” said Angela Walden, founder and CEO, Autism Wings. “This donation will go toward the purchase of what is probably the most crucial element of our services, a recreational vehicle. We will convert this vehicle into a mobile work, play, social, and break space, bringing our services to the front door of youth with autism who live in our community.”

The GIANT Company’s Giving Tuesday donation continues the company’s longstanding tradition of giving back during the holiday season. Last month, the company donated a record-breaking 10,000 turkeys to 28 partner food banks located across its footprint in time for Thanksgiving. Team members from GIANT and MARTIN’S also contributed 500 volunteer hours to help pack boxes and restock shelves in advance of the busy holiday season. The GIANT Company is also hosting an in-store food drive through Thursday, Dec. 3 to further stock the shelves of community hunger relief organizations.

Established in 2012, Giving Tuesday falls on the Tuesday after Thanksgiving and kicks off the charitable season, when many focus on holiday and end-of-year giving. Charities, families, businesses, and community centers alike come together for one common purpose: to celebrate generosity and to give back. For more information, visit www.givingtuesday.org.

About
The
GIANT Company

The GIANT Company
 
believes that no matter where or how, when meals happen, families connect, and when families connect meaningfully, good happens. Guided by its brand platform, For Today’s Table™, the omni-channel retailer proudly serves millions of neighbors across Pennsylvania, Maryland, Virginia and West Virginia. A Great Place to Work™ certified company with more than 35,000 talented team members supporting nearly 190 stores, 132 pharmacies, 105 fuel stations, and over 145 online pickup hubs and grocery delivery service in hundreds of zip
codes, The GIANT Company is changing the customer experience and connecting families for a better future. Founded in 1923 in Carlisle, Pa., The GIANT Company family of brands includes GIANT, MARTIN’S, GIANT Heirloom Market, GIANT Direct and MARTIN’S Direct. The GIANT Company is a company of Ahold Delhaize USA. For more information, visit the
 

GIANT

 
or
 

MARTIN’S

 
websites.

CONTACT:
Ashley Flower
860-966-1727
[email protected]



Shaw Provides Dividend Rate Notice for Cumulative Redeemable Floating Rate Class 2 Preferred Shares, Series B

CALGARY, Alberta, Dec. 01, 2020 (GLOBE NEWSWIRE) — Shaw Communications Inc. (“Shaw”) announced today that it has given the registered shareholders of its Cumulative Redeemable Floating Rate Class 2 Preferred Shares, Series B (the “Series B Shares”) notice of dividend rates.

The Floating Quarterly Dividend Rate for the Series B Shares was set at 2.109% for the Quarterly Floating Rate Period from and including December 31, 2020 to, but excluding, March 31, 2021. The Floating Quarterly Dividend Rate will be reset every quarter.

The Series B Shares are listed on the Toronto Stock Exchange under the ticker symbol SJR.PR.B.

About Shaw Communications Inc.

Shaw Communications Inc. is a leading Canadian connectivity company. The Wireline division consists of Consumer and Business services. Consumer serves residential customers with broadband Internet, Shaw Go WiFi, video and digital phone. Business provides business customers with Internet, data, WiFi, digital phone, and video services. The Wireless division provides wireless voice and LTE data services through an expanding and improving mobile wireless network infrastructure.

Shaw is traded on the Toronto and New York stock exchanges and is included in the S&P/TSX 60 Index (Symbol: TSX – SJR.B, SJR.PR.A, SJR.PR.B, NYSE – SJR, and TSXV – SJR.A). For more information, please visit www.shaw.ca.

For further information, please contact:
Shaw Investor Relations [email protected]



AVITA Therapeutics Appoints Kathy McGee as Chief Operating Officer

VALENCIA, Calif, and MELBOURNE, Australia, Dec. 01, 2020 (GLOBE NEWSWIRE) — AVITA Therapeutics, Inc. (NASDAQ: RCEL, ASX:AVH), a regenerative medicine company that is developing and commercializing a technology platform that enables point-of-care autologous skin restoration for multiple unmet needs, announced today the appointment of Kathy McGee as Chief Operating Officer, effective December 1, 2020.

“Kathy’s extensive healthcare experience and industry insight are a welcome addition to AVITA’s leadership team,” said Dr. Mike Perry, AVITA Therapeutics’ Chief Executive Officer. “In particular her broad operational experience within Regenerative Medicine will be critically important as we seek to bring our pipeline products through development and into the markets.”

Ms. McGee joins AVITA with over 25 years of biopharmaceutical and life sciences experience, most recently serving as President of CnA Consulting Group, which focuses on providing specialized consulting services to the life sciences industry. Prior to CnA Consulting, Ms. McGee was the Vice President of West Coast Operations at Shire Pharmaceuticals Regenerative Medicine Division, formerly Advanced BioHealing, where she was a part of the leadership team responsible for manufacturing operations, strategic planning, capital expansion, and real estate. At Advanced BioHealing, Ms. McGee served as the Senior Vice President of Operations and General Manager, with responsibility for the company’s manufacturing operations in La Jolla, CA. She has also held senior Operations leadership roles at Smith and Nephew and Advanced Tissue Sciences. She earned her Bachelor of Science in chemistry and mathematics from University College Galway Ireland, and holds a Master’s degree in Business and Management from Webster University.

Authorized for release by the Chief Executive Officer of AVITA Therapeutics, Inc.

ABOUT AVITA
THERAPEUTICS, INC.

AVITA Therapeutics is a regenerative medicine company with a technology platform positioned to address unmet medical needs in burns, chronic wounds, and aesthetics indications. AVITA Therapeutics’ patented and proprietary collection and application technology provides innovative treatment solutions derived from the regenerative properties of a patient’s own skin. The medical devices work by preparing a RES® REGENERATIVE EPIDERMAL SUSPENSION, an autologous suspension comprised of the patient’s skin cells necessary to regenerate natural healthy epidermis. This autologous suspension is then sprayed onto the areas of the patient requiring treatment.

AVITA Therapeutics’ first U.S. product, the RECELL® System, was approved by the U.S. Food and Drug Administration (FDA) in September 2018. The RECELL System is indicated for use in the treatment of acute thermal burns in patients 18 years and older. The RECELL System is used to prepare Spray-On Skin™ Cells using a small amount of a patient’s own skin, providing a new way to treat severe burns, while significantly reducing the amount of donor skin required. The RECELL System is designed to be used at the point of care alone or in combination with autografts depending on the depth of the burn injury. Compelling data from randomized, controlled clinical trials conducted at major U.S. burn centers and real-world use in more than 8,000 patients globally, reinforce that the RECELL System is a significant advancement over the current standard of care for burn patients and offers benefits in clinical outcomes and cost savings. Healthcare professionals should read the INSTRUCTIONS FOR USE – RECELL® Autologous Cell Harvesting Device (https://recellsystem.com/) for a full description of indications for use and important safety information including contraindications, warnings and precautions.

In international markets, our products are marketed under the RECELL System brand to promote skin healing in a wide range of applications including burns, chronic wounds and aesthetics. The RECELL System is TGA-registered in Australia and received CE-mark approval in Europe.
To learn more, visit www.avitamedical.com.

CAUTIONARY NOTE REGARDING FORWARD-LOOKING STATEMENTS

This letter includes forward-looking statements. These forward-looking statements generally can be identified by the use of words such as “anticipate,” “expect,” “intend,” “could,” “may,” “will,” “believe,” “estimate,” “look forward,” “forecast,” “goal,” “target,” “project,” “continue,” “outlook,” “guidance,” “future,” other words of similar meaning and the use of future dates.
Forward-looking statements in this letter include, but are not limited to, statements concerning, among other things, our ongoing clinical trials and product development activities, regulatory approval of our products, the potential for future growth in our business, and our ability to achieve our key strategic, operational and financial goal.
Forward-looking statements by their nature address matters that are, to different degrees, uncertain.
Each forward- looking statement contained in this letter is subject to risks and uncertainties that could cause actual results to differ materially from those expressed or implied by such statement. Applicable risks and uncertainties include, among others, the timing of regulatory approvals of our products; physician acceptance, endorsement, and use of our products; failure to achieve the anticipated benefits from approval of our products; the effect of regulatory actions; product liability claims; risks associated with international operations and expansion; and other business effects, including the effects of industry, economic or political conditions outside of the company’s control.
Investors should not place considerable reliance on the forward-looking statements contained in this letter.
Investors are encouraged to read our publicly available filings for a discussion of these and other risks and uncertainties.
The forward-looking statements in this letter speak only as of the date of this release, and we undertake no obligation to update or revise any of these statements.

FOR FURTHER INFORMATION:


U.S. Media

Sam Brown, Inc.

Christy Curran
Phone +1 615 414 8668
[email protected]

O.U.S Media
Monsoon Communications
Rudi Michelson
Phone +61 (0)3 9620 3333
Mobile +61 (0)411 402 737
[email protected]



Investors:

Westwicke
Partners

Caroline Corner
Phone +1 415 202 5678
[email protected]



AT&T SportsNet returns to Verizon Fios

BASKING RIDGE, N.J., Dec. 01, 2020 (GLOBE NEWSWIRE) — Verizon Fios and AT&T SportsNet Pittsburgh have reached a long-term agreement to relaunch the regional sports network to Fios customers in the Pittsburgh and Harrisburg areas. Relaunching AT&T SportsNet, the broadcast home of the Pittsburgh Pirates and Pittsburgh Penguins, allows baseball and hockey fans in the region to enjoy watching their local teams in the upcoming seasons. 

Fios TV customers can watch a wide range of programming on AT&T SportsNet Pittsburgh beginning Tuesday, December 1st. AT&T SportsNet will be viewable in the Pittsburgh area on channels 76 and 1525, and in HD on channel 576. In the Harrisburg area, AT&T SportsNet Pittsburgh will be available on channels 78 and 1527, and in HD on channel 578. AT&T SportsNet alternate is available in both Pittsburgh and Harrisburg on channels 81 and 1528, and in HD on channel 581 when there are programming conflicts on AT&T SportsNet’s primary channels.

Verizon today issued the following statement:

“Verizon is pleased to reach an agreement with AT&T SportsNet Pittsburgh that enables us to offer the channel to Fios TV customers. We look forward to carrying AT&T SportsNet Pittsburgh so Fios customers can focus on cheering for the Pirates and Penguins in the weeks and years to come.”

AT&T SportsNet Pittsburgh issued the following statement:

“We are very pleased that Verizon Fios customers who are fans of the Pittsburgh Pirates and Penguins will again have access to watch their favorite teams’ games.”

Verizon Communications Inc. (NYSE, Nasdaq: VZ) was formed on June 30, 2000 and is celebrating its 20th year as one of the world’s leading providers of technology, communications, information and entertainment products and services. Headquartered in New York City and with a presence around the world, Verizon generated revenues of $131.9 billion in 2019. The company offers data, video and voice services and solutions on its award-winning networks and platforms, delivering on customers’ demand for mobility, reliable network connectivity, security and control.

VERIZON’S ONLINE MEDIA CENTER: News releases, stories, media contacts and other resources are available at https://www.verizon.com/about/media-center. News releases are also available through an RSS feed. To subscribe, visit www.verizon.com/about/rss-feeds/.

Verizon Fios Media Contact:

Andrew Kameka
[email protected]

AT&T SportsNet Media Contact
:

Randi Lackscheide
[email protected]