Horizon Therapeutics plc and Halozyme Therapeutics, Inc. Enter Global Collaboration and License Agreement for ENHANZE® Technology

Horizon Therapeutics plc and Halozyme Therapeutics, Inc. Enter Global Collaboration and License Agreement for ENHANZE® Technology

– Horizon to use ENHANZE® subcutaneous delivery technology for TEPEZZA® (teprotumumab-trbw) –

DUBLIN & SAN DIEGO–(BUSINESS WIRE)–
Horizon Therapeutics plc (Nasdaq: HZNP) and Halozyme Therapeutics, Inc. (Nasdaq: HALO) today announced a global collaboration and license agreement that gives Horizon exclusive access to Halozyme’s ENHANZE® drug delivery technology for subcutaneous (SC) formulation of medicines targeting IGF-1R. Horizon intends to use ENHANZE® to develop a SC formulation of TEPEZZA (teprotumumab-trbw), indicated for the treatment of Thyroid Eye Disease, a serious, progressive and vision-threatening rare autoimmune disease,1 potentially shortening drug administration time, reducing healthcare practitioner time and offering additional flexibility and convenience for patients.

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Under the terms of the agreement, Horizon will make an upfront payment of $30 million to Halozyme and is obligated to make potential future payments of up to $160 million in the aggregate, subject to achievement of specified development, regulatory and sales-based milestones. Halozyme will also be entitled to receive mid-single digit royalties on sales of commercialized medicines using the ENHANZE® technology.

“Our goal with all of our medicines is to optimize the patient experience,” said Tim Walbert, chairman, president and chief executive officer, Horizon. “As we continue to explore subcutaneous administration for TEPEZZA to provide greater flexibility for patients and physicians, access to the ENHANZE® technology, which has been deployed successfully in multiple biologics, represents an important step in our development efforts.”

“We are thrilled to announce our tenth collaboration and license agreement for ENHANZE® and look forward to working closely with Horizon to develop TEPEZZA with ENHANZE®,” said Dr. Helen Torley, president and chief executive officer, Halozyme. “The launch of TEPEZZA has been one of the most successful and exciting launches in rare disease medicine and is making a difference in the lives of patients suffering from Thyroid Eye Disease.”

Horizon represents Halozyme’s tenth global collaboration and license partner for the ENHANZE® technology. These collaborations cover more than 50 therapeutic targets and include five commercialized products to date.

About ENHANZE® Technology

Halozyme’s proprietary ENHANZE® drug-delivery technology is based on its patented recombinant human hyaluronidase enzyme (rHuPH20). rHuPH20 has been shown to remove traditional limitations on the volume of biologics that can be delivered subcutaneously (just under the skin). By using rHuPH20, some biologics and compounds that are administered intravenously may instead be delivered subcutaneously. ENHANZE® may also benefit subcutaneous biologics by reducing the need for multiple injections. This delivery has been shown in studies to reduce health care practitioner time required for administration and shorten time for drug administration.

About Horizon

Horizon is focused on researching, developing and commercializing medicines that address critical needs for people impacted by rare and rheumatic diseases. Our pipeline is purposeful: we apply scientific expertise and courage to bring clinically meaningful therapies to patients. We believe science and compassion must work together to transform lives. For more information on how we go to incredible lengths to impact lives, please visit www.horizontherapeutics.com and follow us on Twitter, LinkedIn, Instagram and Facebook.

Horizon Safe Harbor Statement

This press release contains forward-looking statements, including, but not limited to, statements related to the potential benefits of ENHANZE® and a subcutaneous formulation of TEPEZZA, Horizon’s strategy, plans, objectives, expectations and intentions, including with respect to the potential development of a subcutaneous formulation of TEPEZZA, and other statements that are not historical facts. These forward-looking statements are based on Horizon’s expectations and assumptions as of the date of this press release and inherently involve significant risks and uncertainties. Actual results may differ materially from those in these forward-looking statements as a result of these risks and uncertainties, which include, without limitation, risks associated with the development, regulatory approval and commercialization of novel medicines or formulations of existing medicines, as well as those described in Horizon’s filings with the United States Securities and Exchange Commission, including those factors discussed under the caption “Risk Factors” in those filings. Forward-looking statements speak only as of the date of this press release and Horizon does not undertake any obligation to update or revise these statements, except as may be required by law.

About Halozyme

Halozyme is a biopharmaceutical company bringing disruptive solutions to significantly improve patient experiences and outcomes for emerging and established therapies. Halozyme advises and supports its biopharmaceutical partners in key aspects of new drug development with the goal of improving patients’ lives while helping its partners achieve global commercial success. As the innovators of the ENHANZE® technology, which can reduce hours-long treatments to a matter of minutes, Halozyme’s commercially validated solution has positively impacted more than 400,000 patient lives via five commercialized products across more than 100 global markets. Halozyme and its world-class partners are currently advancing multiple therapeutic programs intended to deliver innovative therapies, with the potential to improve the lives of patients around the globe. Halozyme’s proprietary enzyme rHuPH20 forms the basis of the ENHANZE® technology and is used to facilitate the delivery of injected drugs and fluids, potentially reducing the treatment burden of other drugs to patients. Halozyme has licensed its ENHANZE® technology to leading pharmaceutical and biotechnology companies including Roche, Baxalta, Pfizer, Janssen, AbbVie, Lilly, Bristol-Myers Squibb, Alexion, argenx and Horizon Therapeutics. Halozyme derives revenues from these collaborations in the form of milestones and royalties as the Company’s partners make progress developing and commercializing their products being developed with ENHANZE®. Halozyme is headquartered in San Diego. For more information visit www.halozyme.com.

Halozyme Safe Harbor Statement

In addition to historical information, the statements set forth above include forward-looking statements including, without limitation, statements concerning the possible activity, benefits and attributes of ENHANZE®, the possible method of action of ENHANZE®, its potential application to aid in the dispersion and absorption of other injected therapeutic drugs and statements concerning certain other potential benefits of ENHANZE® including facilitating more rapid delivery of injectable medications through subcutaneous delivery and potentially lowering the treatment burden for patients. These forward-looking statements also include statements regarding the product development and regulatory efforts of Halozyme’s ENHANZE® partner and Halozyme’s potential receipt of payments associated with achievement of certain development, regulatory and sales-based milestones, and royalties on sales of commercialized products. These forward-looking statements involve risks and uncertainties that could cause actual results to differ materially from those in the forward-looking statements. The forward-looking statements are typically, but not always, identified through use of the words “believe,” “enable,” “may,” “will,” “could,” “intends,” “estimate,” “anticipate,” “plan,” “predict,” “probable,” “potential,” “possible,” “should,” “continue” and other words of similar meaning. Actual results could differ materially from the expectations contained in forward-looking statements as a result of several factors, including uncertainties concerning whether development, regulatory and sales-based milestones will be achieved, uncertainties concerning whether collaborative products are ultimately developed or commercialized, unexpected expenditures and costs, unexpected results or delays in development and regulatory review including potential delays caused by the current COVID-19 global pandemic, unexpected regulatory approval requirements, unexpected adverse events or patient outcomes and competitive conditions. These and other factors that may result in differences are discussed in greater detail in Halozyme’s most recent Annual and Quarterly Reports filed with the Securities and Exchange Commission. Except as required by law, Halozyme undertakes no duty to update forward-looking statements to reflect events after the date of this release.

About TEPEZZA

INDICATION

TEPEZZA is indicated for the treatment of Thyroid Eye Disease.

IMPORTANT SAFETY INFORMATION

Warnings and Precautions

Infusion Reactions: TEPEZZA may cause infusion reactions. Infusion reactions have been reported in approximately 4% of patients treated with TEPEZZA. Reported infusion reactions have usually been mild or moderate in severity. Signs and symptoms may include transient increases in blood pressure, feeling hot, tachycardia, dyspnea, headache and muscular pain. Infusion reactions may occur during an infusion or within 1.5 hours after an infusion. In patients who experience an infusion reaction, consideration should be given to premedicating with an antihistamine, antipyretic or corticosteroid and/or administering all subsequent infusions at a slower infusion rate.

Preexisting Inflammatory Bowel Disease: TEPEZZA may cause an exacerbation of preexisting inflammatory bowel disease (IBD). Monitor patients with IBD for flare of disease. If IBD exacerbation is suspected, consider discontinuation of TEPEZZA.

Hyperglycemia: Increased blood glucose or hyperglycemia may occur in patients treated with TEPEZZA. In clinical trials, 10% of patients (two-thirds of whom had preexisting diabetes or impaired glucose tolerance) experienced hyperglycemia. Hyperglycemic events should be managed with medications for glycemic control, if necessary. Monitor patients for elevated blood glucose and symptoms of hyperglycemia while on treatment with TEPEZZA. Patients with preexisting diabetes should be under appropriate glycemic control before receiving TEPEZZA.

Adverse Reactions

The most common adverse reactions (incidence ≥5% and greater than placebo) are muscle spasm, nausea, alopecia, diarrhea, fatigue, hyperglycemia, hearing impairment, dysgeusia, headache and dry skin.

For additional information on TEPEZZA, please see Full Prescribing Information at TEPEZZAhcp.com.

References

  1. Barrio-Barrio J, et al. Graves’ Ophthalmopathy: VISA versus EUGOGO Classification, Assessment and Management. Journal of Ophthalmopathy. 2015;2015:1-16.

Horizon contacts:

Tina Ventura

Senior Vice President, Investor Relations

[email protected]

Ruth Venning

Executive Director, Investor Relations

[email protected]

U.S. Media Contacts:

Geoff Curtis

Executive Vice President, Corporate Affairs & Chief Communications Officer

[email protected]

Ireland Media Contact:

Gordon MRM

Ray Gordon

[email protected]

Halozyme contact:

Al Kildani

Vice President, Investor Relations and Corporate Communications

858-704-8122

[email protected]

KEYWORDS: Ireland Europe

INDUSTRY KEYWORDS: Biotechnology General Health Pharmaceutical Health

MEDIA:

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Benchmark Corp. and Metsi form global partnership to bridge client skills gap to accelerate digital maturity, leverage open source and reduce OPEX

TORONTO, Nov. 23, 2020 (GLOBE NEWSWIRE) — Benchmark Corp., a Canadian software solutions provider focused on open source technology to optimize operations, boost productivity and support scalable growth, and Metsi Technologies, a global digital systems integrator delivering IT automation, integration, and orchestration for software-defined data centers, have joined together to manage critical skills gaps and accelerate digital transformation for enterprise clients.

“It’s a challenging time for clients trying to balance their digital transformation goals, navigate the global pandemic, manage a remote workforce and reduce OPEX,” says Luc Villeneuve, President, Benchmark Corp. “At Benchmark Corp. we pride ourselves on being a trusted partner offering the latest capabilities in DevOps, DevSecOps and containerization to fill skills gaps, and cost-effectively accelerate the journey to the hybrid cloud. We are thrilled to collaborate with a leader like Metsi who brings an outstanding global reputation in automation and cloud acceleration. Their strong partnerships with leaders like Cisco have positioned them as the go-to leader for secure complex cloud integration. This aligns perfectly with our skills, allowing us to offer our clients world-class customized solutions and consultation with white-glove boutique service.”

This partnership is particularly timely as leaders navigate the new normal of Covid-19 managing a remote workforce that requires secure cloud adoption and application modernization, says Rachael Babcock, CEO for the Americas, Metsi Technologies. “Metsi and Benchmark Corp. know IT leaders are dealing with fierce competition to recruit and retain the best talent,” adds Babcock. “Our goal is to distinguish our brands in the marketplace by blending our open source expertise with our vast partner ecosystem of innovation leaders like Cisco, Red Hat, IBM, Centreon, HashiCrop, Sumo Logic, etc. Together we can leap in to fill critical skill gaps and deliver a comprehensive solution that leverages the best expertise in the industry.”

Please watch a short video clip of Luc and Rachael discussing their new partnership.

Adds Mik Hillewaert, Global CEO, Metsi Technologies: “We value our partnership with Benchmark because of their technical thought leadership in automating open source technologies, particularly with cloud adoption and DevOps automation.  Metsi’s extensive expertise in delivering automation with both open and closed source software from leading industry OEMs enables us to deliver a cohesive software automation experience worldwide.”

This is another strategic move by Benchmark Corp. to provide value to our customers by aligning our skills with the most talented partners from around the world, says Kam Sabouri, Managing Director, Benchmark Corp. “I am delighted to partner with Metsi to help our growing customer base solve their greatest challenges with high-quality solutions and talent.”

ABOUT
BENCHMARK CORP.

Founded in 2003, Benchmark is a proven Canadian IT solutions provider that delivers leading-edge expertise and custom solutions, with flexible financing, to its long-term commercial and enterprise customers. We focus on helping customers cost-efficiently transform their data center and meet other business needs with innovative solutions that optimize operations, boost productivity and support scalable growth. www.benchmarkcorp.com.

ABOUT

METSI TECH


N


OLOGIES:


Metsi is a global digital systems integrator, with main offices in the U.S., UK, Germany, and The Netherlands and distributed resources throughout Europe, Africa, and India. Metsi delivers IT automation, integration, and orchestration for Software-Defined Data Centers and is a Cisco Integrator Partner. Metsi’s automation services include workload management and orchestration, hybrid multi-cloud management (Cisco CloudCenter, Morpheus), full stack visibility and performance (AppDynamics, Dynatrace, Tetration, Turbonomic, NetBrain), infrastructure as code, container management (Kubernetes), and IT Self Service (ServiceNow, PMG). Metsi provides integration and automation across the entire IT stack with industry-leading OEMs, including but not limited to, Cisco, Red Hat, AWS, and VMware.

Media contact: Alix Edmiston, [email protected], Cell: 416 809-9996



Cue Biopharma to Present at the Piper Sandler 32nd Annual Healthcare Conference

CAMBRIDGE, Mass., Nov. 23, 2020 (GLOBE NEWSWIRE) — Cue Biopharma, Inc. (Nasdaq: CUE), a clinical-stage biopharmaceutical company engineering a novel class of injectable biologics designed to selectively engage and modulate targeted T cells within the patient’s body, announced today that it participated in a pre-recorded fireside chat as part of the Piper Sandler 32nd Annual Virtual Healthcare Conference, being held on December 1-3, 2020.

The pre-recorded presentation will be available to participants during the conference and on the Events page of the Investors & Media section of the Company’s website www.cuebiopharma.com beginning today, November 23, 2020 at 10:00 a.m. EST. An archived version of the recording will be accessible for 90 days following the event.

About Cue Biopharma

Cue Biopharma, a clinical-stage biopharmaceutical company, is engineering a novel class of injectable biologics to selectively engage and modulate targeted T cells within the patient’s body to transform the treatment of cancer, infectious diseases and autoimmune diseases. The company’s proprietary platform, Immuno-STAT™ (Selective Targeting and Alteration of T cells) is designed to harness the body’s intrinsic immune system without the need for ex vivo manipulation.

Headquartered in Cambridge, Massachusetts, we are led by an experienced management team and independent Board of Directors with deep expertise in the design and clinical development of protein biologics, immunology and immuno-oncology.

For more information, visit www.cuebiopharma.com and follow us on Twitter https://twitter.com/CueBiopharma.

Investor Contact

George B. Zavoico, Ph.D.
VP, Investor Relations & Corporate Development
Cue Biopharma, Inc.
[email protected]

Media Contact

Alison Chen
LifeSci Communications
[email protected] 



Ocular Therapeutix™ to Present at the Piper Sandler 32nd Annual Virtual Healthcare Conference

Ocular Therapeutix™ to Present at the Piper Sandler 32nd Annual Virtual Healthcare Conference

BEDFORD, Mass.–(BUSINESS WIRE)–
Ocular Therapeutix, Inc. (NASDAQ:OCUL) a biopharmaceutical company focused on the formulation, development, and commercialization of innovative therapies for diseases and conditions of the eye, today announced that it will present at the Piper Sandler 32nd Annual Virtual Healthcare Conference being held from December 1 to December 3, 2020.

In addition to a fireside chat, the management team will host virtual investor meetings on Wednesday, December 2nd at the conference. Investors participating in the conference who are interested in meeting with Ocular Therapeutix management should contact their Piper Sandler representative.

A webcast of the pre-recorded fireside chat presentation has been made available ahead of the conference and can be accessed by visiting the Investors section of the Company’s website at investors.ocutx.com. It will be available for replay for 90 days.

About Ocular Therapeutix, Inc.

Ocular Therapeutix, Inc. is a biopharmaceutical company focused on the formulation, development, and commercialization of innovative therapies for diseases and conditions of the eye using its proprietary bioresorbable hydrogel-based formulation technology. Ocular Therapeutix’s first commercial drug product, DEXTENZA, is FDA-approved for the treatment of ocular inflammation and pain following ophthalmic surgery. Ocular Therapeutix recently completed a Phase 3 clinical trial evaluating DEXTENZA for the treatment of ocular itching associated with allergic conjunctivitis. Ocular Therapeutix’s earlier stage development assets currently in Phase 1 clinical trials include OTX-TIC (travoprost intracameral implant) for the reduction of intraocular pressure in patients with primary open-angle glaucoma or ocular hypertension and OTX-TKI (axitinib intravitreal implant) for the treatment of wet AMD and other retinal diseases. Ocular Therapeutix is currently evaluating OTX-CSI (cyclosporine intracanalicular insert) for the chronic treatment of dry eye disease in a Phase 2 clinical trial. Also, Ocular Therapeutix is currently developing OTX-DED (dexamethasone intracanalicular insert) for the short-term treatment of the signs and symptoms of dry eye disease and, in collaboration with Regeneron, OTX-AFS (aflibercept suprachoroidal injection) as an extended-delivery formulation of aflibercept for the treatment of retinal diseases. Ocular Therapeutix’s first product, ReSure® Sealant, is an FDA-approved device to seal corneal incisions following cataract surgery.

Investors

Ocular Therapeutix

Donald Notman

Chief Financial Officer

[email protected]

Media

Ocular Therapeutix

Scott Corning

Senior Vice President, Commercial

[email protected]

or

Westwicke, an ICR Company

Chris Brinzey, 339-970-2843

[email protected]

KEYWORDS: Massachusetts United States North America

INDUSTRY KEYWORDS: Research FDA Clinical Trials Biotechnology General Health Pharmaceutical Health Optical Science Other Science

MEDIA:

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Award-Winning FinTech Monit Announces New Features for Banks to Foster Deeper, More Profitable Relationships with Business Customers

Data-driven Insights Level the Playing Field for Community Banks and Credit Unions Competing with Mega-Banks

BOSTON, Nov. 23, 2020 (GLOBE NEWSWIRE) — Monit, the award-winning mobile predictive financial platform for small businesses, today announced new features for banks that offer Monit to their small business customers. Using predictive intelligence, Monit offers banks a high-level, holistic overview of the health of their aggregated portfolio of small-business customers, as well as digital tools to better serve those customers.

“The industry is seeing a clear trend of mega-banks investing heavily in digital services to support their business customers by connecting to accounting and other critical services while layering predictive analytics and guidance,” said Steve Dow, CEO and co-founder of Monit and a former business banking executive at Webster Bank. “The Monit platform enables community banks and credit unions to punch above their weight by leveraging predictive intelligence to give community bankers new insights to understand what their business customers need and when to offer it. With Monit, bankers can be more than just a vendor to their small businesses and get back to being a trusted advisor to their clients. In doing so, banks will realize deeper relationships and boost their bottom line.”

Monit keeps small business owners on top of their finances in a way that accounting software alone cannot. According to a recent survey, 74 percent of small businesses would switch banks to get access to predictive financial tools, and 90 percent want a “one-stop” digital experience pulling everything together in one place, creating a competitive opportunity for banks. Now, in addition to that advantage, Monit’s predictive intelligence offers community banks the data and insights they need to better serve small business customers. Most small businesses have three to five relationships with banks or other financial institutions, creating giant data blind spots for banks who want to understand and help their small business customers.

Monit’s new bank features help bankers understand, target, and connect with small business customers. First, Monit provides a holistic and complete view of the bank’s aggregated portfolio of customers built from information on each entire business, including data beyond the bank’s internal view of the customer. Second, Monit allows bankers to filter and target customers for bank offers based on specific current and predicted signals about the business, while maintaining privacy. Finally, Monit can deliver to the banker “next-best action” alerts, proactive suggestions on specific clients based on the changing business situation, that can serve as a banker’s to-do list and give bankers insight into which customers to focus on each day.

Eastern Bank is the number one SBA small business lender in the New England region, and began offering Monit to its customers earlier this year. “We see technology as an essential enabler to delivering the highest quality customer experience and increasing the convenience of working with us,” said Ashley Nagle Eknaian, chief digital strategist and head of Eastern Labs at Eastern Bank. “Small business customers tend to continually look for ways to ensure their business is sustainable. Monit’s platform allows us to help them visualize their finances, which can lead to more opportunity to realize their long-term growth plans. It enables us to deepen relationships with our customers, and we see Monit as a real differentiator for us in the market.”

For more information about Monit and its new bank features, go to: https://www.monitapp.io/

Monit will demonstrate its new bank features at FinovateWest Digital. Finovate attendees can watch the demo today, November 23, at 9:05 a.m. PT. at https://informaconnect.com/finovatewest/
For more information about the Monit demo at FinovateWest, go to: https://informaconnect.com/finovatewest/sponsors/monit/
Monit was recently awarded Best in Show at FinovateFall Digital 2020.

About Monit

Monit is a Boston-based predictive intelligence technology company dedicated to the success of business owners and the financial institutions that serve them. Monit’s founding team combines digital enterprise advice capabilities with real-world banking, small business, and regulated financial institution experience. Monit is privately funded with investment from notable individual investors and bank partners, and the principals of the Venture Capital Fund of New England (VCFNE) and Hyperplane VC. Learn more at www.MonitApp.io and engage with Monit on LinkedIn or Twitter.



Media contact:
Chris Fucanan
[email protected]
916-684-9781

Voya Prime Rate Trust Announces Intention to Conduct Tender Offer for its Common Shares

Voya Prime Rate Trust Announces Intention to Conduct Tender Offer for its Common Shares

SCOTTSDALE, Ariz.–(BUSINESS WIRE)–
Voya Prime Rate Trust (NYSE: PPR) (the “Fund”), today announced its intention to commence a tender offer for 15% of its outstanding common shares.

At the Fund’s 2020 annual meeting, shareholders approved a resolution requesting that the Board of Trustees of the Fund (the “Board”) consider authorizing a self-tender offer for 40% of the outstanding common shares of the Fund at or close to the net asset value of the common shares.

As a result, the Board has determined to authorize the Fund to conduct a tender offer for 15% of its outstanding common shares at a price equal to 99% of the Fund’s NAV per share as determined as of the close of the regular trading session of the New York Stock Exchange (“NYSE”) on the day the tender offer expires. The Fund expects to commence the tender offer in early December 2020, with the expiration of the tender offer currently anticipated to occur in January 2021. Additional terms and conditions of the Fund’s tender offer will be set forth in the relevant tender offer materials, which will be distributed to the Fund’s common shareholders. If more than 15% of the Fund’s outstanding common shares are tendered, the Fund will purchase its shares from tendering shareholders on a pro rata basis at a price equal to 99% of the Fund’s NAV per share as determined as of the close of the regular trading session of the NYSE on the day the tender offer expires.

Following the completion of the tender offer, the Board expects to consider authorizing one or more additional tender offers in line with the resolution approved by shareholders.

Important Notice

This press release is for informational purposes only and shall not constitute a recommendation or an offer or a solicitation to buy any common shares. The Fund has not yet commenced the tender offer described in this press release. The offer to purchase Fund common shares will be made pursuant to an offer on Schedule TO. COMMON SHAREHOLDERS ARE URGED TO READ THE TENDER OFFER MATERIALS, INCLUDING THE OFFER TO PURCHASE AND ANY SOLICITATION/RECOMMENDATION STATEMENT REGARDING THE TENDER OFFER, AS THEY MAY BE AMENDED OR SUPPLEMENTED FROM TIME TO TIME, BECAUSE THEY CONTAIN IMPORTANT INFORMATION THAT HOLDERS OF COMMON SHARES SHOULD CONSIDER BEFORE MAKING ANY DECISION REGARDING TENDERING THEIR SHARES. Common shareholders may obtain a free copy of any of these statements and other documents when they are filed with the U.S. Securities and Exchange Commission (“SEC”) at the website maintained by the SEC at www.sec.gov or by directing such requests to the Fund.

About Voya® Investment Management

A leading, active asset management firm, Voya Investment Management manages, as of September 30, 2020, over $238 billion for affiliated and external institutions as well as individual investors. With more than 40 years of history in asset management, Voya Investment Management has the experience and resources to provide clients with investment solutions with an emphasis on equities, fixed income, and multi-asset strategies and solutions. Voya Investment Management was named in 2015, 2016, 2017, 2018 and 2019 as a “Best Places to Work” by Pensions and Investments magazine. For more information, visit voyainvestments.com. Follow Voya Investment Management on Twitter @VoyaInvestments.

SHAREHOLDER INQUIRIES: Shareholder Services at (800) 992-0180; voyainvestments.com 

CONTACT:  Kris Kagel, (800) 992-0180

KEYWORDS: United States North America Arizona

INDUSTRY KEYWORDS: Banking Professional Services Finance

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Shenandoah Telecommunications to Present at the UBS Global TMT Conference

EDINBURG, Va., Nov. 23, 2020 (GLOBE NEWSWIRE) — Shenandoah Telecommunications Company (Shentel) (NASDAQ: SHEN) today announced that Dave Heimbach, Executive Vice President & Chief Operating Officer and Jim Volk, Senior Vice President & Chief Financial Officer, will participate in a fireside chat at the UBS Global TMT Conference on Tuesday, December 8, 2020 at 7:30 a.m. ET. Investors may access a live webcast of the event on Shentel’s website at www.investor.shentel.com. The webcast will be available for replay for a limited time on Shentel’s website following the presentation.

About Shenandoah Telecommunications

Shenandoah Telecommunications Company (Shentel) provides a broad range of diversified communications services through its high speed, state-of-the-art wireless, cable, fiber optic and fixed wireless networks to customers in the Mid-Atlantic United States. The Company’s services include: wireless voice and data; broadband internet, video, and digital voice; fiber optic Ethernet, wavelength and leasing; telephone voice and digital subscriber line; and tower colocation leasing. Shentel is the exclusive personal communications service (“PCS”) Affiliate of Sprint in a multi-state area covering large portions of central and western Virginia, south-central Pennsylvania, West Virginia, and portions of Maryland, Kentucky, and Ohio. For more information, please visit www.shentel.com.

CONTACTS:

Shenandoah Telecommunications Company
Jim Volk
Senior Vice President, Finance and Chief Financial officer
540-984-5168

John Nesbett/Jennifer Belodeau
IMS Investor Relations
203-972-9200
[email protected]



Baxter Announces U.S. FDA 510(k) Clearance of Homechoice Claria with Sharesource

Baxter Announces U.S. FDA 510(k) Clearance of Homechoice Claria with Sharesource

  • Latest offering from global leader in automated peritoneal dialysis (APD) technology
  • Cleared for adult and pediatric populations
  • Available in 38 languages to support expanded ease of use for patients
  • Features Sharesource, the only two-way remote patient management platform available in the U.S. for patients with kidney failure

DEERFIELD, Ill.–(BUSINESS WIRE)–
Baxter International Inc. (NYSE:BAX), a global innovator in renal care, today announced U.S. Food and Drug Administration (FDA) clearance of the Homechoice Claria automated peritoneal dialysis (APD) system with Sharesource connectivity platform. Homechoice Claria combines a simple user interface with the benefits of Sharesource, the only two-way remote patient management platform for patients on peritoneal dialysis in the U.S. Homechoice Claria is cleared for both adult and pediatric populations.1 The clearance follows the recent finalization of the End-Stage Renal Disease (ESRD) Treatment Choices (ETC) payment model, which aims to significantly increase the number of new patients with kidney failure who receive home dialysis and/or organ transplants.

“Our goal remains to expand accessibility to home-based therapy for U.S. patients with kidney failure,” said Gavin Campbell, general manager of Baxter’s U.S. Renal Care business. “Homechoice Claria with Sharesource will support accelerated home dialysis growth by bringing the benefits of a two-way connected automated peritoneal dialysis system combined with a simple, intuitive device to more patients in the U.S.”

Enabling Enhanced Care with Remote Patient Management

With one in four APD patients globally benefitting from Baxter’s two-way remote patient management technology, Sharesource offers patients and clinicians the ability to stay closely connected to proactively address key aspects of peritoneal dialysis (PD) therapy. Through the platform’s accurate, daily treatment data and analytics, clinicians can manage patients remotely and make timely therapy decisions while keeping patients safely at home. Clinicians using Homechoice Claria with Sharesource also have greater visibility to patient adherence patterns, which may allow for early intervention and an increased focus on proactive care.2 To date, more than 6 million home dialysis treatments completed in the U.S. have been enabled by Sharesource, with over 20 million PD treatments managed around the world.

Homechoice Claria offers enhanced features that facilitate added convenience for patients and clinical teams, as well as best-in-class educational companions to further simplify the PD experience. For patients, intuitive control buttons and an easy-to-read screen complement straightforward instructions in 38 languages. To extend patients’ learning beyond the clinic, MyClaria – a web-based app included as part of the Homechoice Claria system – features step-by-step, voice activated and enabled instructions to guide patients through therapy. For clinicians, MySharesource – also a web-based app – is a resource featuring step-by-step guidance and quick demo videos on how to use the Sharesource platform.

“When starting their patients on PD, clinicians are looking for ways to help manage their changing needs over time,” said Amy O’Brien, PD clinical specialist at Baxter. “The combination of features, insights and resources available through Homechoice Claria with Sharesource creates an accurate, efficient tool for therapy management, resulting in peace of mind for patients and the healthcare providers who support them.”

Adding Homechoice Claria to its APD cycler portfolio enhances Baxter’s efforts to bring the benefits of Sharesource remote patient management to as many clinics and patients as possible in the U.S. Baxter will continue offering its Sharesource-enabled APD cycler, Amia, which offers additional features to support patients, including a touchscreen user interface and built-in voice guidance. The introduction of HomechoiceClaria follows several Baxter initiatives across the continuum of care to improve options for patients with kidney failure, including:

  • Launching CKD&Me, an app providing customized disease and therapy education for the individual learning needs of patients with chronic kidney disease.
  • Developing the PD Excellence Academy, a first-of-its-kind curriculum providing education to PD nurses in one easily-accessible online resource.

Homechoice Claria with Sharesource will be available in the U.S. in the coming weeks. More information is available at Claria.Baxter.com.

About Baxter

Every day, millions of patients and caregivers rely on Baxter’s leading portfolio of critical care, nutrition, renal, hospital and surgical products. For more than 85 years, we’ve been operating at the critical intersection where innovations that save and sustain lives meet the healthcare providers that make it happen. With products, technologies and therapies available in more than 100 countries, Baxter’s employees worldwide are now building upon the company’s rich heritage of medical breakthroughs to advance the next generation of transformative healthcare innovations. To learn more, visit www.baxter.com and follow us on Twitter, LinkedIn and Facebook.

Rx Only. For safe and proper use of this device, refer to the full Instructions for Use.

The Homechoice Claria APD system is intended for automatic control of dialysis solution exchanges in the treatment of pediatric and adult renal failure patients undergoing peritoneal dialysis in the home healthcare environment, including comparable use in professional healthcare facilities.

This release includes forward-looking statements concerning Homechoice Claria and Sharesource, including anticipated availability and potential benefits associated with their use. The statements are based on assumptions about many important factors, including the following, which could cause actual results to differ materially from those in the forward-looking statements: satisfaction of regulatory and other requirements; actions of regulatory bodies and other governmental authorities; product quality, manufacturing or supply, or patient safety issues; changes in law and regulations; and other risks identified in Baxter’s most recent filing on Form 10-K and other SEC filings, all of which are available on Baxter’s website. Baxter does not undertake to update its forward-looking statements.

Baxter, Homechoice Claria, Amia, CKD&Me and Sharesource are registered trademarks of Baxter International Inc.

1 Homechoice Claria product indications (please refer to the Instructions for Use for more information)

2 Firanek C. et al, Discrepancy between prescribed and actual APD prescription delivery: Identification using cycler remote management technology. EDTA 5-18-2017. Poster #MP557

Media Contact

Andrea Johnson, (224) 948-5353

[email protected]

Investor Contact

Clare Trachtman, (224) 948-3020

KEYWORDS: Illinois United States North America

INDUSTRY KEYWORDS: Biotechnology Medical Supplies Surgery General Health Health FDA Diabetes Medical Devices

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Kronos Bio Announces Participation in Upcoming Investor Conferences

SAN MATEO, Calif., and CAMBRIDGE, Mass., Nov. 23, 2020 (GLOBE NEWSWIRE) — Kronos Bio, Inc. (Nasdaq: KRON), a company dedicated to transforming the lives of those affected by cancer, today announced that members of the management team will participate in the following investor conferences:

  • A virtual fireside chat at the Evercore ISI 3rd Annual HealthCONx Conference on Wednesday, Dec. 2, 2020, at 2:15 p.m. ET; and
  • Meetings at the Piper Sandler 32nd Annual Virtual Healthcare Conference on Thursday, Dec. 3, 2020, with a pre-recorded fireside chat available today at 10 a.m. ET.

The fireside chats will be available from the Investors & Media section of the company’s website at www.kronosbio.com. A replay of the webcast will be archived and available for one month following the event.

About Kronos Bio, Inc.

Kronos Bio is a clinical-stage biopharmaceutical company dedicated to discovering, developing and commercializing therapies that seek to transform the lives of those affected by cancer. The company focuses on targeting dysregulated transcription factors and the regulatory networks within cells that drive cancerous growth. Kronos Bio’s lead investigational therapy is entospletinib, a selective inhibitor targeting spleen tyrosine kinase (SYK) in development for the frontline treatment of NPM1-mutated acute myeloid leukemia (AML). The company is also developing KB-0742, an oral inhibitor of cyclin dependent kinase 9 (CDK9), for the treatment of MYC-amplified solid tumors.

Kronos Bio is based in San Mateo, Calif., and has a research facility in Cambridge, Mass. For more information, visit www.kronosbio.com or follow the company on LinkedIn.

Contact:

Stephanie Yao
Executive Director, Investor Relations and Corporate Communications
650-525-6605
[email protected]



RAPT Therapeutics to Present at the Piper Sandler 32nd Annual Virtual Healthcare Conference

SOUTH SAN FRANCISCO, Calif., Nov. 23, 2020 (GLOBE NEWSWIRE) — RAPT Therapeutics, Inc. (Nasdaq: RAPT), a clinical-stage, immunology-based biopharmaceutical company focused on discovering, developing and commercializing oral small molecule therapies for patients with significant unmet needs in oncology and inflammatory diseases, today announced that a webcast of Brian Wong, M.D., Ph.D., President and CEO, and Rodney Young, CFO, participating in a fireside chat in conjunction with the Piper Sandler 32nd Annual Virtual Healthcare Conference will be available today at 10:00 a.m. ET. A replay of RAPT’s fireside chat may be accessed on the RAPT Therapeutics website at https://investors.rapt.com/events-and-presentations.

About RAPT Therapeutics, Inc.

RAPT Therapeutics is a clinical stage immunology-based biopharmaceutical company focused on discovering, developing and commercializing oral small molecule therapies for patients with significant unmet needs in oncology and inflammatory diseases. Utilizing its proprietary discovery and development engine, the Company is developing highly selective small molecules designed to modulate the critical immune drivers underlying these diseases. RAPT has discovered and advanced two unique drug candidates, FLX475 and RPT193, each targeting C-C motif chemokine receptor 4 (CCR4), for the treatment of cancer and inflammation, respectively. The Company is also pursuing a range of targets, including hematopoietic progenitor kinase 1 (HPK1) and general control nonderepressible 2 (GCN2), that are in the discovery stage of development.

RAPT
Media Contact:

Angela Bitting
[email protected]
(925) 202-6211

RAPT
Investor Contact:

Sylvia Wheeler
[email protected]