InvestorBrandNetwork Announces DojoLIVE! Interview with IBN Communications Director Jonathan Keim, ‘The Digital Evolution: Maximizing Your Impact’

LOS ANGELES, Nov. 19, 2020 (GLOBE NEWSWIRE) — via InvestorWireInvestorBrandNetwork (“IBN”), a multifaceted financial news and publishing company for private and public entities, today announces that its Communications Director, Jonathan Keim, recently appeared on DojoLIVE!, a lively podcast and interview forum that brings together a broad roster of technology, business and thought leaders from a wide range of software companies and startups.

The broadcast, titled “The Digital Evolution: Maximizing Your Impact,” is available for on-demand viewing on the DojoLIVE! website.

During the interview, Mr. Keim provided a brief overview of InvestorBrandNetwork, examining its growth through the years. Today, its network includes 50+ trusted brands. He then turned his attention to the topic of the day, providing insight into a plethora of ideas and strategies to increase influence and make memorable impressions.

“Some of the different things that have been really effective for us include newsletters and really anything that would be a subscription format, whether it’s podcast subscribers or text blasting. You want to continue to increase the ways that you can reach out to your audiences whenever you want versus hoping they stumble across you again,” Keim stated in the interview.

“Beyond that, engaging in as much conversation as possible, like hash-tagged tweets, becoming a speaker at many different virtual events, guest blogging,” he continued. “One of the keys to our success, specifically, is being very specialized. We have a brand just for psychedelic news, for instance. We also have cannabis and hemp and CBD. Others might try to bring that together into one brand.”

Throughout the interview, Keim delivered an in-depth examination of IBN’s strategy to stand out and increase influence. Over the past 15+ years, IBN has leveraged this strategy to assist 500+ client partners in improving communications within the investment community.

About InvestorBrandNetwork

The InvestorBrandNetwork (“IBN”) consists of financial brands introduced to the investment public over the course of 15+ years. With IBN, we have amassed a collective audience of millions of social media followers. These distinctive investor brands aim to fulfill the unique needs of a growing base of client-partners. IBN will continue to expand our branded network of highly influential properties, leveraging the knowledge and energy of specialized teams of experts to serve our increasingly diversified list of clients.

Through NetworkNewsWire (“NNW”) and its affiliate brands, IBN provides: (1) access to a network of wire solutions via InvestorWire to reach all target markets, industries and demographics in the most effective manner possible; (2) article and editorial syndication to 5,000+ news outlets; (3) enhanced press release solutions to ensure maximum impact; (4) full-scale distribution to a growing social media audience; (5) a full array of corporate communications solutions; and (6) a total news coverage solution.

For more information on IBN, visit https://www.InvestorBrandNetwork.com.

Please see full terms of use and disclaimers on the InvestorBrandNetwork website, applicable to all content provided by IBN wherever published or re-published: https://IBN.fm/Disclaimer

Forward-Looking Statements

This release contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. All forward-looking statements are inherently uncertain as they are based on current expectations and assumptions concerning future events or future performance of the company. Readers are cautioned not to place undue reliance on these forward-looking statements, which are only predictions and speak only as of the date hereof. In evaluating such statements, prospective investors should review carefully various risks and uncertainties identified in this release and matters set in the company’s SEC filings. These risks and uncertainties could cause the company’s actual results to differ materially from those indicated in the forward-looking statements.

Corporate Communications

InvestorBrandNetwork (IBN)
Los Angeles, California
www.InvestorBrandNetwork.com
310.299.1717 Office
[email protected]



Varian and the Cincinnati Children’s/UC Health Proton Therapy Center Announce Initial Patient Treated in the FAST-01 First Human Clinical Trial of FLASH Therapy for Cancer

– First patient in the world to participate in a clinical trial of FLASH therapy

– Physicians and researchers at Cincinnati’s Children’s/UC Health Proton Therapy Center are using a Varian ProBeam® proton therapy system modified to deliver radiation treatment at ultra-high dose rates

– FLASH therapy delivers radiation at ultra-high dose rates up to 100 times faster compared to conventional radiation therapy

– Study was designed in collaboration with the FlashForwardTM Consortium

PR Newswire

PALO ALTO, Calif., and CINCINNATI, Ohio, Nov. 19, 2020 /PRNewswire/ — Varian (NYSE: VAR) and the Cincinnati Children’s/UC Health Proton Therapy Center today announce the start of the first clinical trial of FLASH therapy as part of the recently opened FAST-01 study (FeAsibility Study of FLASH Radiotherapy for the Treatment of Symptomatic Bone Metastases). The clinical trial involves the investigational use of Varian’s ProBeam® particle accelerator modified to enable radiation therapy delivery at ultra-high dose rates (dose delivered in less than 1 second) and is being conducted at the Cincinnati Children’s/UC Health Proton Therapy Center with John C. Breneman M.D., Medical Director of the center, serving as principal investigator.

The first clinical trial patient was treated this week. The FAST-01 study is expected to enroll up to 10 patients with bone metastases to evaluate clinical workflow feasibility, treatment-related side effects, and efficacy of treatment as assessed by measuring pain relief of trial participants. The clinical trial, informed by years of preclinical work, was designed by experts at Varian and multiple centers in the FlashForwardTM Consortium, including Cincinnati’s Children’s/UC Health Proton Therapy Center and the New York Proton Center.

“Treating the first patient in this FLASH clinical trial is a milestone that many thought was still years ahead of us,” said Kolleen Kennedy, Chief Growth Officer and President of Proton Therapy Solutions at Varian. “There was overwhelming support from Dr. Breneman and his team for this clinical trial, which was designed in collaboration with the FlashForward Consortium and with significant contributions from the New York Proton Center. These efforts help Varian safely advance potential therapy options towards our vision of a world without fear of cancer.”

Breneman noted that, because this is the first in human trial of FLASH radiotherapy, it will build a foundation for extending this therapy to other types of cancer treatments.

“Trials using FLASH radiotherapy for lung cancer and other malignancies are currently being developed,” said Breneman, a UC Health radiation oncologist and a professor emeritus at the University of Cincinnati College of Medicine. “Using FLASH treatment for these cancers could deliver higher cancer-killing doses without causing inordinate side effects, which would be a real advance.”

“FLASH therapy has the potential to be practice changing and dramatically improve the experience of cancer care for a new generation of patients. The launch of the first FLASH clinical trial, a project that has come to fruition after years of intensive study, is an important milestone in the progress of radiation therapy,” said FlashForward Consortium member Dr. Charles B. Simone, II, FACRO, Chief Medical Officer at New York Proton Center. “We are optimistic that the results of the FAST clinical development program will transform the way the industry approaches treatment. The New York Proton Center is proud to be a partner in this future-focused study.”

John Perentesis, MD, Director of the Division of Oncology & Cancer Programs at Cincinnati Children’s, said FLASH is potentially a transformational advance for cancer treatment for many patients.”If the side effects of radiation on the normal tissues surrounding a tumor can be significantly reduced, the dose of radiation to treat a cancer can be greatly increased,” Perentesis said. “This would raise hope to cure malignancies that respond to radiation but aren’t completely cured at current doses, including pediatric brain tumors like DIPG/pontine glioma and medulloblastoma, sarcomas, and neuroblastoma.” 

About Varian
At Varian, we envision a world without fear of cancer. For more than 70 years, we have developed, built and delivered innovative cancer care technologies and solutions for our clinical partners around the globe to help them treat millions of patients each year. With an Intelligent Cancer Care approach, we are harnessing advanced technologies like artificial intelligence, machine learning and data analytics to enhance cancer treatment and expand access to care. Our 10,000 employees across 70 locations keep the patient and our clinical partners at the center of our thinking as we power new victories in cancer care. Because, for cancer patients everywhere, their fight is our fight. For more information, visit http://www.varian.com and follow @VarianMedSys on Twitter.

About the Cincinnati Children’s/UC Health Proton Therapy Center
The Cincinnati Children’s/UC Health Proton Therapy Center, which opened in 2016, is one of only 35 in the United States. The Cincinnati center incorporates a $24 million, one-of-a-kind research facility, which includes a fully operational proton treatment room dedicated for just research along with integrated laboratories. The unique capabilities of the research center were instrumental in Cincinnati developing the world’s first clinical trial of FLASH proton therapy. In addition, children and adults from around the world seek treatment for more than 30 types of cancer in two clinical therapy rooms at the center.

About New York Proton Center
The New York Proton Center is creating the gold standard for proton therapy, giving new hope to patients living with cancer. In partnership with leading academic medical centers—Memorial Sloan Kettering Cancer Center, Montefiore Health System, Mount Sinai Health System, and ProHEALTH as manager—the New York Proton Center brings together expert oncologists, clinical care teams, and researchers to improve cancer care and advance the clinical evidence for proton therapy.

About ProBeam

®

Varian’s ProBeam proton therapy system is a cancer treatment system that uses protons rather than X-rays to treat cancerous tumors with great precision. It is effective for certain types of cancers and can treat with a high dose of radiation to the tumor, while delivering lower radiation to the surrounding healthy tissue.


Press Contacts


Investor Relations Contact

Aimee Corso

Health + Commerce on behalf of Varian

+1 (310) 780-2661



[email protected]

Anshul Maheshwari

Vice President, Investor Relations

+1 (650) 424-5631



[email protected]

Barrett J. Brunsman

Cincinnati Children’s


[email protected]

Nathaniel Goehring

+1 (781) 608-8437

BerlinRosen on behalf of NY Proton

Therapy Center


[email protected]

 

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SOURCE Varian

Kapsch Completes New All-Electronic Toll System for New York State Thruway

Kapsch Completes New All-Electronic Toll System for New York State Thruway

New System went live on November 14, 2020

MCLEAN, Va.–(BUSINESS WIRE)–
Kapsch is pleased to announce that the new all-electronic tolling (AET) system developed for the New York State Thruway Authority (NYSTA) is now fully operational and in revenue service. After intensive testing and final configuration, the new system went live on November 14, 2020. All road users now pay their vehicle tolls on NYSTA-operated roads via automatic electronic toll collection (ETC).

The New York State Thruway Authority now operates a completely cashless AET system. Vehicles can pay tolls while traveling at highway speeds below the new high-volume Kapsch gantries, or are tolled at NYSTA-operated entry and exit points that also use the ETC method. Remaining toll plaza infrastructure will eventually be removed. Sensors and lasers automatically determine vehicle class, which define the toll rate applied to each vehicle. Charges are billed to the driver’s E-ZPass account if they have a transponder, or by mail to the vehicle’s registered owner using license plate information.

Unique system features include a redundant and dual central host system, walkable gantries and bracket-mounted equipment for performing tool-less maintenance without lane closures, and automatic classification of the 26 NYSTA vehicle classes using advanced sensor metrics and algorithms. In order to meet the project timeframe, Kapsch deployed teams simultaneously at six sites across New York state where the teams coordinated with Kapsch and NYSTA subcontractors to install and test the AET equipment while keeping roadways open to traffic.

“The launch of this comprehensive and advanced AET system highlights NYSTA’s leadership in providing seamless and efficient transportation for drivers,” said Chris Murray, president of Kapsch TrafficCom North America. “Paying cashless tolls will reduce traffic congestion and vehicle emissions, and contribute to smoother traffic flow along the Thruway in New York state. We are glad for the strong collaboration with NYSTA that led our teams to successfully deliver this ambitious project.”

Kapsch TrafficCom is a globally renowned provider of transportation solutions for sustainable mobility. Innovative solutions in the application fields of tolling, tolling services, traffic management and demand management contribute to a healthy world without congestion.

Kapsch has brought projects to fruition in more than 50 countries around the globe. With one-stop solutions, the company covers the entire value chain of customers, from components to design and implementation to the operation of systems.

As part of the Kapsch Group and headquartered in Vienna, Kapsch TrafficCom has subsidiaries and branches in more than 30 countries. It has been listed in the Prime Market segment of the Vienna Stock Exchange since 2007 (ticker symbol: KTCG). In its 2019/20 financial year, around 5,100 employees generated revenues of EUR 731.2 million.

Further information: www.kapsch.net/ktc

Follow us on Twitter and LinkedIn

Press Contact:

Nicole Busse
Senior Manager, Marketing & Communications

Kapsch TrafficCom North America

8201 Greensboro Drive, Suite 1002

McLean, VA 22102

United States

T +1 703 203 1028

[email protected]

Investor Contact:

Hans Lang

Investor Relations Officer

Kapsch TrafficCom AG

Am Europlatz 2

1120 Vienna

Austria

T +43 50 811 1122

[email protected]

KEYWORDS: New York Virginia United States North America

INDUSTRY KEYWORDS: Data Management Technology Banking Transportation Accounting Professional Services Travel Other Transport Trucking Fleet Management General Automotive Transport Automotive Software Logistics/Supply Chain Management Networks

MEDIA:

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Camping World Holdings Announces Deal to Acquire All RV Needs in the South Medford, Oregon Market

Camping World Holdings Announces Deal to Acquire All RV Needs in the South Medford, Oregon Market

LINCOLNSHIRE, Ill.–(BUSINESS WIRE)–
Camping World Holdings, Inc. (NYSE: CWH) (“Camping World”), the nation’s largest network of RV and outdoor lifestyle – centric retail locations, today announced an agreement to acquire All RV Needs located in Medford, Oregon.

“This acquisition is an incredible fit for our company as it continues to evolve and expand,” said Marcus Lemonis, Chairman of Camping World. “We are excited to grow our presence in Medford, Oregon, while continuing to deliver a high standard of customer service, diverse brands and affordable price points while deepening our roots in the community.”

Located in South Medford, OR off I-5, All RV Needs will be rebranded as Gander RV and offer a wide range of new and used RV’s from top manufacturers and brands.

The acquisition of All RV Needs brings the count of the Company’s retail SuperCenters in the state of Oregon to a total of five and is in line with company’s future growth plans.

Camping World Holdings currently owns and operates over 160 SuperCenters nationwide, specializing in RV sales and service, RV parts and accessories, outdoor lifestyle products and its entire portfolio of Good Sam products and services. From new strategic acquisitions, new store development and facility upgrades, the Company’s network will continue to expand and evolve while serving its customers’ outdoor, RV and camping needs.

Camping World Holdings is always looking for seasoned and professional RV sales associates, technicians, and retail support to assist with locations across the country. Individuals interested in applying for a position may visit http://www.campingworldcareers.com/.

About Camping World Holdings, Inc.

Camping World Holdings, headquartered in Lincolnshire, Illinois, is America’s leading recreational vehicle and outdoor retailer, offering an extensive assortment of recreational vehicles for sale, RV and camping gear, RV maintenance and repair, other outdoor and active sports products, and the industry’s broadest and deepest range of services, protection plans, products and resources. Since the Company’s founding in 1966, Camping World has grown to become one of the most well-known destinations for everything RV, with more than 160 locations in 37 states and a comprehensive e-commerce platform. For more information, visit www.CampingWorld.com.

Cautionary Statement Regarding Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995 concerning Camping World and other matters. All statements other than statements of historical facts contained in this press release may be forward-looking statements. Statements regarding our future results of operations and financial position, our capital return strategy, and expected dividend payments are forward-looking statements. In some cases, you can identify forward-looking statements by terms such as ‘‘may,’’ ‘‘will,’’ ‘‘should,’’ ‘‘expects,’’ ‘‘plans,’’ ‘‘anticipates,’’ ‘‘could,’’ ‘‘intends,’’ ‘‘targets,’’ ‘‘projects,’’ ‘‘contemplates,’’ ‘‘believes,’’ ‘‘estimates,’’ ‘‘predicts,’’ ‘‘potential’’ or ‘‘continue’’ or the negative of these terms or other similar expressions. The forward-looking statements in this press release are only predictions. We have based these forward-looking statements largely on our current expectations and projections about future events and financial trends that we believe may affect our business, financial condition and results of operations. Forward-looking statements involve known and unknown risks, uncertainties and other important factors that may cause our actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements. You should carefully consider the risks and uncertainties that affect our business, including the important factors discussed under the caption “Risk Factors” in our Annual Report on Form 10-K filed for the year ended December 31, 2019, as updated in our Quarterly Report on Form 10-Q for the quarter ended June 30, 2020, and our other reports filed with the SEC. These forward-looking statements speak only as of the date of this communication. Except as required by applicable law, we do not plan to publicly update or revise any forward-looking statements, whether as a result of any new information, future events or otherwise. You are advised, however, to consult any further disclosures we make on related subjects in our public announcements and filings with the Securities and Exchange Commission.

Karen Porter [email protected]

KEYWORDS: Illinois Oregon United States North America

INDUSTRY KEYWORDS: Transportation Travel Automotive Specialty Vacation Recreational Vehicles General Automotive Retail

MEDIA:

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XBiotech Data Shows Effective Anti-Virus Activity for True Human Antibodies in Its Candidate Influenza-COVID-19 Therapeutic Cocktail

Candidate Therapy for Flu+Covid-19 Co-infection Shows Potent Anti-Viral Potential

AUSTIN, Texas, Nov. 19, 2020 (GLOBE NEWSWIRE) — XBiotech Inc. (NASDAQ: XBIT) announced today new data for its breakthrough candidate therapy for treating infections of influenza and COVID-19. The Company continues to analyze components of its so-called FLUVID™ therapy as it develops manufacturing capability for a product candidate. The True Human antibodies targeting the virus causing COVID-19 were found to effectively neutralize a test virus at concentrations about four-times better than the antibodies the FDA is now considering for emergency use authorization. Ongoing research has also found that the True Human antibodies in this therapeutic cocktail that target influenza are capable of rescuing 100% of animals that receive an otherwise lethal dose of flu virus. The latest research findings suggest the FLUVID™ therapy, designed to be effective against all known strains of influenza in addition to the COVID-19 virus, could provide a uniquely effective therapy for treating complex infections from one or more of these viruses. There is no other therapy available to treat both COVID-19 and Influenza infections that occur together.

With the resurgence of the COVID-19 virus during this oncoming flu season, we are faced with the likelihood that many people will be infected by both influenza and COVID-19 viruses. Co-infections, or “superinfections”, may increase severity of disease and further complicate treatment. A therapy that could treat COVID-19+Influenza co-infections is urgently needed.

While the COVID-19 pandemic has only recently emerged, the FLUVID™ candidate therapy is the result of years of Research and Development at XBiotech, incorporating extraordinary influenza True Human antibodies that have been systematically evaluated for their ability to target virtually all known strains of influenza viruses. Whereas the True Human COVID-19 antibodies were derived from patients who recovered rapidly without serious illness and therefore should have potent neutralizing capability against the virus.

The influenza strains that will be targeted by FLUVID include: seasonal H1N1 and H3N2 strains; pandemic strains H1N1, H2N2, H3N2; avian influenza strains H5N1, H5N2 and H7N9; and even H9N2 and H10N8, which are currently in poultry but are believed to have pandemic potential in humans.

Dr. Sushma Shivaswamy, Ph.D., XBiotech’s Chief Scientific Officer, commented, “We continue to see outstanding data as we move this unique and critical therapy toward the clinic. Unlike any other Research and Development program, our pipeline is focused on delivering therapies to the vulnerable demographic that is most in need of the FLUVID™ therapy. We believe strongly in the potential of this product candidate.”

About XBiotech

XBiotech is a fully integrated, global biopharmaceutical company dedicated to pioneering the discovery, development and commercialization of therapeutic antibodies. XBiotech currently is advancing a pipeline of therapies based on harnessing naturally occurring antibodies from patients with immunity to certain diseases. The approach to use natural human immunity as a source of new medicines offers the potential to redefine the standards of care a wide range of diseases. Headquartered in Austin, Texas, XBiotech also is leading the development of innovative manufacturing technology to reduce the cost and complexity of biological drug production. For more information, visit www.xbiotech.com.

About True Human™ Therapeutic Antibodies

XBiotech’s True Human™ antibodies are the only available antibodies derived without modification from humans who possess natural immunity to certain diseases. (Unlike all commercially available antibodies, which are called “Humanized” or “Fully Human”, XBiotech’s True Human™ antibodies are directly sourced from the natural human immune response for specific diseases without modification, and thereby have not been shown to cause immunogenicity.) With discovery and clinical programs across multiple disease areas, XBiotech’s True Human antibodies have the potential to harness the body’s natural immunity to fight disease with increased safety, efficacy and tolerability.

Cautionary Note on Forward-Looking Statements

This press release contains forward-looking statements, including declarations regarding management’s beliefs and expectations that involve substantial risks and uncertainties. In some cases, you can identify forward-looking statements by terminology such as “may,” “will,” “should,” “would,” “could,” “expects,” “plans,” “contemplate,” “anticipates,” “believes,” “estimates,” “predicts,” “projects,” “intend” or “continue” or the negative of such terms or other comparable terminology, although not all forward-looking statements contain these identifying words. Forward-looking statements are subject to inherent risks and uncertainties in predicting future results and conditions that could cause the actual results to differ materially from those projected in these forward-looking statements. These risks and uncertainties are subject to the disclosures set forth in the “Risk Factors” section of certain of our SEC filings. Forward-looking statements are not guarantees of future performance, and 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. Any forward-looking statements that we make in this press release speak only as of the date of this press release. We assume no obligation to update our forward-looking statements whether as a result of new information, future events or otherwise, after the date of this press release.

Contact

Ashley Otero
[email protected]
512-386-2930 



RenovaCare Awarded New Patents Allowing Greater Versatility of SkinGun™; Sterility in Field Environments; Spray Solutions to Now Include Targeted Cells, Drugs or Hormones

ROSELAND, N.J., Nov. 19, 2020 (GLOBE NEWSWIRE) — RenovaCare, Inc. (Symbol: RCAR; www.renovacareinc.com), developer of patented technologies for spraying self-donated stem cells for the regeneration of skin and other organs and tissues, today announced the issuance of two new patents encompassing improvements to the SkinGun™, expanding its potential application beyond the surgical setting into the field, and allowing the use of liquid suspension solutions to include drugs, hormones, and other useful agents. These new patents demonstrate RenovaCare’s commitment to developing new products and expanding its proprietary cell spray technology platforms.

Robin A. Robinson, PhD, Chief Scientific Officer commented, “RenovaCare is leading the development of regenerative medical spray cell therapies with our novel CellMist™ System and SkinGun™ platform technologies. Our newest patents broaden the potential use of our novel SkinGun™ to spray an array of drugs, hormones, medical solutions and other agents. Further, these patented inventions enable the SkinGun™ spray device to be used outside of a surgical setting in out-patient clinics and field settings like emergency situations. The disposable components and an impervious contamination barrier create a sterile environment for the patient and SkinGun™ components.”

“The RenovaCare SkinGun™ was designed to provide a non-invasive gentle spray for expedited burn wound healing. The newly-awarded patents may expand the SkinGun’s potential use to benefit a wider population,” stated Alan L. Rubino, Chairman and Chief Executive Officer.   “While our team remains focused on advancing our core cell spray therapies through the FDA regulatory pathway, I am enthusiastic about the expanded commercial opportunities and meaningful strategic business alliances that our new patents may foster with potential partner companies.”

The RenovaCare patent portfolio is comprised of eight patent families spanning the United States, Europe, and Asia. Already successfully defended, the Company has issued patents extending to 2037. Issued patents include cell isolation techniques for skin and other tissues and a cell spray gun that is highly effective in spraying different types of biologically compatible liquids and cell suspensions of all types. RenovaCare owns all technology developed and under development and has not in-licensed any technology.


About RenovaCare


RenovaCare, Inc. is developing new generation autologous stem cell therapies for the regeneration of human organs and tissues. The Company’s initial product under development targets the body’s largest organ, the skin. The Company’s flagship technology, the CellMist™ System, renders single-cell suspensions of tissue-specific pluripotent cells from donor tissues through sequential protease digestions. The RenovaCare CellMist™ System facilitates rapid healing of wounds or other afflicted tissues when applied topically as a gentle cell mist using the patented RenovaCare SkinGun™. The Company’s SkinGun™ is used to spray a liquid suspension of a patient’s stem cells – the CellMist™ Solution – on to wounds.

Development for next-generation biomedical technologies and devices for addressing unmet medical needs and commercialization is taking place at the RenovaCare R&D Innovation Center, located at StemCell Systems in Berlin, Germany. The Innovation Center houses dedicated RenovaCare cell biology laboratories; additional engineering, fabrication, prototyping and performance testing facilities; and product design studios for medical devices and biomedical products. Experienced contract bioengineers, cell biologists, and support staff work under the direction of a team of MD-PhDs who are experts in regenerative medicine, new product development, and clinical translation.


RenovaCare products are currently in development. They are not available for sale in the United States. There is no assurance that the Company’s planned or filed submissions to the U.S. Food and Drug Administration will be accepted or cleared by the FDA.

For additional information, please call Amit Singh at: 1-888-398-0202 or visit: https://renovacareinc.com

To receive future press releases via email, please visit:
https://renovacareinc.com/investors/register/
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Social Media Disclaimer

Investors and others should note that we announce material financial information to our investors using SEC filings and press releases. We use our website and social media to communicate with our subscribers, shareholders and the public about the company, RenovaCare, Inc. development, and other corporate matters that are in the public domain. At this time, the company will not post information on social media that could be deemed to be material information unless that information was distributed to public distribution channels first.
We encourage investors, the media, and others interested in the company to review the information we post on the company’s website and the social media channels listed below:

  • LinkedIn
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* This list may be updated from time to time.

Legal Notice Regarding Forward-Looking Statements
No statement herein should be considered an offer or a solicitation of an offer for the purchase or sale of any securities. This release contains forward-looking statements that are based upon current expectations or beliefs, as well as a number of assumptions about future events. Although RenovaCare, Inc. (the “Company”) believes that the expectations reflected in the forward-looking statements and the assumptions upon which they are based are reasonable, it can give no assurance that such expectations and assumptions will prove to have been correct. Forward-looking statements, which involve assumptions and describe our future plans, strategies, and expectations, are generally identifiable by use of the words “may,” “will,” “should,” “could,” “expect,” “anticipate,” “estimate,” “believe,” “intend,” or “project” or the negative of these words or other variations on these words or comparable terminology. The reader is cautioned not to put undue reliance on these forward-looking statements, as these statements are subject to numerous factors and uncertainties, including but not limited to: the timing and success of clinical and preclinical studies of product candidates, the potential timing and success of the Company’s product programs through their individual product development and regulatory approval processes, adverse economic conditions, intense competition, lack of meaningful research results, entry of new competitors and products, inadequate capital, unexpected costs and operating deficits, increases in general and administrative costs, termination of contracts or agreements, obsolescence of the Company’s technologies, technical problems with the Company’s research, price increases for supplies and components, litigation and administrative proceedings involving the Company, the possible acquisition of new businesses or technologies that result in operating losses or that do not perform as anticipated, unanticipated losses, the possible fluctuation and volatility of the Company’s operating results, financial condition and stock price, losses incurred in litigating and settling cases, dilution in the Company’s ownership of its business, adverse publicity and news coverage, inability to carry out research, development and commercialization plans, loss or retirement of key executives and research scientists, and other risks. There can be no assurance that further research and development will validate and support the results of our preliminary research and studies. Further, there can be no assurance that the necessary regulatory approvals will be obtained or that the Company will be able to develop commercially viable products on the basis of its technologies. In addition, other factors that could cause actual results to differ materially are discussed in the Company’s most recent Form 10-Q and Form 10-K filings with the Securities and Exchange Commission. These reports and filings may be inspected and copied at the Public Reference Room maintained by the U.S. Securities & Exchange Commission at 100 F Street, N.E., Washington, D.C. 20549. You can obtain information about operation of the Public Reference Room by calling the U.S. Securities & Exchange Commission at 1-800-SEC-0330. The U.S. Securities & Exchange Commission also maintains an Internet site that contains reports, proxy and information statements, and other information regarding issuers that file electronically with the U.S. Securities & Exchange Commission at http://www.sec.gov. The Company undertakes no obligation to publicly release the results of any revisions to these forward-looking statements that may be made to reflect the events or circumstances after the date hereof or to reflect the occurrence of unanticipated events.

A photo accompanying this announcement is available at https://www.globenewswire.com/NewsRoom/AttachmentNg/215f540d-0895-4ce2-b391-ef58b9044617



Wiley Broadens Access to Knewton Alta in Mathematics

Wiley Broadens Access to Knewton Alta in Mathematics

Wiley Continues Accelerating its Strategy to Increase Education Equity, Level Roadblocks and Drive Learner Outcomes

HOBOKEN, N.J.–(BUSINESS WIRE)–
From the 2020 American Mathematical Association of Two Year Colleges conference, John Wiley and Sons Inc. (NYSE:JWA) (NYSE:JWB) today announced it will broaden access to its Knewton Alta Foundations of Math course that covers the entire developmental math curriculum – content that is critical for learners to advance in their future academic and professional achievements.

Beginning in May 2021, the Knewton Alta Foundations of Math course will be freely available to students whose higher ed institution has adopted Knewton Alta for a developmental and gateway math & statistics sequence. The Foundations course can be used to support a prerequisite or corequisite developmental curriculum. Beginning today, Wiley will also offer a new, self-paced Knewton Alta Foundations of Math Self-Study course for all learners in need of support as they prepare for a new math course, math placement exam, or refine their skills after some time away from the discipline.

“At Wiley, our goal is to improve access to high quality education and empower learners to enter the fields that are driving our global economy forward,” said Matt Leavy, Executive Vice President, Wiley in Education Publishing. “We believe technology has the potential to transform what’s possible in education. Platforms, like Knewton Alta, can teach complex subjects like calculus and statistics in a way that better enables students and clears the path for long-term success – putting achievement within reach for all students.”

Success in a gateway math or statistics course is one of the biggest predictors of overall college success, yet math remains a significant obstacle to degree completion and equitable outcomes for millions of students, according to Mathematical Association of America; and research from the National Center of Education Statistics shows many students enrolled in these courses do not complete them leading to unmet learning outcomes, changed career paths, and often accumulating education debt. The research also shows the issue is more prevalent for Black and Latino students, who leave programs at far higher rates than their white peers.

“Students of color and those who live in poverty often do not have equal access to the educational resources needed to succeed in college, particularly those enrolling in mathematics and statistics courses. Wiley is addressing a largely unmet need in underserved communities by helping disadvantaged learners effectively marry preparation with opportunity,” said Donald Doane, Co-Founder, Black Learners Matter. “It’s truly exciting to see this transformative technology being used to tangibly improve learning outcomes for the students who need it most.”

Wiley’s Knewton Alta is expertly designed with adaptive learning technology to deliver a personalized learning experience that is more affordable and accessible, and improves student outcomes in math, statistics, economics, and chemistry. With the company’s acquisition of Knewton Alta last year, Wiley continues to be a source of tech-enabled content, platforms and services that together help learners achieve their goals in new and powerful ways. Today’s announcement reinforces Wiley’s commitment to accelerate the success of today’s learners, educators, and institutions.

For more information, please visit Wiley.com.

About Wiley

Wiley drives the world forward with research and education. Through publishing, platforms and services, we help students, researchers, universities, and corporations to achieve their goals in an ever-changing world. For more than 200 years, we have delivered consistent performance to all of our stakeholders. The Company’s website can be accessed at www.wiley.com.

Tag: All Corporate News

Media:

Lauren Andrich, +1 201 748 5838

[email protected]

Wiley Investors:

Brian Campbell, +1 201 748 6874

[email protected]

KEYWORDS: New Jersey United States North America

INDUSTRY KEYWORDS: Technology Publishing Other Technology Communications Software Continuing Training University Education

MEDIA:

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Hamilton Thorne Reports Financial and Operational Results for the Quarter and Nine Months Ended September 30, 2020

BEVERLY, Mass. and TORONTO, Nov. 19, 2020 (GLOBE NEWSWIRE) — Hamilton Thorne Ltd. (TSX-V:HTL), a leading provider of precision instruments, consumables, software and services to the Assisted Reproductive Technologies (ART), research, and cell biology markets, today reported unaudited financial and operational results for the quarter and nine months ended September 30, 2020.

Highlights

  • Sales increased 10% year over year to $9.8 million for the quarter; sales for the nine-month period increased 12% to $27.5 million; constant currency increase of 8% for the quarter and 13% for the nine-month period
  • Gross profit increased 3% year over year to $4.9 million for the quarter; increased 8% to $12.9 million for the nine-month period
  • Net income increased 41% to $459 thousand for the quarter; net income of $10 thousand for the nine-month period versus a loss in the prior period
  • Adjusted EBITDA decreased 8% to $1.7 million for the quarter; decreased 16% to $4.1 million for the nine-month period
  • Sales declined 7% in USD on an organic basis and were down 9% in constant currency; sales declined 6% on an organic basis for the nine-month period in USD; 5% decline in constant currency
  • Cash generated from operations was $2.8 million for the quarter and $2.0 million for the nine-month period; total cash on hand at September 30, 2020 was $19.98 million

“We are pleased to report a substantial improvement in Company performance in the third quarter,” stated David Wolf, President and Chief Executive Officer. “Sales into the human clinical market were up for the three-month period and up for the nine-month period as, despite the effects of the Covid-19 pandemic, ART activity in our two largest markets, the US and Germany, returned to near-normal levels, along with expanded contribution from our Planer acquisition. Sales into the human clinical market in the third quarter were also positively affected as production delays in our incubator product line that we experienced in Q2 were resolved. Sales into the cell biology/research markets grew substantially during the three- and nine-month periods, primarily due to the contribution from the Planer acquisition, augmented by strong toxicology testing equipment sales. Sales into the animal breeding market were down for both periods after a strong performance in Q2.”

    Three and
Nine
-Month Periods Ending
September
30
    Three Months Nine
Months
Statements of Operations:     20
20
  201
9
  20
20
  201
9
 
Sales   $9,793,572 $8,870,072 $27,521,207 $24,517,310  
Gross profit     4,909,228   4,751,531   13,921,632   12,908,057  
Operating expenses     4,199,819   4,109,461   12,516,473   10,644,601  
Net income (loss)     459,289   326,756   10,348   (137,306)  
Adjusted EBITDA     1,668,075   1,805,848   4,068,950   4,862,949  
Basic earnings per share   $0.00 $0.00 $0.00 $0.00  
Diluted earnings per share   $0.00 $0.00 $0.00 $0.00  

All amounts are in US dollars, unless specified otherwise, and results, with the exception of Adjusted EBITDA, are expressed in accordance with the International Financial Reporting Standards (“IFRS”).

Mr. Wolf continued, “Gross profit margins decreased to 50.1% for the quarter and to 50.6% for the nine months ended September 30, 2020, versus 53.6% and 52.6% for the comparable periods in 2019 primarily due to product mix, the addition of somewhat lower margin sales of Planer products, partially offset by increases in direct sales of higher margin, branded products. Margins were also negatively impacted, primarily in the second quarter, by certain relatively fixed costs of manufacturing spread over a reduced base of sales. Adjusted EBITDA decreased 8% to $1.7 million for the quarter, and decreased 16% to $4.1 million for the nine-month period. The Q3 results are an improvement of $1.1 million from Adjusted EBITDA in the second quarter of 2020 of $573 thousand.”

Michael Bruns, Chief Financial Officer added, “Cash flow generated from operations was $2.8 million for the quarter and $2.0 million for the nine-month period, recovering from the cash usage of $791,000 at June 30. While we currently expect to continue to generate cash in the fourth quarter, given the ongoing uncertainties surrounding the Covid-19 outbreak, it is impossible to predict whether the Company will generate cash from operations in 2021. We currently maintain a strong balance sheet, with cash on hand at September 30 of just under $20 million, and net bank debt of $9.1 million following our accelerated paydown of debt in Q3. I am also pleased to report that we increased our acquisition line of credit with our bank from $3 million to $5 million of availability, further increasing our resources to execute on new acquisitions. We continue to actively manage our acquisition program with a goal of completing one or more meaningful acquisitions every twelve to eighteen months; however, the effects of the Covid-19 outbreak could affect this goal.”

The Company reported that operating expenses were generally in line with expectations, with reduced travel and trade show expenses offset by increased personnel costs associated with maintaining pre Covid-19 investments in sales and support personnel.

COVID
-19 UPDATE

Mr. Wolf added, “The Covid-19 outbreak continues to add substantial uncertainty to the short- and mid-term outlook for our business. While, as reported above, we saw a degree of normalization of our business in our major markets, Covid-19 cases are increasing, in some cases sharply, in parts of those countries, as well as other parts of the world. Overall, we saw growth in our consumables business, while we continued to have meaningful variability in our sales of capital equipment, with significant differences from country to country. Our Services business has also had some slowdown due to travel restrictions and reductions in activity, but we expect this area to be less impacted going forward.”

The main scientific bodies that provide guidance to IVF clinics in Europe and the Americas continue to support the guidance that encourages IVF clinics to maintain operations with enhanced safety measures. Today, with some notable exceptions, clinics in most of our major markets are open, though not always running at full capacity. Moreover, there has been recent positive news on the preliminary success of a number of vaccines under development. Due to the preliminary nature of these reports, as well as the significant logistical hurdles related to scaling up production and distributing the vaccines, for planning purposes, the Company is taking the cautious position that the effects of the Covid-19 pandemic on its markets, and consequently the variability of its business performance, will continue, at least, through the first half of 2021.

“I want to emphasize that we are reporting today on the current state of our business,” Mr. Wolf stated. “There are still significant uncertainties around how quickly all IVF clinic operations will return to pre-pandemic levels, the progression of the Covid-19 virus, and the possibility that further lockdowns, regulation, or economic conditions may lead to future reductions in demand on a regional or worldwide basis. These fluctuations in demand for many of our products and services may last for a period of time that is difficult to determine, and could have an adverse effect on financial results in one or more of our future quarters.”

Conference Call

The Company will hold a conference call on Thursday, November 19, 2020 at 11:00 a.m. EST to review highlights of the results. All interested parties are welcome to join the conference call by dialing toll free 1-855-223-7309 in North America, or 647-788-4929 from other locations, and requesting Conference ID 6491864. The Company’s updated investor presentation and a recording of the call will be available on Hamilton Thorne’s website shortly after the call.

Financial statements and accompanying Management Discussion and Analysis for the periods are available on www.sedar.com and the Hamilton Thorne website.

About Hamilton Thorne Ltd. (
www.hamiltonthorne.ltd
)

Hamilton Thorne is a leading global provider of precision instruments, consumables, software and services that reduce cost, increase productivity, improve results and enable breakthroughs in Assisted Reproductive Technologies (ART), research, and cell biology markets. Hamilton Thorne markets its products and services under the Hamilton Thorne, Gynemed, Planer, and Embryotech Laboratories brands, through its growing sales force and distributors worldwide. Hamilton Thorne’s customer base consists of fertility clinics, university research centers, animal breeding facilities, pharmaceutical companies, biotechnology companies, and other commercial and academic research establishments.

Neither the TSX Venture Exchange, nor its regulation services provider (as that term is defined in the policies of the exchange), accepts responsibility for the adequacy or accuracy of this release.

The Company has included earnings before interest, income taxes, depreciation, amortization, share-based compensation expense, changes in fair value of derivatives and identified acquisition costs related to completed transactions (“Adjusted
EBITDA
”) as a non-IFRS measure, which is used by management as a measure of financial performance. See section entitled “Use of Non-IFRS Measures” and “Results of Operations” in the Company’s Management Discussion and Analysis for the periods covered for further information and a reconciliation of Adjusted EBITDA to Net Income.

Certain information in this press release may contain forward-looking statements. This information is based on current expectations that are subject to significant risks and uncertainties that are difficult to predict. Actual results might differ materially from results suggested in any forward-looking statements. The Company assumes no obligation to update the forward-looking statements, or to update the reasons why actual results could differ from those reflected in the forward-looking statements unless and until required by securities laws applicable to the Company. Additional information identifying risks and uncertainties is contained in filings by the Company with the Canadian securities regulators, which filings are available at

www.sedar.com

.

For more information, please contact:

David Wolf, President & CEO
Hamilton Thorne Ltd.
978-921-2050
[email protected]
Michael Bruns, CFO
Hamilton Thorne Ltd.
978-921-2050
[email protected]
Glen Akselrod
Bristol Investor Relations
905-326-1888
[email protected]



China Biologic Enters into Definitive Merger Agreement for Going Private Transaction

PR Newswire

BEIJING, Nov. 19, 2020 /PRNewswire/ — China Biologic Products Holdings, Inc. (NASDAQ: CBPO, “China Biologic” or the “Company”), a leading fully integrated plasma-based biopharmaceutical company in China, today announced that it has entered into a definitive Agreement and Plan of Merger (the “Merger Agreement”) with CBPO Holdings Limited (“Parent”) and CBPO Group Limited (“Merger Sub”), a wholly owned subsidiary of Parent. Pursuant to the Merger Agreement and subject to the terms and conditions thereof, Merger Sub will merge with and into the Company, with the Company continuing as the surviving entity and becoming a wholly-owned subsidiary of Parent (the “Merger”), in a transaction implying an equity value of the Company of approximately US$4.76 billion.

Pursuant to the Merger Agreement, at the effective time of the Merger (the “Effective Time”), each ordinary share of the Company (each, a “Share”) issued and outstanding immediately prior to the Effective Time will be cancelled and cease to exist in exchange for the right to receive US$120.00 in cash without interest (the “Per Share Merger Consideration”), except for (i) Shares owned by the Company as treasury shares or by any direct or indirect subsidiary of the Company, which will be cancelled and cease to exist without consideration, (ii) Shares held by Parent or any direct or indirect subsidiary of Parent (including the Rollover Shares (as defined below) to be contributed to Parent immediately prior to or at the Effective Time), which will be, at Parent’s option, cancelled and cease to exist without consideration or converted into the same number of shares of the surviving company, and (iii) Shares owned by holders who have validly exercised and not effectively withdrawn or lost their rights to dissent from the Merger pursuant to Section 238 of the Companies Law of the Cayman Islands, which will be cancelled and cease to exist in exchange for the right to receive the payment of fair value of such dissenting Shares determined in accordance with Section 238 of the Companies Law of the Cayman Islands.

The Per Share Merger Consideration represents a 16.8% premium over the closing price of the Shares as quoted by the NASDAQ Global Market on September 17, 2019, the last trading day prior to the Company’s announcement of its receipt of the “going-private” proposal, and a premium of 21.1% over the volume-weighted average price of the Shares during the 30 trading days through September 17, 2019.

Immediately following the consummation of the Merger, Parent will be beneficially owned by (i) Centurium Capital, through its affiliated entities Beachhead Holdings Limited (“Beachhead”), Double Double Holdings Limited (“Double Double”) and/or Point Forward Holdings Limited (“Point Forward”), (ii) CITIC Capital, through its affiliated entity 2019B Cayman Limited (“2019B Cayman”), (iii) Mr. Marc Chan, through his affiliated entity Parfield International Ltd. (“Parfield”), (iv) Hillhouse Capital, through its affiliated entities (“Hillhouse”), (v) V-Sciences Investments Pte Ltd (“V-Sciences”), an indirect wholly-owned subsidiary of Temasek Holdings (Private) Limited, and (vi) Mr. Joseph Chow, CEO and chairman of the board of directors (the “Board”) of the Company, through his affiliated entities Biomedical Treasure Limited (“Biomedical Treasure”), Biomedical Future Limited (“Biomedical Future”), Biomedical Development Limited (“Biomedical Development”), TB MGMT Holding Company Limited (“TB MGMT”), TB Executives Unity Holding Limited (“TB Executives”) and TB Innovation Holding Limited (“TB Innovation”), or their respective affiliates (the foregoing (i) through (vi), together with Parent, Merger Sub and PW Medtech Group Limited (“PWM”), which is bound by certain provisions of that certain amended and restated consortium agreement, dated as of the date hereof, by and among Parent, Merger Sub, PWM and certain other parties and the PWM Merger Voting Undertaking (as defined below) pursuant to the terms thereof, collectively, the “Buyer Consortium”).

Concurrently with the execution of the Merger Agreement, Beachhead, Double Double, Point Forward, 2019B Cayman, Parfield, Hillhouse, V-Sciences, Mr. Joseph Chow, Biomedical Treasure, Biomedical Future, Biomedical Development, certain management members of the Company (such management members, collectively, the “Rollover Management Members”) (all the foregoing persons, collectively, the “Rollover Securityholders”), TB MGMT, TB Executives and TB Innovation entered into a voting and support agreement with Parent, pursuant to which the Rollover Securityholders have agreed to vote all the Shares beneficially owned by them in favor of the authorization and approval of the Merger Agreement and to contribute to Parent immediately prior to or at the Effective Time certain Shares (the “Rollover Shares”) and equity awards of the Company beneficially owned by the Rollover Securityholders.

In addition, on October 26, 2020, (i) each of Biomedical Treasure, Biomedical Future and 2019B Cayman entered into a share purchase agreement with PWM, pursuant to which Biomedical Treasure, Biomedical Future and 2019B Cayman have agreed to purchase from PWM an aggregate of 5,321,000 Shares at a purchase price of US$120.00 per Share (the “PWM Share Sales”), (ii) 2019B Cayman entered into a share purchase agreement with Parfield, pursuant to which 2019B Cayman has agreed to purchase from Parfield an aggregate of 300,000 Shares at a purchase price of US$120.00 per Share (the “Parfield Share Sale”), and (iii) Biomedical Development entered into a share purchase agreement with Double Double, pursuant to which Biomedical Development has agreed to purchase from Double Double an aggregate of 775,000 Shares at a purchase price of US$120.00 per Share (the “Double Double Share Sale”). Concurrently with the execution of the Merger Agreement, PWM delivered a voting undertaking to Parent (the “PWM Merger Voting Undertaking”), pursuant to and subject to the terms and conditions of which, PWM has covenanted to vote all the Shares beneficially owned by it or with respect to which it is otherwise entitled to vote or consent, in favor of the authorization and approval of the Merger Agreement.

As of the date of this press release, members of the Buyer Consortium (including PWM) and the Rollover Management Members beneficially own Shares representing approximately 68.84% of the total outstanding Shares.

The Buyer Consortium intends to fund the Merger through a combination of (i) rollover equity contributions from the Rollover Securityholders, (ii) debt financing provided by one or more third party financial institutions, (iii) available cash of the Company and its subsidiaries, and (iv) if any of the PWM Share Sales and Parfield Share Sale fails to consummate prior to the closing of the Merger, cash contributions by each of Biomedical Treasure, Biomedical Future and 2019B Cayman and/or their respective affiliates.

The Board, acting upon the unanimous recommendation of a special committee of independent directors established by the Board (the “Special Committee”), approved the Merger Agreement and the Merger, and resolved to recommend the Company’s shareholders vote to authorize and approve the Merger Agreement and the Merger. The Special Committee negotiated the terms of the Merger Agreement with the assistance of its financial and legal advisors.

The Merger, which is currently expected to close during the first half of 2021, is subject to customary closing conditions, including, among others, (i) that the Merger Agreement shall be authorized and approved by an affirmative vote of shareholders representing at least two-thirds of the Shares present and voting in person or by proxy at an extraordinary general meeting of the Company’s shareholders and (ii) that the aggregate amount of dissenting Shares shall be less than 8% of the total outstanding Shares immediately prior to the Effective Time. If completed, the Merger will result in the Company becoming a privately-held company and its Shares will no longer be listed on the NASDAQ Global Select Market.

Duff & Phelps, LLC and Duff & Phelps Securities, LLC are serving as the financial advisor to the Special Committee, Davis Polk & Wardwell LLP is serving as U.S. legal counsel to the Special Committee, and Maples and Calder (Hong Kong) LLP is serving as Cayman Islands legal counsel to the Special Committee.

Kirkland & Ellis LLP is serving as co-U.S. legal counsel to the Buyer Consortium, Wilson Sonsini Goodrich & Rosati is serving as co-U.S. legal counsel and Hong Kong legal counsel to the Buyer Consortium, Harney Westwood & Riegels is serving as Cayman Islands legal counsel to the Buyer Consortium, and Fangda Partners is serving as PRC legal counsel to the Buyer Consortium.

Buyer Consortium’s Amendment to Schedule 13E-3 Transaction Statement

In connection with the proposed PWM Share Sales, Parfield Share Sale and Double Double Share Sale (collectively, the “Proposed Buyer Consortium Transfers”), Beachhead, Double Double, Point Forward together with certain other filing persons (the “Filing Persons”) have filed an amendment no. 4 to the transaction statement on Schedule 13E-3 (together with such transaction statement and amendments no. 1, 2 and 3 thereto, the “Buyer Consortium Transaction Statement”) with the SEC under the Securities Exchange Act of 1934, as amended (the “Exchange Act”). The Filing Persons filed the Buyer Consortium Transaction Statement because the Proposed Buyer Consortium Transfers, together with the previously announced and consummated purchases of Shares by members of the Buyer Consortium (all such consummated purchases being collectively, the “Completed Buyer Consortium Transfers,” and together with the Proposed Buyer Consortium Transfers, collectively, the “Buyer Consortium Transfers”), could be viewed as steps in a series of transactions having the reasonable likelihood or purpose of producing a Rule 13e-3 transaction under the Exchange Act. SHAREHOLDERS AND OTHER INVESTORS OF THE COMPANY ARE URGED TO READ THE BUYER CONSORTIUM TRANSACTION STATEMENT, THE EXHIBITS TO THE BUYER CONSORTIUM TRANSACTION STATEMENT AND OTHER MATERIAL FILED WITH OR FURNISHED TO THE SEC CAREFULLY WHEN THEY BECOME AVAILABLE, AS THEY CONTAIN IMPORTANT INFORMATION ABOUT THE BUYER CONSORTIUM TRANSFERS, THE BUYER CONSORTIUM MEMBERS, THE FILING PERSONS, THE COMPANY, AND RELATED MATTERS. All information contained in the Buyer Consortium Transaction Statement has been supplied by the Filing Persons, and the Company has not produced any disclosure with respect to any Filing Persons.

The Buyer Consortium Transaction Statement and its exhibits are available on the Company’s website at http://chinabiologic.investorroom.com/index.php?s=127 and can also be found at the SEC’s website at www.sec.gov. In addition, copies of these documents can be obtained, without charge, by contacting Centurium Capital at the following email address and/or phone number:

Tel: +86 10 5929 3690
E-Mail: [email protected]

As of the date of this release, none of the Proposed Buyer Consortium Transfers has been consummated, and no assurances can be made that any of the Proposed Buyer Consortium Transfers will be consummated. The consummation of each of the Proposed Buyer Consortium Transfers is not subject to approval by the shareholders of the Company.

Additional Information about the Merger

The Company will furnish to the SEC a report on Form 6-K regarding the Merger, which will include as an exhibit thereto the Merger Agreement. All parties desiring details regarding the transactions contemplated by the Merger Agreement are urged to review these documents, which will be available at the SEC’s website (http://www.sec.gov).

In connection with the Merger, the Company will prepare and mail a proxy statement that will include a copy of the Merger Agreement to its shareholders. In addition, certain participants in the Merger will prepare and mail to the Company’s shareholders a Schedule 13E-3 transaction statement (or an amendment to the Buyer Consortium Transaction Statement) that will include the Company’s proxy statement. These documents will be filed with or furnished to the SEC. SHAREHOLDERS AND OTHER INVESTORS OF THE COMPANY ARE URGED TO READ CAREFULLY AND IN THEIR ENTIRETY THESE MATERIALS AND OTHER MATERIALS FILED WITH OR FURNISHED TO THE SEC WHEN THEY BECOME AVAILABLE, AS THEY WILL CONTAIN IMPORTANT INFORMATION ABOUT THE COMPANY, THE PROPOSED TRANSACTIONS AND RELATED MATTERS. In addition to receiving the proxy statement and the Schedule 13E-3 transaction statement (or the amendment to the Buyer Consortium Transaction Statement) by mail, shareholders also will be able to obtain these documents, as well as other filings containing information about the Company, the Merger and related matters, without charge, from the SEC’s website (http://www.sec.gov) or at the SEC’s public reference room at 100 F Street, NE, Room 1580, Washington, D.C. 20549.

The Company and certain of its directors, executive officers and other members of management and employees may, under SEC rules, be deemed to be “participants” in the solicitation of proxies from its shareholders with respect to the Merger and related matters. Information regarding the persons or entities who may be considered “participants” in the solicitation of proxies will be set forth in the proxy statement and the Schedule 13E-3 transaction statement (or the amendment to the Buyer Consortium Transaction Statement) relating to the Merger and related matters, when it is filed with the SEC. Additional information regarding the interests of such potential participants will be included in the proxy statement and the Schedule 13E-3 transaction statement (or the amendment to the Buyer Consortium Transaction Statement) and the other relevant documents filed with the SEC when they become available.

This announcement is neither a solicitation of proxy, an offer to purchase nor a solicitation of an offer to sell any securities and it is not a substitute for any proxy statement or other materials that may be filed with or furnished to the SEC should the proposed merger proceed.

About China Biologic Products Holdings, Inc.

China Biologic Products Holdings, Inc. (NASDAQ: CBPO) is a leading fully integrated plasma-based biopharmaceutical company in China. The Company’s products are used as critical therapies during medical emergencies and for the prevention and treatment of life-threatening diseases and immune-deficiency related diseases. China Biologic is headquartered in Beijing and manufactures over 20 different dosage forms of plasma products through its indirect majority-owned subsidiary, Shandong Taibang Biological Products Co., Ltd. and its wholly owned subsidiary, Guizhou Taibang Biological Products Co., Ltd. The Company also has an equity investment in Xi’an Huitian Blood Products Co., Ltd. Since the acquisition of TianXinFu (Beijing) Medical Appliance Co., Ltd. in 2018, China Biologic is also engaged in the sale of medical devices, primarily regenerative medical biomaterial products. The Company sells its products to hospitals, distributors and other healthcare facilities in China. For additional information, please see the Company’s website www.chinabiologic.com.

Safe Harbor Statement

This news release may contain certain “forward-looking statements”. All statements, other than statements of historical fact included herein, are “forward-looking statements.” These forward-looking statements are often identified by the use of forward-looking terminology such as “intend,” “believe,” “expect,” “are expected to,” “will,” or similar expressions, and involve known and unknown risks and uncertainties. Although the Company believes that the expectations reflected in these forward-looking statements are reasonable, they involve assumptions, risks, and uncertainties, and these expectations may prove to be incorrect. The risks and uncertainties include the possibility that the Merger will not occur as planned if events arise that result in the termination of the Merger Agreement, if the expected financing for the Merger is not available for any reason, or if one or more of the various closing conditions to the Merger are not satisfied or waived, and other risks and uncertainties regarding the Merger Agreement and the Merger that will be discussed in the Schedule 13E-3 to be filed with the SEC. A number of factors could cause actual results to differ materially from those contained in any forward-looking statement. Investors should not place undue reliance on these forward-looking statements, which speak only as of the date of this news release. Other than as required under the securities laws, the Company does not assume a duty to update these forward-looking statements.

Contact:

China Biologic Products Holdings, Inc.
Mr. Ming Yin
Senior Vice President
Email: [email protected]

The Foote Group
Mr. Philip Lisio
Phone: +86-135-0116-6560
Email: [email protected]

Cision View original content:http://www.prnewswire.com/news-releases/china-biologic-enters-into-definitive-merger-agreement-for-going-private-transaction-301177142.html

SOURCE China Biologic Products Holdings, Inc.

Trinity Industries, Inc. to Host 2020 Investor Day Today

Trinity Industries, Inc. to Host 2020 Investor Day Today

DALLAS–(BUSINESS WIRE)–
Trinity Industries, Inc. (NYSE:TRN) will host a virtual Investor Day today including presentations by Jean Savage, Trinity’s CEO and President; Eric Marchetto, EVP and Chief Financial Officer; as well as other members of executive management.

During the presentations, management will discuss their strategic framework for optimization and growth of the rail platform, improving pre-tax return on equity to a mid-teen range through the cycle, and a capital allocation framework for expected cash flow from operations of $1.5 – 2.0 billion generated over the next three years. The presentations will be followed by a question and answer session hosted by Trinity’s management team.

The event is set to begin at 9:00 a.m. Eastern today, November 19, 2020 and is expected run less than 3 hours. The presentation materials were filed in a Form 8K this morning and have been posted to the event webpage for investors to preview.

How to Participate:

To participate in the live video webcast, visit the Investor Relations section of the Company’s website at www.trin.net and access the Events and Presentations webpage.

A replay of the webcast and presentation materials will be available on the website for one year from the date of the event.

About Trinity Industries

Trinity Industries, Inc., headquartered in Dallas, Texas, owns businesses that are leading providers of rail transportation products and services in North America. Our rail-related businesses market their railcar products and services under the trade name TrinityRail®. The TrinityRail platform provides railcar leasing and management services, as well as railcar manufacturing, maintenance and modifications. Trinity also owns businesses engaged in the manufacture of products used on the nation’s roadways and in traffic control, as well as a logistics business that primarily provides support services to Trinity. Trinity reports its financial results in three principal business segments: the Railcar Leasing and Management Services Group, the Rail Products Group, and the All Other Group. For more information, visit: www.trin.net.

Some statements in this release, which are not historical facts, are “forward-looking statements” as defined by the Private Securities Litigation Reform Act of 1995. Forward-looking statements include statements about Trinity’s estimates, expectations, beliefs, intentions or strategies for the future, and the assumptions underlying these forward-looking statements, including, but not limited to, future financial and operating performance, future opportunities and any other statements regarding events or developments that Trinity believes or anticipates will or may occur in the future, including the potential financial and operational impacts of the COVID-19 pandemic. Trinity uses the words “anticipates,” “assumes,” “believes,” “estimates,” “expects,” “intends,” “forecasts,” “may,” “will,” “should,” “guidance,” “projected,” “outlook,” and similar expressions to identify these forward-looking statements. Forward-looking statements speak only as of the date of this release, and Trinity expressly disclaims any obligation or undertaking to disseminate any updates or revisions to any forward-looking statement contained herein to reflect any change in Trinity’s expectations with regard thereto or any change in events, conditions or circumstances on which any such statement is based, except as required by federal securities laws. Forward-looking statements involve risks and uncertainties that could cause actual results to differ materially from historical experience or our present expectations, including but not limited to risks and uncertainties regarding economic, competitive, governmental, and technological factors affecting Trinity’s operations, markets, products, services and prices, and such forward-looking statements are not guarantees of future performance. For a discussion of such risks and uncertainties, which could cause actual results to differ from those contained in the forward-looking statements, see “Risk Factors” and “Forward-Looking Statements” in Trinity’s Annual Report on Form 10-K for the most recent fiscal year, as may be revised and updated by Trinity’s Quarterly Reports on Form 10-Q, and Trinity’s Current Reports on Form 8-K.

Investor Contact:

Jessica L. Greiner

Vice President, Investor Relations and Communications

Trinity Industries, Inc.

(Investors) 214/631-4420

Media Contact:

Jack L. Todd

Vice President, Public Affairs

Trinity Industries, Inc.

(Media Line) 214/589-8909

 

 

KEYWORDS: United States North America Texas

INDUSTRY KEYWORDS: Rail Transport Manufacturing Alternative Energy Energy Other Manufacturing

MEDIA:

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