The New York Academy of Medicine Honors Andrew M. Cuomo, Governor of New York, with Prestigious Public Health Award

The Stephen Smith Medal recognizes Governor Cuomo’s leadership during the COVID-19 pandemic

New York, NY, Nov. 13, 2020 (GLOBE NEWSWIRE) — The New York Academy of Medicine (NYAM) has awarded its prestigious 2020 Stephen Smith Medal for Distinguished Contributions in Public Health to the Honorable Andrew M. Cuomo, Governor of the State of New York, in recognition of his leadership of the state during the COVID-19 pandemic. 

Governor Cuomo accepted the award at NYAM’s 173rd Annual Meeting of the Fellows, which was held virtually on November 12. The event included the induction of 66 new NYAM Fellows and Members, whose names were read by special guests Dr. Howard Zucker, Commissioner of Health for New York State, and Dr. Dave Chokshi, Commissioner of Health for New York City. View the full event video here and the event program here

“Every day during the height of the pandemic in New York, we looked to Governor Cuomo for his leadership and compassion as we weathered this extraordinary challenge,” said NYAM President Judith A. Salerno, MD, MS. “His priority was to safeguard the people of New York, and for that we are forever grateful and inspired by his leadership. NYAM is honored to recognize Governor Cuomo’s significant contributions to public health with the 2020 Stephen Smith Medal.”

Michael J. Dowling, President and CEO of Northwell Health, introduced the award. Mr. Dowling served in New York State government for 12 years, including as deputy secretary to former governor Mario Cuomo. 

“During a crisis like this, leadership really, really matters,” Mr. Dowling said. “Leadership that tells the truth. Leadership that uses facts and science to guide decisions. Leadership that builds trust. Leadership that unifies, that brings people together, that focuses people on the central mission of how we deal with issues such as this. … Here in New York, as I know you will all agree with me, we have been very, very fortunate indeed because we have Governor Andrew Cuomo, a model of such leadership.”

”When Governor Cuomo designated University Hospital of Brooklyn as a COVID-only facility, we understood the magnitude of that designation and the trust he placed in our frontline staff,” said NYAM Board Chair and SUNY Downstate Health Sciences University President Wayne J. Riley, MD. “Under Governor Cuomo’s leadership, working with the New York State Department of Health and other partners, we were able to significantly flatten the curve and the spread of the virus by following and adhering to public health guidelines.”

“During these darkest days of COVID, we also saw the light,” Governor Cuomo said in his acceptance speech. “We saw 30,000 retired doctors and nurses return to service to battle the pandemic. We saw 10,000 healthcare professionals from around the country volunteer to come to New York at the height of the pandemic. We saw healthcare professionals become battlefield heroes in saving lives. And we saw the people of New York State rise to the occasion. … I hope and pray a COVID-19-type crisis never happens again, but I believe it will. And your challenge, our challenge, our society’s challenge is to be better prepared for that day before it comes. That’s my goal, I know that’s your goal, and I know that together we will get it done.”

About the Stephen Smith Medal for Distinguished Contributions in Public Health
The New York Academy of Medicine’s medal for lifetime achievement in public health, first awarded in 2005, was named for Stephen Smith, a NYAM Fellow and pioneer in the field of public health. The recipient should have led or significantly contributed to work that effected a significant change in public health policy or practice to improve population health, including work on the broad determinants of health, with a special emphasis on eliminating health disparities. Past recipients include Mary T. Bassett, the Honorable Michael R. Bloomberg, Thomas Frieden, Paula A. Johnson, Michael Marmot and Linda Rosenstock. 

About The New York Academy of Medicine 
The New York Academy of Medicine (NYAM) tackles the barriers that prevent every individual from living a healthy life. NYAM generates the knowledge needed to change the systems that prevent people from accessing what they need to be healthy such as safe and affordable housing, healthy food, healthcare, and more. Through its high-profile programming for the general public, focused symposia for health professionals, and its base of dedicated Fellows and Members, NYAM engages the minds and hearts of those who also value advancing health equity to maximize health for all. For more information, visit nyam.org and follow @nyamnyc on social media.  

Kiri Oliver
The New York Academy of Medicine
212-822-7278
[email protected]

Atossa Therapeutics Announces Third Quarter 2020 Financial Results and Provides Corporate Update

SEATTLE, Nov. 13, 2020 (GLOBE NEWSWIRE) — Atossa Therapeutics, Inc. (Nasdaq: ATOS), a clinical-stage biopharmaceutical company seeking to discover and develop innovative medicines in areas of significant unmet medical need with a current focus on breast cancer and COVID-19, today announced financial results for the third quarter ended September 30, 2020, and provided an update on recent company developments.

Key recent developments included:

  • Significantly advanced the development of AT-301 proprietary nasal spray as potential at-home treatment against COVID-19, with completion of a randomized, placebo controlled, double-blinded Phase 1 study and a preliminary assessment of the blinded data indicating that AT-301 was safe and well tolerated by participants at two different dose levels in both single and multiple dose forms over 14 days.
  • Applied for regulatory approval from the European Medical Product Authority to commence a Phase 2 clinical study of Endoxifen in Sweden to reduce mammographic breast density (MBD).
  • Announced interim findings following 18 months of an Expanded Access (or “compassionate use”) single-patient study of Endoxifen. The patient in the study had no cancer recurrence and suffered no side effects. Endoxifen did not cause other safety and tolerability concerns in this patient.

“Our COVID-19 nasal spray program has progressed very well during the quarter, with our Phase 1 study of AT-301 nasal spray demonstrating good safety and tolerability at two different dose levels in both single and multiple dose forms over a 14-day trial period,” said Dr. Steven Quay, Atossa’s President and Chief Executive Officer. “We are very encouraged by these preliminary results. In the next 30 days we plan to file a pre-IND meeting request with the FDA and, subject to their input, plan to immediately commence a Phase 2 study, either in the U.S. or abroad, in patients recently diagnosed with COVID-19.

“We believe AT-301 nasal spray is unique among the various therapies under development for COVID-19. While other companies are focused on therapies for patients being treated in hospitals, we are developing AT-301 for at-home use for the vast majority of COVID-19 patients who do not require hospitalization. Although great progress has been made by companies developing vaccines, it has become clear that a vaccine won’t provide a complete solution to the pandemic. No vaccine will be 100 percent effective and surveys have shown that many people won’t take a vaccine even when one becomes available. Similar to the seasonal flu where vaccines don’t provide complete community protection and people also rely on therapies, our AT-301 nasal spray therapy should form an important and necessary component of a comprehensive response to the COVID-19 pandemic,” added Dr. Quay.

Upcoming 2020 milestones include the following:

  • File pre-IND meeting request with FDA for AT-301 nasal spray for potential at-home treatment of COVID-19.
  • Commence Phase 2 study in Sweden for our Endoxifen to reduce MBD.

September
30, 2020 Financial Results 

For the three and nine months ended September 30, 2020 and 2019, we have no source of sustainable revenue and no associated cost of revenue.

Operating Expenses: Total operating expenses were approximately $3,509,000 and $10,382,000 for the three and nine months ended September 30, 2020, respectively, consisting of R&D expenses of approximately $1,659,000 and $4,251,000, respectively, and general and administrative (“G&A”) expenses of approximately $1,850,000 and $6,131,000, respectively. Total operating expenses were approximately $3,298,000 and $14,649,000 for the three and nine months ended September 30, 2019, respectively, consisting of R&D expenses of approximately $1,684,000 and $5,747,000, respectively, and G&A expense of approximately $1,614,000 and $8,901,000, respectively. Total operating expense for the nine months ended September 30, 2020 as compared to the same period in 2019 decreased approximately $4,267,000 or 29% and for the three months ended September 30, 2020 as compared to the same period in 2019 increased approximately $211,000 or 6%.

Research and Development Expenses: R&D expenses for the three months ended September 30, 2020, were approximately $1,659,000, which were comparable to total R&D expenses for the three months ended September 30, 2019, of approximately $1,684,000. R&D expenses for the nine months ended September 30, 2020, were approximately $4,251,000, a decrease of approximately $1,496,000 or 26% from total R&D expenses for the nine months ended September 30, 2019, of approximately $5,747,000. The decrease in R&D expense is attributed primarily to a decrease in stock-based compensation of approximately $2,165,000, which is a non-cash charge, offset by an increase in salaries, professional fees and clinical trials expenses of approximately $669,000, as compared to the same period in 2019. We expect our R&D expenses to increase for the remainder of 2020 as we seek to commence a study of AT-H201, complete our Phase 1 study of AT-301, launch a Phase 2 clinical trial of Endoxifen in women with high breast density, and continue the development of other indications and therapeutics.

General and Administrative Expenses: G&A expenses were approximately $1,850,000 for the three months ended September 30, 2020, an increase of approximately $236,000, or 15% from the total G&A expenses for the three months ended September 30, 2019, of approximately $1,614,000. The $236,000 increase in G&A expenses for the three month period ended September 30, 2020, is mainly attributed to an increase in legal, professional fees and insurance costs. G&A expenses were approximately $6,131,000 for the nine months ended September 30, 2020, a decrease of approximately $2,770,000, or 31% from the total G&A expenses for the nine months ended September 30, 2019, of approximately $8,901,000. G&A expenses consist primarily of personnel and related benefit costs, facilities, professional services, insurance, and public company related expenses. The decrease in G&A expenses for the nine month period ended September 30, 2020, is mainly attributed to a decrease in stock-based compensation expense of approximately $3,535,000, which is a non-cash charge, offset by an increase in legal, professional fees and insurance costs of approximately $765,000 compared to the same period in 2019. 

As of September 30, 2020, the Company had approximately $9.2 million in cash and cash equivalents.

About
Atossa
Therapeutics

Atossa Therapeutics, Inc. is a clinical-stage biopharmaceutical company seeking to discover and develop innovative medicines in areas of significant unmet medical need with a current focus on breast cancer and COVID-19. For more information, please visit www.atossatherapeutics.com.

Forward-Looking Statements

Forward-looking statements in this press release, which Atossa undertakes no obligation to update, are subject to risks and uncertainties that may cause actual results to differ materially from the anticipated or estimated future results, including the risks and uncertainties associated with any variation between interim and final clinical results, actions and inactions by the FDA, the outcome or timing of regulatory approvals needed by Atossa including those needed to commence studies of AT-H201, AT-301 and Endoxifen, lower than anticipated rate of patient enrollment, estimated market size of drugs under development, the safety and efficacy of Atossa’s products, performance of clinical research organizations and investigators, obstacles resulting from proprietary rights held by others such as patent rights, whether reduction in Ki-67 or any other result from a neoadjuvant study is an approvable endpoint for oral Endoxifen, and other risks detailed from time to time in Atossa’s filings with the Securities and Exchange Commission, including without limitation its periodic reports on Form 10-K and 10-Q, each as amended and supplemented from time to time.

Company Contact:
Atossa Therapeutics, Inc.
Kyle Guse CFO and General Counsel
Office: 866 893-4927
[email protected]

Investor Relations Contact:
Core IR
Office:(516) 222-2560
[email protected]

Source: Atossa Therapeutics, Inc.







ATOSSA THERAPEUTICS, INC.

CONDENSED CONSOLIDATED BALANCE SHEETS

    As of
September 30,
2020
    As of
December 31,
 

Assets
  (Unaudited)     2019  
Current assets                
Cash and cash equivalents   $ 9,105,950     $ 12,581,136  
Restricted cash     110,000       110,000  
Prepaid expenses     1,484,251       862,344  
Research and development tax rebate receivable     439,205       739,656  
Other current assets     178,911       26,130  
Total current assets     11,318,317       14,319,266  
                 
Furniture and equipment, net     25,429       34,350  
Intangible assets, net     45,417       68,542  
Right-of-use asset     31,279       50,479  
Other assets     17,218       17,218  
Total Assets   $ 11,437,660     $ 14,489,855  
                 

Liabilities and Stockholders’ Equity
               
Current liabilities                
Accounts payable   $ 682,612     $ 293,171  
Accrued expenses     85,173       77,888  
Payroll liabilities     752,847       899,420  
Lease liability     30,063       39,371  
Other current liabilities     14,671       12,892  
Total current liabilities     1,565,366       1,322,742  
Long term liabilities                
Lease liability long term     1,217       11,108  
Total Liabilities     1,566,583       1,333,850  
                 
Commitments and contingencies                
                 
Stockholders’ equity                
Preferred stock – $0.001 par value; 10,000,000 shares authorized; 623 and 671 shares issued and outstanding as of September 30, 2020 and December 31, 2019, respectively     1       1  
Additional paid-in capital – Series B convertible preferred stock     622,999       670,999  
Common stock – $0.18 par value; 175,000,000 shares authorized; 10,464,250 and 9,130,984 shares issued and outstanding as of September 30, 2020 and December 31, 2019, respectively     1,883,553       1,643,565  
Additional paid-in capital     111,780,197       104,912,480  
Accumulated deficit     (104,415,673 )     (94,071,040 )
Total Stockholders’ Equity     9,871,077       13,156,005  
Total Liabilities and Stockholders’ Equity   $ 11,437,660     $ 14,489,855  

The accompanying notes are an integral part of these condensed consolidated financial statements.







ATOSSA THERAPEUTICS, INC. 
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS
(UNAUDITED)

    For the Three Months Ended September 30,     For the Nine Months Ended September 30,  
                                 
    2020     2019     2020     2019  
Operating expenses                                
Research and development   $ 1,659,075     $ 1,684,215     $ 4,250,934     $ 5,747,399  
General and administrative     1,849,741       1,613,983       6,130,698       8,901,197  
Total operating expenses     3,508,816       3,298,198       10,381,632       14,648,596  
Operating loss     (3,508,816 )     (3,298,198 )     (10,381,632 )     (14,648,596 )
Other income     17,745       12,284       36,999       26,846  
Loss before income taxes     (3,491,071 )     (3,285,914 )     (10,344,633 )     (14,621,750 )
Income taxes                        
Net loss   $ (3,491,071 )   $ (3,285,914 )   $ (10,344,633 )   $ (14,621,750 )
Loss per common share – basic and diluted   $ (0.34 )   $ (0.36 )   $ (1.09 )   $ (1.77 )
Weighted average shares outstanding – basic and diluted     10,162,770       9,130,057       9,496,222       8,283,302  

The accompanying notes are an integral part of these condensed consolidated financial statements.

Progenity to Host Preeclampsia Virtual R&D Day on November 20, 2020

SAN DIEGO, Nov. 13, 2020 (GLOBE NEWSWIRE) — Progenity, Inc. (Nasdaq: PROG), a biotechnology company with an established track record of success in developing and commercializing molecular testing products, today announced that it will host a Preeclampsia Virtual R&D Day on November 20, 2020 from 11 a.m. to 1 p.m. ET (8 a.m. to 10 a.m. PT). Members of Progenity’s senior management team and select guest speakers will provide an in-depth discussion of the company’s ongoing clinical development of the Preecludia™ rule-out test for preeclampsia. Attendees will learn about the pathophysiology of preeclampsia, current clinical management and diagnosis of the condition, its health economic burden, and Progenity’s diagnostic approach.

Interested parties may access a live audio webcast and slides of the presentations on the investor section of Progenity’s website at progenity.com/presentations. Additionally, the live event may be accessed by dialing 833-519-1237 for domestic callers and 914-800-3810 for international callers and entering the conference code: 1190518. A replay of the webcast will be available shortly after the event and can be viewed at the same web link.

About Progenity

Progenity, Inc. is a biotechnology company with an established track record of success in developing and commercializing molecular testing products, as well as innovating in the field of precision medicine. Progenity provides in vitro molecular tests designed to improve lives by providing actionable information that helps guide patients and physicians in making medical decisions during key life stages. The company applies a multi-omics approach, combining genomics, epigenomics, proteomics, and metabolomics to its molecular testing products and to the development of a suite of investigational ingestible devices designed to provide precise diagnostic sampling and drug delivery solutions. Progenity’s vision is to transform healthcare to become more precise and personal by improving diagnoses of disease and improving patient outcomes through localized treatment with targeted therapies. For additional information about Progenity, please visit the company’s website at www.progenity.com.

Investor Contact:

Robert Uhl
Managing Director, Westwicke ICR
[email protected]
(619) 228-5886

Media Contact:

Kate Blom-Lowery
CG Life
[email protected]
(858) 457-2436



Konica Minolta to Show how Security is Anchored in Corporate Culture at the IDC European CISO Summit

Digital Workplace Provider will Host an Expert Talk and Several Discussion Panels

Ramsey, NJ, Nov. 13, 2020 (GLOBE NEWSWIRE) — Konica Minolta Business Solutions, U.S.A., Inc., along with Konica Minolta Business Solutions Europe (Konica Minolta), today announced its participation in the IDC European CISO Summit on November 16–17, 2020.

Malware, ransomware attacks, phishing attacks and cyber-attacks can have dramatic consequences for a company’s business activities. Being fully protected requires a corporate culture in which security is deeply rooted. By participating as a GOLD sponsor in the IDC European CISO Summit, Konica Minolta aims to show those who attend its expert talk and several discussion panels how companies can anchor security into their corporate culture. The IDC European CISO Summit is aimed at a selected group of 100+ CISOs from various companies in Europe and serves as an information-sharing forum and networking platform. Owing to the current global situation, IDC has decided to make the summit a virtual event.

“People have a natural sense of security in the physical world when it comes to hygiene, fear of heights, locked doors or strangers. But once online, their level of caution sometimes drops,” said Yoann Fortini, IT Services Go-To-Market Senior Manager, Konica Minolta Business Solutions Europe GmbH. “But the primary point of failure in cyber-attacks is always the end user — the human being. In the end, however, their actions and the consequences they have damage the company as a whole. This is why the digital transformation is first of all a question of people and culture, then only in the second step a question of technology. Security should follow the same path.”

Security should not be seen as a goal in itself, but as a means to ensure business continuity and optimize business performance. Business strategy and security strategy should be connected. CISOs play a significant role here — by shifting their scope from the security team to the company business, by establishing a new agile security leadership style and by directly influencing the future of work.

That is why, during the European CISO Summit, Yoann Fortini will use his 20-minute TechTalk on November 17 at 12:35 p.m. CET to speak about “Corporate culture and security: friends or foes?” He will talk about the fact that companies go through different stages in their digital transformation and that they have to deal with disparate levels of security maturity, but that all these situations have something in common: security is a question of corporate culture. He will therefore emphasize the concept of security culture and that this is not only in the hands of CISOs, but is ultimately the responsibility of everyone in the company. He will also give his top ten tips on how to create a security culture in an organization.

In addition, Yoann Fortini and Gene Abramov, co-founder and CEO of Depth Security, a cybersecurity consulting company acquired by Konica Minolta Business Solutions U.S.A., Inc. in August 2020, will take part in four IDC roundtables “IDC Connect” under the title “Why CISOs are the new business change makers” on November 16 (11:45 a.m. CET and 1:50 p.m. CET) and November 17 (11:30 a.m. CET and 12:55 p.m. CET). They will talk about how the COVID-19 pandemic has confirmed the relevance of CISOs in particular and about security in general for businesses and the economy. In fact, the role of CISOs will be even further expanded in the near future: from user awareness to business strategy, from day-to-day IT security to advanced cyber security policy. Fortini and Abramov will talk about security as a transversal issue that cannot be considered in isolation, but rather forms the basis for all areas of a company in a connected and integrated ecosystem.

“The challenges and opportunities for CISOs and the cybersecurity industry in 2021, particularly with the uncertainty digital transformation places on security posture, require CISOs to be more adaptive than ever,” said Gene Abramov. “The number of decisions – and the speed at which they make them – have significantly increased in the last eight months, and we look forward to sharing our insight from the field to help them navigate what’s ahead.”

Integrated security services from a certified provider

Last but not least, one of the main paradoxes we see today is that security is considered a high priority in most companies, but that companies do not allocate a sufficient portion of their budget to it. Furthermore, the COVID-19 pandemic is regarded as a kind of fire accelerator that has made the vulnerability of many companies visible, especially through decentralized working. With the support of an external provider, businesses can tackle these challenges. “We are well aware that Konica Minolta is not the provider companies first think of when looking for an expert in cyber security — and if they do consider us, it’s for printer security,” Yoann Fortini admits. “But our approach to security is an integrated and holistic one that involves many factors: Through our acquisitions of IT services companies worldwide in recent years, we have brought a high level of external expertise into the company. We have trained our employees on this basis throughout and we have strong partners at hand. This offers our customers — and our main customer base today is SMEs — an integrated, consolidated ecosystem that considers all aspects of the digital workplace, including cyber security, and does so in an easily accessible and reliable manner that is represented globally and available locally at the same time. Our customers receive packaged solutions so that they can concentrate fully on their core business.”

This year, Konica Minolta Business Solutions Europe was awarded ISO 27001 certification for its established Information Security Management System (ISMS). The certificate was issued on the basis of a thorough audit that included in-depth screening of Konica Minolta’s holistic information security approach across all areas, from HR to customer relations, and across all channels, from digital processes to a clean desk policy in the organization. This makes Konica Minolta Business Solutions Europe an ISO 27001-certified supplier.

More information about the IDC European CISO Summit can be found online.

About Konica Minolta Business Solutions U.S.A., Inc.

Konica Minolta Business Solutions U.S.A., Inc. is reshaping and revolutionizing the Workplace of the Future™ with its expansive smart office product portfolio from IT Services (All Covered), ECM, Managed Print Services and industrial and commercial print solutions. Konica Minolta has been recognized as the #1 Brand for Customer Loyalty in the MFP Office Copier Market by Brand Keys for thirteen consecutive years, and is proud to be ranked on the Forbes 2017 America’s Best Employers list. The World Technology Awards recently named the company a finalist in the IT Software category. Konica Minolta, Inc. has been named to the Dow Jones Sustainability World Index for eight consecutive years and has spent three years on the Global 100 Most Sustainable Corporations in the World list. It partners with its clients to give shape to ideas and work to bring value to our society. For more information, please visit us online and follow Konica Minolta on FacebookYouTubeLinked In and Twitter.

About Konica Minolta Business Solutions Europe

Konica Minolta Business Solutions Europe GmbH, based in Langenhagen, Germany, is a wholly owned subsidiary of Konica Minolta Inc., Tokyo, Japan. Konica Minolta enables its clients to champion the digital era: with its unique imaging expertise and data processing capabilities, Konica Minolta creates relevant solutions for its customers and solves issues faced by society. As a provider of comprehensive IT services, Konica Minolta delivers consultancy and services to optimise business processes with workflow automation. The company further offers its customers solutions and managed services in the field of IT infrastructure and IT security as well as cloud environments. With regard to its office printing solutions, ‘IDC MarketScape: Worldwide Print Transformation 2020 Vendor Assessment’ stated that Konica Minolta is ‘recognised globally as a leader in print transformation’. As a strong partner for the professional printing market, Konica Minolta offers business consulting, state-of-the-art technology and software and has established itself as the production printing market leader for more than a decade in Europe (InfoSource). In the healthcare sector, Konica Minolta drives digitalisation of clinical workflows and offers a broad range of next-level diagnostic solutions. Its Business Innovation Centre in London and four R & D laboratories in Europe enable Konica Minolta to bring innovation forward by collaborating with its customers as well as academic, industrial and entrepreneurial partners. For its innovative service approach that complements their devices perfectly, Konica Minolta was awarded the prestigious ‘Buyers Lab PaceSetter Award for Serviceability and Support 2020/2021’ from Keypoint Intelligence. Konica Minolta Business Solutions Europe is represented by subsidiaries and distributors in more than 80 countries in Europe, Central Asia, the Middle East and Africa. With approximately 10,000 employees (as of April 2020), Konica Minolta Europe earned net sales of over 2.34 billion in financial year 2019/2020. For more information, please visit the newsroom and follow Konica Minolta on Facebook, YouTube and Twitter @KonicaMinoltaEU.

       

# # # # #

Attachment



Maggie Grande
Konica Minolta Business Solutions U.S.A., Inc.
1-551-500-2659
[email protected]

Total To Use Honeywell UOP Technology To Produce Renewable Jet Fuel And Diesel At Its Zero-Crude Platform In France

Honeywell UOP Ecofining™ process to help deliver sustainable jet fuel and renewable diesel in support of France’s sustainability goals

PR Newswire

DES PLAINES, III., Nov. 13, 2020 /PRNewswire/ — Honeywell (NYSE: HON) today announced Total will use Honeywell UOP Ecofining™ process technology to produce renewable fuels, primarily for the aviation industry, at its Grandpuits platform at Seine-et-Marne in north central France.

Honeywell UOP will provide technology licenses, basic engineering, specialty equipment, and catalysts for the project. Once completed, the bio-refinery will process 400,000 tons of feed per year, producing up to 170,000 tons of sustainable aviation fuel, 120,000 tons of renewable diesel and 50,000 tons of renewable naphtha for production of bioplastics.

“Total chose UOP’s Ecofining process to increase its renewable jet fuels production in France,” said Ben Owens, VP and general manager of Honeywell’s Sustainable Technology Solutions business. “UOP’s Ecofining process will help Total to convert its Grandpuits refinery into a zero-crude platform that supports government plans to develop fossil fuel substitutes and achieve carbon neutrality.”

According to the Ministry for Ecological Transition, the deployment of sustainable aviation fuels is one of the top priorities of the French government and part of its broader national commitment to tackle climate change. Earlier this year, France announced plans to replace 2% of its fossil-based jet fuel with sustainable aviation fuels by 2025, rising to 5% by 2030 and to 50% by 2050.

Honeywell pioneered the sustainable aviation fuel market with its UOP Ecofining process. Honeywell Green Jet Fuel™ produced by this process is blended seamlessly with petroleum-based jet fuel at commercial scale. When used in up to a 50% blend with petroleum-based jet fuel, Honeywell Green Jet Fuel requires no changes to aircraft technology and meets all critical specifications for flight. Learn more about UOP renewable energy technologies at www.uop.com/biofuels.

Total is a French broad energy company that produces and markets fuels, natural gas and electricity. Based in Paris, the company is active in more than 130 countries.

Honeywell UOP (www.uop.com) is a leading international supplier and licensor of process technology, catalysts, adsorbents, equipment, and consulting services to the petroleum refining, petrochemical, and gas processing industries. Honeywell UOP is part of Honeywell’s Performance Materials and Technologies strategic business group, which also includes Honeywell Process Solutions (www.honeywellprocess.com), a pioneer in automation control, instrumentation and services for the oil and gas, refining, petrochemical, chemical and other industries.

Honeywell (www.honeywell.com) is a Fortune 100 technology company that delivers industry specific solutions that include aerospace products and services; control technologies for buildings and industry; and performance materials globally. Our technologies help everything from aircraft, buildings, manufacturing plants, supply chains, and workers become more connected to make our world smarter, safer, and more sustainable.  For more news and information on Honeywell, please visit www.honeywell.com/newsroom.

Contacts:

U.S. media contact: 
Tehani Manochio 
(973) 216-0684 
[email protected] 

European media contact:
Martin Orsag
+4 2024 244 2279
[email protected]

Cision View original content:http://www.prnewswire.com/news-releases/total-to-use-honeywell-uop-technology-to-produce-renewable-jet-fuel-and-diesel-at-its-zero-crude-platform-in-france-301172788.html

SOURCE Honeywell

GAMCO Natural Resources, Gold & Income Trust Announces Expected Total Distributions of $0.36 Per Share For 2021

GAMCO Natural Resources, Gold & Income Trust Announces Expected Total Distributions of $0.36 Per Share For 2021

Declares Monthly Distributions of $0.03 Per Share

RYE, N.Y.–(BUSINESS WIRE)–
The Board of Trustees of GAMCO Natural Resources, Gold & Income Trust (NYSE:GNT) (the “Fund”) approved the continuation of its policy of paying monthly cash distributions. The Board of Trustees declared cash distributions of $0.03 per share for each of January, February, and March 2021. This equates to an expected total annual 2021 distribution of $0.36 per common share. Based on current dynamics, the Fund may make distributions in excess of the Fund’s earnings. It is currently expected that distributions to common shareholders in 2021 will primarily constitute a return of capital for tax purposes.

     

Distribution Month

 

Record Date

 

Payable Date

January

 

January 14, 2021

 

January 22, 2021

February

 

February 11, 2021

 

February 19, 2021

March

 

March 17, 2021

 

March 24, 2021

     

The Board of Trustees will continue to monitor the Fund’s distribution level, taking into consideration the Fund’s net asset value and the financial market environment. The distribution rate should not be considered the dividend yield or total return on an investment in the Fund.

Because the Fund’s current monthly distributions are subject to modification by the Board of Trustees at any time and the Fund’s income will fluctuate, there can be no assurance that the Fund will pay distributions at a particular rate or frequency. Shareholders should not draw any conclusions about the Fund’s investment performance from the amount of the current distribution.

Contact John Ball ([email protected] or 914-921-7728) for tax information.

Investors should carefully consider the investment objectives, risks, charges, and expenses of the Fund before investing. More information regarding the Fund’s distribution policy and other information about the Fund is available by calling 800-GABELLI (800-422-3554) or visiting www.gabelli.com.

The Fund’s NAV per share will fluctuate with changes in the market value of the Fund’s portfolio securities. Stocks are subject to market, economic, and business risks that cause their prices to fluctuate. Investors acquire shares of the Fund on a securities exchange at market value, which fluctuates according to the dynamics of supply and demand. When Fund shares are sold, they may be worth more or less than their original cost. Consequently, you can lose money by investing in the Fund.

Covered Call and Other Option Transaction Risks. There are several risks associated with writing covered calls and entering into other types of option transactions. For example, there are significant differences between the securities and options markets that could result in an imperfect correlation between these markets, resulting in a given transaction not achieving its objectives. In addition, a decision as to whether, when, and how to use covered call options involves the exercise of skill and judgment, and even a well-conceived transaction may be unsuccessful because of market behavior or unexpected events. As the writer of a covered call option, the Fund forgoes, during the option’s life, the opportunity to profit from increases in the market value of the security covering the call option above the exercise price of the call option, but has retained the risk of loss should the price of the underlying security decline.

About The GAMCO Natural Resources, Gold & Income Trust

The GAMCO Natural Resources, Gold & Income Trust is a non-diversified, closed-end management investment company with $146 million in total net assets whose primary investment objective is to provide a high level of current income. The Fund invests primarily in equity securities of gold and natural resources companies and intends to earn income primarily through a strategy of writing (selling) primarily covered call options on equity securities in its portfolio. The Fund is managed by Gabelli Funds, LLC, a subsidiary of GAMCO Investors, Inc. (NYSE:GBL).

NYSE – GNT

CUSIP – 36465E101

Investor Relations Contact:

David Schachter

(914) 921-5057

[email protected]

KEYWORDS: United States North America New York

INDUSTRY KEYWORDS: Banking Other Professional Services Professional Services Finance

MEDIA:

AnaptysBio to Present at the 2020 Jefferies London Virtual Healthcare Conference

SAN DIEGO, Nov. 13, 2020 (GLOBE NEWSWIRE) — AnaptysBio, Inc. (Nasdaq: ANAB), a clinical-stage biotechnology company developing first-in-class antibody product candidates focused on emerging immune control mechanisms applicable to inflammation and immuno-oncology indications, today announced that Hamza Suria, chief executive officer of AnaptysBio, will present at the 2020 Jefferies London Virtual Healthcare Conference on Tuesday, November 17, 2020, at 12:35 p.m. ET. The conference will be conducted virtually, and the presentation will be available via https://wsw.com/webcast/jeff141/anab/1804050

A live webcast of the presentation will also be available through the investor section of the AnaptysBio website at https://ir.anaptysbio.com/events. A replay of the webcast will be available for 90 days following the event.

About AnaptysBio

AnaptysBio is a clinical-stage biotechnology company developing first-in-class antibody product candidates focused on emerging immune control mechanisms applicable to inflammation and immuno-oncology indications. The Company’s proprietary anti-inflammatory pipeline includes its anti-IL-36R antibody imsidolimab, previously referred to as ANB019, for the treatment of rare inflammatory diseases, including generalized pustular psoriasis, or GPP, palmoplantar pustulosis, or PPP, EGFRi and ichthyosis; its anti-PD-1 agonist program, ANB030, for treatment of certain autoimmune diseases where immune checkpoint receptors are insufficiently activated; its BTLA modulator program, ANB032, which is broadly applicable to human inflammatory diseases associated with lymphoid and myeloid immune cell dysregulation; and its anti-IL-33 antibody etokimab, previously referred to as ANB020, for the treatment of chronic rhinosinusitis with nasal polyps, or CRSwNP, and eosinophilic asthma. AnaptysBio’s antibody pipeline has been developed using its proprietary somatic hypermutation, or SHM platform, which uses in vitro SHM for antibody discovery and is designed to replicate key features of the human immune system to overcome the limitations of competing antibody discovery technologies. AnaptysBio has also developed multiple therapeutic antibodies in an immuno-oncology collaboration with GlaxoSmithKline, including an anti-PD-1 antagonist antibody (dostarlimab GSK4057190A), an anti-TIM-3 antagonist antibody (cobolimab, GSK4069889A) and an anti-LAG-3 antagonist antibody (GSK4074386), and an inflammation collaboration with Bristol-Myers Squibb, including an anti-PD-1 checkpoint agonist antibody (CC-90006) currently in clinical development.

Contact:

Dennis Mulroy
AnaptysBio, Inc.
858.732.0201
[email protected]

Thermalito Union Elementary School District Approves Purchase of Six All-Electric School Buses From GreenPower

PR Newswire


California Schools Continue Transition to Zero-Emissions Transportation

LOS ANGELES, Nov. 13, 2020 /PRNewswire/ — GreenPower Motor Company Inc. (NASDAQ:GP) (TSXV:GPV) (“GreenPower”) a leading manufacturer and distributor of zero emissions electric powered vehicles serving the cargo delivery, shuttle, transit, and school bus markets, today announced the sale of six electric school buses (B.E.AS.T.), to Thermalito Union Elementary School District through Greenpower’s national distributor Creative Bus Sales.

The B.E.A.S.T. is a purpose-built Type D Battery Electric School bus with a leading class range of up to 150 miles and a 194.5kWh battery pack. The vehicles can charge up to 20KW on standard J1772 protocol and has CCS1 fast charging, with additional standard features like air ride suspension, pass through storage, and air disk brakes. The B.E.A.S.T. offers a Monocoque chassis design built from the ground up to be battery electric.

Butte County Air Quality Management District (AQMD) will be funding the purchase of one school bus through their clean vehicle incentive program. AQMD’s mission is to protect the community and the environment of Butte County from the harmful effects of air pollution. Their clean vehicle incentive programs offer grants to aid in the reduction of emissions and the impact of air quality.

Five of GreenPower’s electric school buses will be funded through the California Clean Energy Jobs Act (CEC) Prop 39. The CEC Prop 39, has awarded schools more than $1.7 billion over the last five years to plan and install energy efficiency upgrades, clean energy generation measures, and zero emissions transportation.

Brendan Riley, President of GreenPower commented, “The sale of six units to the Thermalito Union School District is a great example of how GreenPower is working with customers and our sales partners to leverage multiple incentive programs to bring our all-electric school bus to market. This is a trend we expect to accelerate within California, then spread to other states as a template.”  Mr. Riley continued, “Our sales team has been working exhaustively to further our first mover advantage in the purpose built all-electric school bus market and we have high expectations as the transition to EV accelerates for the sector.”

Ryne Shetterly, VP of Sales and Marketing also commented, “Our purpose-built, zero-emissions, electric school bus was created with the health and safety of children in mind, as our all-electric school buses do not produce the toxic emissions produced by diesel buses. The B.E.A.S.T. showcases how overall safety and efficiency is our number one priority.” Mr. Shetterly adds, “Creative Bus Sales has worked hard with GreenPower to bring together demonstrations to school districts. The sales team at Creative Bus Sales is one of the best in the business and we will continue to proudly partner with them and push deals forward.”


About GreenPower Motor Company Inc. 

GreenPower designs, builds and distributes a full suite of high-floor and low-floor vehicles, including transit buses, school buses, shuttles, cargo van and a double decker. GreenPower employs a clean-sheet design to manufacture all-electric buses that are purpose built to be battery powered with zero emissions. GreenPower integrates global suppliers for key components, such as Siemens or TM4 for the drive motors, Knorr for the brakes, ZF for the axles and Parker for the dash and control systems. This OEM platform  allows GreenPower to meet the specifications of various operators while providing standard parts for ease  of maintenance and accessibility for warranty requirements. For further information go to www.greenpowerbus.com


Forward-Looking Statements 

This document contains forward-looking statements relating to, among other things, GreenPower’s business and operations and the environment in which it operates, which are based on GreenPower’s  operations, estimates, forecasts and projections. Forward-looking statements are not based on historical facts, but rather on current expectations and projections about future events, and are therefore subject to  risks and uncertainties which could cause actual results to differ materially from the future results expressed  or implied by the forward-looking statements. These statements generally can be identified by the use of forward-looking words such as “upon”, “may”, “should”, “will”, “could”, “intend”, “estimate”, “plan”, “anticipate”, “expect”, “believe” or “continue”, or the negative thereof or similar variations. These statements are not guarantees of future performance and involve risks and uncertainties that are difficult to  predict. A number of important factors including those set forth in other public filings (filed under the Company’s profile on www.sedar.com) could cause actual outcomes and results to differ materially from those expressed in these forward-looking statements. Consequently, readers should not place any undue reliance on such forward-looking statements. In addition, these forward-looking statements relate to the date on which they are made. GreenPower disclaims any intention or obligation to update or revise any forward-looking statements whether as a result of new information, future events or otherwise. 

Neither the TSX Venture Exchange nor its Regulation Services Provider (as that term is defined in the policies of the TSX Venture Exchange) accepts responsibility for the adequacy or accuracy of this release. © 2020 GreenPower Motor Company Inc. All rights reserved.

Cision View original content:http://www.prnewswire.com/news-releases/thermalito-union-elementary-school-district-approves-purchase-of-six-all-electric-school-buses-from-greenpower-301172800.html

SOURCE GreenPower Motor Company

Liminal Biosciences to Present at The Stifel Virtual Healthcare Conference

PR Newswire

LAVAL, QC and CAMBRIDGE, England, Nov. 13, 2020 /PRNewswire/ – Liminal BioSciences Inc. (Nasdaq: LMNL) (“Liminal BioSciences” or the “Company”), a clinical-stage biopharmaceutical company, announced that Bruce Pritchard, Chief Executive Officer at Liminal BioSciences is scheduled to present a company overview at The Stifel 2020 Virtual Healthcare Conference on Monday 16th November at 2:40-3:10 PM (EDT).

The presentation will be webcast live on the webcast page of the Investors & Media section of the Company’s website. An archived replay of the webcast will be available on the Company’s website for at least 7 days after the live event concludes.

About Liminal BioSciences Inc.

Liminal BioSciences is a clinical-stage biopharmaceutical company focused on discovering, developing and commercializing novel treatments for patients suffering from diseases of high unmet medical need, primarily related to fibrosis, including respiratory, liver and kidney diseases. Liminal BioSciences has a deep understanding of certain biological targets and pathways that have been implicated in the fibrotic process, including fatty acid receptors such as FFAR1, G-protein-coupled receptor 84 (GPR84), and peroxisome proliferator-activated receptors (PPARs). Our lead small molecule product candidate, fezagepras (PBI-4050), is expected to enter a Phase 1 clinical trial in Q4-2020 in the UK to evaluate multiple ascending doses in normal healthy volunteers, at daily dose exposures higher than those evaluated in our previously completed Phase 2 clinical trials. Fezagepras is expected to be further evaluated in a global Phase 2b clinical trial in patients with idiopathic pulmonary fibrosis (IPF) anticipated to be initiated in H2-2021. In addition, we expect to initiate a Phase 1b/2a clinical trial in the US of fezagepras for patients with high triglyceride levels (hypertriglyceridemia) in H2-2021.

Fezagepras has previously been granted Orphan Drug Designation by the FDA and the European Medical Agency (EMA) for the treatment of IPF. The treatment has also received a Promising Innovative Medicines (PIM) designation by the Medicines and Healthcare products Regulatory Agency (MHRA) for IPF.

Liminal BioSciences has also leveraged its experience in bioseparation technologies through its subsidiary Prometic Bioproduction Inc. to isolate and purify biopharmaceuticals from human plasma. Liminal BioSciences’ lead plasma-derived product candidate is Ryplazim®(plasminogen) (“Ryplazim®“), for which the Company, through its US subsidiary, Prometic Biotherapeutics Inc., resubmitted a BLA in September 2020 with the FDA seeking approval to treat patients with congenital plasminogen deficiency. The PDUFA target action date for this BLA filing is June 5, 2021. Ryplazim® has previously been granted Orphan Drug and Rare Pediatric Disease Designations by the FDA for the treatment of congenital plasminogen deficiency.

Prometic Plasma Resources, a subsidiary of Liminal BioSciences, has joined the CoVIg-19 Plasma Alliance to contribute to the acceleration of the development of a potential new therapy for COVID-19. Liminal BioSciences’ Canadian plasma collection center located in Winnipeg, Manitoba is licensed by the FDA and Health Canada, and is certified by the European Union and the Plasma Protein Therapeutics Association. Liminal BioSciences’ American plasma collection center located in Amherst, New York is licensed by the State of New York and its BLA submission is currently under review by the FDA.

Liminal BioSciences has active business operations in Canada, the United Kingdom and the United States.

Forward Looking Statement

This press release contains forward-looking statements about Liminal BioSciences’ objectives, strategies and businesses that involve risks and uncertainties. Forward–looking information includes statements concerning, among other things, statements regarding our clinical development plans for fezagepras, with respect to the timing for FDA review of the BLA for Ryplazim®, our plans for commercial launch of Ryplazim® in the United States if approved, our regulatory and commercial plans for Ryplazim® outside the United States, the potential of our product candidates and development of R&D programs and the nature and timing of initiation of clinical trials.

These statements are “forward-looking” because they are based on our current expectations about the markets we operate in and on various estimates and assumptions. Actual events or results may differ materially from those anticipated in these forward-looking statements if known or unknown risks affect our business, or if our estimates or assumptions turn out to be inaccurate. At this stage, the product candidates of the Company have not been authorized for sale in any country. Among the factors that could cause actual results to differ materially from those described or projected herein include, but are not limited to, risks associated with FDA review, Liminal BioSciences’ ability to effectively establish a commercial organization, Liminal BioSciences’ ability to develop, manufacture, and successfully commercialize product candidates, if ever, the impact of the COVID-19 pandemic on its business operations, clinical development, regulatory activities and financial and other corporate impacts, the availability of funds and resources to pursue R&D projects, the successful and timely completion of clinical trials, the ability of Liminal BioSciences to take advantage of business opportunities in the pharmaceutical industry, uncertainties associated generally with research and development, clinical trials and related regulatory reviews and approvals and general changes in economic conditions. You will find a more detailed assessment of these risks, uncertainties and other risks that could cause actual events or results to materially differ from our current expectations in the filings the Company makes with the U.S. Securities and Exchange Commission and Canadian Securities Commissions filings and reports filings and reports, including in the Annual Report on Form 20-F, as amended, for the year ended December 31, 2019 and future filings and reports by the Company, from time to time. Such risks may be amplified by the COVID-19 pandemic and its potential impact on Liminal BioSciences’ business and the global economy. As a result, we cannot guarantee that any forward-looking statement will materialize. Existing and prospective investors are cautioned not to place undue reliance on these forward-looking statements and estimates, which speak only as of the date hereof.  We assume no obligation to update any forward-looking statement contained in this Press Release even if new information becomes available, as a result of future events or for any other reason, unless required by applicable securities laws and regulations.

Cision View original content:http://www.prnewswire.com/news-releases/liminal-biosciences-to-present-at-the-stifel-virtual-healthcare-conference-301172751.html

SOURCE Liminal BioSciences Inc.

GAMCO Global Gold, Natural Resources & Income Trust Announces Expected Total Distributions of $0.36 Per Share for 2021

GAMCO Global Gold, Natural Resources & Income Trust Announces Expected Total Distributions of $0.36 Per Share for 2021

Declares Monthly Distributions of $0.03 Per Share

RYE, N.Y.–(BUSINESS WIRE)–
The Board of Trustees of GAMCO Global Gold, Natural Resources & Income Trust (NYSE American: GGN) (the “Fund”) approved the continuation of its policy of paying monthly cash distributions. The Board of Trustees declared cash distributions of $0.03 per share for each of January, February, and March 2021. This equates to an expected total annual 2021 distribution of $0.36 per common share. Based on current dynamics, the Fund may make distributions in excess of the Fund’s earnings. It is currently expected that distributions to common shareholders in 2021 will primarily constitute a return of capital for tax purposes.

Distribution Month

   

Record Date

   

Payable Date

January

   

January 14, 2021

   

January 22, 2021

February

   

February 11, 2021

   

February 19, 2021

March

   

March 17, 2021

   

March 24, 2021

The Board of Trustees will continue to monitor the Fund’s distribution level, taking into consideration the Fund’s net asset value and the financial market environment. The distribution rate should not be considered the dividend yield or total return on an investment in the Fund.

Because the Fund’s current monthly distributions are subject to modification by the Board of Trustees at any time and the Fund’s income will fluctuate, there can be no assurance that the Fund will pay distributions at a particular rate or frequency. Shareholders should not draw any conclusions about the Fund’s investment performance from the amount of the current distribution.

Contact John Ball ([email protected] or 914-921-7728) for tax information.

Investors should carefully consider the investment objectives, risks, charges, and expenses of the Fund before investing. More information regarding the Fund’s distribution policy and other information about the Fund is available by calling 800-GABELLI (800-422-3554) or visiting www.gabelli.com.

The Fund’s NAV per share will fluctuate with changes in the market value of the Fund’s portfolio securities. Stocks are subject to market, economic, and business risks that cause their prices to fluctuate. Investors acquire shares of the Fund on a securities exchange at market value, which fluctuates according to the dynamics of supply and demand. When Fund shares are sold, they may be worth more or less than their original cost. Consequently, you can lose money by investing in the Fund.

Covered Call and Other Option Transaction Risks. There are several risks associated with writing covered calls and entering into other types of option transactions. For example, there are significant differences between the securities and options markets that could result in an imperfect correlation between these markets, resulting in a given transaction not achieving its objectives. In addition, a decision as to whether, when, and how to use covered call options involves the exercise of skill and judgment, and even a well-conceived transaction may be unsuccessful because of market behavior or unexpected events. As the writer of a covered call option, the Fund forgoes, during the option’s life, the opportunity to profit from increases in the market value of the security covering the call option above the exercise price of the call option, but has retained the risk of loss should the price of the underlying security decline.

About The GAMCO Global Gold, Natural Resources & Income Trust

The GAMCO Global Gold, Natural Resources & Income Trust is a non-diversified, closed-end management investment company with $708 million in total net assets whose primary investment objective is to provide a high level of current income. The Fund invests primarily in equity securities of gold and natural resources companies and intends to earn income primarily through a strategy of writing (selling) primarily covered call options on equity securities in its portfolio. The Fund is managed by Gabelli Funds, LLC, a subsidiary of GAMCO Investors, Inc. (NYSE:GBL).

NYSE American – GGN

CUSIP – 36465A109

Investor Relations Contact:

Molly Marion

(914) 921-5681

[email protected]

KEYWORDS: United States North America New York

INDUSTRY KEYWORDS: Banking Other Professional Services Professional Services Finance

MEDIA: