Laird Superfood to Participate in Craig-Hallum and Jefferies Investor Conferences

Laird Superfood to Participate in Craig-Hallum and Jefferies Investor Conferences

Laird Hamilton and Gabrielle Reece at Jefferies Fireside Chat on Wednesday

SISTERS, Ore.–(BUSINESS WIRE)–
Laird Superfood, Inc. (NYSE American: LSF) (“Laird Superfood” or the “Company”) today announced that the Company will participate in two upcoming virtual investor conferences. Founders Laird Hamilton and Gabrielle Reece will take part in a fireside chat as well.

Tomorrow, November 17th, 2020, the Company will host investor meetings at the 11th Annual Craig-Hallum Alpha Select Conference throughout the day. For more information, please contact your Craig-Hallum representative.

On Wednesday, November 18th, 2020, company management will host investor meetings throughout the day, and Founders Laird Hamilton and Gabrielle Reece will take part in a fireside chat at 2:00 p.m. ET, or 11:00 a.m PT, at the Jefferies West Coast Consumer Conference. The discussion can be accessed live at the “Events & Presentations” section of the Laird Superfood Investor Relations site at https://investors.lairdsuperfood.com. The replay will be archived online for 90 days.

About Laird Superfood (NYSE American: LSF)

Laird Superfood, Inc. creates award-winning, plant-based superfood products that are both delicious and functional. The Company’s products are designed to enhance your daily ritual and keep consumers fueled naturally throughout the day. The Company was co-founded in 2015 by the world’s most prolific big-wave surfer, Laird Hamilton. Laird Superfood’s offerings are environmentally conscientious, responsibly tested, and made with real ingredients. Shop all products online at lairdsuperfood.com and join the Laird Superfood community on social media for the latest news and daily doses of inspiration.

ICR

Ashley DeSimone

[email protected]

646.677.1827

KEYWORDS: United States North America Oregon

INDUSTRY KEYWORDS: Retail Health Fitness & Nutrition Supermarket Specialty Food/Beverage

MEDIA:

Physician Advocates for Women’s Sexual Rights Across the Globe in New Book

Dr. Getu Tadesse Mindaye brings awareness to the procedure known as female genital mutilation affecting millions of young girls in ‘Female Genital Mutilations: The Story of Kedra’

AURORA, Colo., Nov. 16, 2020 (GLOBE NEWSWIRE) — “Female Genital Mutilations: The Story of Kedra” by Dr. Getu Tadesse Mindaye shares the story of Kedra and the loss and trauma millions of young girls experience around the world as victims of female genital mutilation (FGM). The book follows a young girl named Kedra, who is a victim of the most dangerous type of FGM called, infibulation. This heart-wrenching book shares Kedra’s battle with society and tradition in order to avoid rejection in her Somalian community in Ethiopia.

Female genital mutilation (FGM) is a procedure that involves partial or total removal of the female external genitalia, has no health benefits and is considered a violation of women’s sexual rights. This procedure is currently happening mostly in East, West and North Africa, as well as the Middle East. After witnessing the aftermath of female genital mutilation being performed on a young girl in the Somali region of Ethiopia, the author wanted to share this hidden reality with the civilized world. During Dr. Tadesse’s time working as a physician in this region, more than 65% of the women came to the clinic with health issues related to the effects of FGM. The book presents in great detail the short and long-term effects of FGM and the aftermath for the victims in the countries where this procedure is being performed.

“While working as a physician in different hospitals throughout the Ethiopian capital I saw many victims of FGM,” said the author. “In 2000, I witnessed the aftermath of a young girl who had the most dangerous type of FGM procedure performed on her. I then wondered who speaks up for this young girl and the millions of others? I want to be the voice for these victims and bring attention and intervention to this violation of human rights.”

Throughout the book, readers will discover the hardships and heartache Kedra experiences in her shocking journey as a woman born in Ethiopia living by her family’s traditions, cultures and religions. This eye-opening story will resonate with readers in unimaginable ways as they come to know this young girl’s suffering and bravery. Ultimately, the author hopes this book will educate readers on this practice and encourage them to help by being the voice for the millions of girls who cannot speak for themselves.

To learn more please visit, www.femalegenitalmutilations.com.

“Female Genital Mutilations: The Story of Kedra”

By Getu Tadesse Mindaye

ISBN: 9781664112056 (softcover); 9781664112063 (hardcover); 9781664112049 (electronic)

Available at Amazon, Barnes & Noble and Xlibris

About the author

Dr. Getu Tadesse Mindaye graduated in medicine at the Medical Faculty of Santiago de Cuba in 1991. After graduating, he went back to his own country of Ethiopia and started working as a physician heading the Infectious Disease Prevention and Control Department. Dr. Tadesse worked with both UNICEF and WHO to eradicate Guinea Worm and polio. He also oversaw the expansion of Ethiopian Public Immunization (EPI) coverage in the region as well as contributed in the prevention of upper respiratory infections and diarrheal diseases. After witnessing the aftermath of genital mutilation being performed on little girls in the Somali region of Ethiopia, he joined a nonprofit organization working against FGM. Dr. Tadesse has given several health education presentations about and against FGM in order to create better awareness of the practice and has requested the Ethiopian government to criminalize FGM. Dr. Tadesse currently resides in Aurora, Colorado with his family.

Xlibris Publishing UK, an Author Solutions, LLC imprint, is a self-publishing services provider dedicated to serving authors throughout the United Kingdom. By focusing on the needs of creative writers and artists and adopting the latest print-on-demand publishing technology and strategies, we provide expert publishing services with direct and personal access to quality publication in hardcover, trade paperback, custom leather-bound and full-color formats. To date, Xlibris has helped to publish more than 60,000 titles. For more information, visit xlibrispublishing.co.uk or call 0800 056 3182 to receive a free publishing guide.

Attachment

Meghan Bowman
LAVIDGE- Phoenix
480-306-6597
[email protected]

Spirit Airlines Brings Back International Service from Orlando with Six Routes Launching in December

MIRAMAR, Fla., Nov. 16, 2020 (GLOBE NEWSWIRE) — Spirit Airlines (NYSE: SAVE) will head back to Latin America from Orlando just in time for the holidays. The Florida-based carrier is re-launching six nonstop international routes aimed at providing More Go for vacationers and people visiting friends and family. It marks the first time Spirit’s bright-yellow planes will fly internationally from Central Florida since border closures began in March.

Spirit plans to reintroduce Latin American destinations from Orlando International Airport (MCO) gradually throughout the month of December, beginning with service to Colombia and Honduras. Within weeks, the airline will add Mexico, Guatemala and El Salvador along with additional Colombian flights.

In the Caribbean, people travelling to Puerto Rico will have more options at the beginning of 2021. Spirit plans to reactivate its service to Aguadilla (BQN) once the airport re-opens in January. Daily flights to the island’s northwestern tip will complement Spirit’s existing service to San Juan (SJU), which runs up to five times each day.

Caribbean & Latin American Service at MCO
Destination Flights Available: Launch Date
:
Bogota (BOG) 4x weekly Dec. 4, 2020
San Pedro Sula (SAP) 3x weekly Dec. 4, 2020*
Cartagena (CTG) 3x weekly Dec. 16, 2020
Cancun (CUN) 6x weekly Dec. 16, 2020
Guatemala City (GUA) 3x weekly Dec. 16, 2020
San Salvador (SAL) 2x weekly Dec. 19, 2020
Aguadilla (BQN) 1x daily Jan. 6, 2021
San Juan (SJU) Up to 5x per day Existing Service
St. Thomas (STT) 4x weekly Existing Service

*
Pending re-opening of the airport following repairs
due to damage from Hurricane Eta
.

“Holidays are the time to see family and friends, and we’re excited to offer so many nonstop international options from Central Florida,” Spirit Airlines Vice President of Network Planning John Kirby said. “We’re the only major airline based in Florida, and the Orlando market is one of our largest gateways. We know how valuable it is for people to jump on a plane and fly nonstop to their destination without having to connect through a busy hub.”

Spirit carried 2.6 million Guests at MCO in 2019. The airline reactivated most of its domestic network from the airport in July as the demand for air travel began to rebound. Resuming international service at MCO bumps up Spirit’s operation at the airport to 38 nonstop destinations throughout the United States, Latin America and the Caribbean. The airline will offer Guests an average of 53 flights each day during the December travel period. That’s a ten-fold increase compared to the five flights available each day when demand for air travel was at its lowest in 2020.

“International service to Orlando International benefits the entire community and our tourism partners,” Greater Orlando Aviation Authority Chief Executive Officer Phil Brown said. “We’re pleased Spirit is taking steps to rebuild that connectivity, including resuming service to international destinations currently suspended during the pandemic.”

Spirit started serving MCO in 1993 and grew into one of Central Florida’s major job providers. The airline employs nearly 1,200 people in the Orlando area directly, and its operations support another 500 contractors in the region.

Guest Safety   
Spirit’s commitment to Safe Travels includes a multi-layered safety approach that requires all Guests and Team Members to wear face coverings. Each passenger agrees to that policy as part of a health and safety acknowledgement prior to boarding the aircraft. Every plane in our Fit Fleet® uses state-of-the-art, high-efficiency particulate air (HEPA) filters that capture 99.97% of particles and filter the air for contaminants every 3 minutes.

Between each flight, enhanced cleaning procedures focus on high-touch areas such as tray tables and armrests using hospital-grade disinfectants. Spirit also uses two EPA-registered fogging treatments. The first applies a safe, high-grade disinfectant that’s effective against coronaviruses. The second uses an antimicrobial product that forms an invisible barrier on all surfaces that kills bacteria and viruses on contact for 30 days. Please visit Spirit’s COVID-19 Information Center for more information on safety enhancements.

About Spirit Airlines:  
Spirit Airlines (NYSE: SAVE) is committed to delivering the best value in the sky. We are the leader in providing customizable travel options starting with an unbundled fare. This allows our Guests to pay only for the options they choose — like bags, seat assignments and refreshments — something we call Á La Smarte. We make it possible for our Guests to venture further and discover more than ever before. Our Fit Fleet® is one of the youngest and most fuel-efficient in the U.S. We serve destinations throughout the U.S., Latin America and the Caribbean, and are dedicated to giving back and improving those communities. Come save with us at spirit.com.

Spirit Media Relations

954.364.0231
[email protected] 



Harmony Gold Mining Company Limited to present at the dbVIC – Deutsche Bank ADR Virtual Investor Conference on 19 November 2020

Company invites individual and institutional investors, as well as advisors, to attend interactive, real-time virtual event

PR Newswire

JOHANNESBURG, Nov. 16, 2020 /PRNewswire/ — Harmony Gold Mining Company Limited  (JSE: HAR) based in South Africa, and focused on gold mining and exploration, today announced that Harmony Financial Director, Boipelo Lekubo will present at the dbVIC – Deutsche Bank American Depositary Receipt (ADR) Virtual Investor Conference on November 19. This virtual investor conference is aimed exclusively at introducing global companies with ADR programs to investors.

DATE:     November 19, 2020
TIME:      9:30 AM ET/4:30pm South Africa Standard Time
LINK:       https://bit.ly/3jNDfgr

This will be a live, interactive online event where investors are invited to ask the company questions in real-time – both in the presentation hall as well as the organization’s “virtual trade booth.” If attendees are not able to join the event live on the day of the conference, an archived webcast will also be made available after the event.

It is recommended that investors pre-register and run the online system check to expedite participation and receive event updates.


Participation is free of charge.

Recent Company Highlights

  • Successful acquisition of Anglogold Ashanti’s remaining South Africa assets as of 1 October 2020, making Harmony South Africa’s largest gold producer by volume
  • Runner-up in the Sunday Times Top 100 companies. The awards acknowledge those JSE-listed companies that have created wealth and value for shareholders. Those with a minimum market capitalisation of R5 billion at 31 August 2020 and a track record of five years trading from 1 September 2015 were ranked on their compound annual growth rate (CAGR) over the five-year period. Also considered were subjective qualifying criteria relating to a company’s perceived compliance with good governance and ethical conduct
  • Harmony has, more than any other gold mining company in South Africa, demonstrated true sustainability over the past 70 years. From the Company’s enduring history, to the product it mines and the way in which it is mined, to the care taken to preserve the environment and the support provided to its communities, Harmony has illustrated time and again, that sustainability is the driving force of its business

About Harmony

Harmony Gold Mining Company Limited (Harmony), a world-class gold mining and exploration company, has operations and assets in South Africa and Papua New Guinea (PNG). Harmony has close to 70 years’ experience in the industry. Company assets include one open pit mine and several exploration tenements in PNG, as well as 10 underground mines and 1 open pit operation and several surface sources in South Africa. In addition, Harmony owns 50% of the significant Wafi-Golpu copper-gold project – a tier 1 asset – in a joint venture in PNG.

The company’s primary stock exchange listing is on the JSE with a secondary listing on the New York Stock Exchange. The bulk of our shareholders are in South Africa and the United States. Additional information on the company is available on the corporate website, www.harmony.co.za.

About Virtual Investor ConferencesSM
Virtual Investor Conferences is the leading proprietary investor conference series that provides an interactive forum for publicly-traded companies to meet and present directly with investors.

A real-time solution for investor engagement, Virtual Investor Conferences is part of OTC Market Group’s suite of investor relations services specifically designed for more efficient Investor Access.  Replicating the look and feel of on-site investor conferences, Virtual Investor Conferences combine leading-edge conferencing and investor communications capabilities with a comprehensive global investor audience network.

 

Cision View original content:http://www.prnewswire.com/news-releases/harmony-gold-mining-company-limited-to-present-at-the-dbvic—deutsche-bank-adr-virtual-investor-conference-on-19-november-2020-301173708.html

SOURCE dbVIC – Deutsche Bank Depositary Receipts Virtual Investor Conference

22nd Century Group to Present at the Virtual Fall Investor Summit on November 17

WILLIAMSVILLE, N.Y., Nov. 16, 2020 (GLOBE NEWSWIRE) — 22nd Century Group, Inc. (NYSE American: XXII), a leading plant-based, biotechnology company that is focused on tobacco harm reduction, very low nicotine content tobacco, and hemp/cannabis research, announced today that the Company will present and meet with investors at the Virtual Fall Investor Summit. The conference is being held virtually November 16 -18, 2020.

22nd Century is scheduled to present on Tuesday, November 17, 2020 at 4:30 p.m. ET. The live webcast and presentation will be accessible in the Investors section of 22nd Century’s website under Events. An archived replay of the webcast will be available shortly after the live event.

Please visit https://investorsummitgroup.com/ to register for the conference and schedule one-on-one meeting with 22nd Century.

About 22nd Century Group, Inc.

22nd Century Group, Inc. (NYSE American: XXII) is a leading plant biotechnology company focused on technologies that alter the level of nicotine in tobacco plants and the level of cannabinoids in hemp/cannabis plants through genetic engineering, gene-editing, and modern plant breeding. 22nd Century’s primary mission in tobacco is to reduce the harm caused by smoking through the Company’s proprietary reduced nicotine content tobacco cigarettes – containing 95% less nicotine than conventional cigarettes. The Company’s primary mission in hemp/cannabis is to develop and commercialize proprietary hemp/cannabis plants with valuable cannabinoid profiles and desirable agronomic traits.

Learn more at xxiicentury.com, on Twitter @_xxiicentury and on LinkedIn.

Investor Relations & Media
Contact:

Mei Kuo
Director, Communications & Investor Relations
22nd Century Group, Inc.
(716) 300-1221
[email protected] 



Spectrum Antimicrobials, Inc. Announces Breakthrough Drug Candidate for Prevention and Treatment of Pulmonary Infections

PETALUMA, Calif., Nov. 16, 2020 (GLOBE NEWSWIRE) — Spectrum Antimicrobials, Inc., a subsidiary of Collidion, Inc. announces the development of a novel antiviral drug candidate designed to treat pulmonary infections. SPC-069 is a new class of therapy designed to treat viral, bacterial, and fungal infections in the lung and respiratory tract. This promising therapy was developed to eradicate not only common pathogens but also those caused by antibiotic resistant strains known as “Super Bugs.” The Company plans to advance this drug candidate into human clinical studies as soon as possible with a partner or upon completion of its financing.

The Company believes SPC-069, has a three-fold mechanism of action against pathogens that may affect the respiratory system. First, it achieves viral and bacterial destruction through a non- selective reaction pathway. This causes fundamental damage to viral structures that are responsible for causing infection. SPC-069’s mechanism of action against bacteria causes damage to the bacterial cell membrane followed by interruption of ATP production, where such damages are irreversible. The secondary mode of action for SPC-069 involves reduction of inflammation through the possible stabilization of mast cells, reducing the overall release of histamines. Lastly, it has a non-selective reaction with general cellular receptors that may be responsible for the reduction of ACE II receptor activity. This may potentially inhibit the spike proteins of the virus from attaching to the receptor which leads to the infection of healthy cells. ACE II has been identified as the primary entry point for coronaviruses which cause respiratory illnesses such as cold and flu.

Hoji Alimi, Founder and CEO of Spectrum Antimicrobials stated, “We are hopeful that further testing will confirm that SPC-069 is safe and effective and will shorten the time for recovery in patients with lung infections caused by either viruses, bacteria or fungi. We believe that clinical studies may provide further evidence that SPC-069 can be used as a preventative therapy against cold, influenzas, bronchitis, and other respiratory ailments. SPC-069 is a patent pending modified hypochlorous acid (HOCl) formulation that has been created with a novel chemistry. HOCl is an endogenous antiviral and antimicrobial chemical that is produced by the immune cells when fighting an infection. SPC-069 essentially reintroduces the modified active chemistry that our bodies naturally produce to fight an infection and protect the respiratory tissues against infections.”

Dr. Sridhar Prasad, Chief Scientific Officer, added, “We have created four other novel antiviral and antibacterial chemistries that can effectively address infection and infection control in a vast number of treatment options as well as applications where control of infection is required. I am especially proud of our scientific talent at Plex Pharmaceuticals who have made significant contributions to our antiviral program goals at Spectrum Antimicrobials.”

Dr. Jerry Stonemetz, Spectrum’s Chief Medical Officer and Medical Director of Perioperative Services at The John Hopkins Hospital affirmed, “These findings may be crucial for the treatment of pulmonary infections since the drug deactivates viruses regardless of their mutations. Once the drug contacts the virus, it damages the virus’ structure, rendering it ineffective and incapable of spreading. This means a great deal for therapeutic treatments of other viral infections as the vaccine industry is continually trying to catch up with the mutating viruses. We hope that further testing will confirm that SPC-069 may very well become the preferred preventative therapy globally against, the coronavirus family that causes cold, influenza, and pneumonia.”

According to the CDC, up to 45 million people in the U.S. contract influenza each year. Up to 800,000 patients are hospitalized and up to 61,000 die each year. SPC-069 may become the first non-antibiotic, non-vaccine class of drug for the potential treatment of such pulmonary infections.

Bill Watson, Co-Founder and Executive Vice President of Business Development and Global Sales added, “Our new drug and device programs have the potential to revolutionize the infection control industry. SPC-069 could be the first broad-spectrum non-selective antimicrobial and antiviral drug developed to treat lung infections. We intend to extend our future clinical programs to include testing of pulmonary infections caused by Candida aureus, which may have morbidity rate of over 60%. While antibiotics are becoming less effective due to emergence of resistance, SPC-069 has the potential to become the next generation treatment option to resolve the microbial attack factors in the lung without concerns of creating new resistant strains of viruses or bacteria.

“This is a pivotal point in the Company’s evolution as we begin to turn our various novel chemistries into products for use in healthcare applications where infection control is mission critical for patient outcome. The initial driver for our product development mission was to create products that would eliminate “Super Bug” infections in wounds. In a study by Washington University in St. Louis, Missouri, as many as 153,000 lives are lost each year in the U.S. and 700,000 globally, due to antibiotic resistant infections, at a cost of $40 billion annually to the U.S. healthcare system. The discoveries made in resolving infection issues in wound care demonstrates the potential for the technology to be repurposed to fight viruses, leading to the application of SPC- 069 to treat respiratory conditions.”

Dr. David Allie, a Spectrum Board Member and Chief of Cardiothoracic and Vascular Surgery at the nation’s first dedicated Cardiovascular & Limb Salvage Center in Lafayette, LA. stated, “I am proud to have been part of the leading physicians who have contributed to the design of the clinical programs for SPC-069 and I remain optimistic that this drug candidate may revolutionize the treatment of pulmonary infections. Clinical success in future trials may lead to creation of other therapies including new treatments for wounds, burns, and surgical site infections. Based on the success of such clinical studies, Spectrum’s wound care solutions may obsolete the use of many other topical wound solutions including all other generic forms of HOCl.”

Mr. Alimi, concluded, “I am confident our breakthrough chemistries may ultimately allow us to optimize the use of SPC-069 and similar chemistries to prevent and treat infections that have been challenging if not impossible to cure. We are facing a moment in history where we hope to utilize our novel chemistries to change the standard of care in infection control, preventing and treating infections in pulmonary, wound care, burns, and surgical procedures.”

About Spectrum Antimicrobials, Inc.

Spectrum Antimicrobials, Inc. is an Infection Control Solutions Company focused on the development and commercialization of platform chemistries and drug formulations created for the treatment and prevention of infection in the healthcare industry. Our product use broad spectrum antimicrobial solutions that are highly effective against bacteria, virus, mold, fungi, and spores, including antibiotic resistant pathogens known as “Superbugs”. These novel platform chemistries were designed as therapeutics to reduce patient treatment times and the economic impact of community and hospital acquired infections. Infection management is one of the most important global challenges in medicine.

Spectrum Antimicrobials is launching a non-alcohol based hand sanitizer and a hard surface disinfectant in the United Kingdom, a novel wound solution in the animal healthcare market in the U.S. under the brand name of VetriceptTM, and a new Pathogen Resistant WaterTM for use in Continuous Positive Airway Pressure (CPAP) machines to prevent the growth of biofilms, mold, fungi and bacteria in solution within the device humidifier. The Company is advancing several of its programs into human clinical studies in 2021 and beyond and plans to launch additional products into the U.S. market and internationally.

For further information, please visit our web site at www.spectrumantimicrobials.comor contact:

William Watson, Executive Vice President
Business Development and Global Sales
[email protected]
408-206-0349

Forward-looking statement disclaimer:

This document contains forward-looking statements. In addition, from time to time, we or our representatives may make forward-looking statements orally or in writing. We base these forward-looking statements on our expectations and projections about future events, which we derive from the information currently available to us. Such forward-looking statements relate to future events or our future performance, including: our financial performance and projections; our growth in revenue and earnings; and our business prospects and opportunities. You can identify forward-looking statements by those that are not historical in nature, particularly those that use terminology such as “may,” “should,” “expects,” “anticipates,” “contemplates,” “estimates,” “believes,” “plans,” “projected,” “predicts,” “potential,” or “hopes” or the negative of these or similar terms.

In evaluating these forward-looking statements, you should consider various factors, including: our ability to change the direction of the Company; our ability to keep pace with new technology and changing market needs; and the competitive environment of our business. These and other factors may cause our actual results to differ materially from any forward-looking statement. Forward-looking statements are only predictions. The forward-looking events discussed in this document and other statements made from time to time by us or our representatives, may not occur, and actual events and results may differ materially and are subject to risks, uncertainties, and assumptions about us. We are not obligated to publicly update or revise any forward-looking statement, whether as a result of uncertainties and assumptions, the forward- looking events discussed in this document and other statements made from time to time by us or our representatives might not occur.



TRACON Pharmaceuticals Announces Submission for Approval of Envafolimab (KN035) with the NMPA in China by its Corporate Partners Alphamab Oncology and 3D Medicines

Submission for Approval Filed in Indication of MSI-H/dMMR Cancer, Including Colorectal and Gastric Cancer

SAN DIEGO, Nov. 16, 2020 (GLOBE NEWSWIRE) — TRACON Pharmaceuticals (NASDAQ:TCON), a clinical stage biopharmaceutical company focused on the development and commercialization of novel targeted cancer therapeutics and utilizing a cost efficient, CRO-independent product development platform to partner with ex-U.S. companies to develop and commercialize innovative products in the U.S., today announced its corporate partners, Alphamab Oncology and 3D Medicines, have submitted a new drug application (NDA) for the approval of envafolimab (KN035) in the indication of MSI-H/dMMR cancer to the National Medical Products Administration (NMPA).

“We congratulate our partners on the regulatory submission of data from the registration trial of envafolimab in MSI-H/dMMR advanced solid tumors including colorectal and gastric cancer, which marks an important milestone in the development and potential commercialization of the program,” said Charles Theuer, M.D., Ph.D., TRACON Chief Executive Officer. “The submission for approval highlights the advanced status of envafolimab product development. Envafolimab is being studied in two additional registration trials, a randomized Phase 3 trial in biliary tract cancer in China being conducted by 3D Medicines and Alphamab, and TRACON’s ENVASARC trial in sarcoma in the U.S., which recently opened multiple sites and expects to dose multiple patients prior to the end of the year.”

About
Envafolimab
(KN035)

Envafolimab (KN035), a novel, single-domain antibody against PD-L1, is the first subcutaneously injected PD-(L)1 inhibitor to be studied in registration trials. Envafolimab is currently being studied in the ENVASARC Phase 2 registration trial in the U.S. sponsored by TRACON, as well as in a Phase 2 registration trial as a single agent in MSI-H/dMMR advanced solid tumor patients and a Phase 3 registration trial in combination with gemcitabine and oxaliplatin in advanced biliary tract cancer patients in China sponsored by TRACON’s corporate partners, Alphamab Oncology and 3D Medicines. Alphamab Oncology and 3D Medicines have submitted an NDA to the NMPA in China for envafolimab in MSI-H/dMMR cancer. In the Phase 2 registration trial, the confirmed objective response rate (ORR) by blinded independent central review in MSI-H/dMMR colorectal cancer (CRC) patients treated with envafolimab who failed a fluoropyrimidine, oxaliplatin and irinotecan was 32%, which was similar to the 28% confirmed ORR reported in the Opdivo package insert in MSI-H/dMMR CRC patients who failed a fluoropyrimidine, oxaliplatin, and irinotecan and the 33% confirmed ORR reported for Keytruda in MSI-H/dMMR CRC patients who failed a fluoropyrimidine, oxaliplatin and irinotecan in cohort A of KEYNOTE-164.

About
ENVASARC
(
NCT04480502)

The ENVASARC registration trial is a multi-center, open-label, randomized, non-comparative, parallel cohort study at approximately 25 top cancer centers in the United States. TRACON expects the trial to enroll 160 patients with UPS or MFS who have progressed following one or two lines of prior treatment and have not received an immune checkpoint inhibitor, with 80 patients enrolled into cohort A of treatment with single agent envafolimab and 80 patients enrolled in cohort B of treatment with envafolimab and Yervoy. The primary endpoint is ORR by blinded independent central review with duration of response a key secondary endpoint.

About TRACON

TRACON develops targeted therapies for cancer utilizing a capital efficient, CRO independent, product development platform. The Company’s clinical-stage pipeline includes: Envafolimab, a subcutaneous PD-L1 single-domain antibody being developed in a registration trial for the treatment of sarcoma; TRC253, a small molecule drug candidate for the treatment of prostate cancer; TRC102, a Phase 2 small molecule drug candidate being developed for the treatment of lung cancer and glioblastoma; and TJ004309, a CD73 antibody in Phase 1 development for the treatment of advanced solid tumors. TRACON is actively seeking additional corporate partnerships whereby it leads U.S. regulatory and clinical development and shares in the cost and risk of clinical development and leads U.S. commercialization.  In these partnerships TRACON believes it can serve as a solution for companies without clinical and commercial capabilities in the U.S.  To learn more about TRACON and its product pipeline, visit TRACON’s website at www.traconpharma.com.

About Alphamab Oncology

Alphamab Oncology is a biopharmaceutical company focusing on innovative biologics medicine for oncology. On December 12, 2019, the Company was listed in the mainboard of Hong Kong Stock Exchange with stock code 9966. Alphamab has fully integrated proprietary biologics platforms in bi-specifics and protein engineering. Its pipeline includes eight anti-tumor drug candidates including mainly bi-specifics, and a Covid-19 multifunctional antibody. Four products have advanced into phase I-III clinical trials in China, the United States, and Japan. The Company also has state-of-the-art manufacturing capabilities designed and built to meet NMPA and EU/FDA’s cGMP standards and a complete quality system which has passed the on-site inspection of a European Union qualified person. Alphamab Oncology is committed to building a global leading, multi-dimensional drug development and commercialization platform, focusing on multifunctional biological innovative drugs, and to benefit patients in China and around the world. Visit http://www.alphamabonc.com for more information.

About 3D Medicines

3D Medicines is a clinical-stage biopharmaceutical company focused on the development of differentiated next-generation immuno-oncology drugs for cancer patients. The world’s first subcutaneous injection PD-L1 antibody Envafolimab (KN035), is currently under clinical development in the United States, China and Japan. 3D Medicines is building a pipeline targeting major indications through combination strategy, either with in-house assets or in collaboration with partners around the world. With a professional team in the China and US, 3D Medicines is capable of conducting global clinical development and registration.

Forward-Looking Statements

Statements made in this press release regarding matters that are not historical facts are “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995. Because such statements are subject to risks and uncertainties, actual results may differ materially from those expressed or implied by such forward‐looking statements. Such statements include, but are not limited to, statements regarding TRACON’s plans to further develop product candidates, expectations regarding the timing and scope of clinical trials and availability of clinical data, expected development and regulatory milestones and timing thereof, and TRACON’s business development strategy and goals to enter into additional collaborations. Risks that could cause actual results to differ from those expressed in these forward‐looking statements include: risks associated with clinical development; whether TRACON or others will be able to complete or initiate clinical trials on TRACON’s expected timelines, if at all, including due to risks associated with the COVID-19 pandemic or other pandemics; the fact that future preclinical studies and clinical trials may not be successful or otherwise consistent with results from prior studies; the fact that TRACON has limited control over whether or when third party collaborators complete on-going trials, initiate additional trials or seek regulatory approval of TRACON’s product candidates; the fact that TRACON’s collaboration agreements are subject to early termination; whether TRACON will be able to enter into additional collaboration agreements on favorable terms or at all; potential changes in regulatory requirements in the United States and foreign countries; TRACON’s reliance on third parties for the development of its product candidates, including the conduct of its clinical trials and manufacture of its product candidates; whether TRACON will be able to obtain additional financing; and other risks described in TRACON’s filings with the Securities and Exchange Commission under the heading “Risk Factors”. All forward‐looking statements contained in this press release speak only as of the date on which they were made and are based on management’s assumptions and estimates as of such date. TRACON undertakes no obligation to update such statements to reflect events that occur or circumstances that exist after the date on which they were made.

Company Contact: Investor Contact:
Mark Wiggins Brian Ritchie
Chief Business Officer LifeSci Advisors LLC
(858) 251-3492 212-915-2578
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Fifth Third Introduces the Fifth Third Cash/Back Card

Fifth Third Introduces the Fifth Third Cash/Back Card

New card offers unlimited 1.67% cash back on every purchase

CINCINNATI–(BUSINESS WIRE)–
Fifth Third Bank today announced its new cash back rewards credit card. The Fifth Third Cash/Back Credit Card is the bank’s new flagship rewards credit card product, offering 1.67% cash back on every purchase, no matter the category.* The new contactless-enabled card gives customers the ability to tap and go in store or load into their digital wallet as a safer way to pay. Customers can also manage the card directly from their Fifth Third Mobile Banking app.

This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20201116005759/en/

Fifth Third Introduces the Fifth Third Cash/Back Card. New card offers unlimited 1.67% cash back on every purchase. (Photo: Business Wire)

Fifth Third Introduces the Fifth Third Cash/Back Card. New card offers unlimited 1.67% cash back on every purchase. (Photo: Business Wire)

“The new card empowers customers to earn 1.67% cash back on all their purchases. It’s that simple,” said Mike Butera, head of consumer products and payments for Fifth Third Bank. “There are no hidden requirements or qualifications. Customers can use one card and know that they are receiving tangible benefits no matter where and what they purchase.”

The new Fifth Third Cash/Back Card offers:

  • Unlimited 1.67% cash back on every purchase.
  • Contactless payment option.
  • No annual fee.
  • No rewards expiration.
  • No rotating categories.

Additionally, Fifth Third is introducing two new products that will offer unlimited 2% cash back on every purchase and no annual fee** for clients who have a Preferred or Private Bank relationship. The card is one more initiative that demonstrates how the Bank is creating solutions to fit neatly into customers’ lives and making banking a Fifth Third better.

“Consumers want one card that earns abundant cash back on all purchases regardless of the category,” Butera said. “The Fifth Third Cash/Back Card keeps things simple: You make purchases, you earn cash back. We are excited to introduce our new flagship rewards card that ensures a seamless experience for our customers, as well as offers more rewards and benefits as their relationship expands with us.”

Customers can learn more and apply for the new Fifth Third Cash/Back Card at 53.com or at any Fifth Third branch location.

*Earn 1.67 Rewards Points (1.67% cash back) for each $1 spent on qualified purchases. The value of each point is $0.01. If earned points result in a fractional amount, then such fractional amount will be rounded to the nearest whole number. For example, if your Rewards Points total 3.216, you will be awarded 3 Rewards Points.

 

**Earn 2 Rewards Points (2% cash back) for each $1 spent on qualified purchases. The value of each point is $0.01.

 

See the rewards terms and conditions at 53.com/myrewards for important information including details about: (1) Purchases: dollar value of goods and services, minus credits and adjustments, excluding fees and other items. (2) Categories: merchants’ card readers are assigned to categories which determine how a transaction is characterized for rewards purposes. We do not control which categories card readers are assigned to. (3) Redemption options. (4) Changes: the program may change. (5) Expiration: points do not expire.

 

Variable APR of 15.49% to 25.49% on purchases when you open your account and on balance transfers after the introductory period. Variable APRs are accurate as of 11/12/2020 and are subject to change with the market based on the prime rate. Cash advance variable APR: 24.99%. Annual Fee: None. Balance transfer fee either $5 or 4% of the amount of each transfer, whichever is greater. Cash advance fee either $10 or 5% of the amount of each cash advance, whichever is greater. Convenience check fee either $5 or 4% of the amount of each check, whichever is greater. International transaction fee: None. Late payment fee of up to $40. Minimum interest charged is $1.50. We may end any promotional (including introductory) APR(s) and apply the standard APR for purchases or balance transfers, as appropriate, if you make a late payment.

About Fifth Third

Fifth Third Bancorp is a diversified financial services company headquartered in Cincinnati, Ohio and the indirect parent company of Fifth Third Bank, National Association, a federally chartered institution. As of Sept. 30, 2020, Fifth Third had $202 billion in assets and operated 1,122 full-service banking centers and 2,414 ATMs with Fifth Third branding in Ohio, Kentucky, Indiana, Michigan, Illinois, Florida, Tennessee, West Virginia, Georgia, North Carolina and South Carolina. In total, Fifth Third provides its customers with access to approximately 52,000 fee-free ATMs across the United States. Fifth Third operates four main businesses: Commercial Banking, Branch Banking, Consumer Lending and Wealth & Asset Management. Fifth Third is among the largest money managers in the Midwest and, as of Sept. 30, 2020, had $422 billion in assets under care, of which it managed $53 billion for individuals, corporations and not-for-profit organizations through its Trust and Registered Investment Advisory businesses. Investor information and press releases can be viewed at www.53.com. Fifth Third’s common stock is traded on the Nasdaq® Global Select Market under the symbol “FITB.” Fifth Third Bank was established in 1858. Deposit and Credit products are offered by Fifth Third Bank, National Association. Member FDIC.

Laura Trujillo (Media Relations)

[email protected] | 513-534-NEWS

Chris Doll (Investor Relations)

[email protected] | 513-534-2345

KEYWORDS: United States North America Ohio

INDUSTRY KEYWORDS: Banking Professional Services Finance

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Fifth Third Introduces the Fifth Third Cash/Back Card. New card offers unlimited 1.67% cash back on every purchase. (Photo: Business Wire)

IIROC Trade Resumption – ACB.WT.U

Canada NewsWire

TORONTO, Nov. 16, 2020 /CNW/ – Trading resumes in:

Company: Aurora Cannabis Inc.

TSX Symbol: ACB.WT.U

All Issues: No

Resumption (ET): 9:45 AM

IIROC can make a decision to impose a temporary suspension (halt) of trading in a security of a publicly-listed company. Trading halts are implemented to ensure a fair and orderly market. IIROC is the national self-regulatory organization which oversees all investment dealers and trading activity on debt and equity marketplaces in Canada.

SOURCE Investment Industry Regulatory Organization of Canada (IIROC) – Halts/Resumptions

ROSEN, A TOP RANKED LAW FIRM, Announces Filing of Securities Class Action Lawsuit Against Interface, Inc.; Encourages Investors with Losses in Excess of $100K to Contact Firm – TILE

ROSEN, A TOP RANKED LAW FIRM, Announces Filing of Securities Class Action Lawsuit Against Interface, Inc.; Encourages Investors with Losses in Excess of $100K to Contact Firm – TILE

NEW YORK–(BUSINESS WIRE)–
Rosen Law Firm, a global investor rights law firm, announces the filing of a class action lawsuit on behalf of purchasers of the securities of Interface, Inc. (NASDAQ: TILE) between March 2, 2018 and September 28, 2020, inclusive (the “Class Period”). The lawsuit seeks to recover damages for Interface investors under the federal securities laws.

To join the Interface class action, go to http://www.rosenlegal.com/cases-register-1788.html or call Phillip Kim, Esq. toll-free at 866-767-3653 or email [email protected] or [email protected] for information on the class action.

According to the lawsuit, defendants throughout the Class Period made false and/or misleading statements and/or failed to disclose that: (1) Interface had inadequate disclosure controls and procedures and internal control over financial reporting; (2) consequently, Interface, among other things, reported artificially inflated income and earnings per share (EPS) in 2015 and 2016; (3) Interface and certain of its employees were under investigation by the SEC with respect to the foregoing since at least November 2017, had impeded the SEC’s investigation, and downplayed the true scope of the Company’s wrongdoing and liability with respect to the SEC investigation; and (4) as a result, the Company’s public statements were materially false and misleading at all relevant times. When the true details entered the market, the lawsuit claims that investors suffered damages.

A class action lawsuit has already been filed. If you wish to serve as lead plaintiff, you must move the Court no later than January 11, 2021. A lead plaintiff is a representative party acting on behalf of other class members in directing the litigation. If you wish to join the litigation, go to http://www.rosenlegal.com/cases-register-1788.html or to discuss your rights or interests regarding this class action, please contact Phillip Kim, Esq. of Rosen Law Firm toll free at 866-767-3653 or via e-mail at [email protected] or [email protected].

NO CLASS HAS YET BEEN CERTIFIED IN THE ABOVE ACTION. UNTIL A CLASS IS CERTIFIED, YOU ARE NOT REPRESENTED BY COUNSEL UNLESS YOU RETAIN ONE. YOU MAY RETAIN COUNSEL OF YOUR CHOICE. YOU MAY ALSO REMAIN AN ABSENT CLASS MEMBER AND DO NOTHING AT THIS POINT. AN INVESTOR’S ABILITY TO SHARE IN ANY POTENTIAL FUTURE RECOVERY IS NOT DEPENDENT UPON SERVING AS LEAD PLAINTIFF.

Follow us for updates on LinkedIn: https://www.linkedin.com/company/the-rosen-law-firm, on Twitter: https://twitter.com/rosen_firm or on Facebook: https://www.facebook.com/rosenlawfirm/.

Rosen Law Firm represents investors throughout the globe, concentrating its practice in securities class actions and shareholder derivative litigation. Rosen Law Firm was Ranked No. 1 by ISS Securities Class Action Services for number of securities class action settlements in 2017. The firm has been ranked in the top 3 each year since 2013. Rosen Law Firm has achieved the largest ever securities class action settlement against a Chinese Company. Rosen Law Firm’s attorneys are ranked and recognized by numerous independent and respected sources. Rosen Law Firm has secured hundreds of millions of dollars for investors. Attorney Advertising. Prior results do not guarantee a similar outcome.

Laurence Rosen, Esq.

Phillip Kim, Esq.

The Rosen Law Firm, P.A.

275 Madison Avenue, 40th Floor

New York, NY 10016

Tel: (212) 686-1060

Toll Free: (866) 767-3653

Fax: (212) 202-3827

[email protected]

[email protected]

[email protected]

www.rosenlegal.com

KEYWORDS: New York United States North America

INDUSTRY KEYWORDS: Other Professional Services Professional Services Legal

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