Monthly Archives: March 2020

Dolphin Entertainment to Host Fourth Quarter and Full Year 2019 Earnings Call

MIAMI, FL / ACCESSWIRE / March 30, 2020 / Dolphin Entertainment, Inc. (NASDAQ:DLPN), a leading independent entertainment marketing and premium content development company, announced today it will report financial results, for its fourth quarter and year ended December 31, 2019, after the market closes today. The Company has scheduled a conference call for Tuesday, March 31, 2020, at 8:45 a.m. ET to review the results.

Conference Call Information

To participate in this event, dial approximately 5 to 10 minutes before the beginning of the call.
Date, Time: March 30, 2020, at 8:45 a.m. ET
Toll-free: 877-407-0782
International: 201-689-8567
Live Webcast: https://www.webcaster4.com/Webcast/Page/2225/33736

Conference Call Replay Information

The replay will be available beginning approximately 1 hour after the completion of the live event.
Toll-free: 877-481-4010
Reference ID: 33736

About Dolphin Entertainment, Inc.

Dolphin Entertainment, Inc. is a leading independent entertainment marketing and premium content development company. Through our subsidiaries 42West and The Door, we provide expert strategic marketing and publicity services to many of the top brands, both individual and corporate, in the entertainment and hospitality industries. The Door and 42West are both recognized global leaders in PR services for their respective industries and, in December 2017, the New York Observer listed them, respectively, as the third and fourth most powerful PR firms of any kind in the United States. Dolphin's recent acquisition of Viewpoint Creative adds full-service creative branding and production capabilities to our marketing group. Dolphin's legacy content production business, founded by Emmy-nominated CEO Bill O'Dowd, has produced multiple feature films and award-winning digital series.

This press release contains 'forward-looking statements' within the meaning of the Private Securities Litigation Reform Act. These forward-looking statements may address, among other things, Dolphin Entertainment Inc.'s offering of common stock as well as expected financial and operational results and the related assumptions underlying its expected results. These forward-looking statements are distinguished by the use of words such as "will," "would," "anticipate," "expect," "believe," "designed," "plan," or "intend," the negative of these terms, and similar references to future periods. These views involve risks and uncertainties that are difficult to predict and, accordingly, Dolphin Entertainment's actual results may differ materially from the results discussed in its forward-looking statements. Dolphin Entertainment's forward-looking statements contained herein speak only as of the date of this press release. Factors or events Dolphin Entertainment cannot predict, including those described in the risk factors contained in its filings with the Securities and Exchange Commission, may cause its actual results to differ from those expressed in forward-looking statements. Although Dolphin Entertainment believes the expectations reflected in such forward-looking statements are based on reasonable assumptions, it can give no assurance that its expectations will be achieved, and Dolphin Entertainment undertakes no obligation to update publicly any forward-looking statements as a result of new information, future events, or otherwise, except as required by applicable law.

Contact:

James Carbonara
Hayden IR
(646)-755-7412
james@haydenir.com

SOURCE: Dolphin Entertainment

ReleaseID: 583091

Dyadic Announces Nonexclusive Research License with WuXi Biologics

JUPITER, FL / ACCESSWIRE / March 30, 2020 / Dyadic International, Inc. ("Dyadic" or the "Company") (NASDAQ:DYAI), a global biotechnology company focused on further improving and applying its proprietary C1 gene expression platform to accelerate development, lower production costs and improve the performance of biologic vaccines, drugs, and other biologic products, at flexible commercial scales, today announced that it has entered into a nonexclusive research collaboration with WuXi Biologics, a leading global open-access biologics technology platform company and Contract Development and Manufacturing Organization (CDMO).

Under the terms of the research license agreement, Dyadic will grant WuXi Biologics restricted access to its proprietary and patented C1 gene expression platform and allow WuXi Biologics to evaluate the C1 technology in a cGMP facility and to perform certain experiments to the C1 cell lines for any other internal noncommercial purpose. WuXi Biologics, one of the global top ten CDMOs, which provides development and manufacturing services to pharmaceutical and biotechnology companies globally, will invest its own resources to evaluate the C1 platform for their customers worldwide.

"We are excited to announce this agreement with one of the world's most prestigious CDMOs. As highlighted by the current coronavirus vaccine and drug situation, there appears to be a growing market demand to find a faster and more efficient gene expression technology platform for vaccine and drug development and manufacturing. We believe that our C1 technology may be ideally suited to help fill this gap for many types of biologic vaccines and drugs and we are continuing to see interest from both our previously announced collaborators as well as other global bio-pharmaceutical companies and governmental agencies," commented Matthew Jones, Dyadic's Managing Director, Business Development and Licensing.

"We believe that today's announcement further highlights the diverse and growing opportunities for Dyadic to leverage its C1 technology platform to begin to help address the cost of goods issues associated with vaccine and drug development and manufacturing as well as to help overcome gene expression challenges that have either been shelved or stalled in R&D. The agreement with WuXi Biologics has the potential to further expand our global footprint and provide another potential catalyst for growth," said Mark Emalfarb, CEO of Dyadic.

"Over the past decade, microbial fermentation has reached a higher level of sophistication, with wider adoption in the biopharmaceutical industry and we are excited to expand our technology platforms into this promising area, utilizing our extensive know-how in biologics discovery, development and manufacturing," said Dr. Chris Chen, CEO of WuXi Biologics. "We have been exploring the right time to work with Dyadic in the hopes of further speeding the adoption and use of their industrially proven C1 gene expression platform. With our decision to expand our technology platforms and CDMO service offerings to include microbial fermentation, coupled with the significant improvements Dyadic has and continues to make to its C1 technology platform, it now seems like the appropriate time to evaluate C1 at WuXi Biologics where it may be better suited to speed the development, lower the cost and improve the performance of a number of biologic vaccines and drugs for our customers."

About WuXi Biologics

WuXi Biologics (stock code: 2269:HK), a Hong Kong-listed company, is a leading global open-access biologics technology platform offering end-to-end solutions to empower organizations to discover, develop and manufacture biologics from concept to commercial manufacturing. Our company history and achievements demonstrate our commitment to providing a truly ONE-stop service offering and strong value proposition to our global clients. As of December 31, 2019, there were a total of 250 integrated projects, including 121 projects in pre-clinical development stage, 112 projects in early-phase (phase I and II) clinical development, 16 projects in late-phase (phase III) development and one project in commercial manufacturing. With total estimated capacity for biopharmaceutical production planned in China, Ireland, Singapore, Germany, and the U.S. exceeding 280,000 liters by 2022, we will provide our biomanufacturing partners with a robust and premier-quality global supply chain network. For more information on WuXi Biologics, please visit www.wuxibiologics.com.

About Dyadic International, Inc.

Dyadic International, Inc. is a global biotechnology company which is developing what it believes will be a potentially significant biopharmaceutical gene expression platform based on the fungus Thermothelomyces heterothallica (formerly Myceliophthora thermophila), named C1. The C1 microorganism, which enables the development and large scale manufacture of low cost proteins, has the potential to be further developed into a safe and efficient expression system that may help speed up the development, lower production costs and improve the performance of biologic vaccines and drugs at flexible commercial scales. Dyadic is using the C1 technology and other technologies to conduct research, development and commercial activities for the development and manufacturing of human and animal vaccines and drugs, such as virus like particles (VLPs) and antigens, monoclonal antibodies, Fab antibody fragments, Fc-Fusion proteins, biosimilars and/or biobetters, and other therapeutic proteins. Certain other research activities are ongoing which include the exploration of using C1 to develop and produce certain metabolites and other biologic products. Dyadic pursues research and development collaborations, licensing arrangements and other commercial opportunities with its partners and collaborators to leverage the value and benefits of these technologies in development and manufacture of biopharmaceuticals. In particular, as the aging population grows in developed and undeveloped countries, Dyadic believes the C1 technology may help bring biologic vaccines, drugs and other biologic products to market faster, in greater volumes, at lower cost, and with new properties to drug developers and manufacturers and, hopefully, improve access and cost to patients and the healthcare system, but most importantly save lives.

Please visit Dyadic's website at http://www.dyadic.com for additional information, including details regarding Dyadic's plans for its biopharmaceutical business.

Safe Harbor Regarding Forward-Looking Statements

This press release contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934, including those regarding Dyadic International's expectations, intentions, strategies and beliefs pertaining to future events or future financial performance. Actual events or results may differ materially from those in the forward-looking statements as a result of various important factors, including those described in the Company's most recent filings with the SEC. Dyadic assumes no obligation to update publicly any such forward-looking statements, whether as a result of new information, future events or otherwise. For a more complete description of the risks that could cause our actual results to differ from our current expectations, please see the section entitled "Risk Factors" in Dyadic's annual reports on Form 10-K and quarterly reports on Form 10-Q filed with the SEC, as such factors may be updated from time to time in Dyadic's periodic filings with the SEC, which are accessible on the SEC's website at http://www.dyadic.com

Contacts:

WuXi Biologics

Media Contact
Kevin Huang PhD
Phone: +86 (510) 85353705
Email: Kevin_Huang@wuxibiologics.com

Ireland Business
Angus Turner
Phone: +44 (0) 7407 733336
Email: Angus_Turner@wuxiapptec.com

Dyadic International, Inc.
Dyadic International, Inc.
Ping Rawson CFO
Phone: +1 (561) 743-8333
Email: prawson@dyadic.com

SOURCE: Dyadic International, Inc.

ReleaseID: 583088

Humanigen Partners With CTI, A Leading Contract Research Organization, For Planned Phase III Study For Lenzilumab For Coronavirus Treatment

Study to Tackle Leading Cause of Death in COVID-19 Patients

Lenzilumab, a monoclonal antibody that neutralizes granulocyte macrophage colony stimulating factor (GM-CSF)
GM-CSF is up-regulated in COVID-19 patients and may cause a harmful immune response leading to acute respiratory distress syndrome (ARDS)
Clinical evidence suggests that this harmful immune response contributes to cytokine storm in COVID-19 patients at risk of developing ARDS
Company plans to study lenzilumab in COVID-19 patients to prevent ARDS and mortality with CTI Clinical Trial and Consulting Services (CTI)

BURLINGAME, CA and COVINGTON, KY / ACCESSWIRE / March 30, 2020 / Humanigen, Inc., (OTCQB:HGEN) ("Humanigen"), a clinical stage biopharmaceutical company focused on preventing and treating cytokine storm with lenzilumab, the company's proprietary Humaneered® anti-human-granulocyte-macrophage colony stimulating factor (GM-CSF) monoclonal antibody, announced that the company has submitted an initial protocol synopsis to the FDA in support of the company's plans to initiate a multi-center, US, Phase III study in COVID-19 patients

The study, if approved, will be a randomized, controlled, clinical trial with lenzilumab for the prevention of ARDS and/or death in hospitalized patients with pneumonia associated with coronavirus 2 (SARS-CoV-2) infection in COVID-19. The study will be conducted in partnership with CTI Clinical Trial and Consulting Services (CTI), a global, privately held, full-service contract research organization specializing in complex programs for critically and chronically ill patients.

"Humanigen has pioneered the field of GM-CSF neutralization and, unlike others, has already conducted two Phase I and two Phase II studies, including in patients with severe respiratory conditions, with excellent safety results," said Dr. Cameron Durrant, chief executive officer of Humanigen. Durrant continued, "We have been working on prevention of cytokine storm for nearly three years. Lenzilumab has an excellent safety and tolerability profile and has not been associated with serious adverse events, including in patients who are immunosuppressed or with severe asthma. Subject to discussion and agreement with regulatory authorities, we intend to progress as quickly as possible with this study."

"The COVID-19 pandemic demands an unprecedented response from the pharmaceutical and biotechnology communities, requiring innovation, collaboration, and prioritization of speed without the cost of safety," remarked Tim Schroeder, founder and CEO of CTI. "We are proud to have the opportunity to collaborate on such a response with the Humanigen team and to work together to develop an effective treatment solution for those hardest hit by COVID-19," he concluded.

More details on the company's programs in COVID-19 can be found on the company's website at www.humanigen.com under the COVID-19 tab.

About COVID-19-Induced ARDS

COVID-19 is an infectious disease caused by SARS-CoV-2. COVID-19 has become a global pandemic, with over 460,000 confirmed cases and over 21,000 deaths reported to date. Patients with severe cases of COVID-19 experience severe viral pneumonia that can progress to acute respiratory distress syndrome (ARDS) and death.

ARDS is an acute, life-threatening inflammatory lung injury characterized by hypoxia – a lack of oxygen to the tissue – and stiff lungs due to increased pulmonary vascular permeability. ARDS necessitates hospitalization and mechanical ventilation. A rapid increase in patients with ARDS presents a major challenge for the global public health system given limited hospital beds and ventilators. When implementing standard of care, including mechanical ventilation, ARDS has an overall mortality rate of greater than 40%.

About Humanigen, Inc.

Humanigen, Inc. is developing its portfolio of clinical and pre-clinical therapies for the treatment of cancers and infectious diseases via its novel, cutting-edge GM-CSF neutralization and gene-knockout platforms. We believe that our GM-CSF neutralization and gene-editing platform technologies have the potential to reduce the inflammatory cascade associated with coronavirus infection as well as the serious and potentially life-threatening CAR-T therapy-related side effects while preserving and potentially improving the efficacy of the CAR-T therapy itself, thus breaking the efficacy/toxicity linkage. The company's immediate focus is to prevent or minimize the cytokine storm that precedes severe lung dysfunction and ARDS in cases of pneumonia-associated SARS-CoV-2 infection and also in combining FDA-approved and development stage CAR-T therapies with lenzilumab, the company's proprietary Humaneered® anti-human-GM-CSF immunotherapy, which is its lead product candidate. A clinical collaboration with Kite, a Gilead Company, was recently announced to evaluate the sequential use of lenzilumab with Yescarta®, axicabtagene ciloleucel, in a multicenter clinical trial in adults with relapsed or refractory large B-cell lymphoma. The company is also focused on creating next-generation combinatory gene-edited CAR-T therapies using strategies to improve efficacy while employing GM-CSF gene knockout technologies to control toxicity. In addition, the company is developing its own portfolio of proprietary first-in-class EphA3-CAR-T for various solid cancers and EMR1-CAR-T for various eosinophilic disorders. The company is also exploring the effectiveness of its GM-CSF neutralization technologies (either through the use of lenzilumab as a neutralizing antibody or through GM-CSF gene knockout) in combination with other CAR-T, bispecific or natural killer (NK) T cell engaging immunotherapy treatments to break the efficacy/toxicity linkage, including to prevent and/or treat graft-versus-host disease (GvHD) in patients undergoing allogeneic hematopoietic stem cell transplantation (HSCT). The company has established several partnerships with leading institutions to advance its innovative cell and gene therapy pipeline. For more information, visit www.humanigen.com.

About CTI

CTI Clinical Trial and Consulting Services is a global, privately held, full-service contract research organization (CRO), delivering a complete spectrum of clinical trial and consulting services throughout the lifecycle of development, from concept to commercialization. CTI's focused therapeutic approach provides pharmaceutical, biotechnology, and medical device firms with clinical and disease area expertise in rare diseases, regenerative medicine/gene therapy, immunology, transplantation, nephrology, hematology/oncology, neurology, infectious diseases, hepatology, cardiopulmonary, and pediatric populations. CTI also offers a fully integrated multi-specialty clinical research site that conducts phase I-IV trials. CTI has a passion for helping life-changing therapies succeed in chronically and critically ill patient populations. With clinical trial experience across 6 continents, CTI partners with research sites, patients, and sponsors to fulfill unmet medical needs. CTI is headquartered in the Greater Cincinnati, OH area, with operations across North America, Europe, Latin America, and Asia-Pacific. For more information visit www.ctifacts.com.

Forward-Looking Statements

This release contains forward-looking statements. Forward-looking statements reflect management's current knowledge, assumptions, judgment and expectations regarding future performance or events. Although management believes that the expectations reflected in such statements are reasonable, they give no assurance that such expectations will prove to be correct and you should be aware that actual events or results may differ materially from those contained in the forward-looking statements. Words such as "will," "expect," "intend," "plan," "potential," "possible," "goals," "accelerate," "continue," and similar expressions identify forward-looking statements, including, without limitation, statements regarding our expectations for a Phase III study and the future development of lenzilumab to minimize or reduce the severity of lung dysfunction associated with severe coronavirus infections or to help CAR-T reach its full potential or to deliver benefit in preventing GvHD. Forward-looking statements are subject to a number of risks and uncertainties including, but not limited to, the risks inherent in Black Horse Capital and its affiliates owning more than 50% of our outstanding common stock, including their ability to control the company; our lack of profitability and need for additional capital to conduct the Phase III study and operate our business as a going concern; our dependence on partners to further the development of our product candidates; the uncertainties inherent in the development and launch of any new pharmaceutical product; the outcome of pending or future litigation; and the various risks and uncertainties described in the "Risk Factors" sections and elsewhere in the Company's periodic and other filings with the Securities and Exchange Commission.

All forward-looking statements are expressly qualified in their entirety by this cautionary notice. You should not place undue reliance on any forward-looking statements, which speak only as of the date of this release. We undertake no obligation to revise or update any forward-looking statements made in this press release to reflect events or circumstances after the date hereof or to reflect new information or the occurrence of unanticipated events, except as required by law.

CONTACT:
Investors and media:
ir@humanigen.com

SOURCE: Humanigen, Inc.

ReleaseID: 583090

Are These Names On Your List Of Penny Stocks To Watch This Week?

CORAL GABLES, FL / ACCESSWIRE / March 30, 2020 / The top website for all things penny stocks, PennyStocks.com just released a new, exclusive & informative article titled: Best Penny Stocks To Buy This Week? 3 With Key Data Planned. The team at PennyStocks.com discusses several penny stocks to watch this week with several scheduled to report key data.

Within this article, PennyStocks.com states how: "Looking for penny stocks to buy can be a task especially if there are many to choose from. When it comes to weekend research one of the main search topics involves potential catalysts. So you might say, "It's the weekend, no one reports news." This is true, however, some companies will update well in advance on key data readout dates. This can give you some insight into putting together a proper list of penny stocks like the one we have put together this morning that includes SuperCom Ltd. (SPCB)."

Read the article from PennyStocks.com titled: Best Penny Stocks To Buy This Week? 3 With Key Data Planned <<

Penny Stocks (PennyStocks.com)

PennyStocks.com is the best place to find the top penny stocks to buy, a full list of penny stocks and small cap stock news, articles & information. Penny stocks are off to a very strong start in 2020 and are expected to continue their bullish run. Subscribe, to our Free Penny Stocks Newsletter and stay updated on the top penny stock picks, exclusive articles & small cap stock alerts.

Contact:

Name: Adam Lawrence
Email: news@pennystocks.com
Phone: (305) 204-3247

Legal Disclaimer

Except for the historical information presented herein, matters discussed in this article contain forward-looking statements that are subject to certain risks and uncertainties that could cause actual results to differ materially from any future results, performance or achievements expressed or implied by such statements. MIDAM VENTURES LLC, which owns www.PennyStocks.com is not registered with any financial or securities regulatory authority and does not provide nor claims to provide investment advice or recommendations to readers of this release. Please Read Our Full Disclosure Located Here: https://pennystocks.com/disclaimer/

SOURCE: PennyStocks.com

ReleaseID: 583092

Experion Increases Cultivation and Processing Capacity

VANCOUVER, BC / ACCESSWIRE / March 30, 2020 / Experion Holdings Ltd. (the "Company" or "Experion") (TSXV:EXP)(OTCQB:EXPFF)(FRANKFURT:MB31) is pleased to announce its wholly owned subsidiary, Experion Biotechnologies Inc., a licensed cannabis company under the Cannabis Act, has received approval from Health Canada amending its license to expand cultivation and processing capacity at its Mission, BC facility.

The Health Canada approved amendment immediately increases the Company's cultivation by 20%. This newly licensed space will begin actively growing premium-quality flower by mid-April. Experion's top shelf cannabis is distributed under its brand, Citizen Stash, which is actively sold in five provinces and two territories across Canada and has experienced strong consumer demand.

Several licensed processing rooms were also approved by the Health Canada amendment now doubling the Company's processing capabilities including post-harvest activities, packaging and labeling, as well as, improving operational efficiencies by enabling a number of these production activities to run in parallel. The increased processing space further enhances Experion's ability to develop and manufacture value-added products such as pre-rolls; ultimately, facilitating the diversification and expansion of its product offerings. The increased capacity also positions the Company to undertake strategic partner relationships and contract manufacturing opportunities including the production of cannabis concentrates like shatter, rosin and kief.

"The approval of this license amendment is a very exciting milestone for Experion," commented Mr. Jarrett Malnarick, CEO of Experion Holdings. "We now have the required space to further our business plan and continue to drive the Company to profitability. As demand for our Citizen Stash branded products continues to grow, coupled with our business model to process and distribute quality cannabis products across Canada, it became clear that additional cultivation and processing space was needed to effectively capitalize on this market opportunity. Now with our strategic grow and supply partners coming online and our newly licensed space, we have the capacity to process hundreds of kilograms of flower per month, launch pre-rolls quickly and offer other value-added products. With cannabis recently identified as an "essential service" in a number of provinces, we remain confident in the future of our Company in these unprecedented times."

About Experion Holdings Ltd.

Experion Holdings Ltd. is the parent company of Experion Biotechnologies Inc., a Health Canada licensed cultivator and processor of Cannabis, based in Mission, BC.

Experion Holdings Ltd. is invested in a portfolio of products to address a wide spectrum of consumer needs' including Adult-use, Wellness and Therapeutic, and Medical products.

Experion trades on the TSX Venture Exchange as a Tier 1 issuer under the symbol "EXP" on the OTCQB Venture under the symbol "EXPFF" and on the Frankfurt Stock Exchange under the symbol "MB31"

For further information, please visit the Company's website www.experionwellness.com or contact Investor Relations, Email: IR@experionwellness.com

Disclosure

This press release contains forward-looking information within the meaning of Canadian securities laws. Although the Company believes that such information is reasonable, it can give no assurance that such expectations will prove to be correct.

Forward looking information is typically identified by words such as: believe, expect, anticipate, intend, estimate, forecast, postulate and similar expressions, or are those, which, by their nature, refer to future events. The Company cautions investors that any forward-looking information provided by the Company are not guarantees of future results or performance, and that actual results may differ materially from those in forward looking information as a result of various factors, including, but not limited to: the state of the financial markets for the Company's equity securities; recent market volatility; the Company's ability to raise the necessary capital or to be fully able to implement its business strategies; the risks identified in the Filing Statement, and other risks and factors that the Company is unaware of at this time. The reader is referred to the Filing Statement dated September 25, 2017 and/or the most recent annual and interim Management's Discussion and Analysis for a more complete discussion of such risk factors and their potential effects, copies of which may be accessed through the Company page on SEDAR at www.sedar.com.

Neither the TSX Venture Exchange nor its Regulation Services Provider (as that term is defined in policies ofthe TSX Venture Exchange) accepts responsibility for the adequacy or accuracy of this release.

SOURCE: Experion Holdings Ltd.

ReleaseID: 583073

SHAREHOLDER ALERT: Purcell Julie & Lefkowitz LLP Is Investigating Murphy Oil Corporation for Potential Breaches of Fiduciary Duty By Its Board of Directors

NEW YORK, NY / ACCESSWIRE / March 30, 2020 / Purcell Julie & Lefkowitz LLP, a class action law firm dedicated to representing shareholders nationwide, is investigating a potential breach of fiduciary duty claim involving the board of directors of Murphy Oil Corporation (NYSE:MUR).

If you are a shareholder of Murphy Oil Corporation and are interested in obtaining additional information regarding this investigation, free of charge, please visit us at:

http://pjlfirm.com/murphy-oil-corporation/

You may also contact Robert H. Lefkowitz, Esq. either via email at rl@pjlfirm.com or by telephone at 212-725-1000. One of our attorneys will personally speak with you about the case at no cost or obligation.

Purcell Julie & Lefkowitz LLP is a law firm exclusively committed to representing shareholders nationwide who are victims of securities fraud, breaches of fiduciary duty and other types of corporate misconduct. For more information about the firm and its attorneys, please visit http://pjlfirm.com. Attorney advertising. Prior results do not guarantee a similar outcome.

SOURCE: Purcell Julie & Lefkowitz LLP

ReleaseID: 583089

Telkonet Announces Fiscal Year 2019 Financial Results with Strong Revenue Growth of 42% Over Prior Year

Teleconference and Webcast to be Held Today at 4:30 P.M. EST

WAUKESHA, WI / ACCESSWIRE / March 30, 2020 / Telkonet, Inc. (OTCQB: TKOI), (the "Company", "Telkonet"), developer of the EcoSmart Platform of intelligent automation designed to optimize occupancy comfort, energy management and operational efficiencies for living environments, announces financial results for the fiscal year ended December 31, 2019. Management will host a teleconference at 4:30pm ET today to discuss these results with the financial community.

"2019 represented a significant increase in industry demand for intelligent automation and Telkonet was well-positioned to take advantage of the opportunity," stated Jason Tienor, Telkonet's President and Chief Executive Officer. "Through innovative products and strong channel support, we continue to broaden our EcoSmart platform and its market penetration in support of our strategic growth goals."

Operating and Financial Highlights Comparison for the Years Ended December 31, 2019 and 2018:

Total revenues increased 42% year over year.
Total revenues increased in all core markets year over year, with the hospitality market leading the way with an increase of $2.1 million, or 30%.
Product revenues derived from value-added resellers and distribution partners were $8.6 million, an increase of 39% compared to prior year.
Material costs as a percentage of product revenues were 42%, an improvement of 8%, compared to the prior year period.
Operating expenses decreased 14% in second half of 2019 compared to first half of 2019, resulting from a number of cost elimination and liquidity actions initiated during the second half of 2019.
Operating losses were $2.0 million for the year, an improvement of $1.0 million year over year.
During the twelve-month period ended December 31, 2019, the Company's cash balances decreased, on average, approximately $0.11 million per month compared to a decrease of approximately $0.31 million per month for the prior year period.
For the three month period ended December 31, 2019, with reported net income of $0.2 million, the Company achieved profitable operations as a single reportable business unit, for the first time.

"Telkonet's fourth quarter performance capped a strong 2019 that demonstrates the development of the Company overall," continues Tienor. "I'm extremely proud of the efforts of the entire organization in meeting our growth demands and have high expectations for the Company's continued performance in 2020."

Financial Results Review

Fiscal Year 2019

Revenue: Total revenue increased $3.6 million to $12 million for the fiscal year ended December 31, 2019 compared to $8.4 million for the comparable period in 2018.

Product Revenue: Product revenue which principally arises from the sales and installation of our EcoSmart energy management platform increased $3.6 million to $11.2 million for the fiscal year ended December 31, 2019 compared to $7.6 million for the comparable period in 2018.

Recurring Revenue: Recurring revenue which principally arises from call center support services decreased $0.05 million to $0.8 million for the fiscal year ended December 31, 2019 compared to fiscal year ended 2018.

Gross Margin: Gross profit percentages decreased to 42% for the fiscal year ended December 31, 2019 from 45% for the comparable period in 2018.

Net Loss: A net loss of $2.0 million was incurred for the fiscal year ended December 31, 2019 compared to a net loss of $3.0 million for the comparable period in 2018.

Teleconference

Date: Monday, March 30, 2020

Time: 4:30 p.m. EST (3:30 p.m. CDT, 1:30 p.m. PST)

Investor Dial-In (Toll Free US & Canada): 877-407-9171

Investor Dial-In (International): 201-493-6757

A replay of the teleconference will be available until April 13, 2020, which can be accessed by dialing (877) 660-6853 if calling within the US & Canada or (201) 612-7415, if calling internationally. Please enter conference ID# 13649459 to access the replay.

NON-GAAP Financial Measures

Telkonet will post to the Company's investor relations web site (www.telkonet.com) any reconciliation of differences between non-GAAP financial information that may be required in connection with issuing the Company's financial results.

The Company, as is common in its industry, uses adjusted EBITDA, a non-GAAP measurement gauge to demonstrate earnings exclusive of interest and non-cash events. The Company manages its business based on its cash flows. The Company, in its daily management of its business affairs and analysis of its monthly, quarterly and annual performance, makes its decisions based on cash flows, not on the amortization of assets obtained through historical activities. The Company, in managing its current and future affairs, cannot affect the amortization of the intangible assets to any material degree, and therefore uses adjusted EBITDA as its primary management guide. Adjusted EBITDA is not, and should not be considered, an alternative to net income (loss), operating income (loss), or any other measure for determining operating performance of liquidity, as determined under accounting principles generally accepted in the United States (GAAP). In assessing the overall health of its business for the years ended December 31, 2019 and 2018, the Company excluded items in the following general category described below:

Stock-based compensation: The Company believes that because of the variety of equity awards used by companies, varying methodologies for determining stock-based compensation and the assumptions and estimates involved in those determinations, the exclusion of non-cash stock-based compensation enhances the ability of management and investors to understand the impact of non-cash stock-based compensation on our operating results. Further, the Company believes that excluding stock-based compensation expense allows for a more transparent comparison of its financial results to the previous period.

Adjusted EBITDA and other non-GAAP financial measures should not be considered in isolation from, or as a substitute for, a measure of financial performance prepared in accordance with GAAP. Further, investors are cautioned that there are inherent limitations associated with the use of the non-GAAP financial measure as an analytical tool. In particular, the non-GAAP financial measure is not based on a comprehensive set of accounting rules or principles and many of the adjustments to the GAAP financial measure reflect the exclusion of items that are recurring and will be reflected in the Company's financial results for the foreseeable future. The Company compensates for these limitations by providing specific information in the reconciliation included in this press release regarding the GAAP amounts excluded from the non-GAAP financial measure.

ABOUT TELKONET

Telkonet, Inc. (OTCQB: TKOI) provides innovative intelligent automation platforms at the forefront of the Internet of Things (IoT) space. Helping commercial audiences better manage operational costs, the Company's EcoSmart intelligent automation platform is supported by a full-suite of IoT-connected devices that provide in-depth energy usage information and analysis, allowing building operators to reduce energy expenses. Vertical markets that benefit from EcoSmart products include hospitality, education, military, government, healthcare and multiple dwelling housing. Telkonet was founded in 1977 and is based in Waukesha, WI. For more information, visit www.telkonet.com.

For news updates as they happen, follow @Telkonet on Twitter.

To receive updates on all of Telkonet's developments, sign up for our email alerts HERE.www.telkonet.com

FORWARD LOOKING STATEMENTS

Statements included in this release may constitute forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Such statements involve a number of risks and uncertainties such as competitive factors, technological development, market demand and the Company's ability to obtain new contracts and accurately estimate net revenue due to variability in size, scope and duration of projects, and internal issues in the sponsoring client. Further information on potential factors that could affect the Company's financial results, can be found in the Company's Annual Report on Form 10-K for the year ended December 31, 2019 and in its Reports on Forms 8-K filed with the Securities and Exchange Commission ("SEC").

Media Contacts:

Telkonet Investor Relations
414.721.7988
ir@telkonet.com

TELKONET, INC.
CONSOLIDATED STATEMENTS OF OPERATIONS
FOR THE YEARS ENDED DECEMBER 31,

 

 
2019
 
 
2018
 

Revenues, net:

 
 
 
 
 
 

Product

 
$
11,212,854
 
 
$
7,616,415
 

Recurring

 
 
769,342
 
 
 
815,564
 

Total Net Revenues

 
 
11,982,196
 
 
 
8,431,979
 

 

 
 
 
 
 
 
 
 

Cost of Sales:

 
 
 
 
 
 
 
 

Product

 
 
6,703,494
 
 
 
4,392,643
 

Recurring

 
 
301,500
 
 
 
269,443
 

Total Cost of Sales

 
 
7,004,994
 
 
 
4,662,086
 

 

 
 
 
 
 
 
 
 

Gross Profit

 
 
4,977,202
 
 
 
3,769,893
 

 

 
 
 
 
 
 
 
 

Operating Expenses:

 
 
 
 
 
 
 
 

Research and development

 
 
1,737,385
 
 
 
1,879,676
 

Selling, general and administrative

 
 
5,155,092
 
 
 
4,843,859
 

Depreciation and amortization

 
 
66,082
 
 
 
67,107
 

Total Operating Expenses

 
 
6,958,559
 
 
 
6,790,642
 

 

 
 
 
 
 
 
 
 

Operating Loss

 
 
(1,981,357
)
 
 
(3,020,749
)

 

 
 
 
 
 
 
 
 

Other Income (Expenses):

Gain on sale of fixed assets

 
 
150
 
 
 

 

Interest income (expense), net

 
 
(53,289
)
 
 
13,622
 

Total Other Income (Expense)

 
 
(53,139
)
 
 
13,622
 

 

 
 
 
 
 
 
 
 

Loss before Provision for Income Taxes

 
 
(2,034,496
)
 
 
(3,007,127
)

Income Tax Provision (Benefit)

 
 
(100,363
)
 
 
9,623
 

Net Loss Attributable to Common Stockholders

 
$
(1,934,133
)
 
$
(3,016,750
)

 

 
 
 
 
 
 
 
 

Net Loss per Common Share:

 
 
 
 
 
 
 
 

 

 
 
 
 
 
 
 
 

Basic – net loss attributable to common stockholders

 
$
(0.01
)
 
$
(0.02
)

 

 
 
 
 
 
 
 
 

Diluted – net loss attributable to common stockholders

 
$
(0.01
)
 
$
(0.02
)

 

 
 
 
 
 
 
 
 

Weighted Average Common Shares Outstanding used in computing basic net loss per share

 
 
135,213,641
 
 
 
134,055,098
 

Weighted Average Common Shares Outstanding used in computing diluted net loss per share

 
 
135,213,641
 
 
 
134,055,098
 

RECONCILIATION OF NET LOSS
TO ADJUSTED EBITDA
FOR THE YEARS ENDED DECEMBER 31,

 

 
2019
 
 
2018
 

Net loss

 
$
(1,934,133
)
 
$
(3,016,750
)

Interest (income) expense, net

 
 
53,139
 
 
 
(13,622
)

Income tax provision (benefit)

 
 
(100,363
)
 
 
9,623
 

Depreciation and amortization

 
 
66,082
 
 
 
67,107
 

EBITDA

 
 
(1,915,275
)
 
 
(2,953,642
)

Adjustments:

 
 
 
 
 
 
 
 

Stock-based compensation

 
 
7,261
 
 
 
6,404
 

 

 
 
 
 
 
 
 
 

Adjusted EBITDA

 
$
(1,908,014
)
 
$
(2,947,238
)

SOURCE: Telkonet, Inc.

ReleaseID: 582177

Heat Biologics Provides Year-End Business Update

Provides update on development of gp96 vaccine for preventing infection from the SARS-CoV-2 coronavirus that causes COVID-19

Reports progress on development of COVID-19 30-minute point of care diagnostic test

Completed enrollment in Phase 2 non-small cell lung cancer trial

Reports over $25 million of cash and short-term investments as of March 23, 2020

DURHAM, NC / ACCESSWIRE / March 30, 2020 / Heat Biologics, Inc. ("Heat") (NASDAQ:HTBX), a clinical-stage biopharmaceutical company specialized in the development of novel therapeutic and prophylactic vaccines, including one for coronavirus COVID-19, today provided financial, clinical and operational updates for the year ended December 31, 2019.

Jeff Wolf, Chief Executive Officer of Heat Biologics, commented, "2019 was an exciting year for Heat, as we advanced our therapeutic pipeline. This past November, we presented additional positive top line Phase 2 data of HS-110 plus BMS checkpoint inhibitor nivolumab (Opdivo®) in advanced NSCLC lung cancer patients at the American Association for Cancer Research (AACR) Special Conference on Tumor Immunology and Immunotherapy. We are highly encouraged by the data as we advance partnership and collaboration discussions. Earlier this year, we announced dosing the first patient in a Phase 1 clinical trial of our co-stimulatory HS-130, in combination with HS-110, for patients with advanced solid tumors refractory to standard of care, which marks a key milestone for Heat."

"We recently announced plans to develop a vaccine for preventing infection from the SARS-CoV-2 coronavirus that causes COVID-19 utilizing our robust gp-96 vaccine platform in collaboration with the University of Miami. Heat's gp96 platform has undergone rigorous testing as a vaccine against SIV/HIV, malaria, zika and other infectious diseases in numerous National Institutes of Health (NIH) and Department of Defense (DOD)-funded mice and primate trials and has been tested in over 300 patients in multiple NIH and Heat-funded oncology trials. We believe this platform has the potential to provide broad protection against COVID-19, and possible future mutations of COVID-19 or other coronaviruses. We are encouraged by the prospects for this program and are moving forward with our partners to advance this vaccine as quickly as possible."

"Earlier this month we also announced a collaboration with the University of Miami to develop a proprietary COVID-19 point-of-care diagnostic test. The new paper-based test is being designed to provide a read-out in a fraction of the time required for most other tests, have no technical hardware requirements, have low cost of goods, be easily manufactured at scale, and provide binary readout if the patient is positive for a disease within 30 minutes. Unfortunately, current diagnostic tests, are in short supply and often take days for results. This diagnostic is being designed for early detection to provide critical and time-sensitive information to help curb the spread of the disease."

Mr. Wolf concluded, "We share our sympathies to those individuals and families impacted by COVID-19 and are committed to helping find solutions to this global pandemic. I'd like to thank all of the Heat and University of Miami professionals that have worked tirelessly to advance our therapeutic and diagnostic platforms. Importantly, we have over $25 million of cash and short-term investments as of March 23, 2020, which should put us on a solid financial footing as we advance our programs. Moreover, we believe that upcoming catalysts and milestones have the potential to drive significant shareholder value."

2019 Financial Results

Research and development expenses decreased by 20% to $13.0 million for the year ended December 31, 2019 compared to $16.2 million for the year ended December 31, 2018. The variance of approximately $3.2 million is primarily due to reduced clinical trial expenses related to HS-110 patient enrollment completion.

General and administrative expense increased approximately 36% to $9.5 million for the year ended December 31, 2019 compared to $7.0 million for the year ended December 31, 2018. The variance of $2.5 million is primarily due to the increase in personnel and stock compensation expense.
Net loss attributable to Heat Biologics was approximately $20.0 million, or ($0.60) per basic and diluted share for the year ended December 31, 2019 compared to a net loss of approximately $15.7 million, or ($0.90) per basic and diluted share for the year ended December 31, 2018.
As of December 31, 2019, the Company had approximately $14.8 million in cash, cash equivalents and short-term investments.

About Heat Biologics, Inc.

Heat Biologics is a biopharmaceutical company developing immunotherapies designed to activate a patient's immune system against cancer and other diseases using its proprietary gp96 platform to activate CD8+ "Killer" T-cells. Heat has completed enrollment in its Phase 2 clinical trial for advanced non-small cell lung cancer with its gp96-based HS-110 therapeutic vaccine. HS-110 is the company's first biologic product candidate in a series of proprietary immunotherapies designed to stimulate a patient's own T-cells. Heat Biologics has also launched a program in collaboration with the University of Miami to develop a vaccine designed to protect against the COVID-19 coronavirus. Heat has numerous other pre-clinical programs at various stages of development. For more information, please visit www.heatbio.com.

Forward Looking Statement

This press release includes forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995 on our current expectations and projections about future events. In some cases, forward-looking statements can be identified by terminology such as "may," "should," "potential," "continue," "expects," "anticipates," "intends," "plans," "believes," "estimates," and similar expressions. These statements are based upon current beliefs, expectation, and assumptions and include statements such as developing a vaccine for treating or preventing infection from the SARS-CoV-2 coronavirus that causes COVID-19 utilizing Heat's robust gp-96 vaccine platform in collaboration with the University of Miami, the platform having the potential to provide broad protection against COVID-19, and possible future mutations of COVID-19 or other coronaviruses, moving forward with Heat's partners to advance this vaccine to clinical trials as quickly as possible, the new paper-based test providing a read-out in a fraction of the time required for most other tests, having no technical hardware requirements, low cost of goods, being easily manufactured at scale, and providing binary readout if the patient is positive for a disease within 30 minutes,upcoming catalysts and milestones having the potential to drive significant shareholder value, and cash being sufficient to advance Heat's programs. These statements are subject to a number of risks and uncertainties, many of which are difficult to predict, including the ability of Heat together with researchers at the University of Miami to develop a proprietary COVID-19 point-of-care diagnostic test that provides a read-out in a fraction of the time required for most other tests, have no technical hardware requirements, low cost of goods, be easily manufactured at scale, and provide binary readout if the patient is positive for a disease within 30 minutes, the ability of Heat's vaccine platform to provide protection against COVID-19, the ability of Heat's therapies to perform as designed, to demonstrate safety and efficacy, as well as results that are consistent with prior results, the ability to enroll patients and complete the clinical trials on time and achieve desired results and benefits, Heat's ability to obtain regulatory approvals for commercialization of product candidates or to comply with ongoing regulatory requirements, regulatory limitations relating to Heat's ability to promote or commercialize its product candidates for specific indications, acceptance of its product candidates in the marketplace and the successful development, marketing or sale of products, Heat's ability to maintain its license agreements, the continued maintenance and growth of its patent estate, its ability to establish and maintain collaborations, its ability to obtain or maintain the capital or grants necessary to fund its research and development activities, its ability to continue to maintain its listing on the Nasdaq Capital Market and its ability to retain its key scientists or management personnel, and the other factors described in Heat's most recent annual report on Form 10-K filed with the SEC, and other subsequent filings with the SEC. The information in this release is provided only as of the date of this release, and Heat undertakes no obligation to update any forward-looking statements contained in this release based on new information, future events, or otherwise, except as required by law.

Media and Investor Relations Contact

David Waldman
+1 919 289 4017
investorrelations@heatbio.com

HEAT BIOLOGICS INC.
Consolidated Balance Sheets

 

 

December 31,

 

 

 

2019

 
 

2018

 

 

 

 

 
 

 

 

Current Assets

 

 

 
 

 

 

Cash and cash equivalents

 
$
9,039,887
 
 
$
22,154,251
 

Short-term investments

 
 
5,713,922
 
 
 
5,570,027
 

Accounts receivable

 
 
34,986
 
 
 
28,538
 

Prepaid expenses and other current assets

 
 
420,328
 
 
 
961,317
 

Total Current Assets

 
 
15,209,123
 
 
 
28,714,133
 

 

 
 
 
 
 
 
 
 

Property and Equipment, net

 
 
559,410
 
 
 
643,146
 

 

 
 
 
 
 
 
 
 

Other Assets

 
 
 
 
 
 
 
 

In-process R&D

 
 
5,866,000
 
 
 
5,866,000
 

Goodwill

 
 
1,452,338
 
 
 
2,189,338
 

Operating lease right-of-use asset

 
 
2,287,500
 
 
 

 

Finance lease right-of-use asset

 
 
187,573
 
 
 

 

Deposits

 
 
394,637
 
 
 
351,220
 

Total Other Assets

 
 
10,188,048
 
 
 
8,406,558
 

 

 
 
 
 
 
 
 
 

Total Assets

 
$
25,956,581
 
 
$
37,763,837
 

 

 
 
 
 
 
 
 
 

Liabilities and Stockholders' Equity

 
 
 
 
 
 
 
 

 

 
 
 
 
 
 
 
 

Current Liabilities

 
 
 
 
 
 
 
 

Accounts payable

 
$
1,503,342
 
 
$
974,619
 

Deferred revenue, current portion

 
 
3,410,319
 
 
 
1,032,539
 

Contingent consideration, current portion

 
 
1,579,334
 
 
 
1,187,000
 

Operating lease liability, current portion

 
 
216,832
 
 
 

 

Finance lease liability, current portion

 
 
49,104
 
 
 

 

Accrued expenses and other liabilities

 
 
1,676,467
 
 
 
1,678,051
 

Total Current Liabilities

 
 
8,435,398
 
 
 
4,872,209
 

 

 
 
 
 
 
 
 
 

Long Term Liabilities

 
 
 
 
 
 
 
 

Other long-term liabilities

 
 

 
 
 
213,724
 

Deferred tax liability

 
 
361,911
 
 
 
316,733
 

Deferred revenue, net of current portion

 
 
200,000
 
 
 
200,000
 

Operating lease liability, net of current portion

 
 
1,519,574
 
 
 

 

Financing lease liability, net of current portion

 
 
142,667
 
 
 

 

Contingent consideration, net of current portion

 
 
2,139,181
 
 
 
1,918,225
 

Total Liabilities

 
 
12,798,731
 
 
 
7,520,891
 

 

 
 
 
 
 
 
 
 

Stockholders' Equity

 
 
 
 
 
 
 
 

Common stock, $.0002 par value; 100,000,000 shares authorized, 33,785,999 and 32,492,144 shares issued and outstanding at December 31, 2019 and December 31, 2018, respectively

 
 
6,757
 
 
 
6,499
 

Additional paid-in capital

 
 
118,173,843
 
 
 
114,883,135
 

Accumulated deficit

 
 
(104,597,748
)
 
 
(84,580,180
)

Accumulated other comprehensive loss

 
 
(11,250
)
 
 
(19,904
)

Total Stockholders' Equity – Heat Biologics, Inc.

 
 
13,571,602
 
 
 
30,289,550
 

Non-Controlling Interest

 
 
(413,752
)
 
 
(46,604
)

Total Stockholders' Equity

 
 
13,157,850
 
 
 
30,242,946
 

 

 
 
 
 
 
 
 
 

Total Liabilities and Stockholders' Equity

 
$
25,956,581
 
 
$
37,763,837
 

HEAT BIOLOGICS INC.
Consolidated Statements of Operations and Comprehensive Loss

 

 

Year ended

 

 

 

December 31,

 

 

 

2019

 
 

2018

 

Revenue:

 

 

 
 

 

 

Grant and licensing revenue

 
$
3,049,104
 
 
$
5,793,849
 

 

 
 
 
 
 
 
 
 

Operating expenses:

 
 
 
 
 
 
 
 

Research and development

 
 
13,013,604
 
 
 
16,233,014
 

General and administrative

 
 
9,431,015
 
 
 
7,025,212
 

Goodwill impairment loss

 
 
737,000
 
 
 

 

Change in fair value of contingent consideration

 
 
613,290
 
 
 
495,936
 

Total operating expenses

 
 
23,794,909
 
 
 
23,754,162
 

 

 
 
 
 
 
 
 
 

Loss from operations

 
 
(20,745,805
)
 
 
(17,960,313
)

 

 
 
 
 
 
 
 
 

Interest income

 
 
431,824
 
 
 
265,752
 

Other (expense) income, net

 
 
(25,557
)
 
 
117,780
 

Total non-operating income

 
 
406,267
 
 
 
383,532
 

 

 
 
 
 
 
 
 
 

Net loss before income taxes

 
 
(20,339,538
)
 
 
(17,576,781
)

Income tax (expense) benefit

 
 
(45,178
)
 
 
985,488
 

Net loss

 
 
(20,384,716
)
 
 
(16,591,293
)

Net loss – non-controlling interest

 
 
(367,148
)
 
 
(857,439
)

Net loss attributable to Heat Biologics, Inc.

 
$
(20,017,568
)
 
$
(15,733,854
)

 

 
 
 
 
 
 
 
 

Net loss per share attributable to Heat Biologics, Inc.-

 
 
 
 
 
 
 
 

Net loss per share attributable to Heat Biologics, Inc.-basic and diluted

 
$
(0.60
)
 
$
(0.90
)

 

 
 
 
 
 
 
 
 

Weighted-average number of common shares used in net loss per share attributable to common stockholders –

 
 
 
 
 
 
 
 

Weighted-average number of common shares used in net loss per share attributable to Heat Biologics, Inc.-basic and diluted

 
 
33,281,817
 
 
 
17,485,461
 

 

 
 
 
 
 
 
 
 

Other comprehensive loss:

 
 
 
 
 
 
 
 

Net loss

 
 
(20,384,716
)
 
 
(16,591,293
)

Unrealized gain on foreign currency translation

 
 
8,654
 
 
 
146,121
 

Total other comprehensive loss

 
 
(20,376,062
)
 
 
(16,445,172
)

Comprehensive loss attributable to non-controlling interest

 
 
(367,148
)
 
 
(857,439
)

Comprehensive loss

 
$
(20,008,914
)
 
$
(15,587,733
)

SOURCE: Heat Biologics, Inc.

ReleaseID: 583087

Innodata Successfully Implements Business Continuity Plan; Commits to Serving Medical Community for Data Analytics for COVID-19 Emergency

NEW YORK, NY / ACCESSWIRE / March 30, 2020 / INNODATA INC. (NASDAQ:INOD) announced today that it had initiated its business continuity plan (BCP) on March 11, 2020, as a result of which 3,600 of Innodata's data analysts and support team members (91% of total) are continuing to work remotely with near full productivity across Innodata's 12 global locations. It also announced that it is offering the global medical community data platforms and services at no-charge or reduced-charge to help fight the COVID-19 emergency.

As a result of having initiated its BCP, Innodata is able to continue operations for most of its customers while safeguarding the health and welfare of its employees. Innodata provides data services that relate to essential services including food distribution, evidence-based medicine, healthcare record management, regulatory change, and global news monitoring.

As the global medical community harnesses medical data analytics in the fight against COVID-19, Innodata is offering healthcare institutions, research institutions, and pharmaceutical companies data extraction, data preparation, and data analytics platforms and services at no-charge or reduced-charge (as circumstances warrant), including but not limited to:

Medical file data extraction and analysis for cohort studies
Data analytics related to clinical trials and treatment efficacy
Data preparation for AI and Machine Learning-based solutions
Supervision and training of AI and Machine Learning models

Institutions may contact us at Covid-19.response@innodata.com.

"As the global community is responding to the emergence and spread of COVID-19, our priorities are the safety of our staff and maintaining business continuity for our valued customers, while supporting wherever possible the global response to this evolving crisis," stated Jack Abuhoff, Innodata CEO.

About Innodata

Innodata (NASDAQ: INOD) is a leading data engineering company. Prestigious companies across the globe turn to Innodata for help with their biggest data challenges. By combining advanced machine learning and artificial intelligence (ML/AI) technologies, a global workforce of over 3,000 subject matter experts, and a high-security infrastructure, we're helping usher in the promise of digital data and ubiquitous AI.

Forward Looking Statements

This press release may contain forward-looking statements within the meaning of Section 21E of the Securities and Exchange Act of 1934, as amended, and Section 27A of the Securities Act of 1933, as amended. Words such as "project," "head start," "believe," "expect," "can," "continue," "could," "intend," "may," "should," "will," "anticipate," "indicate," "point to," "forecast," "predict," "likely," "goals," "optimistic," "foster," "estimate," "plan," "potential," or the negatives thereof and other similar expressions generally identify forward-looking statements, which speak only as of the date hereof.

These forward-looking statements are based on our management's current expectations, assumptions and estimates and are subject to a number of risks and uncertainties, including without limitation, that contracts may be terminated by clients; projected or committed volumes of work may not materialize in whole or in part; the primarily at-will nature of contracts with our Digital Data Solutions clients and the ability of these clients to reduce, delay or cancel projects; the likelihood of continued development of the markets, particularly new and emerging markets, that our services support; continuing Digital Data Solutions segment revenue concentration in a limited number of clients; continuing Digital Data Solutions segment reliance on project-based work; our inability to replace projects that are completed, canceled or reduced; our dependency on third-party content providers in our Agility segment; difficulty in integrating and deriving synergies from acquisitions, joint ventures and strategic investments; potential undiscovered liabilities of companies and businesses that we may acquire; potential impairment of the carrying value of goodwill and other acquired intangible assets of companies and businesses that we acquire; changes in our business or growth strategy; depressed market conditions; changes in external market factors; the ability and willingness of our clients and prospective clients to execute business plans which give rise to requirements for our services; changes in our business or growth strategy; the emergence of new or growing competitors; potential effects on our results of operations from interruptions in, or breaches of, our information technology systems and various other competitive and technological factors; and other risks and uncertainties indicated from time to time in our periodic filings with the Securities and Exchange Commission.

Our actual results could differ materially from the results referred to in forward-looking statements. Factors that could cause or contribute to such differences include, but are not limited to, the risks discussed in Part I, Item 1A. "Risk Factors," Part II, Item 7. Management's Discussion and Analysis of Financial Condition and Results of Operations, and other parts of our Annual Report on Form 10-K, filed with the Securities and Exchange Commission on March 16, 2020, or as updated and amended by our other periodic filings with the Securities and Exchange Commission. In light of these risks and uncertainties, there can be no assurance that the results referred to in the forward-looking statements will occur, and you should not place undue reliance on these forward-looking statements. We undertake no obligation to update or review any guidance or other forward-looking statements, whether as a result of new information, future developments or otherwise, other than as required under the Federal securities laws.

Company Contact

Suzanne Srsich
Innodata Inc.
ssrsich@innodata.com
(201) 371-8033

SOURCE: Innodata Inc.

ReleaseID: 583069

Hemp Naturals, Inc. applauds the use of CBD during the Coronavirus outbreak

MIAMI, FL / ACCESSWIRE / March 30, 2020 / Hemp Naturals Naturals, Inc. (OTC PINK:HPMM) is a developmental stage company that plans to research, develop, acquire and sell products containing CBD, including CBD infused Gummies, CBD infused tinctures, and many more CBD products currently being developed announced today that it is supportive of an article which suggests the best use of CBD during the coronavirus outbreak. More information can be found in this 420 Intel article: "How to Best Use CBD During the Coronavirus Outbreak".

Please see the 420 Intel article below:

"As the world slows down and many people go on lockdown, using CBD oil can be a beneficial tool to promote balance and wellness in you, your family members, and even your pet.

It's clear that we as a human community have not experienced anything quite like what we are facing today. While there have been mass epidemics in the past, the newest coronavirus (COVID-19) has us all collectively taking a pause and learning new ways to take care of ourselves.

During this period of social distancing, self-care is more important than ever. While staying connected through phone calls, social media, and apps like Facetime can prove to be very helpful for mental well being, we want to share a few ways CBD oil can promote health and wellness during these particularly tough times.

How You Can Benefit from Daily Servings of CBD Oil

Everyone is feeling the ramifications of the coronavirus outbreak in ways small and large. With the weight of self-isolation, disruptions to many work schedules, and the uneasiness that comes with daily news updates, it's no wonder we're all feeling a bit unbalanced.

In the midst of all of this, slowing down and putting our health first right now is paramount. You may need to take a step back, limit distractions, and focus on healthy behaviors like meditation, exercise, journaling, sleep, nutritious eating, and limiting screen time.

Adding CBD oil to your everyday self-care routine can also prove to be a highly effective and efficient way to encourage balance in your life right now. CBD oil is an all-natural, non-intoxicating extract of the common hemp plant that provides your body with the balancing benefits of CBD and a wide array of beneficial plant-based nutrients that support a complete diet.

CBD helps naturally promote homeostasis by providing support to your body's endocannabinoid system, a major regulatory network responsible for maintaining homeostasis so that functions can perform more optimally. A long list of functions is kept in check by a well-operating endocannabinoid system, helping you feel better every day.

As you face the unique challenges of this unprecedented time, we have developed a list of ways CBD oil can benefit you while you stay in, stay connected, and stay healthy.

Promoting Balance During These Unsteady Times

Let's be honest, remaining calm during a pandemic when food shelves are empty and work is on hold is a challenge, period. In other words, if you're finding it challenging to stay centered, you are not alone.

By stimulating your endocannabinoid system, CBD oil can naturally promote a sense of balance in the body. A more efficient endocannabinoid system positively impacts various functions, including mood.

It's important to point out here that CBD oil, when derived from hemp, doesn't have any intoxicating properties, so you're not going to experience anything like a "couch-lock" effect. Consumers who regularly use CBD oil often report that they feel "a sense of calm" or "more centered" over time.

If you're looking for a type of CBD oil to help encourage overall balance, try a higher-concentrated product like our RSHO® Blue Label Pure CBD Oil packaged in a convenient oral applicator or our RSHO® Gold Label CBD Oil Liquid. Both can be placed under the tongue for the fastest absorption or added to foods to be absorbed through the digestive system.

Once you ingest the pure CBD oil or CBD oil liquid, the CBD will interact with cannabinoid receptors throughout your body, stimulating your endocannabinoid system and promoting whole-body wellness and homeostasis.

Nourishing Your Regularly-Washed Dry Hands

Yep, we are all back in preschool again when it comes to washing hands. The Center for Disease Control is telling us to do it and do it right this time. Clean hands save lives is the message, and we are on board. But the "wet, lather, scrub, rinse, dry" protocol can take a toll on your hands. And if you've been regularly using hand sanitizers made with harsh alcohol, there is no doubt your hands could use some CBD oil goodness.

CBD oil offers many skincare benefits including nourishing, moisturizing, and rejuvenating the skin. That's right- not all CBD oil has to be ingested or inhaled. A CBD topical is more focused and targeted in delivering its natural balancing and wellness effects. When applied to the skin, CBD never reaches your bloodstream but instead interacts with cannabinoid receptors just below the skin's surface, allowing you to direct the extract's powerful benefits right to where they're needed.

At HempMeds®, some of our most popular CBD skincare products contain ingredients like beeswax, lavender, cedarwood, and camphora essential oils to nourish the skin.

To find some tender love for your hands, check out our RSHO® CBD Oil Salve (50 mg CBD) and our HempMeds® Hydrating & Soothing Hemp Body Lotion (100 mg CBD).

Combatting Restless Nights with Sleep Support

One of the top ways to promote and maintain good health is sleep. If a worldwide pandemic isn't keeping you up at night, hats off to you. For the others who are finding it challenging to get a restful sleep at night, following healthy sleep habits like a mindful strategy shortly before bedtime (yoga, deep breathing, meditation) and reducing screen time is key.

CBD oil naturally promotes better rest at night by supporting balance in the body through its influence on the body's endocannabinoid system. While CBD oil doesn't have any sedation effects, a more efficient EC system positively impacts all the body's regular functions, including sleep habits.

To promote a restful night, check out HempMeds® Sleep Support Capsules, powered by our naturally potent CBD extract and paired with natural sleep-promoting ingredients like passionflower, L-Tryptophan, chamomile, and melatonin to promote healthy sleep patterns.

You can also deliver small servings of CBD oil to your system with Dixie Botanicals® Dew Drops CBD Oil Tinctures, available in vanilla, strawberry, and tangerine flavors.

Promoting a Balanced Immune System

During a viral outbreak, people tend to be more aware of their own physical health. Leading to questions like, was that just a cough? Or, what does this sore throat really mean? The immune system is always an important element of health, but in a time like this, its importance is magnified.

There is no evidence that CBD oil can cure COVID-19, but with its spectrum of cannabinoids and nutrients, it can be a beneficial aspect in supporting a balanced immune system. A well-operating endocannabinoid system keeps the immune system in check, thus promoting a balanced immune response and better health.

If you're looking to use CBD oil to promote immune system support, consider our Immune Support Capsules, made with natural vegan immune-supportive ingredients like turmeric root, black pepper, and our high-quality CBD oil. Another good option is our RSHO® Green Label Liquid, which delivers the exciting natural benefits of raw CBD oil in a convenient liquid form.

Keep Your Pet Balanced

Many people are on lockdown, forced to work from home and avoid social interactions. Having a pet to love and feel the love from, especially during social distancing, is known to be an incredible advantage for mental wellness.

Amid the Coronavirus, many pet owners have more access to spending time with pets. While this can be awesome for some pets, schedule changes and tension in pet owners can lead to challenges for our furry friends. The good news, hemp oil can be beneficial for pets too.

In the same way CBD supports your endocannabinoid system, the cannabinoid can also stimulate a dog or cat's endocannabinoid system and encourage wellness. CBD's influence on the endocannabinoid system promotes pets' cardiovascular function, supports healthy joints, encourages neurological health and emotional behavior, helps maintain stamina, and promotes healthy skin and coat.

To offer your pet extra love, check out our Hemp for Pets™ Relaxation Soft Chews made with full-spectrum hemp oil plus naturally-calming ingredients like chamomile, thiamine, L-tryptophan, and ginger to help ease your dog's nerves during unsettling situations. For your cat, try Hemp for Pets™ Soft Baked Cat Chews.

Safety Tips for Using CBD During the Coronavirus Pandemic

Hopefully, you know now a little more of the ways CBD oil can benefit you during this challenging period of time.

Even with this knowledge, there are some safety tips you'll want to keep in mind as you use CBD oil to reduce their risk of coronavirus transmission.

Before and after use, it's a good idea to thoroughly wash the outside of your CBD oil bottles and their lids.
If you're using a CBD oil tincture, be careful to not allow the end of the dropper to touch the inside of your mouth.
If you generally share a CBD oil tincture or other product with a family member or roommate, you may want to each have your own until the coronavirus pandemic is over.
Wash your hands before taking a CBD oil capsule to avoid transmitting anything from your hands onto the capsule.
With pure CBD oil, it's best to apply the CBD oil from the oral applicator onto a spoon, rather than applying the oil directly into your mouth from the syringe.
If you vape CBD, be sure to regularly wash your CBD vaporizers with isopropyl alcohol and do not share your vape pen with friends or family members."

Cautionary Language Concerning Forward-Looking Statements:

This release contains "forward-looking statements" that include information relating to future events and future financial and operating performance. The words "may," "would," "will," "expect," "estimate," "can," "believe," "potential," and similar expressions and variations thereof are intended to identify forward-looking statements. Forward-looking statements should not be read as a guarantee of future performance or results, and will not necessarily be accurate indications of the times at, or by, which that performance or those results will be achieved. Forward-looking statements are based on information available at the time they are made and/or management's good faith belief as of that time with respect to future events and are subject to risks and uncertainties that could cause actual performance or results to differ materially from those expressed in or suggested by the forward-looking statements. Important factors that could cause these differences include, but are not limited to: fluctuations in demand for Hemp Naturals products, the introduction of new products, the Company's ability to maintain customer and strategic business relationships, the impact of competitive products and pricing, growth in targeted markets, the adequacy of the Company's liquidity and financial strength to support its growth, and other information that may be detailed from time-to-time in Hemp Naturals filings with the United States Securities and Exchange Commission. Examples of such forward-looking statements in this release include statements regarding future sales, costs and market acceptance of products as well as regulatory actions at the State or Federal level. For a more detailed description of the risk factors and uncertainties affecting Hemp Naturals please refer to the Company's Securities and Exchange Commission filings, which are available at www.sec.gov. Hemp Naturals undertakes no obligation to publicly update or revise any forward-looking statements, whether as a result of new information, future events or otherwise.

CONTACT:

Levi Jacobson
Hempofnaturals@gmail.com
hempofnaturals.com

SOURCE: Hemp Naturals Inc. 

ReleaseID: 582941