Takeda Completes Sale of Select OTC and Non-Core Assets to Hypera Pharma

Takeda Completes Sale of Select OTC and Non-Core Assets to Hypera Pharma

OSAKA, Japan–(BUSINESS WIRE)–
Takeda Pharmaceutical Company Limited (TSE:4502/NYSE:TAK) (“Takeda”) today announced the completion of its previously-announced sale of a portfolio of select products sold in Latin America to Hypera S.A. (“Hypera Pharma”) for a total value of $825 million USD. This divestment agreement was first announced in March 2020.

The divested portfolio includes select over-the-counter and prescription pharmaceutical products sold in Brazil, Mexico, and other South American, Central American and Caribbean countries, which are part of Takeda’s Growth & Emerging Markets Business Unit (GEM BU). The products, while addressing key patient needs in these countries, are outside of the business areas Takeda has designated as core to its global long-term growth.

Close to 300 Takeda commercial employees will transition with the divested portfolio at close. As part of a manufacturing and supply agreement, Takeda will continue to exclusively manufacture the divested products.

Takeda intends to use the proceeds from the sale to reduce its debt and accelerate deleveraging towards its target of 2x net debt/adjusted EBITDA within Fiscal Years 2021–2023.

Takeda exceeded its $10 billion non-core asset divestiture target in 2020, announcing 11 deals since January 2019 to date for a total aggregate value of up to approximately $11.6 billion.

About Takeda Pharmaceutical Company Limited

Takeda Pharmaceutical Company Limited (TSE:4502/NYSE:TAK) is a global, values-based, R&D-driven biopharmaceutical leader headquartered in Japan, committed to discover and deliver life-transforming treatments, guided by our commitment to patients, our people and the planet. Takeda focuses its R&D efforts on four therapeutic areas: Oncology, Rare Genetic and Hematology, Neuroscience, and Gastroenterology (GI). We also make targeted R&D investments in Plasma-Derived Therapies and Vaccines. We are focusing on developing highly innovative medicines that contribute to making a difference in people’s lives by advancing the frontier of new treatment options and leveraging our enhanced collaborative R&D engine and capabilities to create a robust, modality-diverse pipeline.

Our employees are committed to improving quality of life for patients and to working with our partners in health care in approximately 80 countries.

For more information, visit https://www.takeda.com.

Important Notice

For the purposes of this notice, “press release” means this document, any oral presentation, any question and answer session and any written or oral material discussed or distributed by Takeda Pharmaceutical Company Limited (“Takeda”) regarding this release. This press release (including any oral briefing and any question-and-answer in connection with it) is not intended to, and does not constitute, represent or form part of any offer, invitation or solicitation of any offer to purchase, otherwise acquire, subscribe for, exchange, sell or otherwise dispose of, any securities or the solicitation of any vote or approval in any jurisdiction. No shares or other securities are being offered to the public by means of this press release. No offering of securities shall be made in the United States except pursuant to registration under the U.S. Securities Act of 1933, as amended, or an exemption therefrom. This press release is being given (together with any further information which may be provided to the recipient) on the condition that it is for use by the recipient for information purposes only (and not for the evaluation of any investment, acquisition, disposal or any other transaction). Any failure to comply with these restrictions may constitute a violation of applicable securities laws.

The companies in which Takeda directly and indirectly owns investments are separate entities. In this press release, “Takeda” is sometimes used for convenience where references are made to Takeda and its subsidiaries in general. Likewise, the words “we,” “us” and “our” are also used to refer to subsidiaries in general or to those who work for them. These expressions are also used where no useful purpose is served by identifying the particular company or companies.

Forward-Looking Statements

This press release and any materials distributed in connection with this press release may contain forward-looking statements, beliefs or opinions regarding Takeda’s future business, future position and results of operations, including estimates, forecasts, targets and plans for Takeda. Without limitation, forward-looking statements often include words such as “targets,” “plans,” “believes,” “hopes,” “continues,” “expects,” “aims,” “intends,” “ensures,” “will,” “may,” “should,” “would,” “could” “anticipates,” “estimates,” “projects” or similar expressions or the negative thereof. These forward-looking statements are based on assumptions about many important factors, including the following, which could cause actual results to differ materially from those expressed or implied by the forward-looking statements: the economic circumstances surrounding Takeda’s global business, including general economic conditions in Japan and the United States; competitive pressures and developments; changes to applicable laws and regulations; the success of or failure of product development programs; decisions of regulatory authorities and the timing thereof; fluctuations in interest and currency exchange rates; claims or concerns regarding the safety or efficacy of marketed products or product candidates; the impact of health crises, like the novel coronavirus pandemic, on Takeda and its customers and suppliers, including foreign governments in countries in which Takeda operates, or on other facets of its business; the timing and impact of post-merger integration efforts with acquired companies; the ability to divest assets that are not core to Takeda’s operations and the timing of any such divestment(s); and other factors identified in Takeda’s most recent Annual Report on Form 20-F and Takeda’s other reports filed with the U.S. Securities and Exchange Commission, available on Takeda’s website at: https://www.takeda.com/investors/reports/sec-filings/ or at www.sec.gov. Takeda does not undertake to update any of the forward-looking statements contained in this press release or any other forward-looking statements it may make, except as required by law or stock exchange rule. Past performance is not an indicator of future results and the results or statements of Takeda in this press release may not be indicative of, and are not an estimate, forecast, guarantee or projection of Takeda’s future results.

Japanese Media

Kazumi Kobayashi

[email protected]

+81 (0) 3-3278-2095

Investor Relations:

Christopher O’Reilly

[email protected]

+81 (0) 3-3278-2306

Media outside Japan

Justine Grosvenor

[email protected]

+1 872 226 6701

KEYWORDS: Japan Asia Pacific

INDUSTRY KEYWORDS: Biotechnology Pharmaceutical Health

MEDIA:

Eagle Financial Bancorp, Inc. Announces Cash Dividend, 2021 Annual Meeting Date and Fourth Quarter 2020 Results

Eagle Financial Bancorp, Inc. Announces Cash Dividend, 2021 Annual Meeting Date and Fourth Quarter 2020 Results

CINCINNATI–(BUSINESS WIRE)–
Eagle Financial Bancorp, Inc. (the “Company”) (OTCQB: EFBI), the holding company for Eagle Savings Bank, today announced that its Board of Directors declared a cash dividend of $0.05 per common share. The dividend will be paid on or about February 28, 2021, to stockholders of record as of the close of business on February 15, 2021.

The Company also announced today that the 2021 annual meeting of stockholders of Eagle Financial Bancorp, Inc. will be held on April 20, 2021.

In addition, the Company announced today its results of operations for the quarter ended December 31, 2020. A copy of the announcement can be found on the Company’s website at www.eaglesavings.com under the heading “Investor Relations – Financial Reports.”

About Eagle Savings Bank

Eagle Savings Bank, an Ohio chartered savings association headquartered in Cincinnati, Ohio, was originally chartered in 1882. At December 31, 2020 Eagle Financial Bancorp, Inc., our holding company, had $160.4 million of total assets, $128.4 million of total deposits and $29.0 million of total stockholders’ equity. We provide financial services primarily to individuals, families and businesses through our main office and two branch offices located in Hamilton County, Ohio.

Forward-looking statements

This news release may contain certain forward-looking statements, such as statements of the Company’s plans, objectives, expectations, estimates and intentions. Forward-looking statements may be identified by the use of words such as “expects,” “subject,” “believe,” “will,” “intends,” “will be” or “would.” These statements are subject to change based on various important factors (some of which are beyond the Company’s control) and actual results may differ materially. Accordingly, readers should not place undue reliance on any forward-looking statements (which reflect management’s analysis of factors only as of the date of which they are given). These factors include general economic conditions, trends in interest rates, the ability of our borrowers to repay their loans, the ability of the Company to effectively manage its growth, the results of regulatory examinations, and the effect of the Coronavirus Disease 2019 (COVID-19) pandemic on our Company, the communities where we have our branches, the state of Ohio and the United States, including its effect on the economy and overall financial stability. The effects of the COVID-19 pandemic may also exacerbate the effects of the other factors listed herein. The foregoing list of important factors is not exclusive. Other factors including uncertainties and risks that may affect our results are disclosed in our SEC filings, including under the heading “Risk Factors.”

Gary J. Koester

President and CEO

(513) 574-0700

[email protected]

KEYWORDS: Ohio United States North America

INDUSTRY KEYWORDS: Banking Professional Services Finance

MEDIA:

EHang announces US$40 million Investment from Carmignac

GUANGZHOU, China, Jan. 30, 2021 (GLOBE NEWSWIRE) — EHang Holdings Limited (Nasdaq: EH) (“EHang” or the “Company”), the world’s leading autonomous aerial vehicle (AAV) technology platform company, today announced that Carmignac, a leading European asset management firm, invested US$40 million on behalf of its funds in the Company through a private placement of newly issued Class A ordinary shares of the Company. The transaction was closed on January 29, 2021.

EHang intends to use the proceeds to further strengthen the technology advancement and business development of EHang to reinforce its leading position in the global urban air mobility (UAM) industry.

The issuance of the securities is made in reliance on, and in compliance with Regulation S under the Securities Act of 1933, as amended.

About EHang

EHang (Nasdaq: EH) is the world’s leading autonomous aerial vehicle (AAV) technology platform company. Our mission is to make safe, autonomous, and eco-friendly air mobility accessible to everyone. EHang provides customers in various industries with AAV products and commercial solutions: air mobility (including passenger transportation and logistics), smart city management, and aerial media solutions. As the forerunner of cutting-edge AAV technologies and commercial solutions in the global Urban Air Mobility (UAM) industry, EHang continues to explore the boundaries of the sky to make flying technologies benefit our life in smart cities. For more information, please visit www.ehang.com.

Safe Harbor Statement

This press release contains statements that may constitute “forward-looking” statements pursuant to the “safe harbor” provisions of the U.S. Private Securities Litigation Reform Act of 1995. These forward-looking statements can be identified by terminology such as “will,” “expects,” “anticipates,” “aims,” “future,” “intends,” “plans,” “believes,” “estimates,” “likely to” and similar statements. Management has based these forward-looking statements on its current expectations, assumptions, estimates and projections. While they believe these expectations, assumptions, estimates and projections are reasonable, such forward-looking statements are only predictions and involve known and unknown risks and uncertainties, many of which are beyond management’s control. These statements involve risks and uncertainties that may cause EHang’s actual results, performance or achievements to differ materially from any future results, performance or achievements expressed or implied by these forward-looking statements.

Press Contact: [email protected]
Investor Contact: [email protected] / In the U.S.: [email protected] / In China: [email protected]



Baker Hughes Declares Quarterly Dividend

Baker Hughes Declares Quarterly Dividend

HOUSTON & LONDON–(BUSINESS WIRE)–
Baker Hughes (NYSE: BKR) announced today that the Baker Hughes Board of Directors declared a cash dividend of $.18 per share of Class A common stock payable on February 19, 2021 to holders of record on February 9, 2021.

About Baker Hughes:

Baker Hughes (NYSE: BKR) is an energy technology company that provides solutions to energy and industrial customers worldwide. Built on a century of experience and with operations in over 120 countries, our innovative technologies and services are taking energy forward – making it safer, cleaner and more efficient for people and the planet. Visit us at bakerhughes.com.

Investor Relations

Jud Bailey

+1 281-809-9088

[email protected]

Media Relations

Thomas Millas

+1 713-879-2862

[email protected]

KEYWORDS: Texas Europe United States United Kingdom North America

INDUSTRY KEYWORDS: Other Energy Energy

MEDIA:

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Sproutly Announces Financial Results for the Third Quarter Of 2021

Sproutly Announces Financial Results for the Third Quarter Of 2021

NOT FOR DISSEMINATION IN THE US OR THROUGH US NEWSWIRE SERVICES

VANCOUVER, British Columbia–(BUSINESS WIRE)–
Sproutly Canada, Inc. (CSE: SPR) (OTCQB: SRUTF) (FRA: 38G) (“Sproutly” or the “Company”) today announced the Company’s financial results for the third quarter ended November 30, 2020.

“This was a significant quarter for us in that we received our Cannabis 2.0 sales license which then subsequently allowed us to sign two LOI’s as we further transition into a 2.0 product focused company,” said Dr. Arup Sen, Chief Executive Officer of Sproutly. “With the 2.0 license and these partnerships, we are ideally positioned to leverage our THR facility to produce differentiated cannabis and hemp products that use the natural water soluble and oil ingredients with our APP technology in Canada.”

Highlights for the Third Quarter Ended November 30, 2020

  • The Company’s wholly-owned subsidiary, Toronto Herbal Remedies Inc., (“THR”), a licensed producer and processor under the Cannabis Act, received its cannabis extract sales license from Health Canada. THR is authorized to manufacture and sell Cannabis 2.0 products directly to provincial distributors and other authorized Canadian retail supply channels. THR’s ability to sell Cannabis 2.0 products allows it to utilize its licensed APP technology and offer the Company’s strain specific cannabis extracts, edible and beverage products in Canada through its existing provincial sales relationships.
  • THR entered into a cannabis supply agreement with the province of Ontario through the OCS. Ontario will be the 6th province in Canada to carry the Company’s CALIBER branded products, following Saskatchewan, Manitoba, and British Columbia earlier this year as well as Alberta and New Brunswick in 2019.
  • The Company amended the maturity date of its previously issued convertible debentures from October 24, 2020 to April 24, 2021 and reduced the conversion price from $0.105 to $0.06 per share.
  • The Company and Infusion Biosciences Inc. (“Infusion”) extended the maturity dates of both the $1 million private loan issued by Infusion to the Company on January 28, 2020, and the $855,000 private loan issued by Infusion to the Company on August 27, 2020, by six months to April 24, 2021.
  • The Company settled an aggregate of $182,340 of payroll indebtedness owed to certain current and former employees for past services rendered through the issuance of 2,604,867 common shares at a deemed issuance price of $0.07 per share.
  • The Company settled an aggregate of approximately $69,300 of indebtedness owed to one arms-length creditor for past services rendered through the issuance of 1,386,000 common shares at a deemed issuance price of $0.05 per share.

Subsequent Events

  • The Company executed a Letter of Intent to enter into a commercial relationship with Cannabis Manufacturer’s Guild Ltd. (“CMG”). The agreement will allow Sproutly to expand and diversify its flower and Cannabis 2.0 product offerings utilizing brands developed by CMG and its affiliates (the “Acquired Products”), through THR. The agreement allows Sproutly to sell the Acquired Products and facilitate potential business-to-business sales of Sproutly’s proprietary whole plant extracts to CMG’s network of Guild members.
  • The Company executed a Letter of Intent to enter into a commercial relationship with CannaHive Inc. The agreement will allow the Company to further expand its Cannabis 2.0 product offerings at THR. Sproutly will leverage CannaHive’s proprietary manufacturing and packaging equipment and intellectual property to produce cannabis dissolvable powder at THR’s licensed facility. These relationships will provide synergies for the branding, commercialization, and distribution of a portfolio of cannabis products through THR’s existing agreements with multiple provinces in Canada.

Consolidated Financial Statements and Management’s Discussion and Analysis

The Company’s unaudited consolidated interim financial statements and accompanying notes at and for the period ended November 30, 2020, and the Company’s Management’s Discussion and Analysis for the period ended November 30, 2020 are available under the Company’s profile on SEDAR at www.sedar.com.

About Sproutly Canada, Inc.

Sproutly’s core objective is to become the leading supplier of unique ingredients and customized formulations to the cannabis beverage and edibles market. Our water-soluble Infuz2O and BioNatural Oils will deliver unique brands to international markets that are striving to produce a diverse portfolio of differentiated consumer products. Sproutly’s business focus is to execute on partnerships with local and globally established consumer brands to leverage their existing customer bases, further expand brand loyalty, assist with marketing, and support distribution networks to deliver the benefits of the APP technology with speed and efficiency worldwide.

For more information on Sproutly, please visit www.sproutly.ca.

Forward-Looking Statements

Cautionary Note Regarding Forward-Looking Statements: This release includes certain statements and information that may constitute forward-looking information within the meaning of applicable Canadian securities laws or forward-looking statements within the meaning of the United States Private Securities Litigation Reform Act of 1995. Forward-looking statements relate to future events or future performance and reflect the expectations or believes regarding future events of management of Sproutly Canada. Generally, forward-looking statements and information can be identified by the use of forward-looking terminology such as “intends” or “anticipates”, or variations of such words and phrases or statements that certain actions, events or results “may”, “could”, “should”, “would” or “occur”. This information and these statements, referred to herein as “forward-looking statements”, are not historical facts, are made as of the date of this news release and include without limitation, statements regarding discussions of future plans, estimates and forecasts and statements as to management’s expectations and intentions with respect to, among other things, the date of trading of the Sproutly Shares on the CSE and final regulatory approvals. These forward-looking statements involve numerous risks and uncertainties and actual results might differ materially from results suggested in any forward-looking statements. These assumptions, risks and uncertainties include, among other things, the state of the economy in general and capital markets in particular, and other factors, many of which are beyond the control of Sproutly Canada. Although management of the Company has attempted to identify important factors that could cause actual results to differ materially from those contained in forward-looking statements or forward-looking information, there may be other factors that cause results not to be as anticipated, estimated or intended. There can be no assurance that such statements will prove to be accurate, as actual results and future events could differ materially from those anticipated in such statements. Accordingly, readers should not place undue reliance on forward-looking statements and forward-looking information. Readers are cautioned that reliance on such information may not be appropriate for other purposes. The Company does not undertake to update any forward-looking statement, forward-looking information or financial out-look that are incorporated by reference herein, except in accordance with applicable securities laws. We seek safe harbor.

Contact: Dr. Arup Sen, Chief Executive Officer of Sproutly Canada

Email: [email protected]

KEYWORDS: North America Canada

INDUSTRY KEYWORDS: Retail Alternative Medicine Health Food/Beverage

MEDIA:

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BREAKING NOTICE: ROSEN, A GLOBALLY RECOGNIZED FIRM, Encourages Minerva Neurosciences, Inc. Investors with Large Losses to Secure Counsel Before Important February 8 Deadline – NERV

NEW YORK, Jan. 29, 2021 (GLOBE NEWSWIRE) — WHY: Rosen Law Firm, a global investor rights law firm, reminds purchasers of the securities of Minerva Neurosciences, Inc. (NASDAQ: NERV) between May 15, 2017 and November 30, 2020, inclusive (the “Class Period”), of the important February 8, 2021 lead plaintiff deadline.

SO WHAT: If you purchased Minerva securities during the Class Period you may be entitled to compensation without payment of any out of pocket fees or costs through a contingency fee arrangement.

WHAT TO DO NEXT: To join the Minerva class action, go to http://www.rosenlegal.com/cases-register-2004.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. A class action lawsuit has already been filed. If you wish to serve as lead plaintiff, you must move the Court no later than February 8, 2021. A lead plaintiff is a representative party acting on behalf of other class members in directing the litigation.

WHY ROSEN LAW: We encourage investors to select qualified counsel with a track record of success in leadership roles. Often, firms issuing notices do not have comparable experience or resources. The Rosen Law Firm represents investors throughout the globe, concentrating its practice in securities class actions and shareholder derivative litigation. Rosen Law Firm has achieved the largest ever securities class action settlement against a Chinese Company. 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 and has recovered hundreds of millions of dollars for investors. In 2019 alone the firm secured over $438 million for investors. In 2020 founding partner Laurence Rosen was named by law360 as a Titan of Plaintiffs’ Bar. Many of the firm’s attorneys have been recognized by Lawdragon and Super Lawyers.

DETAILS OF THE CASE: According to the lawsuit, defendants throughout the Class Period made false and/or misleading statements and/or failed to disclose: (1) the truth about the feedback received from the FDA concerning the “end-of-Phase 2” meeting; (2) that the Phase 2b study did not use the commercial formulation of roluperidone and was conducted solely outside of the United States; (3) the failure of the Phase 3 study to meet its primary and key secondary endpoints rendered that study incapable of supporting substantial evidence of effectiveness; (4) Minerva’s plan to use the combination of the Phase 2b and Phase 3 studies would be “highly unlikely” to support the submission of an New Drug Application (“NDA”); (5) that reliance on these two trials in the submission of an NDA would lead to “substantial review issues” because the trials were inadequate and not well-controlled; and (6) as a result, defendants’ 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.

To join the Minerva class action, go to http://www.rosenlegal.com/cases-register-2004.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.

No Class Has Been Certified. Until a class is certified, you are not represented by counsel unless you retain one. You may select 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/.

Attorney Advertising. Prior results do not guarantee a similar outcome.

——————————-

Contact Information:

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



Barricade Building Products Puts Sheathing Innovations at the Forefront at IBSx 2021

Barricade®, an INDEVCO North America brand, will highlight certified 3-in-1 and 4-in-1 sheathing products that are not tied to raw material and market fluctuations.

Richmond, Virginia, Jan. 29, 2021 (GLOBE NEWSWIRE) — Richmond, Virginia, January 25, 2021 – At this year’s virtual NAHB International Builder Show, Barricade Building Products will address market needs for alternatives to high-priced OSB and exterior insulation products.

From February 9-12 during IBSx 2021 Virtual Experience, Barricade will emphasize the certified performance of Thermo-Brace lightweight structural sheathing and Thermo-Brace S.I.B. structural insulative board. Barricade developed the latter in partnership with BASF, using Neopor GPS graphite polystyrene rigid foam insulation.

At its industrial complex north of Richmond in Doswell, Virginia, Barricade Building Products manufactures sheathing and other building envelope system products for national distribution. Geoff Baldwin, President of INDEVCO North America Building Products Division, explains, “We’re focused on innovating lighter weight, safer, and healthier products that help builders meet needs of consumers for energy-efficient homes that reduce costs and impact the environment.”

Thermo-Brace Lightweight Sheathing as an OSB Replacement 

Barricade Thermo-Brace, a 3-in-1 sheathing, offers stable raw material pricing, significantly less weight, moisture impenetrability, and ease of use. These qualities offer faster installation and reduced labor costs for builders.

Mike Fields, Barricade Vice President of Sales, explains, “Thermo-Brace is recognized by the International Residential Code to have a higher shear value level than OSB testing standards. In addition, we’ve designed this sheathing to be water resistant and lightweight for easy carry and install, whether on-site or in a modular construction facility.”

Besides the standard 4×8 feet sheet size, Thermo-Brace sheathing also comes in a unique 48 ¾ inch width for overlapping sheets, which eliminates the need for House Wrap. Custom lengths range up to 12’ to reduce waste and trim time.

Thermo-Brace S.I.B. Sheathing for Steel Stud Modular Construction

Barricade Thermo-Brace S.I.B., a 4-in-1 reversible structural insulative sheathing, has an additional energy-efficient insulative barrier comprised of BASF Neopor® GPS insulative foam. Thermo-Brace S.I.B. offers a tight, secure install for modular builders and panelizers who rely on lightweight, high-performance material.

Darcy Overby, Barricade Sales Manager, notes, “The unique thing is that Thermo-Brace S.I.B. is reversable, unlike any other sheathing product available. And both sides can be applied to steel stud applications.”

Easy-to-install Thermo-Brace S.I.B. saves installation time and costs and protects against external elements. Multi-functional design reduces labor and material costs, resulting in efficient and manageable projects. The outside weather-resistant barrier (WRB) layers of Thermo-Brace S.I.B. prevent water, moisture vapor, and mold and eliminate the need for additional outside protection.

Homeowners will experience energy savings with an indoor air quality seal when homes have Thermo-Brace S.I.B. installed. The inner foam layer resists conductive and convective heat flow with its long-term thermal resistance.

 

Builders, modular construction companies, panelizers, and lumber and building material (LBM) distributors can find additional information about Barricade’s complete Building Envelope System and system warranties at Barricade’s virtual IBSx 2021 booth.

 

For more information about Thermo-Brace lightweight sheathing and Thermo-Brace S.I.B. sheathing, visit

https://barricadebp.com/structural-sheathing/barricade-thermo-brace

https://barricadebp.com/structural-sheathing/barricade-thermo-brace-s-i-b

 

About Barricade Building Products

Barricade Building Products manufactures a comprehensive portfolio of Building Envelope System products with a 10-year system warranty in Doswell, Virginia outside Richmond. The system includes Structural Sheathing, Structural Insulative Board, Construction Seam Tapes, House Wrap, including Drainable Wrap and Digitally-Printed House Wrap, Window and Door Flashing, Roof Underlayment, Floor Underlayment, and Interior Board.

 

Barricade Building Products is a member of INDEVCO North America, Inc. Building Products Division. Barricade® is an INDEVCO North America brand.

Attachments



Kelsey Russell - Communications Specialist
Barricade Building Products
804-876-9170
[email protected]

Mike Fields - VP of Sales
Barricade Building Products
804-334-1379
[email protected]

Valorem Announces Acquisition of British Columbia Gold Project

VANCOUVER, British Columbia, Jan. 29, 2021 (GLOBE NEWSWIRE) — VALOREM RESOURCES INC. (the “Company” or “Valorem”) (CSE: VALU) (Frankfurt: 1XW1) is pleased to announce that the Company has entered into an acquisition agreement dated January 29, 2021 (the “Agreement”) to acquire the British Columbia project (the “BC Property”) located in the Cariboo District, British Columbia. The BC Property comprises multiple tenure blocks totaling more than 4,000 ha, which strategically target the Transitional or Basalt Siltstone of the Barkerville Terrain.

Pursuant to the Agreement, the Company will acquire the BC Property by way of a three-cornered amalgamation, whereby the Company will acquire 100% of the issued and outstanding shares of 1267818 B.C. Ltd. and will assume all of its assets, namely the BC Property. As consideration for the BC Property, the Company will issue a total of 30,000,000 common shares to five independent shareholders of 1267818 B.C. Ltd. (representing approximately 37.32% of the Company’s issued and outstanding shares). No new insiders and no control persons will be created in connection with the acquisition of the BC Property.

The Company has also arranged a non-brokered private placement of up to 17,391,304 units at a price of 11.5 cents per unit to raise gross proceeds of up to $2-million. Each unit consists of one common share of the company and one transferable share purchase warrant. Each warrant will entitle the holder thereof to acquire one additional share at a price of 15 cents for term of one year following closing.

This financing is subject to regulatory approval, and all securities to be issued pursuant to the financing are subject to a four-month hold period under applicable Canadian securities laws. A finder’s fee commensurate with regulatory policies may be paid, if applicable.

About Valorem Resources Inc.

Valorem explores and develops precious metal Property in the Americas.

For further details and maps, please see:
https://valoremresources.com/

ON BEHALF OF THE BOARD – Valorem Resources Inc.

Tony Louie, Interim CEO and Director
Email: [email protected]
Phone: 604-319-8712

This news release includes certain statements that may be deemed “forward-looking statements”. All statements in this release, other than statements of historical facts, including the likelihood of commercial mining and possible future financings are forward-looking statements. Although the Company believes the expectations expressed in such forward-looking statements are based on reasonable assumptions, such statements are not guarantees of future performance and actual results or developments may differ materially from those in the forward-looking statements. Factors that could cause actual results to differ materially from those in forward-looking statements include unsuccessful exploration results, changes in metals prices, changes in the availability of funding for mineral exploration, unanticipated changes in key management personnel and general economic conditions. Mining is an inherently risky business. Accordingly, the actual events may differ materially from those projected in the forward-looking statements. For more information on the Company and the risks and challenges of its business, investors should review the Company’s annual filings which are available at www.sedar.com.



Glancy Prongay & Murray LLP, a Leading Securities Fraud Law Firm, Announces the Filing of a Securities Class Action on Behalf of AstraZeneca PLC (AZN) Investors

Glancy Prongay & Murray LLP, a Leading Securities Fraud Law Firm, Announces the Filing of a Securities Class Action on Behalf of AstraZeneca PLC (AZN) Investors

LOS ANGELES–(BUSINESS WIRE)–Glancy Prongay & Murray LLP (“GPM”), a leading national shareholder rights law firm, announces that a class action lawsuit has been filed on behalf of investors who purchased AstraZeneca PLC (“AstraZeneca” or the “Company”) (NASDAQ: AZN) American Depositary Shares (“ADSs” or “shares”) between May 21, 2020 and November 20, 2020 (the “Class Period”). AstraZeneca investors have until March 29, 2021 to file a lead plaintiff motion.

If you suffered a loss on your AstraZeneca investments or would like to inquire about potentially pursuing claims to recover your loss under the federal securities laws, you can submit your contact information at https://www.glancylaw.com/cases/astrazeneca/. You can also contact Charles H. Linehan, of GPM at 310-201-9150, Toll-Free at 888-773-9224, or via email at [email protected] to learn more about your rights.

On November 23, 2020, AstraZeneca announced the results of an interim analysis of its ongoing clinical trials for AZD1222. Though the Company claimed that the drug candidate was highly effective in preventing COVID-19, the primary endpoint of the trials, AstraZeneca disclosed that the interim analysis involved two smaller scale trials in different locales that used two different dosing regimens. One clinical trial provided patients a half dose of AZD1222 followed by a full dose, while the other trial provided two full doses. AstraZeneca contradictorily claimed that the half dosing regimen was substantially more effective at preventing COVID-19 at 90% efficacy than the full dosing regimen, which had achieved just 62% efficacy. The Company noted the combined “average efficacy of 70%” among two trials.

The unexplained discrepancies, omissions and the need for multiple trials in separate locales raised red flags for investors and distinguished AstraZeneca’s trial procedures from those of other biopharmaceutical companies, such as Pfizer and Moderna.

On this news, the price of AstraZeneca’s American Depositary Shares (“ADSs”) fell $2.10, or 5%, over three consecutive trading sessions to close at $52.60 per ADS on November 25, 2020.

The complaint filed alleges that throughout the Class Period, Defendants made materially false and/or misleading statements, as well as failed to disclose material adverse facts about the Company’s business, operations, and prospects. Specifically, Defendants failed to disclose to investors that: (1) initial clinical trials for AZD1222 had suffered from a critical manufacturing error, resulting in a substantial number of trial participants receiving half the designed dosage; (2) clinical trials for AZD1222 consisted of a patchwork of disparate patient subgroups, each with subtly different treatments, undermining the validity and import of the conclusions that could be drawn from the clinical data across these disparate patient populations; (3) certain clinical trial participants for AZD1222 had not received a second dose at the designated time points, but rather received the second dose up to several weeks after the dose had been scheduled to be delivered according to the original trial design; (4) AstraZeneca had failed to include a substantial number of patients over 55 years of age in its clinical trials for AZD1222, despite this patient population being particularly vulnerable to the effects of COVID-19 and thus a high priority target market for the drug; (5) AstraZeneca’s clinical trials for AZD1222 had been hamstrung by widespread flaws in design, errors in execution, and a failure to properly coordinate and communicate with regulatory authorities and the general public; (6) as a result of the foregoing, the clinical trials for AZD1222 had not been conducted in accordance with industry best practices and acceptable standards and the data and conclusions that could be derived from the clinical trials was of limited utility; and (7) as a result of the foregoing, AZD1222 was unlikely to be approved for commercial use in the United States in the short term, one of the largest potential markets for the drug.

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If you purchased AstraZeneca shares during the Class Period, you may move the Court no later than March 29, 2021 to ask the Court to appoint you as lead plaintiff. To be a member of the Class you need not take any action at this time; you may retain counsel of your choice or take no action and remain an absent member of the Class. If you wish to learn more about this action, or if you have any questions concerning this announcement or your rights or interests with respect to these matters, please contact Charles Linehan, Esquire, of GPM, 1925 Century Park East, Suite 2100, Los Angeles California 90067 at 310-201-9150, Toll-Free at 888-773-9224, by email to [email protected], or visit our website at www.glancylaw.com. If you inquire by email please include your mailing address, telephone number and number of shares purchased.

This press release may be considered Attorney Advertising in some jurisdictions under the applicable law and ethical rules.

Glancy Prongay & Murray LLP, Los Angeles

Charles H. Linehan, 310-201-9150 or 888-773-9224

1925 Century Park East, Suite 2100

Los Angeles, CA 90067

www.glancylaw.com

[email protected]

KEYWORDS: California United States North America

INDUSTRY KEYWORDS: Legal Professional Services

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SHAREHOLDER ALERT: WeissLaw LLP Investigates Alussa Energy Acquisition Corp.

PR Newswire

NEW YORK, Jan. 29, 2021 /PRNewswire/ — WeissLaw LLP is investigating possible breaches of fiduciary duty and other violations of law by the board of directors of Alussa Energy Acquisition Corp. (“ALUS” or the “Company”) (NYSE: ALUS) in connection with the Company’s proposed merger with FREYR A/S (“FREYR”), a privately-held developer of clean battery cell production capacity.  Under the terms of the merger agreement, ALUS will acquire FREYR through a reverse merger that will result in FREYR becoming a public company traded on the NYSE.  The transaction implies a pro forma equity value of $1.4 billion for the combined company.


If you own ALUS shares and wish to discuss this investigation or have any questions concerning this notice or your rights or interests, visit our website:


https://www.weisslawllp.com/ALUS/


Or please contact:


Joshua Rubin, Esq.

WeissLaw LLP
1500 Broadway, 16th Floor
New York, NY  10036
(212) 682-3025
(888) 593-4771
[email protected]

WeissLaw LLP is investigating whether ALUS’s board acted in the best interest of ALUS’s public shareholders in agreeing to the proposed transaction, whether the board was fully informed as to the valuation of FREYR, and whether all information regarding the process undertaken by the board and the valuation of the transaction will be fully and fairly disclosed to ALUS’s public shareholders. 

WeissLaw LLP has litigated hundreds of stockholder class and derivative actions for violations of corporate and fiduciary duties.  We have recovered over a billion dollars for defrauded clients and obtained important corporate governance relief in many of these cases.  If you have information or would like legal advice concerning possible corporate wrongdoing (including insider trading, waste of corporate assets, accounting fraud, or materially misleading information), consumer fraud (including false advertising, defective products, or other deceptive business practices), or anti-trust violations, please email us at [email protected]

Cision View original content to download multimedia:http://www.prnewswire.com/news-releases/shareholder-alert-weisslaw-llp-investigates-alussa-energy-acquisition-corp-301218316.html

SOURCE WeissLaw LLP