Monthly Archives: August 2020

Avidian Gold Commences Drone Magnetic and Fixed-Wing LiDAR Surveys at Golden Zone Property, Alaska

TORONTO, ON / ACCESSWIRE / August 13, 2020 / Avidian Gold Corp. ("Avidian" or the "Company") (TSX-V:AVG) is pleased to announce that it has contracted Eagle Mapping Services Ltd (Eagle Mapping) to complete a fixed-wing Light Detection and Ranging (LiDAR) survey over the entire Golden Zone Property and Pioneer Exploration Consultants Ltd. to conduct a drone magnetic survey over key portions of the Golden Zone Property in Alaska.

The ongoing surveys at Golden Zone are part of the effort by Avidian to continue to expand the existing 267,400 ounce Indicated Breccia Pipe gold resource. The road accessible property is strategically located midway between Anchorage and Fairbanks and 16 km west of paved State Highway 3, the Alaska Railroad and the 345 kV Alaska Intertie power lines (see Figure 1).

Dr. Tom Setterfield, Vice President of Exploration for Avidian states: "The LiDAR survey will provide important information on the structural setting of the Breccia Pipe gold deposit and provide a structural template to seek similar deposits elsewhere on the property. It will also provide key structural information at regional to prospect scales, which will allow us to put all our known mineralization into its proper structural context. In addition to providing structural information, the magnetic survey will help Avidian to interpret the location of concealed intrusions, which are key to the mineralization processes at Golden Zone, and to locate alteration-related addition or destruction of magnetic minerals".

The technical information contained in this news release has been approved by Steve Roebuck, P.Geo. and President of Avidian Gold, who is a Qualified Person as defined in National Instrument 43-101 – Standards of Disclosure for Mineral Projects.

About Avidian Gold Corp.

Avidian brings a disciplined and veteran team of project managers together with a focus on advanced stage gold exploration projects in Alaska. Avidian's Golden Zone project hosts a NI 43-101 Indicated gold resource of 267,400 ounces (4,187,000 tonnes at 1.99 g/t Au) plus an Inferred gold resource of 35,900 ounces (1,353,000 tonnes at 0.83 g/t Au)*. Additional projects include the Amanita and the Fish Creek gold properties which are both adjacent to Kinross Gold's Fort Knox gold mine in Alaska and the Jungo gold/copper property in Nevada. *Technical Report on the Golden Zone Property, August 17, 2017, L. McGarry P.Geo & I. Trinder P.Geo, A.C.A Howe International Ltd.

Avidian is the majority owner of High Tide Resources, a private company with an option on the Labrador West iron ore property and owner of the base metal Strickland Property and the Black Raven gold property, all located in Newfoundland and Labrador, Canada.

Avidian is focused on and committed to the development of advanced stage mineral projects throughout first world mining friendly jurisdictions using industry best practices combined with a strong social license from local communities. Further details on the Corporation and the individual projects, including the NI 43-101 Technical report on the Golden Zone property, can be found on the Corporation's website at www.avidiangold.com.

Figure 1: Map of Golden Zone Property, Alaska

For further information, please contact:

Steve Roebuck, President
E: sroebuck@avidiangold.com or +1(905) 741-5458
Email: info@avidiangold.com

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

Forward-looking information

This News Release includes certain "forward-looking statements". These statements are based on information currently available to the Company and the Company provides no assurance that actual results will meet management's expectations. Forward-looking statements include estimates and statements that describe the Company's future plans, objectives or goals, including words to the effect that the Company or management expects a stated condition or result to occur. Forward-looking statements may be identified by such terms as "believes," "anticipates," "expects," "estimates," "may," "could," "would," "will," or "plan". Since forward-looking statements are based on assumptions and address future events and conditions, by their very nature they involve inherent risks and uncertainties. Actual results relating to, among other things, results of exploration, project development, reclamation and capital costs of the Company's mineral properties, and the Company's financial condition and prospects, could differ materially from those currently anticipated in such statements for many reasons such as: changes in general economic conditions and conditions in the financial markets; changes in demand and prices for minerals; litigation, legislative, environmental and other judicial, regulatory, political and competitive developments; technological and operational difficulties encountered in connection with the activities of the Company; and other matters discussed in this news release. This list is not exhaustive of the factors that may affect any of the Company's forward-looking statements. These and other factors should be considered carefully and readers should not place undue reliance on the Company's forward-looking statements. The Company does not undertake to update any forward-looking statement that may be made from time to time by the Company or on its behalf, except in accordance with applicable securities law.found on the Corporation's website at www.avidiangold.com.

SOURCE: Avidian Gold Corp.

ReleaseID: 601393

Capstone Turbine (NASDAQ:CPST) Secures Consecutive 200-Kilowatt Orders for a Wastewater Treatment Plant & Recreational Waterpark in Poland

VAN NUYS, CA / ACCESSWIRE / August 13, 2020 / Capstone Turbine Corporation (www.capstoneturbine.com) (NASDAQ:CPST), the world's leading clean technology manufacturer of microturbine energy systems, announced today that it received two consecutive orders that include a C200S for a wastewater treatment facility and a C200R for a recreational waterpark in Poland. ASPAMET, Capstone's exclusive distributor in Poland (www.aspamet.pl), secured the orders, which are expected to be commissioned in early 2021.

"During our recent earnings call, I outlined our six-part revenue growth strategy, which included an initiative to grow our global distributor business. I highlighted that we are specifically interested in growing our distributor businesses in untapped markets such as Eastern Europe, Northern Africa, parts of Asia, and the Middle East as these geographies represent a tremendous upside for us and are currently underserved," said Darren Jamison, Capstone's President and Chief Executive Officer. "ASPAMET has developed a nice pipeline of projects, and I'm excited to see these two great projects added to their growing list of successful sites helping to accelerate microturbine adoption in the region," added Mr. Jamison.

Destined for a municipal water and treatment facility in the city of Mińsk Mazowiecki, the C200S microturbine will replace an aging reciprocating engine. Once commissioned, the microturbine will operate on the biogas, or "organic waste," produced on-site from municipal solid waste. The C200S microturbine will be deployed in a combined heat and power (CHP) configuration. The clean heat exhaust from the microturbines will be captured using heat exchangers and used for digester heating, hot water production, and the preheating of sludge to support the water treatment process, all while providing the highest system efficiency possible.

Wastewater treatment plants are considered to be some of the largest consumers of energy for cities and municipalities. Improving energy efficiency in wastewater treatment facilities can produce a range of environmental and economic benefits, including lowering carbon emissions, reducing energy costs, and improving energy and water security.

Plant operators selected Capstone Turbine's innovative microturbine solution as a trusted source of reliable technology. In Poland, Capstone Turbine is known for several successful biogas-fueled microturbine projects, including at a nearby waste treatment facility in Kraków. These regional site applications further confirmed to plant operators the high reliability and very high availability of Capstone's microturbine technology in the field.

The second order for a low-pressure natural gas-fueled C200R microturbine will be installed in a large recreational water park with amenities that include numerous swimming pools, an early education center, recreation facility, ice rink, and go-kart track. The C200R's ultra-low exhaust emissions and relatively low noise levels were of particular interest to park operators as some of the facility will be utilized for a kindergarten classroom for the local community.

The C200 microturbine will serve as the primary source of electrical power for the energy intensive site and will be installed in a CHP application designed to cover all basic energy and heating needs. Along with industry-leading reliability and resiliency, the C200R features low-emissions, low maintenance costs, and a low carbon footprint.

Both sites received incentive funding from the European Union with a grant that supports energy-related projects that will benefit the environment by reducing greenhouse gas emissions, increasing the use of renewable energy, or improving energy efficiency. The water park received additional funding from the Polish National Fund for Environmental Protection and Water Management.

"The investment will ensure energy independence in the reality of rapidly changing electricity prices. Environmental parameters of Capstone turbines perfectly fit into the character of both site installations," said Tomasz Bak, Electrical Engineer at ASPAMET.

About Capstone Turbine Corporation
Capstone Turbine Corporation (www.capstoneturbine.com) (NASDAQ:CPST) is the world's leading producer of highly efficient, low-emission, resilient microturbine energy systems. Capstone microturbines serve multiple vertical markets worldwide, including natural resources, energy efficiency, renewable energy, critical power supply, transportation and microgrids. Capstone offers a comprehensive product lineup, via our direct sales team, as well as our global distribution network. Capstone provides scalable solutions from 30 kWs to 10 MWs that operate on a variety of fuels and are the ideal solution for today's multi-technology distributed power generation projects.

For customers with limited capital or short-term needs, Capstone offers rental systems, for more information, contact: rentals@capstoneturbine.com. To date, Capstone has shipped nearly 10,000 units to 83 countries and in FY20, saved customers an estimated $219 million in annual energy costs and 368,000 tons of carbon.

For more information about the company, please visit www.capstoneturbine.com. Follow Capstone Turbine on Twitter, LinkedIn, Instagram, Facebook and YouTube.

Forward-Looking Statements
This press release contains "forward-looking statements," as that term is used in the federal securities laws. Forward-looking statements may be identified by words such as "expects," "believes," "objective," "intend," "targeted," "plan" and similar phrases. These forward-looking statements are subject to numerous assumptions, risks and uncertainties described in Capstone's filings with the Securities and Exchange Commission that may cause Capstone's actual results to be materially different from any future results expressed or implied in such statements. Capstone cautions readers not to place undue reliance on these forward-looking statements, which speak only as of the date of this release. Capstone undertakes no obligation, and specifically disclaims any obligation, to release any revisions to any forward-looking statements to reflect events or circumstances after the date of this release or to reflect the occurrence of unanticipated events.

"Capstone" and "Capstone Microturbine" are registered trademarks of Capstone Turbine Corporation. All other trademarks mentioned are the property of their respective owners.

CONTACT:
Capstone Turbine Corporation
Investor and investment media inquiries:
818-407-3628
ir@capstoneturbine.com

Integra Investor Relations
Shawn M. Severson
415-226-7747
cpst@integra-ir.com

SOURCE: Capstone Turbine Corporation

ReleaseID: 601539

Jerash Reports $0.07 GAAP EPS Fiscal First Quarter, Enters PPE Market

Expands New Customer Sales; Increased Outlook for Fiscal Second Quarter

FAIRFIELD, NJ / ACCESSWIRE / August 13, 2020 / Jerash Holdings (US), Inc. (NASDAQ:JRSH) (the "Company" or "Jerash"), a producer of high-quality textile goods for leading global brands, today reported results for its first quarter of fiscal year 2021, ended June 30, 2020.

First Quarter of Fiscal 2021 and Recent Highlights

Increased sales to new global brand customers won in fiscal 2020 in both dollar value and as a percentage of sales;
Entered the personal protective equipment (PPE) market, including shipments of initial orders to customers and a rapidly growing pipeline of orders and prospective orders;
Received approvals to export various PPE products to Europe, the Middle East and the United States;
Reported $18.7 million in revenue, a decrease of 17.0% from the prior-year first quarter, reflecting higher than anticipated reinstatement of customer orders during the COVID-19 pandemic;
Reported GAAP net income of $0.8 million, or $0.07 per diluted share, compared with net income of $1.5 million, or $0.14 per diluted share in the prior-year first quarter; and
Ended the quarter with cash of $18.5 million and working capital of $48.7 million.

Management Commentary
Sam Choi, Chairman and Chief Executive Officer, stated: "Jerash posted stronger than anticipated first quarter revenue as customers reinstated orders and prioritized production in Jordan to maximize the benefit of our duty-free status. We also shipped increased order volumes to new customers won in the past year, further diversifying our customer base and positioning Jerash for additional growth.

"We also made important progress on strategic initiatives, including entry into the high-quality face mask and PPE markets. Our new PPE subsidiary has now shipped initial orders to multiple customers and has a rapidly growing book of new orders and prospective orders from a variety of customers for export to Europe, the Middle East and North America. We are also in the process of securing clearances from the US Food and Drug Administration to further expand the products we can ship to the US and other markets. We are actively seeking acquisition candidates to bring additional scale, customer relationships and technical capabilities to Jerash, including both traditional garments and the PPE sectors. With $18.5 million of cash on our balance sheet, no debt and $48.7 million in working capital deployed to fuel our business, we are well positioned to pursue these opportunities ahead.

"For our September quarter, we expect to report sequential revenue growth and further expansion of new customer order activity. We also expect to report sequential improvement in gross margins through increased utilization of our factory capacity. We also remain vigilant in protecting our workers, with additional safety measures in place and no COVID-19 cases reported to date at our facilities."

PPE Production Update
Jerash has commenced shipments of both branded (washable) and disposable face masks to customers and is currently launching sales in additional PPE categories, including medical scrubs and surgical gowns. The Company is using both internal and partnership initiatives, including subcontract manufacturing capabilities, in order to produce PPE for certain markets, including Europe, the Middle East, and the United States.

In order to advance its PPE market development efforts, Jerash incorporated a new entity, Jerash The First Medical Supplies Manufacturing Company Limited, which has received temporary permission from Jordan's Food and Drug Administration to manufacture and export non-surgical PPE. This subsidiary has already accepted subcontracting orders of surgical masks and medical gowns for customers in Jordan, the Middle East and Europe beginning in July 2020. Jerash intends to pursue additional certifications and partnerships, including US FDA approvals, for this subsidiary and is presently engaged in these efforts.

First Quarter of Fiscal 2021 Financial Results and Second Quarter Outlook
"First quarter revenue demonstrated rapid reinstatement of orders initially suspended during the COVID-19 pandemic by our existing customers plus the addition of new orders from customers won over the past year," said Gilbert Lee, Chief Financial Officer. "Building on this momentum, we expect fiscal second quarter sales and margins to improve sequentially as factory utilization and bookings continue to increase.For the quarter ending September 30, we anticipate revenue of about $25 million, or 34% sequential growth over the first quarter, subject to potential adjustments in delivery schedules. This estimate does not include certain orders that may ship in the last week of September or sales from additional PPE activity."

For the first quarter of fiscal 2021, Jerash reported revenue of $18.7 million, a decrease of 17.0% from $22.5 million in fiscal 2020. The decrease in sales reflected the impact of the global COVID-19 pandemic on Jerash's customers. A number of Jerash's customers initially cancelled or deferred orders originally scheduled for the June quarter. Subsequently, most of these orders were reinstated for delivery in the second or third quarter as customers prioritized their supply chains, resulting in increased revenue activity as the quarter progressed. A portion of the revenue decline was offset by a 15.5% increase in sales to new customers won in fiscal 2020, advancing Jerash's goal to further diversify its customer base.

Gross margin for the first quarter was 16.3%, compared with 20.0% in the first quarter of fiscal 2020. Gross margin was primarily impacted by reduced factory utilization and workforce disruptions due to the shelter in place orders as part of Jordan's response to the COVID-19 pandemic. Production volumes have risen since May, and the full workforce is now allowed by the Jordanian government to return to work.

Operating expenses for the first quarter of fiscal 2021 were $1.9 million, a decline of 27.9% compared with $2.6 million in the first quarter of fiscal 2020. Operating expenses included lower selling costs as well as general and administrative cost reductions implemented by the company in response to the COVID-19 pandemic.

Operating income for the first quarter was $1.2 million, compared with $1.9 million in the first quarter of fiscal 2020.

GAAP net income for the first fiscal quarter was $0.8 million, or $0.07 per diluted share, a decrease from net income of $1.5 million, or $0.14 per diluted share in the first quarter of the prior year.

COVID-19 Update
Jerash was impacted in both the March and June quarters by business closure mandates across the country of Jordan beginning March 18. As a result of the shutdown, shipments were delayed and production at the factories halted until the government approved re-opening. Jerash's dormitory workforce was allowed to resume production within the industrial zone on April 4, but local employees were not allowed to return until June 1. Jerash enacted a number of additional screening, cleaning and monitoring programs designed to protect the health and well-being of its workforce. Jerash has been recognized as a model employer by the country of Jordan for its efforts, and no cases of COVID-19 were reported among its Jordanian employees.

Balance Sheet, Cash Flow and Dividends
Working capital increased by $0.6 million sequentially, to $48.7 million at June 30, compared with $48.1 million as of March 31, 2020. Cash and restricted cash at June 30, 2020 was $18.5 million, compared with $16.9 million at June 30. 2019. Inventory was $18.1 million, primarily comprised of fabric, work in progress and finished garments, and accounts receivable were $15.9 million.

Said Lee: "Cash flows improved by approximately $800,000 year-over-year in the first quarter, which is traditionally a seasonal high quarter for inventory and accounts receivable due to customer order patterns. As of August 12, the Company had collected more than 80% of our June 30 receivables balance, consistent with prior years."

Jerash approved payment of a regular quarterly dividend of 5 cents per share on the Company's common stock on or about August 24, 2020, to stockholders of record on August 17, 2020.

Conference Call
The Company will conduct a conference call and webcast to review its fiscal first quarter 2021 results on Thursday, August 13, 2020, at 10:00 a.m. ET. Interested parties can access the call by dialing +1-862-298-0970. Callers should dial in at least 5 minutes prior to the call start time. A live and archived webcast will be available online in the investor relations section of Jerash's website at www.jerashholdings.com.

About Jerash Holdings (US), Inc.
Jerash Holdings (US), Inc. (NASDAQ:JRSH) is a manufacturer utilized by many well-known brands and retailers, such as Walmart, Costco, Hanes, New Balance, G-III, VF Corporation (which owns brands such as The North Face, Timberland, JanSport, etc.), and PVH Corp. (which owns brands such as Calvin Klein, Tommy Hilfiger, IZOD, etc.). Its production facilities comprise four factory units, one workshop, and three warehouses and it currently employs approximately 4,100 people. The total annual capacity at its facilities was approximately 8.0 million pieces as of June 30, 2020. Additional information is available at www.jerashholdings.com.

Forward Looking Statements
This news release contains forward-looking statements that involve risks and uncertainties, which may cause actual results to differ materially from the statements made. When used in this document, the words "may", "would", "could", "will", "intend", "plan", "anticipate", "believe", "estimate", "expect", "seek", "potential," "outlook" and similar expressions are intended to identify forward-looking statements. Such statements reflect Jerash's current views with respect to future events and are subject to such risks and uncertainties. Many factors could cause actual results to differ materially from the statements made, including those risks described from time to time in filings made by Jerash with the Securities and Exchange Commission. In addition, there is uncertainty about the further spread of the COVID-19 virus or the occurrence of a second wave of cases and the impact it may have on the Company's operations, the demand for the Company's products, global supply chains and economic activity in general. These and other risks and uncertainties are detailed in the Company's filings with the Securities and Exchange Commission. Should one or more of these risks or uncertainties materialize, or should assumptions underlying the forward-looking statements prove incorrect, actual results may vary materially from those described herein as intended, planned, anticipated or expected. Statements contained in this news release regarding past trends or activities should not be taken as a representation that such trends or activities will continue in the future. Jerash does not intend and does not assume any obligation to update these forward-looking statements, other than as required by law.

Contact:
Matt Kreps
Darrow Associates Investor Relations
(214) 597-8200
mkreps@darrowir.com

JERASH HOLDINGS (US), INC.,
SUBSIDIARIES AND AFFILIATE

CONDENSED CONSOLIDATED BALANCE SHEETS

 

 
June 30,
2020
 
 
March 31,
2020
 

 

 
(Unaudited)
 
 
 
 

ASSETS

 
 
 
 
 
 

Current Assets:

 
 
 
 
 
 

Cash

 

17,754,673
 
 

26,130,411
 

Accounts receivable, net

 
 
15,867,632
 
 
 
5,335,748
 

Inventories

 
 
18,077,080
 
 
 
22,633,772
 

Prepaid expenses and other current assets

 
 
2,239,343
 
 
 
2,761,877
 

Advance to suppliers, net

 
 
3,168,395
 
 
 
2,116,367
 

Total Current Assets

 
 
57,107,123
 
 
 
58,978,175
 

 

 
 
 
 
 
 
 
 

Restricted cash

 
 
786,298
 
 
 
786,298
 

Long-term deposits

 
 
329,697
 
 
 
253,414
 

Deferred tax assets, net

 
 
139,895
 
 
 
139,895
 

Property, plant and equipment, net

 
 
5,927,631
 
 
 
6,174,164
 

Right of use assets

 
 
1,083,809
 
 
 
1,147,090
 

Total Assets

 

65,374,453
 
 

67,479,036
 

 

 
 
 
 
 
 
 
 

LIABILITIES AND EQUITY

 
 
 
 
 
 
 
 

 

 
 
 
 
 
 
 
 

Current Liabilities:

 
 
 
 
 
 
 
 

Credit facilities

 


 
 

235
 

Accounts payable

 
 
3,764,543
 
 
 
6,376,320
 

Accrued expenses

 
 
2,127,629
 
 
 
2,245,402
 

Income tax payable- current

 
 
1,282,329
 
 
 
1,088,497
 

Other payables

 
 
1,088,461
 
 
 
929,783
 

Operating lease liabilities – current

 
 
187,909
 
 
 
210,081
 

Total Current Liabilities

 
 
8,450,871
 
 
 
10,850,318
 

 

 
 
 
 
 
 
 
 

Operating lease liabilities – non-current

 
 
655,598
 
 
 
649,935
 

Income tax payable – non-current

 
 
1,227,632
 
 
 
1,227,632
 

Total Liabilities

 
 
10,334,101
 
 
 
12,727,885
 

 

 
 
 
 
 
 
 
 

Commitments and Contingencies (See Note 15)

 
 
 
 
 
 
 
 

 

 
 
 
 
 
 
 
 

Equity

 
 
 
 
 
 
 
 

Preferred stock, $0.001 par value; 500,000 shares authorized; none issued and outstanding

 


 
 


 

Common stock, $0.001 par value; 30,000,000 shares authorized; 11,325,000 shares issued and outstanding

 
 
11,325
 
 
 
11,325
 

Additional paid-in capital

 
 
15,277,176
 
 
 
15,235,025
 

Statutory reserve

 
 
212,739
 
 
 
212,739
 

Retained earnings

 
 
39,244,786
 
 
 
38,997,177
 

Accumulated other comprehensive loss

 
 
(8,877
)
 
 
(8,324
)

Total Jerash Holdings (US), Inc.'s Stockholder's Equity

 
 
54,737,149
 
 
 
54,447,942
 

 

 
 
 
 
 
 
 
 

Non-controlling interest

 
 
303,203
 
 
 
303,209
 

Total Equity

 
 
55,040,352
 
 
 
54,751,151
 

 

 
 
 
 
 
 
 
 

Total Liabilities and Equity

 

65,374,453
 
 

67,479,036
 

 

 

JERASH HOLDINGS (US), INC.,
SUBSIDIARIES AND AFFILIATE

CONDENSED CONSOLIDATED STATEMENTS OF INCOME AND COMPREHENSIVE INCOME

(Unaudited)

 

 
For the Three Months
Ended June 30,
 

 

 
2020
 
 
2019
 

 

 
 
 
 
 
 

Revenue, net

 

18,706,755
 
 

22,527,325
 

Cost of goods sold

 
 
15,655,185
 
 
 
18,014,622
 

Gross Profit

 
 
3,051,570
 
 
 
4,512,703
 

 

 
 
 
 
 
 
 
 

Selling, general and administrative expenses

 
 
1,850,827
 
 
 
2,623,682
 

Stock-based compensation expenses

 
 
42,151
 
 
 

 

Total Operating Expenses

 
 
1,892,978
 
 
 
2,623,682
 

 

 
 
 
 
 
 
 
 

Income from Operations

 
 
1,158,592
 
 
 
1,889,021
 

 

 
 
 
 
 
 
 
 

Other Expense:

 
 
 
 
 
 
 
 

Other expense, net

 
 
2,739
 
 
 
4,533
 

Total other expense, net

 
 
2,739
 
 
 
4,533
 

 

 
 
 
 
 
 
 
 

Net income before provision for income taxes

 
 
1,155,853
 
 
 
1,884,488
 

 

 
 
 
 
 
 
 
 

Income tax expense

 
 
342,000
 
 
 
335,000
 

 

 
 
 
 
 
 
 
 

Net Income

 
 
813,853
 
 
 
1,549,488
 

 

 
 
 
 
 
 
 
 

Net loss attributable to non-controlling interest

 
 
6
 
 
 

 

Net income attributable to Jerash Holdings (US), Inc.'s Common Stockholders

 

813,859
 
 

1,549,488
 

 

 
 
 
 
 
 
 
 

Net Income

 

813,853
 
 

1,549,488
 

Other Comprehensive (Loss) Income:

 
 
 
 
 
 
 
 

Foreign currency translation (loss) gain

 
 
(553
)
 
 
811
 

Total Comprehensive (Loss) Income

 
 
813,300
 
 
 
1,550,299
 

Comprehensive loss attributable to non-controlling interest

 
 

 
 
 

 

Comprehensive Income Attributable to Jerash Holdings (US), Inc.'s Common Stockholders

 

813,300
 
 

1,550,299
 

 

 
 
 
 
 
 
 
 

Earnings Per Share Attributable to Common Stockholders:

 
 
 
 
 
 
 
 

Basic

 

0.07
 
 

0.14
 

Diluted

 

0.07
 
 

0.14
 

 

 
 
 
 
 
 
 
 

Weighted Average Number of Shares

 
 
 
 
 
 
 
 

Basic

 
 
11,325,000
 
 
 
11,325,000
 

Diluted

 
 
11,330,210
 
 
 
11,472,363
 

 

 
 
 
 
 
 
 
 

Dividend per share

 

0.05
 
 

0.05
 

 

SOURCE: Jerash Holdings

ReleaseID: 601530

Aztec Commences Phase 1 Drill Program on the Tombstone Property, Tombstone Silver Mining District, Arizona

VANCOUVER, BC / ACCESSWIRE / August 13, 2020 / Aztec Minerals Corp. (TSXV:AZT)(OTCQB:AZZTF), announces that reverse circulation (RC) drilling has commenced at its Tombstone project covering much of the historic Tombstone silver-gold-zinc-lead-copper district located in southeastern Arizona.

Aztec holds an option to acquire a 75% interest in the Tombstone property, which includes many of the original patented mining claims in the district. The fully financed Phase 1 RC drill program will consist of around 20 drill holes totaling 2,900 metres. The main target is shallow, bulk tonnage, heap leach, epithermal gold-silver oxide mineralization around and below and adjacent to the previously mined Contention pit.

Three, four-hole patterns or "spokes" will be drilled to test segments of the North-Northeast trending Contention structure along 800 meters (m) of strike length and across the 50 to 100 m width of the steeply west dipping structural corridor with argillized porphyry dyking. Three additional holes will test the following: a geophysical NSAMT conductor target, a covered geologic dyke target, and a series of gold-rich quartz veins hosted in strongly altered rhyolite. Additionally, the collaring of two holes for subsequent core drilling later this year to test for deeper, high grade, "Taylor"-style carbonate replacement silver-lead-zinc-copper-gold deposits (CRD).

Aztec CEO, Simon Dyakowski commented, "Since acquiring an option on the Tombstone project, Aztec has generated several exciting new targets through its methodical evaluation of historic exploration and production data followed by systematic exploration programs. The Phase 1 RC drill program represents Aztec's first opportunity to test for shallow, bulk tonnage, heap leach, gold-silver oxide mineralization".

Tombstone Project Overview

The Tombstone project is located 100 kilometers (km) southeast of Tucson, Arizona. The historic Tombstone silver district is renowned for its high grade, oxidized, silver-gold-lead-zinc-copper epithermal and CRD mineralization hosted in veins, mantos, pipes and disseminated orebodies that were mined in the late 1800's and early 1900's.

Although the historic silver mines at Tombstone were generally small but high grade, Aztec believes they could be related to much more extensive epithermal and CRD mineralization. Since 2017, Aztec has completed geological mapping, geochemical sampling and geophysical surveying to identify the most prospective areas for epithermal gold-silver mineralization around and below the Contention open pit.

Tombstone Project Highlights

Well located property on patented land (164 hectares), covers much of the historic Tombstone silver mining district, great infrastructure, local town, road access, full services, water, power
Historic silver district produced 32 million oz silver from 1878-1939 in high grade, oxidized, silver-gold-lead-zinc-copper vein and CRD deposits, followed by small open pit heap leach production in late 1980's for open pit, heap leach, epithermal gold-silver oxide ore
Seven prospective targets in Cretaceous and Paleozoic rocks related to major NW and NNE trending structures hosting porphyritic intrusions crosscutting a possible caldera ring structure
Distinct magnetic anomalies confirm multiple target areas, Contention pit hosts dikes along strongest structure, excellent potential for CRD deposits
Distinct NSAMT anomalies indicate discrete sub-horizontal conductors at depths of 600 and 700m in the south half of the Contention Pit and are interpreted to represent massive or semi-massive CRD sulphide bodies and occur well below any historic mining or drilling
Aztec high-grade samples in Contention Pit, grade up to 3,178 gpt silver and 23.5 gpt gold, epithermal stockwork mineralization open along strike. Out of 94 samples collected from within the pit, silver assays ranges from <0.1 to 3,178 gpt (114.5 average) and gold assays range from <0.005 to 23.5 gpt (1.60 gpt average)
*Historic drilling by USMX aimed at exploring for shallow epithermal gold-silver mineralization around the Contention pit in 1993, well after the mine had closed. Their result returned multiple intersections including 1.61 gpt Au, 91.2 gpt Ag over 44.2m. USMX drilled 7,350 m in 86 shallow RC holes at the north end of the pit to delineate shallow, bulk tonnage, heap leach, epithermal gold-silver mineralization. Historic drilling highlights were as follows:

*44.2 m @ 1.61 gpt gold and 91.2 gpt silver in hole TR-01
*68.6 m @ 1.42 gpt gold and 28.6 gpt silver in hole TR-02
*38.1 m @ 1.73 gpt gold and 35.3 gpt silver in hole TR-08
*35.1 m @ 1.54 gpt gold and 24.1 gpt silver in hole TR-12
*30.5 m @ 2.65 gpt gold and 37.6 gpt silver in hole TR-41
*41.1 m @ 1.20 gpt gold and 49.1 gpt silver in hole TR-70

These USMX drill intercepts indicate the presence of bulk tonnage, epithermal oxide gold-silver mineralization around the center and northern part of the Contention pit and much of the remainder of the pit remains undrilled. This drilling campaign will attempt to verify the historic results by twinning some of their drill holes in addition to drilling new and un-explored areas.

*Aztec will attempt to verify these historic results with this drilling campaign. Aztec has in its possession the historic drill logs, maps and reports but does not have any information on the quality assurance or quality control measures taken and recognizes these results are non NI-43-101 compliant.

Joey Wilkins, B.Sc., P.Geo., the VP Exploration & Chief Geologist of Aztec, is the Qualified Person who reviewed and approved the technical disclosures in this news release.

"Simon Dyakowski"

Simon Dyakowski, Chief Executive Officer
Aztec Minerals Corp.

About Aztec Minerals – Aztec is a mineral exploration company focused on the discovery of large polymetallic mineral deposits in the Americas. Our core asset is the prospective Cervantes porphyry gold-copper property in Sonora, Mexico. The historic, district-scale Tombstone properties host both bulk tonnage epithermal gold-silver as well as CRD silver-lead-zinc mineralization in Cochise County, Arizona. Aztec's shares trade on the TSX-V stock exchange (symbol AZT) and on the OTCQB (symbol AZZTF).

For more information, please contact:

Simon Dyakowski, CEO or Bradford Cooke, Chairman
Tel: (604) 619-7469
Fax: (604) 685-9744
Email: simon@aztecminerals.com
Website: www.aztecminerals.com

Neither the TSXV nor its Regulation Services Provider (as that term is defined in the policies of the TSXV) accepts responsibility for the adequacy or accuracy of this release. No stock exchange, securities commission or other regulatory authority has approved or disapproved the information contained herein.

Forward-Looking Statements:

Certain statements contained in this press release may constitute forward-looking statements under Canadian securities legislation. Generally, forward-looking information can be identified by the use of forward-looking terminology such as "expects" or "it is expected", or variations of such words and phrases or statements that certain actions, events or results "will" occur. These forward-looking statements are subject to a number of risks and uncertainties. Actual results may differ materially from results contemplated by the forward-looking statements. Factors that could cause actual results to differ materially from those in forward-looking statements. Accordingly, the actual events may differ materially from those projected in the forward-looking statements. When relying on forward-looking statements to make decisions, investors and others should carefully consider the foregoing factors and other uncertainties and should not place undue reliance on such forward-looking statements. The Company does not undertake to update any forward-looking statements, except as may be required by applicable securities laws.

SOURCE: Aztec Minerals Corp.

ReleaseID: 601520

Jaguar Health, Inc. Reports 2020 Second Quarter Financial Results

Q2 2020 Mytesi net sales and gross sales were approximately $3.2 million and approximately $6.3 million, respectively

Reminder: Company to host investor call Thursday, August 13th at 8:30 a.m. Eastern regarding Q2 2020 financials & business updates

Save the Date: Company to host virtual Diarrhea Dialogues disease education event for investors and business development contacts on October 20, 2020 focused on cancer therapy-related diarrhea

SAN FRANCISCO, CA / ACCESSWIRE / August 13, 2020 / Jaguar Health, Inc. (NASDAQ:JAGX) ("Jaguar" or the "Company") today reported consolidated second quarter 2020 financial results.

2020 Second Quarter Company Financial Results:

Mytesi Net Product Revenue: Net sales during the second quarter of 2020 were approximately $3.2 million and $1.7 million in the second quarter of 2019. This Q2 2020 result represents 186% of the same period in 2019, or an increase of $1.5 million quarter over quarter. Net sales during the first quarter of 2020 were approximately $830,000. Net sales for the second quarter of 2020 represented 378% of the first quarter of 2020, or an increase of $2.3 million quarter over quarter.

Mytesi Gross Product Revenue (Non-GAAP): Gross sales during the second quarter of 2020 were approximately $6.3 million and $2.4 million in the second quarter of 2019. This Q2 2020 result represents 268% of the same period in 2019, or an increase of $3.9 million quarter over quarter. Gross sales during the first quarter of 2020 was approximately $1.3 million. Gross sales for the second quarter of 2020 represented 482% of the first quarter of 2020, or an increase of approximately $5.0 million quarter over quarter. The gross sales for Neonorm were immaterial for all periods.

Total Mytesi Bottles Sold: The total Mytesi bottles sold for the second quarter of 2020 represented 104.3% of the bottles sold for the same period in 2019. The total Mytesi bottles sold for the second quarter of 2020 represented 155% of the bottles sold for the first quarter of 2020.

 
 
 
 
 
 
 
 
 
 

 

 
Three Months Ended
 
 
 
 
 
 
 

Financial Highlights

 
June 30,
 
 
 
 
 
 
 

(in thousands, except per share amounts)

 
2020
 
 
2019
 
 
$ change
 
 
% change
 

Net product revenue

 
$
3,167
 
 
$
1,706
 
 
$
1,461
 
 
 
85.6
%

Loss from operations

 
$
(8,451
)
 
$
(10,622
)
 
$
2,171
 
 
 
-20.4
%

Net loss

 
$
(9,238
)
 
$
(16,721
)
 
$
7,483
 
 
 
-44.8
%

Net loss attributable to common shareholders

 
$
(10,597
)
 
$
(16,721
)
 
$
6,124
 
 
 
-36.6
%

Net loss per share, basic and diluted

 
$
(0.44
)
 
$
(15.11
)
 
$
14.67
 
 
 
-97.1
%

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Operating Expenses: Total operating expenses for the second quarter of 2020 were $11.6 million as compared to $12.3 million in the same period last year, a 6%, or $0.7 million, decrease year over year. The decrease in total operating expenses was due to a $4.0 million impairment charge in the second quarter of 2019 and none in the same period this year, an approximately $1.0 million decrease in cost of product revenue, research & development, and sales & marketing expenses offset by a warrant inducement expense of $3.7 million and an increase in general & administrative expense of $0.6 million.

Cost of Product Revenue: Total cost of product revenue for the quarters ended June 30, 2020 and June 30, 2019 was $1.0 million (33% of revenue) and $1.3 million (74% of revenue), respectively, an 18%, or $0.2 million, decrease quarter over quarter. The decrease in cost of product revenue was due to a non-recurring write-off of non-conforming inventory and equipment maintenance in the three months ended June 30, 2019.

Research and Development: The R&D expense was $1.4 million for the second quarter of 2020 compared to $1.7 million for the second quarter of 2019, a 17%, or $0.3 million, decrease quarter over quarter. A decrease of approximately $0.6 million of contract manufacturing expenses for enhanced manufacturing process improvements is offset by $0.3 million in increased consulting, formulation, and regulatory fees.

Sales and Marketing: Sales and Marketing expenses were $1.7 million for the second quarter of 2020 as compared to $2.2 million for the second quarter of 2019, a 20%, or $0.4 million, decrease quarter over quarter. The decrease in Sales and Marketing expenses was due to a salesforce reduction of $0.6 million offset by an increase in direct marketing, consulting and stock-based compensation of $0.2 million.

General and Administrative: The G&A expense was $3.8 million for the second quarter of 2020 compared to $3.2 million for the second quarter of 2019, a 17.5%, or $0.6 million, increase year over year. The increase in G&A expenses was due to an increase in accounting, legal fees and stock-based compensation of $0.6 million, offset by a decrease in third-party consulting, travel, IT and facilities expenses of $0.5 million.

Impairment of Intangible Assets: An impairment charge of $4.0 million associated with our indefinite-lived intangible assets was recorded during the three months ended June 20, 2019 and none in the three months ended June 30, 2020.

Series 3 Warrant Inducement Expense: In May 2020, the exercise price of Series 1, 2, and Bridge Warrants was reduced to $0.49 per share with an inducement offer of Series 3 warrants exercisable into one share of common stock under a cashless exercise feature to those warrant holders who immediately exercised. The Series 3 warrants were valued and charged as an operating expense of approximately $3.7 million.

Loss from Operations: For the second quarter of 2020, the loss from operations was $8.5 million compared to a loss of $10.6 million of the second quarter of 2019, a 20%, or $2.1 million, decrease quarter over quarter. The increase of the Mytesi list price resulted in a decrease of our loss in operations and a decrease of total operating expenses by 6% or $0.7 million as compared to the three months ended June 30, 2019.

Net Loss: The net loss for the second quarter of 2020 was $9.2 million compared to a net loss of $16.7 million in the second quarter of 2019, a 45%, or approximately $7.5 million decrease quarter over quarter. The decrease in net loss was due to the increase of the Mytesi list price, a decrease in operating loss of $2.2 million, and interest expense that was lower by $3.2 million. A $2.7 million loss on extinguishment of debt was recorded during the three months ended June 30, 2019 and none in the same period this year.

Net Loss Attributable to Common Shareholders: For the second quarter of 2020, net loss attributable to common shareholders was $10.6 million compared to $16.7 million for the second quarter of 2019. A deemed dividend of $1.4 million associated with the Company's convertible preferred stock and warrants were recorded during the three months ended June 30, 2020.

Non-GAAP EBITDA: Non-GAAP EBITDA for the second quarter of 2020 and the second quarter of 2019 was a net loss of $7.6 million and $12.2 million, respectively. Excluding the loss on extinguishment of debt, and other non-recurring expenses, non-GAAP Recurring EBITDA was a loss of approximately $3.9 million and $5.5 million for the second quarter of 2020 and the second quarter of 2019, respectively.

 
 
 
 

 

 
Three Months Ended
 

 

 
June 30,
 

 

 
2020
 
 
2019
 

 

 
(unaudited)
 

Net loss (in thousands):

 
$
(9,238
)
 
$
(16,721
)

Adjustments:

 
 
 
 
 
 
 
 

Interest expense

 
 
479
 
 
 
3,657
 

Property and equipment depreciation

 
 
11
 
 
 
15
 

Amortization of intangible assets

 
 
422
 
 
 
422
 

Share-based compensation expense

 
 
749
 
 
 
446
 

Income taxes

 
 

 
 
 

 

Non-GAAP EBITDA

 
$
(7,577
)
 
$
(12,181
)

Impairment of indefinite-lived intangible assets

 
 

 
 
 
4,000
 

Loss on extinguishment of debt

 
 

 
 
 
2,663
 

Modification & Extinguishment of Warr-Finance

 
 
3,696
 
 
 

 

Non-GAAP Recurring EBITDA

 
$
(3,881
)
 
$
(5,518
)

 
 
 
 
 
 
 
 
 

Note Regarding Use of Non-GAAP Measures

The Company supplements its condensed consolidated financial statements presented on a GAAP basis by providing gross sales, non-GAAP EBITDA and non-GAAP recurring EBITDA, which are considered non-GAAP under applicable SEC rules. Jaguar believes that the disclosure items of these non-GAAP measures provide investors with additional information that reflects the basis upon which Company management assesses and operates the business. These non-GAAP financial measures are not in accordance with GAAP and should not be viewed in isolation or as substitutes for GAAP net sales and GAAP net loss and are not substitutes for, or superior to, measures of financial performance in conformity with GAAP.

Gross sales percentages are based on gross sales figures that represent Mytesi orders placed by wholesalers with Jaguar's third-party logistics warehouse, which generate invoiced sales and cash flow for Napo Pharmaceuticals, Inc. ("Napo"), Jaguar's wholly owned subsidiary. Gross sales are used internally by management as an indicator of and to monitor operating performance, including sales performance of Mytesi, salesperson performance, and product growth or declines. The Company believes that the presentation of gross sales provides a closer to real-time useful measure of our operating performance. Gross sales is not a measure that is recognized under accounting principles generally accepted in the United States of America ("GAAP") and should not be considered as an alternative to net sales, which is determined in accordance with GAAP, and should not be used alone as an indicator of operating performance in place of net sales. Additionally, gross sales may not be comparable to similarly titled measures used by other companies, as gross sales have been defined by the Company's internal reporting practices. In addition, gross sales may not be realized in the form of cash receipts as promotional payments and allowances may be deducted from payments received from certain customers. Mytesi gross sales are reduced by Medicare, ADAP 340B chargebacks, returns, and wholesale distribution fees based on historical trends to determine net sales.

The Company defines non-GAAP EBITDA as net loss before interest expense and other expense, property and equipment, amortization of intangible assets, share-based compensation expense and provision for or benefit from income taxes. The Company defines non-GAAP Recurring EBITDA as non-GAAP EBITDA adjusted for certain non-recurring revenues and expenses. Company management believes that non-GAAP EBITDA and non-GAAP Recurring EBITDA are meaningful indicators of Jaguar's performance and provide useful information to investors regarding the Company's results of operations and financial condition.

Dial-In Instructions for Conference Call
When: Thursday, August 13 at 8:30 a.m. Eastern Time
Dial-in (US Toll Free): 800-289-0438
Dial-in (International): 323-794-2423
Conference ID number: 1021156
Live webcast on the investor relations section of Jaguar's website (click here)

Replay Instructions
Dial-in (US Toll Free): 844-512-2921
Dial-in (International): 412-317-6671
Replay Pin Number: 1021156
Replay of the webcast on the investor relations section of Jaguar's website (click here)

SAVE THE DATE:

Virtual Diarrhea Dialogues Disease Education Event Scheduled for October 20, 2020

Jaguar is planning to host a virtual "Diarrhea Dialogues" disease education event for investors and business development contacts on Tuesday, October 20, 2020. Leading oncologists, patient advocates, and supportive care experts will address the importance of supportive care for people related to chronic lower GI tract distress, specifically with regard to debilitating diarrhea experienced as a result of cancer therapy. Jaguar will be issuing further details regarding the event, along with information about how investors and business development contacts can register to participate, as we get closer to the October date.

About Jaguar Health, Inc. and Napo Pharmaceuticals, Inc.

Jaguar Health, Inc. is a commercial stage pharmaceuticals company focused on developing novel, plant-based, non-opioid, and sustainably derived prescription medicines for people and animals with GI distress, specifically chronic, debilitating diarrhea. Our wholly owned subsidiary, Napo Pharmaceuticals, Inc., focuses on developing and commercializing proprietary plant-based human gastrointestinal pharmaceuticals from plants harvested responsibly from rainforest areas. Our Mytesi® (crofelemer) product is approved by the U.S. FDA for the symptomatic relief of noninfectious diarrhea in adults with HIV/AIDS on antiretroviral therapy and the only oral plant-based prescription medicine approved under FDA Botanical Guidance.

For more information about Jaguar, please visit https://jaguar.health. For more information about Napo, visit www.napopharma.com.

About Mytesi®

Mytesi (crofelemer) is an antidiarrheal indicated for the symptomatic relief of noninfectious diarrhea in adult patients with HIV/AIDS on antiretroviral therapy (ART). Mytesi is not indicated for the treatment of infectious diarrhea. Rule out infectious etiologies of diarrhea before starting Mytesi. If infectious etiologies are not considered, there is a risk that patients with infectious etiologies will not receive the appropriate therapy and their disease may worsen. In clinical studies, the most common adverse reactions occurring at a rate greater than placebo were upper respiratory tract infection (5.7%), bronchitis (3.9%), cough (3.5%), flatulence (3.1%), and increased bilirubin (3.1%).

See full Prescribing Information at Mytesi.com. Crofelemer, the active ingredient in Mytesi, is a botanical (plant-based) drug extracted and purified from the red bark sap of the medicinal Croton lechleri tree in the Amazon rainforest. Napo has established a sustainable harvesting program for crofelemer to ensure a high degree of quality and ecological integrity.

Forward-Looking Statements

Certain statements in this press release constitute "forward-looking statements." These include statements regarding the belief that Jaguar will host an investor call on Thursday, August 13, 2020 at 8:30 a.m. Eastern Time, and the expectation that the Company will host a virtual “Diarrhea Dialogues” disease education event on Tuesday, October 20, 2020. In some cases, you can identify forward-looking statements by terms such as "may," "will," "should," "expect," "plan," "aim," "anticipate," "could," "intend," "target," "project," "contemplate," "believe," "estimate," "predict," "potential" or "continue" or the negative of these terms or other similar expressions. The forward-looking statements in this release are only predictions. Jaguar has based these forward-looking statements largely on its current expectations and projections about future events. These forward-looking statements speak only as of the date of this release and are subject to several risks, uncertainties and assumptions, some of which cannot be predicted or quantified and some of which are beyond Jaguar's control. Except as required by applicable law, Jaguar does not plan to publicly update or revise any forward-looking statements contained herein, whether as a result of any new information, future events, changed circumstances or otherwise.

Contact:
Peter Hodge
Jaguar Health, Inc.
phodge@jaguar.health

Jaguar-JAGX

SOURCE: Jaguar Health, Inc.

ReleaseID: 601540

eMagin Corporation Announces Second Quarter 2020 Results

Revenue of $7.7 million, up 44 % year-over-year and 15% sequentially from Q1

HOPEWELL JUNCTION, NY / ACCESSWIRE / August 13, 2020 / eMagin Corporation, or the "Company", (NYSE American:EMAN), a leader in the development, design and manufacture of Active Matrix OLED microdisplays used in Military and Commercial AR/VR devices, and other near-eye imaging products, today announced results for the second quarter 2020.

"We have been deemed an essential business by the U.S. government and as such, have continued to manufacture and ship products during the COVID-19 pandemic. Despite operating with an enhanced number of employee health and safety measures including social distancing, we were still able to significantly increase our revenue in the quarter both sequentially and year-over-year," said CEO Andrew G. Sculley. "Our revenue increased 44% on a year-over-year basis and 15% sequentially, at the high end of our guidance that we gave on July 22nd. In addition to our revenue growth, we had solid bookings and growth of our backlog to $14.5 million of which $13.2 million is shippable within the next twelve months. Our quarterly operating loss declined from $2.9 million in 2019 to $1.3 million. Because of the significant opportunities related to our direct patterning technology (" dPdTM") and the progress that we have been making, we increased our R&D activities and expenditures during the quarter."

"We received a significant affirmation of the strength of our products and technology in the quarter from the U.S. government. In the past two months, we received two Department of Defense awards totaling $39.1 million. eMagin is the only US manufacturer of OLED microdisplays and our displays are used in many important U.S. Military programs."

"The funding provided by these awards will enable us to procure key equipment and tooling, including dPd equipment, and we are currently defining the specifications and expect to place orders for new equipment beginning in the next few weeks. Our first deliveries of equipment under this three-year program would most likely occur in the second quarter of 2021. Upon receipt of the equipment, there is typically an additional period needed to test and qualify the machinery and the processes. The production tool for dPd is expected to be functional and manufacturing qualified products in the third quarter of 2023."

"We have several contracts with Tier One customers in the consumer space and are seeing renewed or increased interest in our dPd technology from these and other high-profile Tier One players. We believe that our technology can be broadly applied and licensed to other OLED manufacturers, and is ideal for AR/VR."

"During the quarter, we continued to ship a significant amount of product for the ENVG-B program as well as produce displays for the F-35 program. Our success in these programs has led to additional design work as well as significant new bookings for other military programs worldwide. We have a number of new customers and projects spanning a broad range of applications from military and medical to law enforcement, industrial, and consumer."

"In terms of operations, we have fabricated full color displays using the newly upgraded and installed dPd tool in the second quarter. We plan to ship in small quantities to customers in the third quarter," continued Mr. Sculley. "In addition, we are continually making improvements in production processes. Despite some delays earlier in the quarter related to COVID-19, our manufacturing line and production equipment have been running without major issues. We are in the process of implementing some of the processes from our yield improvement efforts and we have initiated an effort to explore an overall productivity improvement in the operations area that we believe has the potential to significantly impact the bottom line."

"At the end of the quarter, we had $5.4 million in cash, and borrowings outstanding and borrowings available under our ABL facility of $0.4 million and $3.1 million, respectively. Included in this amount is $1.96 million from a PPP loan, which the Company will use to maintain full employment and expects to be forgiven."

"Subsequent to the quarter, we further strengthened our overall financial position as we were awarded funds over a three year period from the Department of Defense for new equipment and tooling. Finally, we raised an additional $6.5 million remaining under our ATM facility which improves our liquidity."

"I want to again extend our thanks and appreciation to our team members at eMagin. This has been a very challenging environment, but the teams have not let this significantly impact our production and ongoing success," concluded Mr. Sculley.

Second Quarter Results
Total revenues for the second quarter of 2020 were $7.7 million, an increase of approximately $2.3 million from revenues of $5.4 million reported in the prior year period, and an increase of $1.0 million from the first quarter of 2020.

Total revenue consists of both product revenue and contract revenue. Product revenues for the second quarter of 2020 were $6.3 million, an increase of $1.3 million from product revenues of $5.0 million reported in the prior year period. The increase in display revenue for the quarter resulted from increased demand from military customers and higher average selling prices. The increase in product revenue was achieved despite some minor disruptions resulting from the Covid-19 pandemic. Contract revenues were $1.4 million compared to $0.4 million reported in the prior year reflecting the contribution from contract R&D work for the consumer market.

Total gross margin for the second quarter was 26% on gross profit of $2.0 million compared to a gross margin of 4% on gross profit of $0.2 million in the prior year period. The total gross margin of 26% in the second quarter of 2020 reflects favorable margins on contract revenues for the consumer market. Second quarter 2020 product gross margin of 20% compares favorably to 1% in the prior year which was impacted by lower throughput due to manufacturing challenges that had continued from the first quarter of 2019.

Operating expenses for the second quarter of 2020, including R&D expenses, were $3.3 million as compared to $3.1 million reported in the prior year period. Operating expenses as a percentage of sales were 43% in the second quarter of 2020 compared to 57% reported in the prior year period. R&D expenses were higher in the second quarter, primarily reflecting a focus on R&D projects related to dPd technology and our XLE display development, partially offset by costs charged to contract R&D work for the consumer market. SG&A expenses were slightly lower in the second quarter versus the year ago period due to salary reductions implemented in October 2019, a reduction in non-cash stock compensation for the Board of Directors implemented in December 2019 and lower travel and other discretionary expenses.

Operating loss for the second quarter of 2020 was $1.3 million compared to an operating loss of $2.9 million in the prior year period. Net loss for the second quarter of 2020 was $2.8 million or $0.05 per share compared to a loss of $2.3 million or $0.05 per share in the prior year period. Net loss for the current and prior year periods reflects a $1.5 million non-cash loss and $0.5 million non-cash gain related to the change in fair value of a warrant liability, respectively.

Adjusted EBITDA the second quarter was negative $0.8 million compared to a negative $2.3 million in the prior year period.

At June 30, 2020, the Company had cash and cash equivalents of $5.4 million and working capital of $12.0 million. Borrowings and availability under the ABL facility were $0.4 million and $3.1 million respectively at June 30, 2020. In December 2019, eMagin entered into an At the Market sales agreement with H.C. Wainwright & Co. for the sale of common stock. During the quarter, the Company raised $1.8 million under its ATM facility.

Outlook for third quarter
At June 30, 2020, the Company's backlog of open orders was $14.5 million, including $13.2 million shippable within twelve months. This compares to a backlog of orders shippable within twelve months of $11.7 million as of December 31, 2019. As deemed an essential business, the Company continues to ship and produce product and has not experienced any major material supply chain disruptions.

Conference Call Information
eMagin will hold a Webcast at 9:00 am (New York time) on August 13, 2020 to discuss its second quarter results. To access the live webcast or archive, please visit the Company's website at ir.emagin.com or www.earnings.com. An archive of the webcast will be available one hour after the live call.

About eMagin Corporation
The leader in OLED microdisplay technology for the next generation of computing and imaging devices, serving world-class customers in the military and consumer, medical and industrial markets. We invent, engineer and manufacture display technologies of the future in the USA, including our Direct Patterning Technology (dPd) that will transform the way the world consumes information. Since 2001, our microdisplays have been, and continue to be, used in AR/VR, aircraft helmets, heads-up display systems, thermal scopes, night vision goggles, future weapon systems and a variety of other applications. www.emagin.com

Important Cautionary Information 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 eMagin Corporation'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. For a more complete description of the risks factors that could cause our actual results to differ from our current expectations, including impacts of the COVID-19 pandemic, please see the section entitled "Risk Factors" in eMagin's Annual Report on Form 10-K for the fiscal year ended December 31, 2019, and in any Form 10-Q filed or to be filed by eMagin, and in other documents we file with the SEC from time to time.

CONTACT
eMagin Corporation
Mark A. Koch
Acting Chief Financial Officer
845-838-7951
mkoch@emagin.com

Affinity Growth Advisors
Betsy Brod
212-661-2231
betsy.brod@affinitygrowth.com

 

eMAGIN CORPORATION

CONDENSED CONSOLIDATED BALANCE SHEETS

(In thousands, except share data)

(Unaudited)

 

 
June 30,
 
 
December 31,
 

 

 
2020
 
 
2019
 

ASSETS

 
 
 
 
 
 

Current assets:

 
 
 
 
 
 

Cash and cash equivalents

 

5,447
 
 

3,515
 

Accounts receivable, net

 
 
6,085
 
 
 
3,966
 

Unbilled accounts receivable

 
 
16
 
 
 
155
 

Inventories

 
 
8,470
 
 
 
8,832
 

Prepaid expenses and other current assets

 
 
1,389
 
 
 
1,130
 

Total current assets

 
 
21,407
 
 
 
17,598
 

Equipment, furniture and leasehold improvements, net

 
 
7,817
 
 
 
8,100
 

Operating lease right – of – use assets

 
 
3,358
 
 
 
3,729
 

Intangibles and other assets

 
 
130
 
 
 
160
 

Total assets

 

32,712
 
 

29,587
 

 

 
 
 
 
 
 
 
 

LIABILITIES AND SHAREHOLDERS' EQUITY

 
 
 
 
 
 
 
 

Current liabilities:

 
 
 
 
 
 
 
 

Accounts payable

 

1,809
 
 

1,302
 

Accrued compensation

 
 
1,914
 
 
 
1,778
 

Paycheck Protection Program loan – current

 
 
496
 
 
 

 

Revolving credit facility, net

 
 
420
 
 
 
2,891
 

Common stock warrant liability

 
 
1,524
 
 
 
23
 

Other accrued expenses

 
 
1,598
 
 
 
1,401
 

Deferred revenue

 
 
289
 
 
 
277
 

Operating lease liability – current

 
 
809
 
 
 
775
 

Other current liabilities

 
 
508
 
 
 
342
 

Total current liabilities

 
 
9,367
 
 
 
8,789
 

Finance lease liability – long term

 
 
16
 
 
 
24
 

Paycheck Protection Program loan – long term

 
 
1,467
 
 
 

 

Deferred Income – Government awards – long term

 
 
2,263
 
 
 

 

Operating lease liability – long term

 
 
2,654
 
 
 
3,067
 

Total liabilities

 
 
15,767
 
 
 
11,880
 

 

 
 
 
 
 
 
 
 

Commitments and contingencies

 
 
 
 
 
 
 
 

 

 
 
 
 
 
 
 
 

Shareholders' equity:

 
 
 
 
 
 
 
 

Preferred stock, $.001 par value: authorized 10,000,000 shares:

 
 
 
 
 
 
 
 

Series B Convertible Preferred stock, (liquidation preference of $5,659) stated value $1,000 per share, $.001 par value: 10,000 shares designated and 5,659 issued and outstanding as of June 30, 2020 and December 31, 2019.

 
 

 
 
 

 

Common stock, $.001 par value: authorized 200,000,000 shares, issued 61,407,331 shares, outstanding 61,245,265 shares as of June 30, 2020 and issued 50,250,378 shares, outstanding 50,088,312 shares as of December 31, 2019.

 
 
61
 
 
 
50
 

Additional paid-in capital

 
 
262,194
 
 
 
258,767
 

Accumulated deficit

 
 
(244,810
)
 
 
(240,610
)

Treasury stock, 162,066 shares as of June 30, 2020 and December 31, 2019.

 
 
(500
)
 
 
(500
)

Total shareholders' equity

 
 
16,945
 
 
 
17,707
 

Total liabilities and shareholders' equity

 

32,712
 
 

29,587
 

 

 

eMAGIN CORPORATION

CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS

(In thousands, except per share data)

(Unaudited)

 

 
Three Months Ended
 
 
Six Months Ended
 

 

 
June 30,
 
 
June 30,
 

 

 
2020
 
 
2019
 
 
2020
 
 
2019
 

Revenues:

 
 
 
 
 
 
 
 
 
 
 
 

 

 
 
 
 
 
 
 
 
 
 
 
 

Product

 

6,260
 
 

4,958
 
 

11,894
 
 

10,465
 

Contract

 
 
1,440
 
 
 
403
 
 
 
2,537
 
 
 
1,008
 

Total revenues, net

 
 
7,700
 
 
 
5,361
 
 
 
14,431
 
 
 
11,473
 

 

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Cost of revenues:

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

 

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Product

 
 
4,978
 
 
 
4,898
 
 
 
9,768
 
 
 
9,324
 

Contract

 
 
746
 
 
 
238
 
 
 
1,253
 
 
 
588
 

Total cost of revenues

 
 
5,724
 
 
 
5,136
 
 
 
11,021
 
 
 
9,912
 

 

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Gross profit

 
 
1,976
 
 
 
225
 
 
 
3,410
 
 
 
1,561
 

 

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Operating expenses:

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

 

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Research and development

 
 
1,599
 
 
 
1,300
 
 
 
2,579
 
 
 
2,897
 

Selling, general and administrative

 
 
1,712
 
 
 
1,777
 
 
 
3,510
 
 
 
3,716
 

Total operating expenses

 
 
3,311
 
 
 
3,077
 
 
 
6,089
 
 
 
6,613
 

 

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Loss from operations

 
 
(1,335
)
 
 
(2,852
)
 
 
(2,679
)
 
 
(5,052
)

 

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Other income (expense):

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Change in fair value of common stock warrant liability

 
 
(1,481
)
 
 
536
 
 
 
(1,501
)
 
 
1,330
 

Interest expense, net

 
 
(18
)
 
 
(21
)
 
 
(35
)
 
 
(55
)

Other income, net

 
 
3
 
 
 

 
 
 
15
 
 
 

 

Total other (expense) income

 
 
(1,496
)
 
 
515
 
 
 
(1,521
)
 
 
1,275
 

Loss before provision for income taxes

 
 
(2,831
)
 
 
(2,337
)
 
 
(4,200
)
 
 
(3,777
)

Income taxes

 
 

 
 
 

 
 
 

 
 
 

 

 

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Net loss

 

(2,831
)
 

(2,337
)
 

(4,200
)
 

(3,777
)

 

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Loss per share, basic and diluted

 

(0.05
)
 

(0.05
)
 

(0.08
)
 

(0.08
)

 

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Weighted average number of shares outstanding:

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

 

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Basic and Diluted

 
 
56,755
 
 
 
48,818
 
 
 
54,197
 
 
 
46,980
 

 

Non-GAAP Financial Measures
To supplement the Company's consolidated financial statements presented on a GAAP basis; the Company has provided non-GAAP financial information, namely earnings before interest, taxes, depreciation and amortization, and non-cash compensation expense ("Adjusted EBITDA"). The Company's management believes that this non-GAAP measure provides investors with a better understanding of how the results relate to the Company's historical performance. The additional adjusted information is not meant to be considered in isolation or as a substitute for GAAP financial statements. Management believes that these adjusted measures reflect the essential operating activities of the Company. A reconciliation of non-GAAP financial information appears below (in thousands).

 

 

 
Three Months Ended
 
 
Six Months Ended
 

 

 
June 30,
 
 
June 30,
 

 

 
2020
 
 
2019
 
 
2020
 
 
2019
 

Net loss

 

(2,831
)
 

(2,337
)
 

(4,200
)
 

(3,777
)

Non-cash compensation

 
 
44
 
 
 
97
 
 
 
87
 
 
 
290
 

Change in fair value of common stock warrant liability

 
 
1,481
 
 
 
(536
)
 
 
1,501
 
 
 
(1,330
)

Depreciation and intangibles amortization expense

 
 
479
 
 
 
499
 
 
 
959
 
 
 
987
 

Interest expense

 
 
18
 
 
 
21
 
 
 
35
 
 
 
55
 

Adjusted EBITDA

 

(809
)
 

(2,256
)
 

(1,618
)
 

(3,775
)

 

SOURCE: eMagin Corporation

ReleaseID: 601497

Aemetis, Inc. Reports Second Quarter 2020 Financial Results

Earnings of $0.10 per Share; Net Income of $2.2 Million; Adjusted EBITDA of $11.2 Million Driven by Sales of High Grade Alcohol for Hand Sanitizer

CUPERTINO, CA / ACCESSWIRE / August 13, 2020 / Aemetis, Inc. (NASDAQ:AMTX), an advanced renewable fuels and biochemicals company, today announced its financial results for the three and six months ended June 30, 2020.

Aemetis' second quarter of 2020 included significant announcements and financial achievements related principally to sales of high-grade alcohol, including:

Gross Profit of $14.1 million
Net Income of $2.2 million
Adjusted EBITDA of $11.2 million
Announced plans to produce US Pharmacopeia (USP) grade alcohol

"As a result of the global COVID-19 pandemic, demand for high grade alcohol for sanitizer production and shipments of alcohol to bulk sanitizer alcohol customers increased dramatically in the second quarter," said Eric McAfee, Chairman and CEO of Aemetis. "In the final weeks of Q1, we adopted a variety of process improvements and plant upgrades to produce large volumes of high grade alcohol for hand sanitizer. Due to pandemic-related demand as well as what we expect will be longer-term behavioral changes by consumers to reduce the spread of viruses, we anticipate continued market growth for hand sanitizers, personal care and cleaning markets, which contain high grade alcohol," added McAfee.

"As the largest capacity high grade alcohol producer in the Western US," McAfee stated, "Aemetis is implementing systems and equipment that we believe will enable us to produce USP grade alcohol in Q1 2021. We are also developing expanded marketing channels in the US, Canada and other countries for the sale of bulk sanitizer alcohol, bulk blended liquid and gel sanitizer, along with private label and Aemetis-branded and packaged sanitizer products."

Today, Aemetis will host an earnings review call at 11:00 a.m. Pacific time (PT).
Live Participant Dial In (Toll Free): +1-844-602-0380
Live Participant Dial In (International): +1-862-298-0970
Webcast URL: https://www.webcaster4.com/Webcast/Page/2211/36421

For details on the call, please visit http://www.aemetis.com/investors/conference-calls/

Financial Results for the Three Months Ended June 30, 2020

Revenues were $47.8 million for the second quarter of 2020 compared to $50.6 million for the second quarter of 2019, driven by the entry into the high-grade alcohol market, but were slightly offset by the delay in the India Government Oil Marketing Company biodiesel bidding process.

Gross profit for the second quarter of 2020 rose to $14.1 million, compared to a gross profit of $3.3 million during the second quarter of 2019. North America segment accounted for $13.9 million of the reported, consolidated gross profit.

Selling, general and administrative expenses were $4.0 million during the second quarter of 2020, compared to $3.9 million during the second quarter of 2019.

Operating income increased to $10.0 million for the second quarter of 2020, compared to an operating loss of $0.8 million for the second quarter of 2019.

Interest expense during the second quarter of 2020 was $6.2 million, excluding accretion in connection with Series A preferred units in the Aemetis Biogas LLC subsidiary, compared to $6.6 million during the second quarter of 2019. The Aemetis Biogas subsidiary recognized $1.4 million of accretion in connection with preference payments on its preferred stock.

Net income was $2.2 million for the second quarter of 2020, compared to a net loss of $13.9 million for the second quarter of 2019.

Adjusted EBITDA increased to $11.2 million for the three months ended June 30, 2020.

Cash at the end of the second quarter of 2020 increased to $3.4 million, compared to $0.6 million at the end of 2019.

Financial Results for the Six Months Ended June 30, 2020

Revenues were $87.3 million for the first half of 2020, compared to $92.5 million for the first half of 2019.

Selling, general and administrative expenses were $8.0 million during the first half of 2020, compared to $8.2 million during the first half of 2019.

Operating income increased to $5.5 million for the first half of 2020, compared to an operating loss of $5.4 million for the first half of 2019.

Interest expense was $13.1 million during the first half of 2020, excluding accretion of Series A preferred units in the Aemetis Biogas LLC subsidiary, compared to interest expense of $12.8 million during the first half of 2019. Additionally, the Aemetis Biogas subsidiary recognized $2.3 of accretion in connection with preference payments on its preferred stock.

Net loss for the first half of 2020 was $9.9 million, compared to a net loss of $24.6 million in 2019, when the Company recorded a one-time charge for loss contingency on litigation. The 2020 margin improvement was due in large part to selling high-grade alcohol into the hand sanitizer market.

Adjusted EBITDA was $8.2 million for the six months ended June 30, 2020.

About Aemetis

Headquartered in Cupertino, California, Aemetis is an advanced renewable fuels and biochemicals company focused on the acquisition, development and commercialization of innovative technologies that replace traditional petroleum-based products by the conversion of ethanol and biodiesel plants into advanced biorefineries. Founded in 2006, Aemetis owns and operates a 65 million gallon per year ethanol production facility in California's Central Valley near Modesto. Aemetis also owns and operates a 50 million gallon per year renewable chemical and advanced fuel production facility on the East Coast of India producing high quality distilled biodiesel and refined glycerin for customers in India and Europe. Aemetis is building a biogas anaerobic digester network and pipeline to convert dairy animal waste gas to Renewable Natural Gas (RNG), and is developing a plant to convert waste orchard wood into high grade cellulosic alcohol. Aemetis holds a portfolio of patents and related technology licenses for the production of renewable fuels and biochemicals. For additional information about Aemetis, please visit www.aemetis.com.

NON-GAAP FINANCIAL INFORMATION

We have provided non-GAAP measures as a supplement to financial results based on GAAP. A reconciliation of the non-GAAP measures to the most directly comparable GAAP measures is included in the accompanying supplemental data. Adjusted EBITDA is defined as net income/(loss) plus (to the extent deducted in calculating such net income) interest expense, loss on extinguishment, income tax expense, intangible and other amortization expense, accretion expense, depreciation expense, loss contingency on litigation and share-based compensation expense.

Adjusted EBITDA is not calculated in accordance with GAAP and should not be considered as an alternative to net income/(loss), operating income or any other performance measures derived in accordance with GAAP or to cash flows from operating, investing or financing activities as an indicator of cash flows or as a measure of liquidity. Adjusted EBITDA is presented solely as a supplemental disclosure because management believes that it is a useful performance measure that is widely used within the industry in which we operate. In addition, management uses Adjusted EBITDA for reviewing financial results and for budgeting and planning purposes. EBITDA measures are not calculated in the same manner by all companies and, accordingly, may not be an appropriate measure for comparison between companies.

Safe Harbor Statement

This news release contains forward-looking statements, including statements regarding our assumptions, projections, expectations, targets, intentions or beliefs about future events or other statements that are not historical facts. Forward-looking statements in this news release include, without limitation, expectations for growth in India and development of our cellulosic ethanol business in North America. Words or phrases such as "anticipates," "may," "will," "should," "believes," "estimates," "expects," "intends," "plans," "predicts," "projects," "showing signs," "targets," "view," "will likely result," "will continue" or similar expressions are intended to identify forward-looking statements. These forward-looking statements are based on current assumptions and predictions and are subject to numerous risks and uncertainties. Actual results or events could differ materially from those set forth or implied by such forward-looking statements and related assumptions due to certain factors, including, without limitation, competition in the ethanol, biodiesel and other industries in which we operate, commodity market risks including those that may result from current weather conditions, financial market risks, customer adoption, counter-party risks, risks associated with changes to federal policy or regulation, demand for high grade alcohol and related products, including hand sanitizers, and other risks detailed in our reports filed with the Securities and Exchange Commission, including our Annual Report on Form 10-K for the year ended December 31, 2019, our Quarterly Report on Form 10-Q for the quarters ended March 31, 2020 and June 30, 2020 and in our subsequent filings with the SEC. We are not obligated, and do not intend, to update any of these forward-looking statements at any time unless an update is required by applicable securities laws.

(Tables follow)

AEMETIS, INC.
CONSOLIDATED CONDENSED STATEMENTS OF OPERATIONS
(unaudited, in thousands except per share data)

 
 
Three months ended
 
 
Six months ended
 

 

 
June 30,
 
 
June 30,
 

 

 
2020
 
 
2019
 
 
2020
 
 
2019
 

Revenues

 
$
47,824
 
 
$
50,619
 
 
$
87,304
 
 
$
92,507
 

Cost of goods sold

 
 
33,765
 
 
 
47,346
 
 
 
73,678
 
 
 
89,585
 

Gross profit

 
 
14,059
 
 
 
3,273
 
 
 
13,626
 
 
 
2,922
 

 

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Research and development expense

 
 
21
 
 
 
90
 
 
 
138
 
 
 
123
 

Selling, general and admin. expense

 
 
4,049
 
 
 
3,945
 
 
 
7,985
 
 
 
8,186
 

Operating income (loss)

 
 
9,989
 
 
 
(762
)
 
 
5,503
 
 
 
(5,387
)

 

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Interest expense

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Interest rate expense

 
 
5,574
 
 
 
5,190
 
 
 
11,160
 
 
 
10,176
 

Amortization expense

 
 
614
 
 
 
1,396
 
 
 
1,904
 
 
 
2,619
 

Accretion of Series A preferred units

 
 
1,362
 
 
 
471
 
 
 
2,322
 
 
 
920
 

Loss contingency on litigation

 
 

 
 
 
6,200
 
 
 

 
 
 
6,200
 

Other (income) expense

 
 
303
 
 
 
(89
)
 
 
240
 
 
 
(712
)

Income (loss) before income taxes

 
 
2,136
 
 
 
(13,930
)
 
 
(10,123
)
 
 
(24,590
)

 

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Income tax expense (benefit)

 
 
(56
)
 
 

 
 
 
(263
)
 
 
7
 

 

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Net income (loss)

 
$
2,192
 
 
$
(13,930
)
 
$
(9,860
)
 
$
(24,597
)

 

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Non-controlling interest

 
 

 
 
 
(994
)
 
 

 
 
 
(1,932
)

Net income (loss) attributable to Aemetis, Inc.

 
 
2,192
 
 
 
(12,936
)
 
 
(9,860
)
 
 
(22,665
)

 

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Net income (loss) per common share

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Basic

 
$
0.11
 
 
$
(0.63
)
 
$
(0.48
)
 
$
(1.11
)

Diluted

 
$
0.10
 
 
$
(0.63
)
 
$
(0.48
)
 
$
(1.11
)

 

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Weighted average shares outstanding

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Basic

 
 
20,683
 
 
 
20,375
 
 
 
20,668
 
 
 
20,371
 

Diluted

 
 
21,153
 
 
 
20,375
 
 
 
20,668
 
 
 
20,371
 

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

AEMETIS, INC.
CONSOLIDATED CONDENSED BALANCE SHEETS
(in thousands)

 

 

June 30, 2020

(Unaudited)

 
 
December 31, 2019
 

Assets

 
 
 
 
 
 

Current assets:

 
 
 
 
 
 

Cash and cash equivalents

 

3,410
 
 

656
 

Accounts receivable

 
 
5,202
 
 
 
2,036
 

Inventories

 
 
7,290
 
 
 
6,518
 

Prepaid and other current assets

 
 
2,034
 
 
 
3,366
 

Total current assets

 
 
17,936
 
 
 
12,576
 

 

 
 
 
 
 
 
 
 

Property, plant and equipment, net

 
 
98,525
 
 
 
84,226
 

Right-of-use and other assets

 
 
5,697
 
 
 
3,094
 

Total assets

 

122,158
 
 

99,896
 

 

 
 
 
 
 
 
 
 

Liabilities and stockholders' deficit

 
 
 
 
 
 
 
 

Current liabilities:

 
 
 
 
 
 
 
 

Accounts payable

 

16,367
 
 

15,968
 

Current portion of long term debt

 
 
7,569
 
 
 
5,792
 

Short term borrowings

 
 
16,096
 
 
 
16,948
 

Mandatorily redeemable Series B stock

 
 
3,200
 
 
 
3,149
 

Accrued property taxes and other current liabilities

 
 
16,766
 
 
 
15,962
 

Total current liabilities

 
 
59,998
 
 
 
57,819
 

 

 
 
 
 
 
 
 
 

Total long term liabilities

 
 
226,359
 
 
 
196,449
 

 

 
 
 
 
 
 
 
 

Stockholders' deficit:

 
 
 
 
 
 
 
 

Series B convertible preferred stock

 
 
1
 
 
 
1
 

Common stock

 
 
21
 
 
 
21
 

Additional paid-in capital

 
 
87,580
 
 
 
86,852
 

Accumulated deficit

 
 
(247,281
)
 
 
(237,421
)

Accumulated other comprehensive loss

 
 
(4,520
)
 
 
(3,825
)

Total stockholders' deficit

 
 
(164,199
)
 
 
(154,372
)

Total liabilities and stockholders' deficit

 

122,158
 
 

99,896
 

 
 
 
 
 
 
 
 
 

RECONCILIATION OF ADJUSTED EBITDA TO NET LOSS
(unaudited, in thousands)

 

 

Three Months Ended

June 30,

 
 

Six Months Ended

June 30,

 

 

 
2020
 
 
2019
 
 
2020
 
 
2019
 

Net income (loss) attributable to Aemetis, Inc.

 

2,192
 
 

(12,936
)
 

(9,860
)
 

(22,665
)

Adjustments:

 
 
 
 
 
 
 
 
 
 
 
 

Interest expense

 
 
6,188
 
 
 
5,694
 
 
 
13,064
 
 
 
11,075
 

Loss contingency on litigation

 
 

 
 
 
6,200
 
 
 

 
 
 
6,200
 

Depreciation expense

 
 
1,172
 
 
 
1,096
 
 
 
2,262
 
 
 
2,234
 

Accretion of Series A preferred units

 
 
1,362
 
 
 
471
 
 
 
2,322
 
 
 
920
 

Share-based compensation

 
 
325
 
 
 
196
 
 
 
635
 
 
 
486
 

Intangibles and other

amortization expense

 
 
12
 
 
 
12
 
 
 
24
 
 
 
24
 

Income tax expense (benefit)

 
 
(56
)
 
 

 
 
 
(263
)
 
 
7
 

Total adjustments

 
 
9,003
 
 
 
13,669
 
 
 
18,044
 
 
 
20,946
 

Adjusted EBITDA

 

11,195
 
 

733
 
 

8,184
 
 

(1,719
)

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

PRODUCTION AND PRICE PERFORMANCE
(unaudited)

 

 

Three months ended

June 30,

 
 

Six months ended

June 30,

 

 

 
2020
 
 
2019
 
 
2020
 
 
2019
 

Ethanol

 
 
 
 
 
 
 
 
 
 
 
 

Gallons sold (in millions)

 
 
13.8
 
 
 
16.2
 
 
 
29.6
 
 
 
32.4
 

Average sales price/gallon

 

2.63
 
 

1.84
 
 

2.08
 
 

1.76
 

Percentage of nameplate capacity

 
 
100
%
 
 
118
%
 
 
108
%
 
 
118
%

WDG

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Tons sold (in thousands)

 
 
90.9
 
 
 
106.9
 
 
 
198.0
 
 
 
213.8
 

Average sales price/ton

 

82
 
 

81
 
 

80
 
 

81
 

Delivered cost of corn

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Bushels ground (in millions)

 
 
4.9
 
 
 
5.7
 
 
 
10.6
 
 
 
11.3
 

Average delivered cost / bushel

 

4.46
 
 

5.37
 
 

4.84
 
 

5.29
 

Biodiesel

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Metric tons sold (in thousands)

 
 
2.6
 
 
 
13.0
 
 
 
6.3
 
 
 
18.2
 

Average sales price/metric ton

 

835
 
 

833
 
 

786
 
 

830
 

Percentage of nameplate capacity

 
 
7
%
 
 
35
%
 
 
8
%
 
 
24
%

Refined glycerin

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Metric tons sold (in thousands)

 
 
0.4
 
 
 
0.6
 
 
 
0.6
 
 
 
2.0
 

Average sales price/metric ton

 

901
 
 

560
 
 

772
 
 

618
 

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

External Investor Relations Contact:

Kirin Smith
PCG Advisory Group
(646) 863-6519

Investor Relations/ Media Contact:

Todd Waltz
(408) 213-0940
investors@aemetis.com

SOURCE: Aemetis, Inc.

ReleaseID: 601527

Ophthalmic Drugs Market to Grow with 4.2% CAGR through 2025; Concerns of Covid-19 Transmission Through Tear Secretions Hinder Adoption Rates

Ophthalmic drug manufacturers are leveraging the growing rate of FDA approvals for novel drug offerings to introduce new products and revenue streams in the market.

ROCKVILLE, MD / ACCESSWIRE / August 13, 2020 / The global ophthalmic drugs market is anticipated to show a moderate growth rate of 4.2% CAGR between the forecasting years from 2020 to 2025. The coronavirus pandemic is likely to have a detrimental impact on the ophthalmic drugs market. Government guidelines postponing elective ophthalmic procedures and consultations are hurting demand for ophthalmic drugs. In addition, fears over covid-19 transmission through ocular secretions is also hampering short term prospects.

"Growing use of novel therapeutics in the field of ophthalmology, coupled with higher numbers of eye ailments, are major drivers for the ophthalmic drugs industry. Further, faster approvals for new offerings and growing patient awareness treatment options will contribute to market developments," says the FACT.MR analyst.

Request a sample of the report to gain more market insights at

https://www.factmr.com/connectus/sample?flag=S&rep_id=4799

Ophthalmic Drugs Market- Key Takeaways

OTC drug variants are witnessing strong growth owing to the expiration of patents, and popularity of generic options.
Ophthalmic drugs for retinal disorders are gaining ground, supported by industry collaborations and associated academic research.
North America holds a major share of the ophthalmic drugs market, owing to favorable government policies and faster access to new technologies for eyecare infrastructure.

Ophthalmic Drugs Market- Driving Factors

Rising incidences of eye conditions such as diabetic retinopathy, macular degeneration, and presbyopia contribute to demand for ophthalmic drugs.
Rapid tech advancements in drug delivery systems account greater adoption of ophthalmic drug offerings.

Ophthalmic Drugs Market- Major Restraints

Long timelines for regulatory approvals in many parts of the world remains a key challenge for manufacturers.
Substantial risk of side effects from the administration of ophthalmic drugs holds back market growth.

COVID-19 Impact on Ophthalmic Drugs Market

The coronavirus pandemic is having a negative impact on the ophthalmic drugs market owing to suspension of non-critical operations in the ophthalmic sector of the healthcare industry. In addition, the industry is facing challenges in supply chains, owing to disruptions of raw material production. Concerns over ocular transmission of the virus also hurts short term prospects. However, the market is likely to witness strong recovery post pandemic, driven by high numbers of eye disorder incidences and resurgence of ophthalmic treatment services.

Explore the global Ophthalmic Drugs market with 90 figures, 55 data tables, along with the table of contents of the report. You can also find detailed segmentation on https://www.factmr.com/report/4799/opthalmic-drugs-market

Competitive Landscape

Santen Pharmaceutical Co., Novartis AG, Allergan, and Regeneron Pharmaceuticals Inc. are some of the leading ophthalmic drug manufacturers in the global market.

Ophthalmic drugs market players displaying greater bias towards the development and launch of new drug formulations to widen their portfolio of solutions for ocular ailments.

For instance, Eyevance has announced the FDA approval of Zerviate, a cetirizine ophthalmic solution aimed towards treating allergic conjunctivitis. Horizon Therapeutics has announced the approval of Teprotumumab for thyroid eye disease in adults. Further, Allergan has also announced the approval of Artemis, a new biodegradable glaucoma implant drug.

About the Report

This study offers readers a comprehensive market forecast of the ophthalmic drugs market. Global, regional and country-level analysis of the top industry trends impacting the ophthalmic drugs market is covered in this FACT.MR study. The report offers insights on the ophthalmic drugs market on the basis of disease indication (dry eye, glaucoma, infection, retinal disorders, allergy, uveitis, and others), therapeutic class (anti-inflammatory drugs, anti-infective drugs, anti-glaucoma drugs, anti-allergy drugs, anti-VEGF drugs, and others) product type (prescription drugs and OTC drugs) and distribution channel (hospital pharmacies, online pharmacies, and independent pharmacies), across five regions (North America, Latin America, Europe, Asia Pacific, and Middle East & Africa).

Explore FACT.MR's Comprehensive Coverage of Healthcare Landscape

OTC Vitamins & Dietary Supplements Market– Get the latest insights on the global OTC vitamins & dietary supplements market through FACT.MR's report covering analysis for projection period (2017-2022).

OTC Cough, Cold & Allergy Medicine Market– FACT.MR's study on the global OTC cough, cold & allergy medicine market covers trends, tech innovations, players, and strategies for 2017-2022.

OTC Analgesics Market– Obtain analysis on the global OTC analgesics market through FACT.MR's latest report covering competitive analysis, key regions, along with segmental analysis for 2017-2022.

About Fact.MR

Expert analysis, actionable insights, and strategic recommendations of the veteran research team at FACT.MR helps clients from across the globe with their unique business intelligence requirements. With a repository of over a thousand reports and 1 million+ data points, the team has scrutinized the healthcare sector across 50+ countries for over a decade. The team provides unmatched end-to-end research and consulting services.

Contact:

Fact.MR
11140 Rockville Pike
Suite 400
Rockville, MD 20852
United States
Email: sales@factmr.com
Web: https://www.factmr.com/
PR- https://www.factmr.com/media-release/1567/global-opthalmic-drugs-market

SOURCE: Fact.MR

ReleaseID: 601556

Immigration Lawyer Carlos E. Sandoval Releases Notice on Upcoming Immigration Fees Increase

MIAMI, FL / ACCESSWIRE / August 13, 2020 / Florida Immigraton Attorney Carlos E. Sandoval released details regarding the recently announced immigration fees increase set to take effect October 2, 2020.

On July 31, 2020, USCIS officially announced the highly anticipated increase in the fees applicable to certain immigration processes and Naturalization applications. According to DHS, the adjusted weighted average increase of 20% will be applied to help recover USCIS operational costs.

This decision comes months after USCIS notified Congress of a projected budget shortfall and requested emergency funding of $1.2 billion. At the time, USCIS also notified that if no action were to be taken by Congress, a significant portion of its workforce would need to furlough employees. The furloughs would negatively impact the already delayed applications' processing times and pending petitions with USCIS.

Certain immigration benefits, however, will foresee either a lower or higher percentage increase including:

I-130 Petition for Alien Relative going from $535 to $550 (3%)
I-485 Application to Register for Permanent Residency going from $1140 to $1130 (-1%)
I-601A Provisional Unlawful Presence Waiver going from $630 to $960 (52%)
I-765 Application for Employment Authorization (Non-DACA) going from $410 to $550 (34%)
N-400 Application for Naturalization going from $725 to $1245 for online filing* (81%)
I-881 Application for Suspension of Deportation going rom $285 to $1810 (535%)

"Although delayed responses are still expected, it is highly recommended to submit applications prior to October 2, 2020 to avoid the fee increase," advised Sandoval. "It is also important to ensure government fees are paid accurately and in full as applications with incorrect or incomplete fees may be rejected." he added.

Individuals needing assistance with their applications and verification of accurate fees may contact Attorney Sandoval's office at 954-306-6921.

For a full list of changes and a complete table of final fees, please visit: https://s3.amazonaws.com/public-inspection.federalregister.gov/2020-16389.pdf

About Carlos E. Sandoval, Attorney at Law

Carlos E. Sandoval is a member of the Florida Bar, the American Immigration Lawyers Association, the Broward County Hispanic Bar Association and the Broward County Bar Association. Carlos, who speaks fluent English and Spanish, is licensed to practice law by the Florida Supreme Court and the Federal Court for the Southern and Central Districts of Florida.

He focuses his practice in all areas of immigration and employment law. For more information or a consultation, call (954) 306-6921, or visit http://www.carlosesandoval.com

For media inquiries, please call the NALA at 805.650.6121, ext. 361.

SOURCE: Carlos E. Sandoval

ReleaseID: 601384

Xenetic Biosciences, Inc. Reports Second Quarter 2020 Financial Results and Provides Corporate Update

– Successfully established two strategic academic collaborations in Q2 2020 to advance development of XCART™, its differentiated CAR T therapy platform –
– Strengthened panel of experts on the Scientific Advisory Board, bringing valuable expertise across all phases of preclinical and clinical development –

FRAMINGHAM, MA / ACCESSWIRE / August 13, 2020 / Xenetic Biosciences, Inc. (NASDAQ:XBIO) ("Xenetic" or the "Company"), a biopharmaceutical company focused on advancing XCART™, a personalized CAR T platform technology engineered to target patient- and tumor-specific neoantigens, today reported its financial results for the second quarter ended June 30, 2020 and provided a corporate update.

"The second quarter was marked by the achievement of important milestones for the Company. We previously announced that we would seek to utilize academic collaborators, which we believe provides many significant advantages to our overall XCART program, including access to leading CAR T experts as well as manufacturing facilities with the ability to carry out our early development activities," commented Jeffrey Eisenberg, Chief Executive Officer of Xenetic. "Now that we have entered into strategic collaboration agreements with Scripps Research and Pharmsynthez, we believe we are well-positioned to efficiently advance our XCART program through preclinical development and into the clinic. We will be working closely with both institutions to develop the manufacturing methods for XCART and generate key preclinical data to support a potential Phase 1 dosing study."

XCART Platform Technology Overview: Significantly differentiated, proprietary approach to personalized CAR T therapy for the treatment of multiple tumor types of B-cell Non-Hodgkin lymphomas, an area of significant unmet need, with the potential to address an initial global market opportunity of over $5 billion annually.[1] Xenetic believes XCART has the potential to transform CAR T therapy.

Program Highlights:

Collaboration with Pharmsynthez and multiple academic institutions in Russia and Belarus to optimize the overall XCART workflow, including clinical manufacturing processes, and to ultimately dose B-cell non-Hodgkin lymphoma (NHL) patients.
Research and development collaboration with Scripps Research covering design and implementation of the preclinical development program, as well as method development activities supporting process development for clinical manufacturing.

PolyXen® Platform Technology: Patent-protected platform technology designed for protein or peptide therapeutics, enabling next-generation biological drugs by prolonging a drug's circulating half-life and potentially improving other pharmacological properties.

Program Highlights:

Exclusive License Agreement with Takeda Pharmaceuticals Co. Ltd. ("Takeda") in the field of coagulation disorders. Takeda currently has one active development program underway utilizing the PolyXen platform technology.
Royalty payments doubled during the second quarter as the relevant product has now launched worldwide and continues to be rolled out by Takeda's sublicensee.

Summary of Financial Results for Second Quarter 2020

Net loss for the six months ended June 30, 2020 was approximately $2.1 million compared to a net loss of approximately $2.7 million for the same period in 2019. As of June 30, 2020, working capital was $8.3 million compared to $9.7 million as of December 31, 2019. The decrease in working capital was primarily due to the Company's net loss for the six months ended June 30, 2020. The Company ended the quarter with approximately $8.1 million of cash.

About Xenetic Biosciences

Xenetic Biosciences, Inc. is a biopharmaceutical company focused on progressing XCART™, a personalized CAR T platform technology engineered to target patient- and tumor-specific neoantigens. The Company is initially advancing cell-based therapeutics targeting the unique B-cell receptor on the surface of an individual patient's malignant tumor cells for the treatment of B-cell lymphomas. XCART™ has the potential to fuel a robust pipeline of therapeutic assets targeting high-value oncology indications.

Additionally, Xenetic is leveraging PolyXen®, its proprietary drug delivery platform, by partnering with biotechnology and pharmaceutical companies. PolyXen® has demonstrated its ability to improve the half-life and other pharmacological properties of next-generation biologic drugs. The Company has an exclusive license agreement with Takeda Pharmaceuticals Co. Ltd. in the field of coagulation disorders and receives royalty payments under this agreement.

For more information, please visit the Company's website at www.xeneticbio.com and connect on Twitter, LinkedIn, and Facebook.

Forward-Looking Statements

This press release contains forward-looking statements for purposes of the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. All statements contained in this press release other than statements of historical facts may constitute forward-looking statements within the meaning of the federal securities laws. These statements can be identified by words such as "expects," "plans," "projects," "will," "may," "anticipates," "believes," "should," "intends," "estimates," and other words of similar meaning, including, but not limited to, statements regarding: our belief that academic collaborators provide many significant advantages to our overall XCART program, including access to leading CAR T experts as well as manufacturing facilities with the ability to carry out our early development activities; our belief that we are well‐positioned to efficiently advance our XCART program through preclinical development and into the clinic; our expectations regarding working closely with our academic collaborators to develop the manufacturing methods for XCART and generate key preclinical data to support a potential Phase 1 dosing study; expectations regarding the collaboration with Pharmsynthez optimizing the overall XCART workflow and ultimately dosing NHL patients; our plans to initially apply the XCART technology to advance cell-based therapeutics by targeting the unique B-cell receptor on the surface of an individual patient's malignant tumor cells for the treatment of B-cell lymphomas; our expectations that XCART has the potential to fuel a robust pipeline of therapeutic assets targeting high-value oncology indications; our belief that our significantly differentiated, proprietary approach to personalized CAR T therapy for the treatment of multiple tumor types of B-cell Non-Hodgkin lymphomas, an area of significant unmet need, has the potential to address an initial global market opportunity of over $5 billion annually; our belief that XCART has the potential to transform CAR T therapy; our plans to leverage PolyXen® by partnering with biotechnology and pharmaceutical companies; and our expectation regarding receipt of royalty payments under the exclusive license agreement with Takeda Pharmaceuticals Co. Ltd. Any forward-looking statements contained herein are based on current expectations, and are subject to a number of risks and uncertainties. Many factors could cause our actual activities, performance, achievements, or results to differ materially from the activities and results anticipated in forward-looking statements. Important factors that could cause actual activities, performance, achievements, or results to differ materially from such plans, estimates or expectations include, among others, (1) unexpected costs, charges or expenses resulting from the acquisition of XCART; (2) uncertainty of the expected financial performance of the Company following completion of the acquisition of XCART; (3) failure to realize the anticipated potential of the XCART technology; (4) the ability of the Company to implement its business strategy; (5) failure of Scripps Research and/or Pharmsynthez or the other academic institutions in Belarus and Russia (as applicable) to perform their obligations under the respective agreements; (6) failure of the Company and Pharmsynthez to reach agreements with the contract sites on terms favorable to the Company, or at all; and (7) other risk factors as detailed from time to time in the Company's reports filed with the SEC, including its annual report on Form 10-K, periodic quarterly reports on Form 10-Q, periodic current reports on Form 8-K and other documents filed with the SEC. The foregoing list of important factors is not exclusive. In addition, forward-looking statements may also be adversely affected by general market factors, general economic and business conditions, including potential adverse effects of public health issues, such as the COVID-19 outbreak on economic activity, competitive product development, product availability, federal and state regulations and legislation, the regulatory process for new product candidates and indications, manufacturing issues that may arise, patent positions and litigation, among other factors. The forward-looking statements contained in this press release speak only as of the date the statements were made, and the Company does not undertake any obligation to update forward-looking statements, except as required by law.

Contact:

JTC Team, LLC
Jenene Thomas
(833) 475-8247
xbio@jtcir.com

[1] Market Reports World GLOBAL NON-HODGKIN LYMPHOMA THERAPEUTICS MARKET – SEGMENTED BY TYPE OF TREATMENT – GROWTH, TRENDS AND FORECASTS (2018 – 2023); BioPharm Insight Surveillance, Epidemiology, and End Results (SEER) 9 registries, National Cancer Institute, 2017

SOURCE: Xenetic Biosciences, Inc.

ReleaseID: 601404