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Classified in: Health, Science and technology, Business, Covid-19 virus
Subjects: ERN, ACC

BiondVax Announces First Quarter 2021 Financial Results and Provides Business Update


JERUSALEM, June 23, 2021 /PRNewswire/ -- BiondVax Pharmaceuticals Ltd. (Nasdaq: BVXV), a biopharmaceutical company focused on developing, manufacturing and ultimately commercializing products for the prevention and treatment of infectious diseases and related illnesses, today published its first quarter financial results for the quarter ended March 31, 2021. A summary is included in the tables below.

 

BiondVax Pharmaceuticals Logo

First Quarter 2021 Financial Summary
Results are in New Israel Shekels (NIS) and convenience translation to $US is provided using the exchange rate of 3.334 (NIS/$US), the rate as of the close of business on March 31, 2020.

The decrease in total operating expenses, including the R&D expenses, compared to the first quarter of 2020 was primarily attributable to expenses related to a Phase 3 clinical trial and related operations at our manufacturing facility. As previously reported, the trial concluded in Q4 2020. As of March 31, 2021, BiondVax had cash and cash equivalents of NIS 48.6 million ($14.6 million) as compared to NIS 9.4 million as of December 31, 2020. The increase was primarily attributable to a follow-on offering on Nasdaq conducted by the Company in February 2021, providing net proceeds of approximately $12.8 million after fees and underwriter discounts. As previously reported, as of May 12, 2021, the Company had cash and cash equivalents of NIS 46 million (approximately $14 million).

Q1 Business Highlights

About BiondVax

BiondVax Pharmaceuticals Ltd. (Nasdaq: BVXV) is a biopharmaceutical company focused on developing, manufacturing and ultimately commercializing products for the prevention and treatment of infectious diseases and related illnesses. The Company had been developing M?001, a novel influenza vaccine candidate that was designed to provide multi-strain and multi-season protection against current and future seasonal and pandemic influenza. In seven Phase 1/2 and Phase 2 clinical trials designed to test for immunogenicity, the Company was able to demonstrate M-001 was effective in stimulating an immune response to a broad range of influenza virus strains. In October 2020, the Company completed a Phase 3 clinical trial of M?001 which failed to meet the trial's primary and secondary efficacy endpoints. The Company is now pursuing opportunities in the infectious disease space towards development of a pipeline of diversified products and platforms.

Contact Details

Company: Joshua E. Phillipson | +972 8 930 2529 | [email protected]

Investor Relations: Kenny Green (Israel) | +1 646 201 9246 | [email protected]

Forward Looking Statements

This press release contains forward-looking statements within the meaning of the Private Litigation Reform Act of 1995. Words such as "expect," "believe," "intend," "plan," "continue," "may," "will," "anticipate," and similar expressions are intended to identify forward-looking statements, including statements regarding future business strategies that BiondVax may explore. These forward-looking statements reflect management's current views with respect to certain current and future events and are subject to various risks, uncertainties and assumptions that could cause the results to differ materially from those expected by the management of BiondVax Pharmaceuticals Ltd. Risks and uncertainties include, but are not limited to, the risk that BiondVax may not be able to secure additional capital on attractive terms, if at all; the risk that the European Investment Bank may accelerate the loans under its finance contract with BiondVax; the risk that BiondVax may not execute a strategic alternative to M-001 or implement a strategy that will diversify BiondVax's risk, and, if executed, may not be successful; risks relating to the COVID-19 (coronavirus) pandemic; BiondVax's ability to acquire rights to additional product opportunities; BiondVax's ability to enter into collaborations on terms acceptable to BiondVax or at all;  timing of receipt of regulatory approval of BiondVax's manufacturing facility in Jerusalem, if at all or when required; the risk that the manufacturing facility will not be able to be used for a wide variety of applications and other vaccine and treatment technologies, and the risk that drug development involves a lengthy and expensive process with uncertain outcomes. More detailed information about the risks and uncertainties affecting the Company is contained under the heading "Risk Factors" in the Company's Annual Report on Form 20-F filed with the Securities and Exchange Commission on May 13, 2021. BiondVax undertakes no obligation to revise or update any forward-looking statement for any reason.

BALANCE SHEETS

In thousands, except share and per share data









Convenience









Translation


December 31,



March 31,


March
31,


2020



2020


2021


2021


Audited



Unaudited


Unaudited


N I S


U.S. dollars

CURRENT ASSETS:









Cash and cash equivalents

9,421



42,505


48,577


14,570

Other receivables

1,204



1,540


481


144











10,625



44,045


49,058


14,714

LONG?TERM ASSETS:









Property, plant and equipment

39,607



35,989


39,252


11,773

Right-of-use assets

6,206



6,899


5,978


1,793

Other long-term assets

473



899


436


131











46,286



43,787


45,666


13,697











56,911



87,832


94,724


28,411










CURRENT LIABILITIES:









Trade payables

1,868



3,278


2,085


625

Operating lease liabilities

654



684


641


192

Loan from others

60,421



-


62,346


18,700

Other payables

1,246



807


1,640


492











64,189



4,769


66,712


20,009

LONG?TERM LIABILITIES:









Liability in respect of government grants

-



12,991


-


-

Operating lease liabilities

6,088



6,641


5,978


1,793

Loan from others

-



117,784


-


-

Warrants

-



6,861


-


-

Other payables

1,135



-


1,135


340

Severance pay liability, net

95



90


95


29











7,318



144,367


7,208


2,162

SHAREHOLDERS' EQUITY:









Ordinary shares of no par value: Authorized:
700,000,000 shares at March 31, 2021
(unaudited) and 600,000,000 at March 31,
2020 (unaudited) and December 31, 2020;
Issued and outstanding: 573,285,824 shares at
March 31, 2021 (unaudited) 410,213,977
shares at March 31, 2020 (unaudited), and
461,285,824 shares at December 31, 2020

*)   -



*)   -


*)   -


*)   -

Share premium

310,197



262,729


353,783


106,114

Accumulated deficit

(324,793)



(324,033)


(332,979)


(99,874)











(14,596)



(61,304)


20,804


6,240











56,911



87,832


94,724


28,411

*) Represents less than 1 NIS\USD 

 

STATEMENTS OF COMPREHENSIVE LOSS

In thousands, except share and per share data








Convenience

translation


Year ended

December 31,


Three months ended

March 31,


Three months

ended

March 31,


2020


2020


2021


2021


Audited


Unaudited


Unaudited


NIS


U.S. dollars

Operating expenses:








Research and development, net of participations

51,463


19,068


2,750


825

Marketing, general and administrative

16,687


981


4,005


1,201

Other income

(75,484)


-


-


-









Total operating expenses (income)

(7,334)


20,049


6,755


2,026








-

Operating income (loss)

7,334


(20,049)


(6,755)


(2,026)









Financial income

3,843


16,502


1,182


354

Financial expense

(15,632)


(148)


(2,613)


(784)









Net loss and total comprehensive loss               

(4,455)


(3,695)


(8,186)


(2,456)

 

Basic and Diluted net loss per share

(0.01)


(0.01)


(0.02)


(0.005)









Weighted average number of shares outstanding used to compute basic and diluted loss per share

443,260,878


408,596,752


530,840,391


530,840,391















 

SOURCE BiondVax Pharmaceuticals Ltd.


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