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BrainStorm Announces Second Quarter 2021 Financial Results and Provides a Corporate Update

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BrainStorm Cell Therapeutics (NASDAQ: BCLI) reported its financial results for the first quarter ended June 30, 2021, indicating a net loss of approximately $6.3 million, down from $7.4 million the previous year. Cash and equivalents totaled around $35.0 million, a decline from $40.0 million as of March 31, 2021. The company successfully received GMP approval for expanded manufacturing capacity in Israel and has strengthened its NurOwn® intellectual property with multiple patents in key markets. Ongoing discussions with ALS experts aim to enhance the regulatory strategy for NurOwn.

Positive
  • GMP approval received for three cleanrooms at Tel Aviv Sourasky Medical Center.
  • Expansion of NurOwn® intellectual property portfolio with multiple patents granted.
  • Reduction in research and development expenses from $5.7 million to $3.6 million year-over-year.
  • Decrease in net loss per share from $0.25 to $0.17 year-over-year.
Negative
  • Cash and equivalents decreased from $40.0 million to $35.0 million in Q2 2021.
  • General and administrative expenses increased from $1.7 million to $2.5 million year-over-year.

NEW YORK, Aug. 5, 2021 /PRNewswire/ -- BrainStorm Cell Therapeutics Inc. (NASDAQ: BCLI), a leading developer of cellular therapies for neurodegenerative diseases, announced today financial results for the first quarter ended June 30, 2021 and provided a corporate update.

BrainStorm Cell Therapeutics Logo

"We continue to take important steps to advance NurOwn in ALS and progressive MS and position ourselves for sustained success," said Chaim Lebovits, Chief Executive Officer of BrainStorm. "Our discussions with leading ALS experts have provided invaluable insights that we will leverage as we assess NurOwn's potential regulatory pathways in major markets. We also doubled our capacity to supply NurOwn® across Israel and Europe, supporting our readiness to provide broad patient access following any potential approval. Looking ahead, we will continue to work expeditiously with key opinion leaders and the broader ALS community to address the urgent unmet needs of ALS patients, who remain our greatest inspiration."  

Second Quarter 2021 and Subsequent Corporate Highlights

  • Increased commercial manufacturing capacity with the receipt of Good Manufacturing Practice (GMP) approval from the Israel Ministry of Health for three state-of-the-art cleanrooms leased by the Company at the Tel Aviv Sourasky Medical Center ("Sourasky Hospital") in Tel Aviv, Israel.
  • Announced the expansion of the NurOwn® intellectual property portfolio with the grant and allowance of multiple patents and applications in key territories including the U.S., European Union, Canada, Israel, and Hong Kong.
  • Presented preclinical data showing that intrathecal administration of NurOwn-derived exosomes resulted in statistically significant improvements in multiple lung parameters in a mouse model of acute respiratory distress syndrome (ARDS) at the ISCT 2021 New Orleans VIRTUAL Meeting.

Cash and Liquidity as of June 30, 2021

The Company's cash, cash equivalents and short-term bank deposits as of June 30, 2021, totaled approximately $35.0 million.

During the quarter ended June 30, 2021, the Company did not sell any ordinary shares pursuant to its ATM offering established in September 2020.  Since commencement of the ATM offering in September 2020, the Company has raised gross proceeds, before payment of commissions and offering expenses, of approximately $29.1 million under this facility.

Financial Results for the Three Months Ended June 30, 2021

Cash, cash equivalents, and short-term bank deposits were approximately $35.0 million as of June 30, 2021, compared to approximately $40.0 million on March 31, 2021.

Research and development expenses, net for the three months ended June 30, 2021 and 2020 were approximately $3.6 million and $5.7 million, respectively.

Excluding participation from IIA and other grants, research and development expenses decreased by approximately $2.2 million from $6.0 million in the second quarter of 2020 to $3.8 million in the second quarter of 2021.

General and administrative expenses for the three months ended June 30, 2021 and 2020 were approximately $2.5 million and $1.7 million, respectively.

Net loss for the three months ended June 30, 2021 was approximately $6.3 million, as compared to a net loss of approximately $7.4 million for the three months ended June 30, 2020.

Net loss per share for the three months ended June 30, 2021 and 2020 was $0.17 and $0.25, respectively.

Conference Call & Webcast

Thursday, August 5, 2021 at 8:00 a.m. Eastern Time
From the U.S.:  888-506-0062
International:     973-528-0011
Entry Code:       298566
Webcast URL:   https://www.webcaster4.com/Webcast/Page/2354/41929

Those that wish to listen to the replay of the conference call can do so by dialing the numbers below. The replay will be available for 14 days.
From the U.S.:         877-481-4010
International:            919-882-2331 
Replay Passcode:    41929 

About NurOwn®

The NurOwn® technology platform (autologous MSC-NTF cells) represents a promising investigational therapeutic approach to targeting disease pathways important in neurodegenerative disorders. MSC-NTF cells are produced from autologous, bone marrow-derived mesenchymal stem cells (MSCs) that have been expanded and differentiated ex vivo. MSCs are converted into MSC-NTF cells by growing them under patented conditions that induce the cells to secrete high levels of neurotrophic factors (NTFs). Autologous MSC-NTF cells are designed to effectively deliver multiple NTFs and immunomodulatory cytokines directly to the site of damage to elicit a desired biological effect and ultimately slow or stabilize disease progression.

About BrainStorm Cell Therapeutics Inc.

BrainStorm Cell Therapeutics Inc. is a leading developer of innovative autologous adult stem cell therapeutics for debilitating neurodegenerative diseases. The Company holds the rights to clinical development and commercialization of the NurOwn® technology platform used to produce autologous MSC-NTF cells through an exclusive, worldwide licensing agreement. Autologous MSC-NTF cells have received Orphan Drug designation status from the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA) for the treatment of amyotrophic lateral sclerosis (ALS). BrainStorm has completed a Phase 3 pivotal trial in ALS (NCT03280056); this trial investigated the safety and efficacy of repeat-administration of autologous MSC-NTF cells and was supported by a grant from the California Institute for Regenerative Medicine (CIRM CLIN2-0989). BrainStorm completed under an investigational new drug application a Phase 2 open-label multicenter trial (NCT03799718) of autologous MSC-NTF cells in progressive multiple sclerosis (MS).

For more information, visit the company's website at www.brainstorm-cell.com.

Safe-Harbor Statement 

Statements in this announcement other than historical data and information, including statements regarding future NurOwn® manufacturing and clinical development plans, constitute "forward-looking statements" and involve risks and uncertainties that could cause BrainStorm Cell Therapeutics Inc.'s actual results to differ materially from those stated or implied by such forward-looking statements. Terms and phrases such as "may," "should," "would," "could," "will," "expect," "likely," "believe," "plan," "estimate," "predict," "potential," and similar terms and phrases are intended to identify these forward-looking statements. The potential risks and uncertainties include, without limitation, BrainStorm's need to raise additional capital; the prospects for regulatory approval of BrainStorm's NurOwn® treatment candidates for the treatment of ALS and MS; the initiation, completion, and results of BrainStorm's preclinical and clinical development programs; research, regulatory and personnel issues; if approved, development of a global market for our treatment candidates; the ability to secure and maintain research institutions to conduct our clinical trials; if approved and commercialized, the ability to generate any significant revenue; the ability of BrainStorm's NurOwn® treatment candidate to achieve broad acceptance as a treatment option for ALS or other neurodegenerative diseases; BrainStorm's ability to manufacture, or to use third parties to manufacture, and, if approved, commercialize the NurOwn® treatment candidates; obtaining patents that provide meaningful protection, competition and market developments; BrainStorm's ability to protect our intellectual property from infringement by third parties; heath reform legislation; currency exchange rates; and product liability claims and litigation; and other factors detailed in BrainStorm's annual report on Form 10-K and quarterly reports on Form 10-Q available at http://www.sec.gov. These factors should be considered carefully, and readers should not place undue reliance on BrainStorm's forward-looking statements. The forward-looking statements contained in this press release are based on the beliefs, expectations and opinions of management as of the date of this press release. We do not assume any obligation to update forward-looking statements to reflect actual results or assumptions if circumstances or management's beliefs, expectations or opinions should change, unless otherwise required by law. Although we believe that the expectations reflected in the forward-looking statements are reasonable, we cannot guarantee future results, levels of activity, performance or achievements.

Contacts
Investor Relations:
Eric Goldstein
LifeSci Advisors, LLC
Phone: +1 646.791.9729
egoldstein@lifesciadvisors.com

Media:
Paul Tyahla
SmithSolve
Phone: + 1.973.713.3768
Paul.tyahla@smithsolve.com


 

BRAINSTORM CELL THERAPEUTICS INC. AND SUBSIDIARIES
INTERIM CONDENSED CONSOLIDATED BALANCE SHEETS

U.S. dollars in thousands

(Except share data)










June 30, 


December 31, 



2021


2020



U.S. $ in thousands

ASSETS














Current Assets:







Cash and cash equivalents


$

30,565


$

37,829

Short-term deposit (Note 4)



4,047



4,107

Other accounts receivable



183



304

Prepaid expenses and other current assets (Note 5)



392



1,002

Total current assets



35,187



43,242








Long-Term Assets:







Prepaid expenses and other long-term assets



108



26

Operating lease right of use asset (Note 6)



5,886



6,872

Property and Equipment, Net



1,054



1,119

Total Long-Term Assets



7,048



8,017








Total assets


$

42,235


$

51,259








LIABILITIES AND STOCKHOLDERS' EQUITY














Current Liabilities:







Accounts payable


$

3,000


$

5,417

Accrued expenses



1,712



1,261

Operating lease liability (Note 6)



2,037



2,655

Other accounts payable



1,310



1,900

Total current liabilities



8,059



11,233








Long-Term Liabilities:







Operating lease liability (Note 6)



4,004



4,562

Total long-term liabilities



4,004



4,562








Total liabilities


$

12,063


$

15,795








Stockholders' Equity:







Stock capital: (Note 7)



12



12

Common Stock of $0.00005 par value - Authorized: 100,000,000 shares at June 30, 2021 and December 31, 2020 respectively; Issued and outstanding: 36,318,561 and 35,159,977 shares at June 30, 2021 and December 31, 2020 respectively.







Additional paid-in-capital



192,294



184,655

Treasury stocks



(116)



(116)

Accumulated deficit



(162,018)



(149,087)

Total stockholders' equity



30,172



35,464








Total liabilities and stockholders' equity


$

42,235


$

51,259

 

 

BRAINSTORM CELL THERAPEUTICS INC. AND SUBSIDIARIES
INTERIM CONDENSED CONSOLIDATED STATEMENTS OF COMPREHENSIVE LOSS
(UNAUDITED)

U.S. dollars in thousands

(Except share data)
















Six months ended


Three months ended



June 30, 


June 30, 



2021


2020


2021


2020



Unaudited


Unaudited

Operating expenses:


























Research and development, net (Note 8)


$

7,940


$

11,642


$

3,599


$

5,694

General and administrative



5,110



4,066



2,522



1,706














Operating loss



(13,050)



(15,708)



(6,121)



(7,400)














Financial expenses (income), net



(119)



(200)



148



(6)














Net loss


$

(12,931)


$

(15,508)


$

(6,269)


$

(7,394)














Basic and diluted net loss per share from continuing operations


$

(0.36)


$

(0.56)


$

(0.17)


$

(0.25)














Weighted average number of shares outstanding used in computing basic and diluted net loss per share



36,056,391



27,452,750



36,318,561



29,274,130

 

Cision View original content:https://www.prnewswire.com/news-releases/brainstorm-announces-second-quarter-2021-financial-results-and-provides-a-corporate-update-301349131.html

SOURCE BrainStorm Cell Therapeutics Inc.

FAQ

What were the financial results for BrainStorm Cell Therapeutics in Q2 2021?

BrainStorm reported a net loss of approximately $6.3 million for the quarter, an improvement from a $7.4 million loss in the same period of 2020.

How much cash did BrainStorm Cell Therapeutics have as of June 30, 2021?

As of June 30, 2021, BrainStorm had approximately $35.0 million in cash, cash equivalents, and short-term bank deposits.

What significant developments occurred for NurOwn in Q2 2021?

The company received Good Manufacturing Practice approval for expanded manufacturing capacity in Israel and added multiple patents to its NurOwn portfolio in key markets.

What improvements did BrainStorm Cell Therapeutics see in its expenses?

Research and development expenses decreased from $5.7 million to $3.6 million year-over-year, while net loss per share improved from $0.25 to $0.17.

How did BrainStorm Cell Therapeutics plan to enhance its regulatory strategy?

The company is leveraging insights from discussions with leading ALS experts to assess NurOwn's potential regulatory pathways in major markets.

Brainstorm Cell Therapeutics Inc.

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Biotechnology
Biological Products, (no Disgnostic Substances)
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