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UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM 8-K
CURRENT REPORT
Pursuant to Section 13 or 15(d) of the
Securities Exchange Act of 1934
Date of Report (Date of earliest event reported):
August 14, 2024
Brainstorm Cell Therapeutics Inc.
(Exact name of registrant as specified in its
charter)
Delaware |
|
001-36641 |
|
20-7273918 |
(State or other jurisdiction of
incorporation) |
|
(Commission File No.) |
|
(IRS Employer Identification No.) |
1325 Avenue of Americas, 28th Floor |
|
New York, NY |
10019 |
(Address of principal executive offices) |
(Zip Code) |
(201) 488-0460
(Registrant’s telephone number, including
area code)
N/A
(Former name or former address, if changed
since last report)
Check the appropriate box below if the Form 8-K filing is intended
to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:
| ¨ |
Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425) |
| ¨ |
Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12) |
| ¨ |
Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b)) |
| ¨ |
Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c)) |
Securities registered pursuant to Section
12(b) of the Act:
Title of each class |
Trading Symbol(s) |
Name of each exchange on which registered |
Common Stock, $0.00005 par value |
BCLI |
NASDAQ Stock Market LLC
(Nasdaq Capital Market) |
Indicate by check mark whether the registrant is an emerging
growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities
Exchange Act of 1934 (§240.12b-2 of this chapter).
Emerging growth company ¨
If an emerging growth company, indicate by check mark if the
registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards
provided pursuant to Section 13(a) of the Exchange Act. ¨
Item 2.02. Results of Operations and Financial
Condition.
On August 14, 2024, Brainstorm Cell Therapeutics
Inc. issued a press release announcing its financial results for the quarter ended June 30, 2024. The full text of the press release
is being furnished as Exhibit 99.1 to this current report on Form 8-K and is incorporated herein by reference.
The information in this Item 2.02, including
Exhibit 99.1 attached hereto, shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934,
or the Exchange Act, or otherwise subject to the liabilities of that section, nor shall it be deemed incorporated by reference in any
filing under the Securities Act of 1933, as amended, or the Exchange Act, except as expressly set forth by specific reference in such
a filing.
Item 9.01 Financial Statements and Exhibits.
(d) Exhibits.
SIGNATURES
Pursuant to the requirements
of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto
duly authorized.
|
BRAINSTORM CELL THERAPEUTICS INC. |
|
|
|
Date: August 14, 2024 |
By: |
/s/ Chaim Lebovits |
|
|
Chaim Lebovits |
|
|
President and Co-Chief Executive Officer |
Exhibit 99.1
BrainStorm Cell Therapeutics Announces Second
Quarter 2024 Financial Results and Provides Corporate Update
Company reached alignment with the U.S. FDA on
the Chemistry, Manufacturing, and Controls (CMC) aspects of its planned Phase 3b clinical trial for NurOwn® in ALS
SPA in place for Phase 3b NurOwn®
trial in ALS
Enhanced leadership team with appointment of Hartoun
Hartounian Ph.D. as EVP and Chief Operating Officer, and promotion of Dr. Bob Dagher to
EVP and Chief Medical Officer
Conference call and webcast at 8.30am ET today
NEW YORK, Aug 14, 2024 /PRNewswire/
-- BrainStorm Cell Therapeutics Inc. (NASDAQ: BCLI), a leading developer of adult stem cell therapeutics for neurodegenerative
diseases, today announced financial results for the Second Quarter ended June 30, 2023 and provided a corporate update.
“We continue to make excellent progress
in our preparations for the planned Phase 3b trial of NurOwn in ALS, with important recent developments on regulatory and operational
fronts,” said Chaim Lebovits, President and CEO of BrainStorm. “We believe that the regulatory aspects of the program have
been substantially derisked, having secured agreement with the FDA on a Special Protocol Assessment and also reached alignment on the
CMC aspects. We have selected a leading Clinical Research Organization and are actively working to establish multiple trial sites. If
successful, this trial has the potential to significantly improve the lives of ALS patients by providing a much-needed therapeutic option."
Second Quarter 2024 and Recent Highlights
Clinical and regulatory
| · | In
June 2024, BrainStorm reached alignment with the U.S. Food and Drug Administration (FDA)
on the Chemistry, Manufacturing, and Controls (CMC) aspects of its planned Phase 3b clinical
trial for NurOwn®, its investigational therapy for amyotrophic lateral sclerosis (ALS).
This followed the announcement, in April 2024, that the FDA had granted BrainStorm a
Special Protocol Assessment (SPA) agreement for the Phase 3b trial. The SPA agreement
validates the clinical trial protocol and statistical analysis of the trial, demonstrating
their adequacy for addressing objectives that support a future BLA (Biologics License Application)
in ALS. |
| · | The
Company has selected a leading Clinical Research Organization (CRO) to support the initiation
and execution of the Phase 3b trial. We are actively engaging with over 12 leading ALS centers
of excellence to establish trial sites. Manufacturing processes are well-advanced and on
track to meet production timelines. |
| · | In
May 2024, new biomarker data on NurOwn from the prior Phase 3 study and Expanded Access Program
(EAP) were featured in a presentation at the 3rd Annual ALS Drug Development Summit, which
took place in Boston MA. The data suggested that patients who received extended
treatment with NurOwn continued to see benefits. The summit was attended by advocacy groups,
physicians, research organizations, industry representatives, key thought leaders and decision
makers dedicated to ALS research. |
| · | In
April 2024, Phase 3 biomarker data on NurOwn in ALS were published in Muscle and
Nerve in a paper entitled "Debamestrocel multimodal effects on biomarker pathways
in amyotrophic lateral sclerosis are linked to clinical outcomes". |
Corporate
| · | In
June 2024, BrainStorm completed a successful registered direct offering, with a single institutional
investor, raising gross proceeds of $4.0 million. |
| · | In
June 2024, appointed Hartoun Hartounian Ph.D. as EVP and Chief Operating Officer. Dr.
Hartounian brings a distinguished track record with over 32 years of experience in the biopharmaceutical
industry, with a focus on cell and gene therapy. |
| · | In
April 2024, promoted Dr. Bob Dagher to
Executive Vice President and Chief Medical Officer. Dr. Dagher has over 20 years' of experience
in clinical research and development, with a proven track record of leading successful clinical
trials and fostering innovation in drug development. |
Financial
Results for the Second Quarter Ended June 30, 2024
| · | Cash,
cash equivalents, and restricted cash amounted to approximately $3.65 million, as of June
30, 2024. |
| · | Research
and development expenses, net, in the second quarter ended June 30, 2024 were $0.9 million,
compared to $2.8 million for the quarter ended June 30, 2023. |
| · | General
and administrative expenses for the second quarter ended June 30, 2024 and 2023 were $2.0
million and $2.7 million, respectively. |
| · | Net
loss for the second quarter ended June 30, 2024 was $2.5 million as compared to a net loss
of $5.3 million for the quarter ended June 30, 2023. |
| · | Net
loss per share for the second quarter ended June 30, 2024 and June 30, 2023 was $0.04 and
$0.13, respectively. |
Conference Call and Webcast
BrainStorm
management will discuss the second quarter results and recent progress in a conference call and webcast for the investment community
at 830am ET today. Investors may participate by dialing the following numbers:
Toll Free: |
877-545-0523 |
International: |
973-528-0016 |
Participant Access Code: |
308245 |
Webcast URL: |
https://www.webcaster4.com/Webcast/Page/2354/51009 |
The
replay of the conference call can be accessed by dialing the numbers below and will be available for 14 days.
Replay
Numbers
Toll Free: |
877-481-4010 |
International: |
919-882-2331 |
Replay Passcode: |
51009 |
About
BrainStorm Cell Therapeutics Inc.
BrainStorm
Cell Therapeutics Inc. is a leading developer of innovative autologous adult stem cell therapeutics for debilitating neurodegenerative
diseases. BrainStorm 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 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), and
another grant from the ALS Association and I AM ALS. BrainStorm completed under an investigational new drug application a Phase 2 open-label
multicenter trial (NCT03799718) of autologous MSC-NTF cells in progressive MS and was supported by a grant from the National MS Society
(NMSS).
Notice Regarding
Forward-Looking Statements
This press release contains
"forward-looking statements" that are subject to substantial risks and uncertainties, including statements regarding meetings
with the U.S. Food and Drug Administration (FDA), Special Protocol Assessment (SPA), ADCOM meeting related to NurOwn, the timing
of a PDUFA action date for the BLA for NurOwn, the clinical development of NurOwn as a therapy for the treatment of ALS, the future availability
of NurOwn to patients, and the future success of BrainStorm. All statements, other than statements of historical fact, contained in this
press release are forward-looking statements. Forward-looking statements contained in this press release may be identified by the use
of words such as "anticipate," "believe," "contemplate," "could," "estimate," "expect,"
"intend," "seek," "may," "might," "plan," "potential," "predict,"
"project," "target," "aim," "should," "will" "would," or the negative of
these words or other similar expressions, although not all forward-looking statements contain these words. Forward-looking statements
are based on BrainStorm's current expectations and are subject to inherent uncertainties, risks and assumptions that are difficult to
predict. These potential risks and uncertainties include, without limitation, management's ability to successfully achieve its goals,
BrainStorm's ability to raise additional capital, BrainStorm's ability to continue as a going concern, prospects for future regulatory
approval of NurOwn, whether BrainStorm's future interactions with the FDA will have productive outcomes, 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
Media:
Lisa Guiterman
Phone: +1 202-330-3431
lisa.guiterman@gmail.com
IR:
Michael Wood
Phone: +1 646-597-6983
mwood@lifesciadvisors.com
BRAINSTORM CELL THERAPEUTICS INC. AND
SUBSIDIARIES
INTERIM CONDENSED CONSOLIDATED BALANCE SHEETS
U.S. dollars in thousands
(Except share data)
| |
June 30, | | |
December 31, | |
| |
2024 | | |
2023 | |
| |
Unaudited | | |
Audited | |
| |
U.S. $ in thousands | |
ASSETS | |
| | |
| |
| |
| | |
| |
Current Assets: | |
| | | |
| | |
Cash and cash equivalents | |
$ | 3,469 | | |
$ | 1,300 | |
Other accounts receivable | |
| 33 | | |
| 51 | |
Prepaid expenses and other current assets (Note 4) | |
| 314 | | |
| 548 | |
Total current assets | |
$ | 3,816 | | |
$ | 1,899 | |
Long-Term Assets: | |
| | | |
| | |
Prepaid expenses and other long-term assets | |
$ | 20 | | |
$ | 22 | |
Restricted Cash | |
| 179 | | |
| 185 | |
Operating lease right of use asset (Note 5) | |
| 1,110 | | |
| 1,416 | |
Property and Equipment, Net | |
| 558 | | |
| 686 | |
Total Long-Term Assets | |
$ | 1,867 | | |
$ | 2,309 | |
| |
| | | |
| | |
Total assets | |
$ | 5,683 | | |
$ | 4,208 | |
| |
| | | |
| | |
LIABILITIES AND STOCKHOLDERS’ DEFICIT | |
| | | |
| | |
| |
| | | |
| | |
Current Liabilities: | |
| | | |
| | |
Accounts payables | |
$ | 5,340 | | |
$ | 4,954 | |
Accrued expenses | |
| 718 | | |
| 1,240 | |
Operating lease liability (Note 5) | |
| 566 | | |
| 603 | |
Employees related liability | |
| 1,067 | | |
| 1,003 | |
Total current liabilities | |
$ | 7,691 | | |
$ | 7,800 | |
| |
| | | |
| | |
Long-Term Liabilities: | |
| | | |
| | |
Operating lease liability (Note 5) | |
| 396 | | |
| 672 | |
Warrants liability (Note 6) | |
| 1,123 | | |
| 594 | |
Total long-term liabilities | |
$ | 1,519 | | |
$ | 1,266 | |
| |
| | | |
| | |
Total liabilities | |
$ | 9,210 | | |
$ | 9,066 | |
| |
| | | |
| | |
Stockholders’ Deficit: | |
| | | |
| | |
Stock capital: (Note 7) | |
| 14 | | |
| 13 | |
Common Stock of $0.00005 par value - Authorized: 100,000,000 shares at June 30, 2024 and December 31, 2023 respectively; Issued and outstanding: 79,646,942 and 60,489,208 shares at June 30, 2024 and December 31, 2023 respectively. | |
| | | |
| | |
Additional paid-in-capital | |
| 217,530 | | |
| 210,258 | |
Treasury stocks | |
| (116 | ) | |
| (116 | ) |
Accumulated deficit | |
| (220,955 | ) | |
| (215,013 | ) |
Total stockholders’ deficit | |
$ | (3,527 | ) | |
$ | (4,858 | ) |
| |
| | | |
| | |
Total liabilities and stockholders’ deficit | |
$ | 5,683 | | |
$ | 4,208 | |
The accompanying notes are an integral part of the
consolidated financial statements.
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, | |
| |
2024 | | |
2023 | | |
2024 | | |
2023 | |
| |
Unaudited | | |
Unaudited | |
Operating expenses: | |
| | | |
| | | |
| | | |
| | |
| |
| | | |
| | | |
| | | |
| | |
Research and development, net | |
$ | 1,883 | | |
$ | 5,718 | | |
$ | 922 | | |
$ | 2,794 | |
General and administrative | |
| 3,573 | | |
| 4,882 | | |
| 2,060 | | |
| 2,655 | |
| |
| | | |
| | | |
| | | |
| | |
Operating loss | |
| (5,456 | ) | |
| (10,600 | ) | |
| (2,982 | ) | |
| (5,449 | ) |
| |
| | | |
| | | |
| | | |
| | |
Financial income, net | |
| 43 | | |
| 212 | | |
| 30 | | |
| 120 | |
| |
| | | |
| | | |
| | | |
| | |
Gain (loss) on change in fair value of Warrants liability (Note 6) | |
| 529 | | |
| - | | |
| (411 | ) | |
| - | |
| |
| | | |
| | | |
| | | |
| | |
Net loss | |
$ | (5,942 | ) | |
$ | (10,388 | ) | |
$ | (2,541 | ) | |
$ | (5,329 | ) |
| |
| | | |
| | | |
| | | |
| | |
Basic and diluted net loss per share from continuing operations | |
$ | (0.09 | ) | |
$ | (0.27 | ) | |
$ | (0.04 | ) | |
$ | (0.13 | ) |
| |
| | | |
| | | |
| | | |
| | |
Weighted average number of shares outstanding used in computing basic and diluted net loss per share | |
| 67,977,012 | | |
| 38,224,230 | | |
| 71,215,481 | | |
| 39,696,665 | |
The accompanying notes are an integral part of the consolidated financial
statements.
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