UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM 6-K
Report of Foreign Private Issuer
Pursuant to Rule 13a-16 or 15d-16
of the Securities Exchange Act of 1934
For the month of November 2024
Commission File Number: 001-37643
PURPLE BIOTECH LTD.
(Translation of registrant’s name into English)
4 Oppenheimer Street, Science Park, Rehovot
7670104, Israel
(Address of principal executive offices)
Indicate by check mark whether the registrant files or will file annual
reports under cover Form 20-F or Form 40-F.
Form 20-F ☒ Form 40-F ☐
On November 15, 2024, Purple Biotech Ltd. (the
“Company” or the “Registrant”) issued a press release, “Purple Biotech Reports Third Quarter 2024
Financial Results”, which is attached hereto as Exhibit 99.1.
Incorporation by Reference
This Report on Form 6-K, including all exhibits attached hereto, is
hereby incorporated by reference into each of the Registrant’s Registration Statement on Form S-8 filed with the Securities and
Exchange Commission on May 20, 2016 (Registration file number 333-211478), the Registrant’s Registration Statement on Form S-8 filed
with the Securities and Exchange Commission on June 6, 2017 (Registration file number 333-218538), the Registrant’s Registration
Statement on Form F-3, as amended, originally filed with the Securities and Exchange Commission on July 16, 2018 (Registration file number
333-226195), the Registrant’s Registration Statement on Form S-8 filed with the Securities and Exchange Commission on March 28,
2019 (Registration file number 333-230584), the Registrant’s Registration Statement on Form F-3 filed with the Securities and Exchange
Commission on September 16, 2019 (Registration file number 333-233795), the Registrant’s Registration Statement on Form F-1 filed
with the Securities and Exchange Commission on December 27, 2019 (Registration file number 333-235729), the Registrant’s Registration
Statement on Form F-3 filed with the Securities and Exchange Commission on May 13, 2020 (Registration file number 333-238229), the Registrant’s
Registration Statement on Form S-8 filed with the Securities and Exchange Commission on May 18, 2020 (Registration file number 333-238481),
each of the Registrant’s Registration Statements on Form F-3 filed with the Securities and Exchange Commission on July 10, 2020
(Registration file numbers 333-239807 and 333-233793), the Registrant’s Registration Statement on Form S-8 filed with the Securities
and Exchange Commission on April 4, 2022 (Registration file number 333-264107) and the Registrant’s Registration Statement on Form F-3 filed with the Securities and Exchange Commission on March 23, 2023 (Registration file number 333-270769), the Registrant’s
Registration Statement on Form F-3, as amended, originally filed with the Securities and Exchange Commission on December 8, 2022 (Registration
file number 333-268710), the Registrant’s Registration Statement on Form F-1, as amended, originally filed with the Securities
and Exchange Commission on October 30, 2023 (Registration file number 333-275216) and the Registrant’s Registration Statement on
Form F-1, filed with the Securities and Exchange Commission on July 22, 2024 (Registration file number 333- 280947), to be a part
thereof from the date on which this report is submitted, to the extent not superseded by documents or reports subsequently filed or furnished.
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, thereunto
duly authorized.
| November 15, 2024 |
PURPLE BIOTECH LTD. |
| |
|
|
| |
By: |
/s/ Gil Efron |
| |
|
Gil Efron |
| |
|
Chief Executive Officer |
2
Exhibit 99.1
Purple Biotech Reports Third Quarter 2024 Financial
Results
Topline data from Phase 2 CM24 pancreatic cancer
trial expected by the end of 2024
New CM24 biomarkers data presented during the
third quarter of 2024 including two predicting serum biomarkers identified and associated with CM24 novel targets
CAPTN-3 tri-specific antibody platform data
presented at the ENA Symposium October 2024
REHOVOT, Israel, November 15, 2024 -- Purple
Biotech Ltd. (“Purple Biotech” or “the Company”) (NASDAQ/TASE: PPBT), a clinical-stage company developing first-in-class
therapies that overcome tumor immune evasion and drug resistance, today announced financial results for the three and nine months ended
September 30, 2024.
“Marking what we believe to be the most
significant value-driving event for Purple Biotech’s clinical programs to date, we are on track to complete CM24’s Phase 2
study in pancreatic cancer and report topline results by the end of this year,” stated Purple Biotech’s CEO, Gil Efron. “The
interim Phase 2 CM24 data released so far demonstrated efficacy, and new biomarker data indicate potential to further improve outcomes
in a future study through the use of one or more serum biomarkers for patient selection. This would position CM24 as a potentially promising
CEACAM1 and Neutrophils Extracellular Trap (NET) targeted therapy. While we advance CM24 as a second line treatment for pancreatic cancer,
we are planning to address additional unmet needs in other indications based on CM24’s demonstrated mechanism of action in our Phase
2 study. Our cash runway now extends into the fourth quarter of 2025. We continue to advance our clinical assets and believe we will be
soon well positioned for partnerships across our pipeline.”
Q3 2024 and Recent Clinical & Corporate
Highlights:
| ● | Phase 2 CM24 pancreatic cancer study on track for conclusion with topline data expected in 2024: Serum
biomarkers may improve outcomes in future studies |
New positive biomarker findings for CM24, a multi-functional
CEACAM1 inhibitor, were presented at the American Association for Cancer Research® (AACR) Special Conference on Advances in Pancreatic
Cancer Research in a poster titled “Exploratory biomarker evaluation of the randomized Phase 2 cohort of CM24 in combination with
nivolumab and chemotherapy in advanced/metastatic pancreatic cancer”.
The summary of findings presented at AACR include
the following:
| ü | High CEACAM1 and low PDL1 expression in tumors, as well as their combination were identified as potential
biomarkers associated with improved overall survival (OS) of pancreatic ductal adenocarcinoma (PDAC) patients (HR=0.1 and prolongation
of 4.1 months in median OS, P = 0.01, for the combination), which support the CM24/nivolumab combined treatment |
| ü | Improved OS was demonstrated for patients with selected pretreatment serum neutrophil extracellular trap
(NET) marker myeloperoxidase (MPO) levels (HR=0.38 and prolongation of 3.3 months in median OS, P = 0.1), with a similar trend
in patients with NET-positive tumors |
| ü | The results presented in the poster propose NETs as a novel mechanism of action and a potential biomarker
for CM24-based therapy |
| ü | New biomarker data supports the potential for future biomarker-guided studies and the exploration of CM24’s
efficacy in other cancers where the novel target CEACAM1 plays a key role in cancer progression and immune evasion. |
More recent biomarker data specific to serum CEACAM1,
associated with a 79% reduction in risk of death were announced by Purple Biotech in November 2024:
PDAC patients who had pretreatment serum CEACAM1
levels between 6K and 15K pg/mL demonstrated the best outcomes following treatment with CM24 and nivolumab in combination with irinotecan/fluoropyrimidine
based chemotherapy compared to chemotherapy alone.
| ü | Median progression free survival (PFS) of this group was 4.6 months (hazard ratio [HR] < 0.1, P = 0.003) |
| ü | Risk of death was reduced by 79% (HR = 0.21, P = 0.04) |
| ü | Median OS increased from 3.6 months with chemotherapy alone to 8.7 months with the combination therapy. |
The Phase 2 randomized study is evaluating CM24
in combination with Bristol Myers Squibb’s PD-1 inhibitor nivolumab plus standard of care (SoC) chemotherapy as a second line treatment
of patients with PDAC. In the experimental arms of the study patients were treated with CM24 plus nivolumab and one of two SoC chemotherapies,
gemcitabine/nab-paclitaxel or Nal-IRI/5FU/LV, while patients in the control arms are administered with either respective chemotherapies
alone. Sixty-three patients have been enrolled across 18 centers in the U.S., Spain and Israel. The gemcitabine/nab-paclitaxel-based part
of the study was impacted by informative censoring of the control arm that led to an imbalance between the control and experimental cohorts,
rendering this part of the study unsuitable for analysis; this part of the study has no impact on the CM24+nivolumab+Nal-IRI/5FU/LV portion
of the study.
| ● | NT219 Phase 2 study in head and neck cancer planned to commence H1 2025 |
A Phase 2 study of NT219, a first-in-class, small
molecule dual inhibitor of IRS1/2 and STAT3, is planned to commence in the first half of 2025. The recommended Phase 2 dose of 100 mg/kg
was achieved in the prior Phase 1/2 dose escalation study, which demonstrated anti-tumor activity at the target exposure level and was
well tolerated in combination with cetuximab as a second line treatment of recurrent metastatic squamous cell carcinoma of the head and
neck.
| ● | CAPTN-3 tri-specific platform data presented at key molecular targets and cancer therapeutics conference
|
New data regarding Purple Biotech’s novel
tri-specific antibody platform, CAPTN-3, were presented at the 36th European Organization for Research and Treatment of Cancer, National
Cancer Institute, American Association for Cancer Research (EORTC-NCI-AACR) Symposium on Molecular Targets and Cancer Therapeutics (the
“Triple Meeting”) in a poster titled “CAPTN-3: A novel platform of conditionally activated T cell and NK cell engagers”.
CAPTN-3 demonstrated sustained tumor regression in a triple negative breast cancer in-vivo model as well as dose dependent activity and
synergistic effect of the engager arms in non-small cell lung cancer patient-derived explants. Purple Biotech’s lead tribody candidate,
IM1240, demonstrated that cytokine release is 5T4-dependent and suppressed by the conditionally activated capping technology, suggesting
a potentially beneficial safety profile of this tribody. The data further demonstrated additional tribodies, suggesting CAPTN-3’s
plug and play platform capability. Purple Biotech continues to accumulate data supporting the benefit of dual engagement of both T cells
and NK cells.
Financial Results for the Three Months Ended
September 30, 2024
Research and Development Expenses were
$1.3 million, a decrease of $3.3 million, or 71.7%, compared to $4.6 million in the same period of 2023, mainly due to reduced clinical
trials expenses.
Sales, General and Administrative Expenses were
$0.8 million, compared to $1.2 million in the same period of 2023, a decrease of $0.4 million, or 33.3%, mainly due to a decrease in salary
and salary related costs and share based payment expenses.
Operating Loss was $2.1 million, a decrease
of $3.6 million, or 63.2%, compared to $5.7 million in the same period of 2023, mainly due to the decrease in research and development
expenses.
Adjusted Operating Loss (as
reconciled below) was $2 million, a decrease of $3.3 million, compared to $5.3 million in the same period of 2023.
Net Loss for the three months ended September
30, 2024, was $0.7 million, or $0.39 per basic and diluted ADS, compared to a net loss of $5 million, or $4.63 per basic and diluted ADS,
in the same period of 2023. The decrease in net loss was mainly due to the decrease in research and development expenses and an increase
in financial income related to changes in fair value of warrants.
Adjusted Net Loss (as reconciled below)
for the three months ended September 30, 2024, was $2.4 million, a decrease of $2.4 million or 50% compared to $4.8 million for the three
months ended September 30, 2023.
As of September 30, 2024, Purple Biotech had cash
and cash equivalents and short-term deposits of $6.3 million. Purple Biotech now has a cash runway into the fourth quarter of 2025.
During the three months ended September 30, 2024,
the Company sold, under the Open Market Sale Agreement with Jefferies LLC, approximately 76 thousand ADSs, at an average price of $6.5
per ADS. Net proceeds to the Company were approximately $0.5 million, net of issuance expenses.
Financial Results for the Nine Months Ended
September 30, 2024
Research and Development Expenses were
$7.2 million, a decrease of $4.6 million, or 39%, compared to $11.8 million in the same period of 2023. The decrease was mainly due to
reduced clinical trials expenses.
Sales, General and Administrative Expenses were
$2.6 million, a decrease of $1.6 or 38.1%, compared to $4.2 million in the same period of 2023, mainly due to a decrease in salary and
salary related expenses and share based payment expenses.
Operating Loss was $10 million, a decrease
of $6 million, or 37.5%, compared to $16 million in the same period of 2023, mainly due to the decrease in research and development expenses.
Adjusted Operating Loss (as reconciled
below) was $9.4 million, a decrease of $4.9 million, compared to $14.3 million in the same period of 2023.
Net Loss for the nine months ended September
30, 2024 was $6.9 million, or $4.57 loss per basic and diluted ADS, compared to a net loss of $15.1 million, or $14.47 loss per basic
and diluted ADS, in the same period of 2023. The decrease in net loss was mainly due to a $6 million decrease in operating expenses and
$3.3 million income from change in fair value of warrants.
Adjusted net loss (as reconciled below)
for the nine months ended September 30, 2024 was $9.5 million, compared to $13.7 million for the nine months ended September 30, 2023.
Non-IFRS Financial Measures.
This press release includes information about certain
financial measures that are not prepared in accordance with International Financial Reporting Standards (“IFRS”), including
adjusted operating loss and adjusted net loss. These non-IFRS measures are not based on any standardized methodology prescribed by IFRS
and are not necessarily comparable to similar measures presented by other companies. Adjusted operating loss and adjusted net loss adjust
for non-cash share-based compensation expenses and adjusted net loss also adjusts for non-cash financial instruments evaluation income.
The Company’s management and board of directors utilize these non-IFRS financial measures to evaluate the Company’s performance. The Company
provides these non-IFRS measures of the Company’s performance to investors because management believes that these non-IFRS financial measures,
when viewed with the Company’s results under IFRS and the accompanying reconciliations, are useful in identifying underlying trends in
ongoing operations. However, these non-IFRS measures are not measures of financial performance under IFRS and, accordingly, should not
be considered as alternatives to IFRS measures as indicators of operating performance. Further, these non-IFRS measures should not be
considered measures of the Company’s liquidity. A reconciliation of certain IFRS to non-IFRS financial measures has been provided in the
tables included in this press release.
About Purple Biotech
Purple Biotech Ltd. (NASDAQ/TASE: PPBT) is a clinical-stage
company developing first-in-class therapies that seek to overcome tumor immune evasion and drug resistance. The Company’s oncology pipeline
includes CM24, NT219 and IM1240. CM24 is a humanized monoclonal antibody that blocks CEACAM1, that supports tumor immune evasion and survival
through multiple pathways. CEACAM1 on tumor cells, immune cells and neutrophils extracellular traps is a novel target for the treatment
of multiple cancer indications. As a proof of concept of these novel pathways, the Company is advancing CM24 as a combination therapy
with anti-PD-1 checkpoint inhibitors in a Phase 2 study for the treatment of pancreatic ductal adenocarcinoma (PDAC). The Company has
entered into a clinical collaboration agreement with Bristol Myers Squibb for the Phase 2 clinical trials to evaluate the combination
of CM24 with the PD-1 inhibitor nivolumab in addition to chemotherapy. NT219 is a dual inhibitor, novel small molecule that simultaneously
targets IRS1/2 and STAT3. A Phase 1 dose escalation study was concluded as a monotherapy and in combination with cetuximab in which NT219
demonstrated anti-tumor activity in combination with cetuximab in second line patients with recurrent and/or metastatic SCCHN (R/N SCCHN).
The Company is advancing CAPTN-3, a preclinical platform of conditionally-activated tri-specific antibody that engages both T cells and
NK cells to induce a strong, localized immune response within the tumor microenvironment. The cleavable capping technology confines the
compound’s therapeutic activity to the local tumor microenvironment, and thereby potentially increases the anticipated therapeutic window
in patients. The third arm specifically targets the Tumor Associated Antigen (TAA). The technology presents a novel mechanism of action
by unleashing both innate and adaptive immune systems to mount an optimal anti-tumoral immune response. IM1240 is the first tri-specific
antibody in development that targets 5T4 expressed in a variety of solid tumors and is correlated with advanced disease, increased invasiveness
and poor clinical outcomes. The Company’s corporate headquarters are located in Rehovot, Israel. For more information, please visit https://purple-biotech.com/.
Forward-Looking Statements and Safe Harbor Statement
Certain statements in this press release that are
forward-looking and not statements of historical fact are forward-looking statements within the meaning of the safe harbor provisions
of the Private Securities Litigation Reform Act of 1995. Such forward-looking statements include, but are not limited to, statements that
are not statements of historical fact, and may be identified by words such as “believe”, “expect”, “intend”,
“plan”, “may”, “should”, “could”, “might”, “seek”, “target”, “will”,
“project”, “forecast”, “continue” or “anticipate” or their negatives or variations of these words
or other comparable words or by the fact that these statements do not relate strictly to historical matters. You should not place undue
reliance on these forward-looking statements, which are not guarantees of future performance. Forward-looking statements reflect our current
views, expectations, beliefs or intentions with respect to future events, and are subject to a number of assumptions, involve known and
unknown risks, many of which are beyond our control, as well as uncertainties and other factors that may cause our actual results, performance
or achievements to be significantly different from any future results, performance or achievements expressed or implied by the forward-looking
statements. Important factors that could cause or contribute to such differences include, among others, risks relating to: the plans,
strategies and objectives of management for future operations; product development for NT219, CM24 and IM1240; the process by which such
early stage therapeutic candidates could potentially lead to an approved drug product is long and subject to highly significant risks,
particularly with respect to a joint development collaboration; the fact that drug development and commercialization involves a lengthy
and expensive process with uncertain outcomes; our ability to successfully develop and commercialize our pharmaceutical products; the
expense, length, progress and results of any clinical trials; the impact of any changes in regulation and legislation that could affect
the pharmaceutical industry; the difficulty in receiving the regulatory approvals necessary in order to commercialize our products; the
difficulty of predicting actions of the U.S. Food and Drug Administration or any other applicable regulator of pharmaceutical products;
the regulatory environment and changes in the health policies and regimes in the countries in which we operate; the uncertainty surrounding
the actual market reception to our pharmaceutical products once cleared for marketing in a particular market; the introduction of competing
products; patents obtained by competitors; dependence on the effectiveness of our patents and other protections for innovative products;
our ability to obtain, maintain and defend issued patents; the commencement of any patent interference or infringement action against
our patents, and our ability to prevail, obtain a favorable decision or recover damages in any such action; and the exposure to litigation,
including patent litigation, and/or regulatory actions, and other factors that are discussed in our Annual Report on Form 20-F for the
year ended December 31, 2023 and in our other filings with the U.S. Securities and Exchange Commission (“SEC”), including our
cautionary discussion of risks and uncertainties under “Risk Factors” in our Registration Statements and Annual Reports. These
are factors that we believe could cause our actual results to differ materially from expected results, performance or achievements. Other
factors besides those we have listed could also adversely affect us. Any forward-looking statement in this press release speaks only as
of the date which it is made. We disclaim any intention or obligation to publicly update or revise any forward-looking statement or other
information contained herein, whether as a result of new information, future events or otherwise, except as required by applicable law.
You are advised, however, to consult any additional disclosures we make in our reports to the SEC, which are available on the SEC’s website,
https://www.sec.gov.
CONTACTS:
IR@purple-biotech.com
Purple Biotech Ltd.
Consolidated Unaudited Statements of Financial
Position as of:
| | |
September 30, | | |
December 31, | |
| | |
2024 | | |
2023 | |
| | |
USD thousand | | |
USD thousand | |
| Assets | |
| | |
| |
| Cash and cash equivalents | |
| 5,438 | | |
| 14,489 | |
| Short term deposits | |
| 848 | | |
| 850 | |
| Other investments | |
| 14 | | |
| 73 | |
| Other current assets | |
| 638 | | |
| 376 | |
| | |
| | | |
| | |
| Total current assets | |
| 6,938 | | |
| 15,788 | |
| | |
| | | |
| | |
| Non-current assets | |
| | | |
| | |
| Right of use assets | |
| 202 | | |
| 316 | |
| Fixed assets, net | |
| 123 | | |
| 154 | |
| Intangible assets | |
| 27,842 | | |
| 28,044 | |
| | |
| | | |
| | |
| Total non–current assets | |
| 28,167 | | |
| 28,514 | |
| | |
| | | |
| | |
| Total assets | |
| 35,105 | | |
| 44,302 | |
| | |
| | | |
| | |
| Liabilities | |
| | | |
| | |
| Lease liability - short term | |
| 184 | | |
| 188 | |
| Accounts payable | |
| 1,912 | | |
| 3,532 | |
| Other payables | |
| 1,803 | | |
| 3,463 | |
| Warrants | |
| 1,560 | | |
| 2,518 | |
| | |
| | | |
| | |
| Total current liabilities | |
| 5,459 | | |
| 9,701 | |
| | |
| | | |
| | |
| Non-current liabilities | |
| | | |
| | |
| Lease liability | |
| 38 | | |
| 163 | |
| Post-employment benefit liabilities | |
| 141 | | |
| 141 | |
| | |
| | | |
| | |
| Total non-current liabilities | |
| 179 | | |
| 304 | |
| | |
| | | |
| | |
| Equity | |
| | | |
| | |
| Share capital, no par value | |
| - | | |
| - | |
| Share premium | |
| 143,647 | | |
| 133,184 | |
| Receipts on account of warrants | |
| 21,145 | | |
| 28,467 | |
| Capital reserve for share-based payments | |
| 9,002 | | |
| 10,088 | |
| Capital reserve from transactions with related parties | |
| 761 | | |
| 761 | |
| Capital reserves from hedging | |
| (2 | ) | |
| 19 | |
| Capital reserve from transactions with non-controlling interest | |
| (859 | ) | |
| (859 | ) |
| Accumulated loss | |
| (144,283 | ) | |
| (137,453 | ) |
| | |
| | | |
| | |
| Equity attributable to owners of the Company | |
| 29,411 | | |
| 34,207 | |
| Non-controlling interests | |
| 56 | | |
| 90 | |
| | |
| | | |
| | |
| Total equity | |
| 29,467 | | |
| 34,297 | |
| | |
| | | |
| | |
| Total liabilities and equity | |
| 35,105 | | |
| 44,302 | |
Purple Biotech Ltd.
Consolidated Unaudited Statement of Operations
for the nine and three months ended September 30, 2024
| | |
For the nine months ended
September 30, | | |
For the three months ended
September 30, | |
| | |
2024 | | |
2023 | | |
2024 | | |
2023 | |
| | |
USD
thousand | | |
USD
thousand | | |
USD
thousand | | |
USD
thousand | |
| | |
| | |
| | |
| | |
| |
| Research and development expenses | |
| 7,162 | | |
| 11,792 | | |
| 1,348 | | |
| 4,589 | |
| Sales, general and administrative expenses | |
| 2,625 | | |
| 4,212 | | |
| 785 | | |
| 1,158 | |
| Impairment loss | |
| 202 | | |
| - | | |
| - | | |
| - | |
| | |
| | | |
| | | |
| | | |
| | |
| Operating loss | |
| 9,989 | | |
| 16,004 | | |
| 2,133 | | |
| 5,747 | |
| | |
| | | |
| | | |
| | | |
| | |
| Change in fair value of warrants | |
| (3,265 | ) | |
| - | | |
| (1,846 | ) | |
| - | |
| Finance expense | |
| 552 | | |
| 223 | | |
| 511 | | |
| 16 | |
| Finance income | |
| (412 | ) | |
| (1,109 | ) | |
| (130 | ) | |
| (708 | ) |
| | |
| | | |
| | | |
| | | |
| | |
| Finance income, net | |
| (3,125 | ) | |
| (886 | ) | |
| (1,465 | ) | |
| (692 | ) |
| | |
| | | |
| | | |
| | | |
| | |
| Loss for the period | |
| 6,864 | | |
| 15,118 | | |
| 668 | | |
| 5,055 | |
| | |
| | | |
| | | |
| | | |
| | |
| Other Comprehensive Loss: | |
| | | |
| | | |
| | | |
| | |
| Items that will be transferred to
profit or loss: | |
| | | |
| | | |
| | | |
| | |
| Loss (profit) on cash flow hedges | |
| 21 | | |
| (4 | ) | |
| - | | |
| - | |
| | |
| | | |
| | | |
| | | |
| | |
| Total comprehensive loss for the period | |
| 6,885 | | |
| 15,114 | | |
| 668 | | |
| 5,055 | |
| | |
| | | |
| | | |
| | | |
| | |
| Loss attributable to: | |
| | | |
| | | |
| | | |
| | |
| Owners of the Company | |
| 6,830 | | |
| 15,052 | | |
| 663 | | |
| 5,036 | |
| Non-controlling interests | |
| 34 | | |
| 66 | | |
| 5 | | |
| 19 | |
| | |
| | | |
| | | |
| | | |
| | |
| | |
| 6,864 | | |
| 15,118 | | |
| 668 | | |
| 5,055 | |
| | |
| | | |
| | | |
| | | |
| | |
| Total comprehensive loss attributable to | |
| | | |
| | | |
| | | |
| | |
| Owners of the Company | |
| 6,851 | | |
| 15,048 | | |
| 663 | | |
| 5,036 | |
| Non-controlling interests | |
| 34 | | |
| 66 | | |
| 5 | | |
| 19 | |
| | |
| | | |
| | | |
| | | |
| | |
| | |
| 6,885 | | |
| 15,114 | | |
| 866 | | |
| 5,055 | |
| | |
| | | |
| | | |
| | | |
| | |
| Loss per share data (*) | |
| | | |
| | | |
| | | |
| | |
| Basic and diluted loss per ADS - USD | |
| 4.57 | | |
| 14.47 | | |
| 0.39 | | |
| 4.63 | |
| | |
| | | |
| | | |
| | | |
| | |
| Number of ADSs used in calculation | |
| 1,502,321 | | |
| 1,045,054 | | |
| 1,732,565 | | |
| 1,091,823 | |
| (*) | Restated
to reflect reverse split of 1:20 approved in August 2024 . |
Reconciliation of Adjusted Operating Loss
| | |
For the nine months ended
September 30, | | |
For the three months ended
September 30, | |
| | |
2024 | | |
2023 | | |
2024 | | |
2023 | |
| | |
USD
thousand | | |
USD
thousand | | |
USD
thousand | | |
USD
thousand | |
| | |
| | |
| | |
| | |
| |
| Operating loss for the period | |
| 9,989 | | |
| 16,004 | | |
| 2,133 | | |
| 5,747 | |
| Less ESOP expenses | |
| (616 | ) | |
| (1,694 | ) | |
| (132 | ) | |
| (449 | ) |
| | |
| 9,373 | | |
| 14,310 | | |
| 2,001 | | |
| 5,298 | |
Reconciliation of Adjusted Net Loss
| | |
For the nine months ended
September 30, | | |
For the three months ended
September 30, | |
| | |
2024 | | |
2023 | | |
2024 | | |
2023 | |
| | |
USD
thousand | | |
USD
thousand | | |
USD
thousand | | |
USD
thousand | |
| | |
| | |
| | |
| | |
| |
| Loss for the period | |
| 6,864 | | |
| 15,118 | | |
| 668 | | |
| 5,055 | |
| Less ESOP expenses | |
| (616 | ) | |
| (1,694 | ) | |
| (132 | ) | |
| (449 | ) |
| Less finance income from financial instruments | |
| 3,206 | | |
| 293 | | |
| 1,838 | | |
| 213 | |
| | |
| 9,454 | | |
| 13,717 | | |
| 2,374 | | |
| 4,819 | |
Consolidated
Unaudited Statements of Cash Flow
| | |
For the nine months ended
September 30, | |
| | |
2024 | | |
2023 | |
| | |
USD
thousand | | |
USD
thousand | |
| Cash flows from operating activities: | |
| | |
| |
| Loss for the period | |
| (6,864 | ) | |
| (15,118 | ) |
| Adjustments: | |
| | | |
| | |
| Depreciation | |
| 146 | | |
| 149 | |
| Impairment loss | |
| 202 | | |
| - | |
| Finance income, net | |
| (3,125 | ) | |
| (886 | ) |
| Share-based payments | |
| 616 | | |
| 1,694 | |
| | |
| | | |
| | |
| | |
| (9,025 | ) | |
| (14,161 | ) |
| | |
| | | |
| | |
| Changes in assets and liabilities: | |
| | | |
| | |
| Changes in other investments and other current assets | |
| (22 | ) | |
| 219 | |
| Changes in accounts payables | |
| (1,628 | ) | |
| 415 | |
| Changes in other payables | |
| (1,678 | ) | |
| (1,255 | ) |
| Changes in post-employment benefit liabilities | |
| - | | |
| (161 | ) |
| | |
| | | |
| | |
| | |
| (3,328 | ) | |
| (782 | ) |
| | |
| | | |
| | |
| Net cash used in operating activities | |
| (12,353 | ) | |
| (14,943 | ) |
| | |
| | | |
| | |
| Cash flows from investing activities: | |
| | | |
| | |
| Acquisition of subsidiary, net of cash acquired | |
| - | | |
| (3,549 | ) |
| Proceed from other investments | |
| 187 | | |
| 875 | |
| Interest received | |
| 282 | | |
| 675 | |
| Decrease in short-term deposits | |
| 2 | | |
| 15,809 | |
| Acquisition of fixed assets | |
| - | | |
| (3 | ) |
| | |
| | | |
| | |
| Net cash provided by investing activities | |
| 471 | | |
| 13,807 | |
| | |
| | | |
| | |
| Cash flows from financing activities: | |
| | | |
| | |
| Proceeds from issuance ADSs | |
| 1,442 | | |
| 1,559 | |
| ADS issuance expenses paid | |
| (160 | ) | |
| (188 | ) |
| Proceeds from warrants transaction | |
| 2,028 | | |
| - | |
| Warrants issuance expenses paid | |
| (308 | ) | |
| - | |
| Repayment of lease liability | |
| (135 | ) | |
| (126 | ) |
| Interest paid | |
| (32 | ) | |
| (42 | ) |
| | |
| | | |
| | |
| Net cash provided by financing activities | |
| 2,835 | | |
| 1,203 | |
| | |
| | | |
| | |
| Net increase in cash and cash equivalents | |
| (9,047 | ) | |
| 67 | |
| Cash and cash equivalents at the beginning of the period | |
| 14,489 | | |
| 15,030 | |
| Effect of translation adjustments on cash and cash equivalents | |
| (4 | ) | |
| 7 | |
| | |
| | | |
| | |
| Cash and cash equivalents at the end of the period | |
| 5,438 | | |
| 15,104 | |
9
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