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 2023
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 21, 2023, Purple Biotech Ltd. (the
“Company” or the “Registrant”) issued a press release, “Purple Biotech Reports Third
Quarter 2023 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) and 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), 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 21, 2023 |
PURPLE BIOTECH LTD. |
|
|
|
By: |
/s/ Lior Fhima |
|
|
Lior Fhima |
|
|
Chief Financial Officer |
2
Exhibit 99.1
Purple Biotech Reports Third Quarter 2023 Financial
Results
Initial Activity in Head and Neck
Cancer Demonstrated in NT219 Phase 1/2 Dose Escalation Study
Patients’ Enrollment in the
Phase 2 Randomized CM24 Pancreatic Cancer Trial Ahead of Timelines
Cash Runway Extended to 2H 2025 through
Recent Financing
REHOVOT, Israel, Nov. 21, 2023 (GLOBE NEWSWIRE) -- Purple Biotech
Ltd. (“Purple Biotech” or “the Company”) (NASDAQ/TASE: PPBT), a clinical-stage company developing first-in-class therapies
that harness the power of the tumor microenvironment to overcome tumor immune evasion and drug resistance, today announced financial results
for the third quarter and nine months ended September 30, 2023.
“We are pleased to report that we expect to
complete patient enrollment in our Phase 2 randomized CM24 pancreatic cancer study soon, ahead of our previous plan and that might result
in earlier than anticipated analysis of interim and top line overall survival (OS) data during 2024. The interim data look will occur
in 2024 when sufficient progression free survival (PFS) and OS events are registered and enable a meaningful data interpretation for a
larger number of patients. Recently reported biomarker data demonstrates CM24’s mechanism of action for this important indication
in dire need of a more effective drug that prolongs survival,” stated Purple Biotech CEO, Gil Efron.
“Our Phase 1/2 dose escalation study of NT219
in head and neck cancer demonstrated initial activity at the dose level of 50 mg/kg. We continue dose optimization at a higher dose level
and expect to report additional data during the first half of 2024 in parallel to preparing to enter a Phase 2 study.”
“With a cash runway that extends more than
two years, through the second half of 2025, Purple Biotech is very well positioned to execute on multiple value-driving milestones. Moreover,
we expect 2024 to be a year with major clinical data catalysts.”
Q3 2023 and Recent Corporate
Highlights:
| ● | CM24 Pancreatic Cancer Program Advances |
| o | Phase 2 enrollment ahead of schedule |
| o | Interim results for PFS and OS expected in H1 2024 with topline results expected in H2 2024 |
| o | Biomarker data supporting MOA presented at AACR |
Patient enrollment
in the Phase 2 study of CM24 was accelerated and the Company’s plan to enroll approximately 60 patients is expected to be completed
soon, ahead of schedule. Since OS and PFS are event-based endpoints, a meaningful estimate of the endpoint can be achieved once sufficient
events occur in the study arms. We expected this to happen in 2024 when enough PFS and OS events are registered and enable meaningful
data interpretation for a larger number of patients. The acceleration allows the Company to reduce the total cost of the trial and to
report, possibly earlier than expected, an interim OS analysis, the study’s primary endpoint, together with the analysis of PFS
during 1H 2024. The randomized Phase 2 study (NCT04731467), in clinical collaboration with Bristol Myers Squibb (BMS), is evaluating CM24
in combination with BMS’s nivolumab plus chemotherapy in PDAC patients as a second line treatment as compared to chemotherapy alone.
New biomarker
data for CM24 were presented at the American Association for Cancer Research (AACR) Special Conference: Pancreatic Cancer in a scientific
poster titled “Phase 1 Study of CM24 in Combination with Nivolumab in Patients with Advanced Pancreatic Cancer - Survival, Exploratory
Biomarkers and Effect on Neutrophil Extracellular Traps (NETs)”. The study showed a high expression of CEACAM1, CM24’s target,
on neutrophils and Neutrophil Extracellular Traps (NETs), and that there are enhanced levels of serum NETs in PDAC patients. This study
demonstrated for the first time that CM24 treatment significantly reduced the level of NET marker in patients’ serum, suggesting CM24’s
novel mechanism of action (MOA) in treating pancreatic cancer.
| ● | NT219 Positive Phase 1/2 Interim Results in
Head & Neck Cancer |
| o | Anti-tumor activity with confirmed partial responses in highest, to date, dose cohort |
| o | Phase 2 study is being designed |
| o | Fortified IP protection with new patent |
Initial anti-tumor
activity was demonstrated at the 50mg/kg dose level of NT219 at 50mg/kg in combination with cetuximab in the Phase 1 dose escalation study.
A dose-dependent increase in drug exposure of NT219 was reported and target engagement was observed in tumor samples, with 2 of the 4
evaluable recurrent and metastatic squamous cell carcinoma of the head and neck patients dosed at 50mg/kg demonstrated confirmed partial
response.
A new patent was
granted in China for NT219’s pharmaceutical composition. The new patent protects the method which prevents the conversion of NT219
from its active form to a less active form and supports maintenance of the active form during manufacturing, storage, and handling until
administered to the patient.
Financial Results for the three Months Ended
September 30, 2023
Research and Development Expenses were
$4.6 million, an increase of $1.1 million, or 31.43%, compared to $3.5 million in the same period of 2022. The increase was mainly due
to clinical trials expenses in our CM24 study.
Selling, General and Administrative Expenses
were $1.2 million, a decrease of $0.4 million, or 25%, compared to $1.6 million in the same period of 2022. The decrease was mainly
due to a decrease in share based payment expenses.
Operating Loss was $5.7 million, an increase
of $0.7 million, or 14%, compared to $5.0 million in the same period of 2022. The increase was mainly due to the increase in research
and development expenses.
On a non-IFRS basis (as reconciled below), adjusted
operating loss was $5.3 million, an increase of $0.9 million, compared to $4.4 million in the same period of 2022.
Net Loss for the three months ended
September 30, 2023 was $5 million, or $0.23 per basic and diluted ADS, compared to a net loss of $4.8 million, or $0.27 per basic and
diluted ADS, in the three months ended September 30, 2022. Adjusted net loss for the three months ended September 30, 2023 was
$4.6 million, an increase from $4.1 million in the three months ended September 30, 2022.
Financial Results for the Nine Months Ended
September 30, 2023
Research and Development Expenses were
$11.8 million, an increase of $0.3 million, or 2.6%, compared to $11.5 million in the same period of 2022. The increase was mainly due
to clinical trials expenses in our CM24 study offset by lower CMC costs in 2023.
Selling, General and Administrative Expenses
were $4.2 million, a decrease of $0.3 million, or 6.67%, compared to $4.5 million in the same period of 2022. The decrease was mainly
due to a decrease in share base payment and insurance costs.
Operating Loss was $16 million, compared to
$16 million in the same period of 2022.
On a non-IFRS basis (as reconciled below), adjusted
operating loss was $14.3 million, a decrease of $0.1 million, compared to $14.4 million in the same period of 2022.
Net Loss for the nine months ended
September 30, 2023 was $15.1 million, or $0.72 loss per basic and diluted ADS, compared to a net loss of $15.7 million, or $0.87 loss
per basic and diluted ADS, in the same period of 2022. The decrease in net loss was mainly due to an increase of $0.6 million in finance
income. Adjusted net loss for the nine months ended September 30, 2023 was $13.4 million, a decrease from $14.1 million in the
nine months ended September 30, 2022.
As of September 30, 2023, the Company had $15.9
million in cash, cash equivalents and short-term deposits. In October 2023 the Company raised an additional gross amount of $5 million
which extended the cash runway to the second half of 2025.
During the nine months ended September 30, 2023,
the Company sold, under the Open Market Sale Agreementsm with Jefferies LLC, approximately 1,040 thousand ADSs, at a weighted
average price of $1.499 per ADS. Net proceeds to the Company, were approximately $1.5 million, net of direct issuance expenses.
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 share-based compensation expenses. 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 its 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 NT219, CM24 and IM1240. NT219 is a dual inhibitor, novel small molecule that simultaneously targets IRS1/2 and STAT3. In a Phase
1/2 study of NT219, the Company is currently advancing it in a dose escalation as a monotherapy treatment of solid tumors, and in a dose
escalation in combination with cetuximab for the treatment of recurrent and metastatic squamous cell carcinoma of the head and neck (SCCHN)
or colorectal adenocarcinoma (CRC). These studies will be followed by an expansion phase of NT219 at its recommended Phase 2 level in
combination with cetuximab in patients with recurrent and metastatic SCCHN. CM24 is a humanized monoclonal antibody that blocks CEACAM1,
an immune checkpoint protein that supports tumor immune evasion and survival through multiple 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. IM1240 is a preclinical, conditionally-activated
tri-specific antibody that engages both T cells and NK cells to mount a strong, localized immune response within the tumor microenvironment.
The third arm specifically targets the Tumor Associated Antigen (TAA) 5T4 that is expressed in a variety of solid tumors and is correlated
with advanced disease, increased invasiveness and poor clinical outcomes. IM1240 has a cleavable capping technology that confines the
compound’s therapeutic activity to the local tumor microenvironment, and thereby potentially increases the anticipated therapeutic window
in patients. 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, 2022 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. 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:
Company Contact:
Lior Fhima
Chief Financial Officer
IR@purple-biotech.com
Purple Biotech Ltd.
Consolidated Unaudited Statements of Financial
Position as of:
| |
September 30, | | |
December 31, | |
| |
2023 | | |
2022 | |
| |
USD
thousand | | |
USD
thousand | |
Assets | |
| | |
| |
Cash and cash equivalents | |
| 15,104 | | |
| 15,030 | |
Short term deposits | |
| 842 | | |
| 16,652 | |
Other investments | |
| 138 | | |
| 431 | |
Other current assets | |
| 634 | | |
| 1,143 | |
| |
| | | |
| | |
Total current assets | |
| 16,718 | | |
| 33,256 | |
| |
| | | |
| | |
Non-current assets | |
| | | |
| | |
Right of use assets | |
| 354 | | |
| 467 | |
Fixed assets, net | |
| 156 | | |
| 215 | |
Intangible assets | |
| 28,044 | | |
| 20,684 | |
| |
| | | |
| | |
Total non–current assets | |
| 28,554 | | |
| 21,366 | |
| |
| | | |
| | |
Total assets | |
| 45,272 | | |
| 54,622 | |
| |
| | | |
| | |
Liabilities | |
| | | |
| | |
Lease liability - short term | |
| 178 | | |
| 194 | |
Accounts payable | |
| 2,593 | | |
| 2,132 | |
Other payables | |
| 3,449 | | |
| 4,732 | |
| |
| | | |
| | |
Total current liabilities | |
| 6,220 | | |
| 7,058 | |
| |
| | | |
| | |
Non-current liabilities | |
| | | |
| | |
Lease liability | |
| 192 | | |
| 321 | |
Post-employment benefit liabilities | |
| 141 | | |
| 145 | |
| |
| | | |
| | |
Total non-current liabilities | |
| 333 | | |
| 466 | |
| |
| | | |
| | |
Equity | |
| | | |
| | |
Share capital, no par value | |
| - | | |
| - | |
Share premium | |
| 133,024 | | |
| 126,407 | |
Receipts on account of warrants | |
| 28,017 | | |
| 28,017 | |
Capital reserve for share-based payments | |
| 10,284 | | |
| 10,164 | |
Capital reserve from transactions with related parties | |
| 761 | | |
| 761 | |
Capital reserves from hedging | |
| (2 | ) | |
| (6 | ) |
Capital reserve from transactions with non-controlling interest | |
| (859 | ) | |
| (859 | ) |
Accumulated loss | |
| (132,627 | ) | |
| (117,573 | ) |
| |
| | | |
| | |
Equity attributable to owners of the Company | |
| 38,598 | | |
| 46,911 | |
Non-controlling interests | |
| 121 | | |
| 187 | |
| |
| | | |
| | |
Total equity | |
| 38,719 | | |
| 47,098 | |
| |
| | | |
| | |
Total liabilities and equity | |
| 45,272 | | |
| 54,622 | |
Purple Biotech Ltd.
Consolidated Unaudited Statement of Operations
for the nine and three months ended September 30, 2023
| |
For the nine months ended
September 30, | | |
For the three months ended
September 30, | |
| |
2023 | | |
2022 | | |
2023 | | |
2022 | |
| |
USD
thousand | | |
USD
thousand | | |
USD
thousand | | |
USD
thousand | |
| |
| | |
| | |
| | |
| |
Research and development expenses | |
| 11,792 | | |
| 11,500 | | |
| 4,589 | | |
| 3,465 | |
Sales, general and administrative expenses | |
| 4,212 | | |
| 4,502 | | |
| 1,158 | | |
| 1,616 | |
| |
| | | |
| | | |
| | | |
| | |
Operating loss | |
| 16,004 | | |
| 16,002 | | |
| 5,747 | | |
| 5,081 | |
| |
| | | |
| | | |
| | | |
| | |
Finance expense | |
| 223 | | |
| 108 | | |
| 16 | | |
| 16 | |
Finance income | |
| (1,109 | ) | |
| (393 | ) | |
| (708 | ) | |
| (248 | ) |
| |
| | | |
| | | |
| | | |
| | |
Finance expense (income), net | |
| (886 | ) | |
| (285 | ) | |
| (692 | ) | |
| (232 | ) |
| |
| | | |
| | | |
| | | |
| | |
Loss for the period | |
| 15,118 | | |
| 15,717 | | |
| 5,055 | | |
| 4,849 | |
| |
| | | |
| | | |
| | | |
| | |
Other Comprehensive Loss: | |
| | | |
| | | |
| | | |
| | |
Items that will be transferred to profit or loss: | |
| | | |
| | | |
| | | |
| | |
| |
| | | |
| | | |
| | | |
| | |
Loss (Profit) on cash flow hedges | |
| (4 | ) | |
| 17 | | |
| - | | |
| (4 | ) |
| |
| | | |
| | | |
| | | |
| | |
Total comprehensive loss for the period | |
| 15,114 | | |
| 15,734 | | |
| 5,055 | | |
| 4,845 | |
| |
| | | |
| | | |
| | | |
| | |
Loss attributable to: | |
| | | |
| | | |
| | | |
| | |
Owners of the Company | |
| 15,052 | | |
| 15,657 | | |
| 5,036 | | |
| 4,824 | |
Non-controlling interests | |
| 66 | | |
| 60 | | |
| 19 | | |
| 25 | |
| |
| | | |
| | | |
| | | |
| | |
| |
| 15,118 | | |
| 15,717 | | |
| 5,055 | | |
| 4,849 | |
| |
| | | |
| | | |
| | | |
| | |
Total comprehensive loss attributable to | |
| | | |
| | | |
| | | |
| | |
Owners of the Company | |
| 15,048 | | |
| 15,674 | | |
| 5,036 | | |
| 4,820 | |
Non-controlling interests | |
| 66 | | |
| 60 | | |
| 19 | | |
| 25 | |
| |
| | | |
| | | |
| | | |
| | |
| |
| 15,114 | | |
| 15,734 | | |
| 5,055 | | |
| 4,845 | |
| |
| | | |
| | | |
| | | |
| | |
Loss per share data | |
| | | |
| | | |
| | | |
| | |
Basic and diluted loss per ADS - USD | |
| 0.72 | | |
| 0.87 | | |
| 0.23 | | |
| 0.27 | |
| |
| | | |
| | | |
| | | |
| | |
Number of ADSs used in calculation | |
| 20,901,078 | | |
| 17,977,244 | | |
| 21,836,454 | | |
| 18,073,331 | |
Reconciliation of Adjusted Operating Loss
| |
For the nine months ended
September 30, | | |
For the three months ended
September 30, | |
| |
2023 | | |
2022 | | |
2023 | | |
2022 | |
| |
USD
thousand | | |
USD
thousand | | |
USD
thousand | | |
USD
thousand | |
| |
| | |
| | |
| | |
| |
Operating loss for the period | |
| 16,004 | | |
| 16,002 | | |
| 5,747 | | |
| 5,081 | |
Less ESOP expenses | |
| (1,694 | ) | |
| (1,573 | ) | |
| (449 | ) | |
| (707 | ) |
| |
| 14,310 | | |
| 14,429 | | |
| 5,298 | | |
| 4,374 | |
Reconciliation of Adjusted Net Loss
| |
For the nine months ended
September 30, | | |
For the three months ended
September 30, | |
| |
2023 | | |
2022 | | |
2023 | | |
2022 | |
| |
USD
thousand | | |
USD
thousand | | |
USD
thousand | | |
USD
thousand | |
| |
| | |
| | |
| | |
| |
Loss for the period | |
| 15,118 | | |
| 15,717 | | |
| 5,055 | | |
| 4,849 | |
Less ESOP expenses | |
| (1,694 | ) | |
| (1,573 | ) | |
| (449 | ) | |
| (707 | ) |
| |
| 13,424 | | |
| 14,144 | | |
| 4,606 | | |
| 4,142 | |
Consolidated
Unaudited Statements of Cash Flow
| |
For the nine months ended September 30, | |
| |
2023 | | |
2022 | |
| |
USD thousand | | |
USD thousand | |
Cash flows from operating activities: | |
| | |
| |
Loss for the period | |
| (15,118 | ) | |
| (15,717 | ) |
Adjustments: | |
| | | |
| | |
Depreciation | |
| 149 | | |
| 151 | |
Finance income, net | |
| (886 | ) | |
| (285 | ) |
Share-based payments | |
| 1,694 | | |
| 1,573 | |
| |
| | | |
| | |
| |
| (14,161 | ) | |
| (14,278 | ) |
| |
| | | |
| | |
Changes in assets and liabilities: | |
| | | |
| | |
Changes in other investments and other current assets | |
| 219 | | |
| (124 | ) |
Changes in accounts payables | |
| 415 | | |
| 1,534 | |
Changes in other payables | |
| (1,255 | ) | |
| 495 | |
Changes in post-employment benefit liabilities | |
| (161 | ) | |
| (148 | ) |
| |
| | | |
| | |
| |
| (782 | ) | |
| 1,757 | |
| |
| | | |
| | |
Net cash used in operating activities | |
| (14,943 | ) | |
| (12,521 | ) |
| |
| | | |
| | |
Cash flows from investing activities: | |
| | | |
| | |
Acquisition of subsidiary, net of cash acquired | |
| (3,549 | ) | |
| - | |
Proceed from other investments | |
| 875 | | |
| - | |
Acquisition of intangible asset | |
| - | | |
| (202 | ) |
Interest received | |
| 675 | | |
| 324 | |
Decrease (increase) in short-term deposits | |
| 15,809 | | |
| (2,481 | ) |
Decrease in long-term deposits | |
| - | | |
| 14,300 | |
Acquisition of fixed assets | |
| (3 | ) | |
| (26 | ) |
| |
| | | |
| | |
Net cash provided by investing activities | |
| 13,807 | | |
| 11,915 | |
| |
| | | |
| | |
Cash flows from financing activities: | |
| | | |
| | |
Proceeds from issuance ADSs | |
| 1,559 | | |
| 1,312 | |
ADS issuance expenses paid | |
| (188 | ) | |
| (114 | ) |
Repayment of lease liability | |
| (126 | ) | |
| (124 | ) |
Interest paid | |
| (42 | ) | |
| (49 | ) |
| |
| | | |
| | |
Net cash provided by financing activities | |
| 1,203 | | |
| 1,025 | |
| |
| | | |
| | |
Net increase in cash and cash equivalents | |
| 67 | | |
| 419 | |
Cash and cash equivalents at the beginning of the period | |
| 15,030 | | |
| 10,890 | |
Effect of translation adjustments on cash and cash equivalents | |
| 7 | | |
| (235 | ) |
| |
| | | |
| | |
Cash and cash equivalents at the end of the period | |
| 15,104 | | |
| 11,074 | |
8
Purple Biotech (NASDAQ:PPBT)
過去 株価チャート
から 5 2024 まで 6 2024
Purple Biotech (NASDAQ:PPBT)
過去 株価チャート
から 6 2023 まで 6 2024