Purple Biotech Reports Third Quarter 2024 Financial Results
Purple Biotech (NASDAQ/TASE: PPBT) reported Q3 2024 financial results and clinical updates. The company expects topline data from Phase 2 CM24 pancreatic cancer trial by end of 2024. New biomarker data showed patients with specific serum CEACAM1 levels demonstrated 79% reduction in death risk. Q3 financial highlights include reduced R&D expenses to $1.3M (71.7% decrease), operating loss of $2.1M (63.2% decrease), and net loss of $0.7M. Cash position stands at $6.3M with runway extending into Q4 2025. The company plans to commence Phase 2 study of NT219 in head and neck cancer in H1 2025.
Purple Biotech (NASDAQ/TASE: PPBT) ha riportato i risultati finanziari e gli aggiornamenti clinici del terzo trimestre del 2024. L'azienda si aspetta dati preliminari dal trial di fase 2 su CM24 per il cancro al pancreas entro la fine del 2024. Nuovi dati sui biomarcatori hanno mostrato che i pazienti con specifici livelli di CEACAM1 nel siero hanno dimostrato una riduzione del rischio di morte del 79%. I punti salienti finanziari del terzo trimestre includono una riduzione delle spese per R&S a 1,3 milioni di dollari (decremento del 71,7%), una perdita operativa di 2,1 milioni di dollari (decremento del 63,2%) e una perdita netta di 0,7 milioni di dollari. La posizione di cassa è di 6,3 milioni di dollari, con un finanziamento che si estende fino al quarto trimestre del 2025. L'azienda prevede di avviare lo studio di fase 2 su NT219 nel cancro testa-collo nel primo semestre del 2025.
Purple Biotech (NASDAQ/TASE: PPBT) reportó los resultados financieros y las actualizaciones clínicas del tercer trimestre de 2024. La compañía espera datos preliminares del ensayo de fase 2 de CM24 para el cáncer de páncreas para finales de 2024. Nuevos datos de biomarcadores mostraron que los pacientes con niveles específicos de CEACAM1 en suero demostraron una reducción del riesgo de muerte del 79%. Los aspectos financieros destacados del tercer trimestre incluyen una reducción de gastos de I+D a 1,3 millones de dólares (una disminución del 71,7%), una pérdida operativa de 2,1 millones de dólares (una disminución del 63,2%) y una pérdida neta de 0,7 millones de dólares. La posición de efectivo se sitúa en 6,3 millones de dólares, con un tiempo de ejecución que se extiende hasta el cuarto trimestre de 2025. La compañía planea comenzar el estudio de fase 2 de NT219 en cáncer de cabeza y cuello en el primer semestre de 2025.
퍼플 바이오텍 (NASDAQ/TASE: PPBT)는 2024년 3분기 재무 결과 및 임상 업데이트를 보고했습니다. 이 회사는 2024년 말까지 췌장암 임상 시험인 CM24의 2상 데이터가 발표될 것으로 예상하고 있습니다. 새로운 바이오마커 데이터에 따르면, 특정 혈청 CEACAM1 수준을 가진 환자들이 사망 위험이 79% 감소한 것으로 나타났습니다. 3분기 재무 하이라이트에는 130만 달러로 감소한 연구 개발 비용(71.7% 감소), 210만 달러의 운영 손실(63.2% 감소), 70만 달러의 순손실이 포함됩니다. 현재 현금 보유액은 630만 달러이며, 자금은 2025년 4분기까지 연장됩니다. 이 회사는 2025년 상반기에 NT219의 두경부암 2상 연구를 시작할 계획입니다.
Purple Biotech (NASDAQ/TASE: PPBT) a rapporté les résultats financiers et les mises à jour cliniques du troisième trimestre 2024. L'entreprise s'attend à des données préliminaires de l'essai de phase 2 sur le CM24 pour le cancer du pancréas d'ici la fin de 2024. De nouvelles données sur les biomarqueurs ont montré que les patients avec des niveaux spécifiques de CEACAM1 dans le sérum ont présenté une réduction du risque de décès de 79 %. Les points forts financiers du troisième trimestre comprennent une réduction des dépenses en R&D à 1,3 million de dollars (baisse de 71,7 %), une perte opérationnelle de 2,1 millions de dollars (baisse de 63,2 %) et une perte nette de 0,7 million de dollars. La position de liquidités s'élève à 6,3 millions de dollars, avec une marge de manœuvre s'étendant jusqu'au quatrième trimestre 2025. L'entreprise prévoit de commencer l'étude de phase 2 sur NT219 dans le cancer de la tête et du cou au premier semestre 2025.
Purple Biotech (NASDAQ/TASE: PPBT) hat die Finanzberichte und klinischen Updates für das dritte Quartal 2024 veröffentlicht. Das Unternehmen erwartet bis Ende 2024 erste Daten aus der Phase-2-Studie zu CM24 bei Bauchspeicheldrüsenkrebs. Neue Biomarkerdaten zeigten, dass Patienten mit spezifischen CEACAM1-Spiegeln im Serum ein um 79 % reduziertes Sterberisiko aufwiesen. Zu den finanziellen Höhepunkten des dritten Quartals gehören reduzierte F&E-Ausgaben von 1,3 Millionen US-Dollar (71,7 % Rückgang), ein operativer Verlust von 2,1 Millionen US-Dollar (63,2 % Rückgang) und ein Nettovolumen von 0,7 Millionen US-Dollar. Die Barreserven belaufen sich auf 6,3 Millionen US-Dollar, mit einem Liquiditätsbedarf, der bis ins vierte Quartal 2025 reicht. Das Unternehmen plant, im 1. Halbjahr 2025 die Phase-2-Studie zu NT219 bei Kopf- und Halskrebs zu beginnen.
- Significant reduction in operating loss by 63.2% to $2.1M
- R&D expenses decreased by 71.7% to $1.3M
- Net loss decreased to $0.7M from $5M year-over-year
- Biomarker data showed 79% reduction in death risk for specific patient group
- Cash runway extended into Q4 2025
- Cash position relatively low at $6.3M
- Ongoing share dilution through Open Market Sale Agreement
- Gemcitabine/nab-paclitaxel study arm rendered unsuitable for analysis due to control arm issues
Insights
Purple Biotech's Q3 results show significant financial improvements, with operating loss decreasing by
The Phase 2 CM24 pancreatic cancer trial shows promising biomarker data, with serum CEACAM1 levels between 6K-15K pg/mL demonstrating significant clinical benefits. Key findings include a
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, Nov. 15, 2024 (GLOBE NEWSWIRE) -- 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:
- 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
- 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
- The results presented in the poster propose NETs as a novel mechanism of action and a potential biomarker for CM24-based therapy
- 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
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.
- Median progression free survival (PFS) of this group was 4.6 months (hazard ratio [HR] < 0.1, P = 0.003)
- Risk of death was reduced by
79% (HR = 0.21, P = 0.04)
- 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
Sales, General and Administrative Expenses were
Operating Loss was
Adjusted Operating Loss (as reconciled below) was
Net Loss for the three months ended September 30, 2024, was
Adjusted Net Loss (as reconciled below) for the three months ended September 30, 2024, was
As of September 30, 2024, Purple Biotech had cash and cash equivalents and short-term deposits of
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
Financial Results for the Nine Months Ended September 30, 2024
Research and Development Expenses were
Sales, General and Administrative Expenses were
Operating Loss was
Adjusted Operating Loss (as reconciled below) was
Net Loss for the nine months ended September 30, 2024 was
Adjusted net loss (as reconciled below) for the nine months ended September 30, 2024 was
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:
| 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 | |||
FAQ
What were Purple Biotech's (PPBT) key financial results for Q3 2024?
When will Purple Biotech (PPBT) report topline data from its CM24 pancreatic cancer trial?
What is Purple Biotech's (PPBT) cash position as of Q3 2024?
What were the biomarker results for CM24 in pancreatic cancer patients?
