Purple Biotech Provides Corporate Update and Reports Second Half and Full Year 2020 Financial Results

Rhea-AI Summary

Purple Biotech (PPBT) announced significant advancements in its anti-cancer therapies and financial results for 2020. Key highlights include the completion of patient recruitment for the NT219 clinical trial and imminent Phase 1b/2 studies for CM24. The company raised $68.5 million in 2020, ending with $60.8 million in cash, sufficient to support operations until 2024. Despite increased R&D expenses leading to a higher operating loss of $12.6 million, cash resources appear robust, supporting ongoing clinical initiatives aimed at improving cancer treatment outcomes.

Positive

• Raised $68.5 million in 2020, ending with $60.8 million in cash.
• Completed patient recruitment for NT219 clinical trial; demonstrated safety.
• Imminent start of Phase 1b/2 studies for CM24.

Negative

• Operating loss increased by 76% to $12.6 million in 2020.
• No revenue growth; revenues remained at $1.0 million for 2020.
• R&D expenses surged by 180% to $7.5 million, impacting profitability.

Rehovot, Israel, March 02, 2021 (GLOBE NEWSWIRE) -- Purple Biotech Ltd. (“Purple Biotech”) (NASDAQ/TASE: PPBT), a clinical-stage company developing first-in-class, effective, and durable therapies by overcoming tumor immune evasion and drug resistance, today provided a corporate update and announced financial results for the six and 12-months ended December 31, 2020.

“We have recently achieved substantial progress in multiple key aspects of our business,” said Isaac Israel, Chief Executive Officer. “Most importantly, our promising anti-cancer product development pipeline continues to advance our Phase 1/2 clinical studies for NT219, a dual inhibitor, novel small molecule targeting IRS1/2 and STAT3. We completed patient recruitment of the second dose level in the single agent dose-escalation phase, demonstrating the drug to be safe and well tolerated in the treated patients. We expect to begin imminently our Phase 1b/2 studies for CM24, our monoclonal antibody drug candidate blocking CEACAM1, a novel immune checkpoint that supports tumor immune evasion and survival through multiple pathways. Our robust clinical development activities are supported by a strong balance sheet, as we raised $68.5 million in 2020, ended the year with $60.8 million in cash, and we believe we are well-funded to support our currently planned corporate initiatives until 2024.”

“As part of the completion of our transformation to a corporate mission dedicated to developing first-in-class oncology therapies, we were honored to ring the Nasdaq stock market opening bell on January 5, 2021 to commemorate the successful evolution of our business and the Company’s name change to Purple Biotech. We are firmly committed to improving the lives of cancer patients globally, and look forward to executing on the opportunities that lie ahead of us in 2021 and beyond,” concluded Mr. Israel.

Recent Corporate Highlights

CM24:

• Expanded the planned Phase 1b/2 clinical trial evaluating CM24 in combination with nivolumab in advanced non-small cell lung cancer (NSCLC) with a new cohort that will evaluate CM24 in combination with both nivolumab and nab-paclitaxel (Abraxane®) in patients with pancreatic cancer under a clinical collaboration agreement with Bristol Myers Squibb.
• Advanced preparations to initiate the Phase 1b/2 study, which is expected to begin imminently. 
• Received notifications from the U.S. Patent and Trademark Office, European Patent Office and the Chinese Patent Office to grant the patent application entitled "Humanized antibodies against CEACAM1," covering the humanized antibodies capable of specific binding to human CEACAM1 molecules, pharmaceutical compositions and methods of their use in treating and diagnosing cancer and other condition. 
• Presented at the American Society of Clinical Oncology (ASCO) 2020 Virtual Scientific Program positive results of a Phase 1 study consisting of a monotherapy dose escalating of CM24, as CM24 was found to be safe and well tolerated in all patients. In the study of efficacy evaluable patients (n=24), subjects were highly refractory to prior therapy, having received between two and eight prior therapies (with a median of four). Eight of the evaluable patients (33%) achieved stable disease, with most of these patients treated at the higher dose levels of 3mg/kg and 10mg/kg.  Pharmacokinetic analysis revealed non-linearity, and modeling suggested that a higher dose level is required to achieve full saturation of CEACAM1 receptors.

NT-219:

• Initiated and dosed the first patient in the Phase 1/2 clinical trial of NT219.
• Presented new data supporting the mechanism of action of NT219 at the Epigenetics and Metabolism AACR Special Virtual Conference by researchers at Tel-Aviv University.
• Received notifications from the U.S. Patent and Trademark Office and the Chinese Patent Office to grant a patent application entitled "Combinations of IRS/STAT3 Dual Modulators and Anti-Cancer Agents for Treating Cancer,” covering the various combinations of NT219 with multiple EGFR inhibitors, including cetuximab (Erbitux®), which will be administrated in combination with NT219 for the treatment of recurrent or metastatic squamous cell carcinoma of the head as well as for neck cancer as part of our ongoing Phase 1/2 study, and osimertinib (TAGRISSO®), a 3^rd generation EGFR inhibitor approved in the U.S. for first-line treatment of EGFR-mutated non-small-cell lung carcinoma (NSCLC).

             
CONSENSI®:

• Growth of sales of Consensi® in the U.S. has been slow primarily due to the COVID-19 environment, with minor sales of the drug in the second half of 2020. In addition, our distribution partner has not fulfilled all of its obligations as per the distribution agreement. We are currently evaluating a re-launch program that will be designed to boost sales and maximize the value of Consensi® post-COVID-19. At this time, we are not able to provide revenue projections for the rest of 2021 and beyond.

Financial Results for the Six Months Ended December 31, 2020
Research and Development Expenses were $4.4 million, an increase of $3.4 million, or 342%, compared to $1.0 million in the same period of 2019. The increase was due to expenses related to the NT219 clinical trials initiated in 2020 and the preparation for the anticipated initiation of the CM24 clinical trials, including manufacturing costs.

Selling, General and Administrative (SG&A) Expenses were $4.1 million, compared to $2.8 million in the same period of 2019, an increase of $1.3 million. The increase was due mainly to a $0.9 million increase in expenses related to stock options granted to directors and employees in the second and third quarters of 2020 and a $0.3 million increase in director and officer insurance expenses.

Operating Loss was $8.3 million, an increase of $4.7 million, or 131%, compared to $3.6 million in the same period of 2019.

On a non-IFRS basis (as reconciled below), adjusted operating loss was $6.4 million, an increase of $3.6 million, compared to $2.8 million in the same period of 2019.

Net Loss for the second half of 2020 was $0.3 million, or $0.48 per diluted share, compared to a net loss of $3.3 million, or $1.70 per diluted share, in the second half of 2019. The decrease in net loss was due to $7.5 million in income from a change in the fair value of derivatives, partially offset by an increase of $4.5 million in operating expenses.

Financial Results for the Full Year Ended December 31, 2020
Revenues were $1.0 million for the year ended December 31, 2020, unchanged from the $1.0 million reported for the year ended December 31, 2019.

Research and Development Expenses were $7.5 million, an increase of $4.8 million, or 180%, compared to $2.7 million for the year ended December 31, 2019. The increase was due to expenses related to the NT219 clinical trials initiated in 2020 and the preparation for the anticipated initiation of the CM24 clinical trials, including manufacturing costs.

SG&A Expenses were $6.3 million, compared to $6.1 million for the year ended December 31, 2019.

Operating Loss was $12.6 million, an increase of $5.5 million, or 76%, compared to $7.2 million for the year ended December 31, 2019.

On a non-IFRS basis (as reconciled below), adjusted operating loss was $10.0 million, compared to $5.9 million, an increase of $4.1 million, for the year ended December 31, 2019.

Net Loss for the year ended December 31, 2020, was $28.1 million, or $2.44 per diluted share, compared to a net loss of $5.9 million, or $3.00 per diluted share, in the same period of 2019. The increase was due to $17.1 million increase in expenses on account of warrants mainly from a change in the fair value of derivatives and an increase of $4.8 million in R&D expenses.

As of December 31, 2020, Purple Biotech had cash and cash equivalents and short- and long-term deposits of $60.8 million, compared to $4.4 million at December 31, 2019. Purple Biotech believes that its cash position will provide sufficient resources for its currently anticipated ongoing needs until fiscal year 2024.

About Purple Biotech
Purple Biotech Ltd. (the “Company”; NASDAQ/TASE: PPBT) is a clinical-stage company focusing on advancing first-in-class therapies to overcome tumor immune evasion and drug resistance in order to create successful long-lasting treatments for people with cancer. The Company’s oncology pipeline includes NT219 and CM24. NT219 is a small molecule targeting the novel cancer drug resistance pathways IRS1/2 and STAT3. The Company is currently advancing NT219 as a monotherapy treatment of advanced solid tumors and in combination with cetuximab for the treatment of recurrent or metastatic squamous cell carcinoma of head and neck cancer (SCCHN) in a phase 1/2 study. CM24 is a monoclonal antibody blocking CEACAM1, a novel immune checkpoint that supports tumor immune evasion and survival through multiple pathways. The Company plans to advance CM24 as a combination therapy with anti-PD-1 checkpoint inhibitors in selected cancer indications in a phase 1 study followed by a phase 2 for the treatment of non-small cell lung cancer and pancreatic cancer. The Company has entered into a clinical collaboration agreement, as amended, with Bristol Myers Squibb for the planned phase 1/2 clinical trials to evaluate the combination of CM24 with the PD-1 inhibitor nivolumab (Opdivo®) in patients with non-small cell lung cancer and in combination with nivolumab in addition to nab-paclitaxel (ABRAXANE®) in patients with pancreatic cancer. The Company is also the owner of Consensi®, a fixed-dose combination of celecoxib and amlodipine besylate, for the simultaneous treatment of osteoarthritis pain and hypertension that was approved by the FDA for marketing in the U.S. Consensi® is being sold in the U.S. by Burke Therapeutics, the marketing partner of the Company’s U.S. distributor, Coeptis Pharmaceuticals. The Company has also partnered to commercialize Consensi in China and South Korea. The Company has recently relocated its corporate headquarters to Rehovot, Israel. For more information, please visit http://www.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 and CM24; the process by which early stage therapeutic candidates such as NT219 and CM24 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, 2019 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 Securities and Exchange Commission, which are available on the SEC's website, http://www.sec.gov.

Company Contact:
Gil Efron
Deputy CEO & Chief Financial Officer
IR@ purple-biotech.com

Investor Relations Contact:
Chuck Padala
chuck@lifesciadvisors.com
+1 646-627-8390

Purple Biotech Ltd

Consolidated Unaudited Statements of Financial Position

		As of December 31,
		2020				2019
		USD thousands				USD thousands
Assets
Cash and cash equivalents			11,247				4,385
Short term deposits			46,558				10
Trade receivables			500				-
Financial assets			-				2,000
Other current assets			977				1,907
Total current assets			59,282				8,302
Non-current assets
Right to use assets			790				206
Fixed assets, net			178				38
Long term deposits			3,071				-
Intangible assets			20,482				6,172
Total assets			83,803				14,718
Liabilities
Lease liability – short term			207				195
Accounts payable			1,198				1,245
Other payables			1,693				2,106
Total current liabilities			3,098				3,546
Non-current liabilities
Lease liability			688				28
Post-employment benefit liabilities			265				285
Total non–current liabilities			953				313
Equity
Share capital, no par value			-				-
Share premium			118,909				46,986
Receipts on account of warrants			29,984				9,874
Capital reserve for share-based payments			8,115				3,181
Capital reserve from transactions with related parties			761				761
Capital reserve from transactions with non- controlling interest			(859	)			(859	)
Accumulated loss			(77,521	)			(49,522	)
Equity attributable to owners of the Company			79,389				10,421
Non-controlling interests			363				438
Total equity			79,752				10,859
Total liabilities and equity			83,803				14,718

Purple Biotech Ltd.

Consolidated Unaudited Statements of Operations

 

		For the year ended December 31,								For the six months ended December 31,
		2020				2019				2020				2019
		USD thousands				USD thousands				USD thousands				USD thousands
Revenues			1,000				1,000				-				-
Research and development expenses			7,488				2,674				4,355				986
Sales, general and administrative expenses			6,306				6,078				4,072				2,773
Reimbursement of legal fees			(182	)			(596	)			(117	)			(166	)
Total operating expenses			13,612				8,156				8,310				3,593
Operating loss			12,612				7,156				8,310				3,593
Expenses (income) on account of warrants			15,655				(1,509	)			(7,928	)			(517	)
Finance expenses			61				181				46				73
Finance income			(254	)			(151	)			(170	)			(78	)
Finance expenses (income), net			15,462				(1,479	)			(8,052	)			(522	)
Tax expenses			-				216				-				216
Loss for the year			28,074				5,893				258				3,287
Loss attributable to:
Owners of the Company			27,999				5,850				220				3,275
Non-controlling interests			75				43				38				12
			28,074				5,893				258				3,287
Loss per share data
Basic loss per ADS – USD			2.44				3.00	(*)			0.02				1.70	(*)
Diluted loss per ADS – USD			2.44				3.00	(*)			0.48				1.70	(*)
Number of shares used in calculating basic loss per ADS			11,500,113				1,936,778	(*)			16,928,162				1,954,866	(*)
Number of shares used in calculating diluted loss per ADS			11,500,113				1,936,778	(*)			17,160,018				1,954,866	(*)

(*) Restated to reflect a 1:10 reverse ratio of the ADSs, that took place in August 2020.

Purple Biotech Ltd.

Consolidated Unaudited Statements of Cash Flow

		For the year ended December 31,								For the six months ended December 31,
		2020				2019				2020				2019
		USD thousands				USD thousands				USD thousands				USD thousands
Cash flows from operating activities:
Loss for the period			(28,074	)			(5,893	)			(258	)			(3,287	)
Adjustments:
Depreciation			235				178				143				84
Finance expense (income), net			15,462				(1,479	)			(8,052	)			(522	)
Share-based payments			2,645				1,273				1,895				773
			(9,732	)			(5,921	)			(6,272	)			(2,952	)
Changes in assets and liabilities:
Changes in trade receivables and other current assets			501				62				880				(891	)
Changes in accounts payable			(2,330	)			503				(1,437	)			361
Changes in other payables			(511	)			(77	)			(641	)			149
Changes in post-employment benefit liabilities			(20	)			(148	)			19				22
			(2,360	)			340				(1,179	)			(359	)
Net cash used in operating activities			(12,092	)			(5,581	)			(7,451	)			(3,311	)
Cash flows from investing activities:
Cash assumed as part of acquisition of FameWave			69				-				-				-
Investment in financial asset			-				(2,100	)			-				(100	)
Decrease (increase) in deposits			(49,618	)			1,511				(49,618	)			5,011
Interest received			110				151				71				121
Acquisition of fixed assets			(156	)			(11	)			(156	)			(3	)
Net cash provided by (used in) investing activities			(49,595	)			(449	)			(49,703	)			5,029
Cash flows from financing activities:
Proceeds from issuance of ADSs			27,925				2,594				-				-
ADS issuance expenses paid			(2,074	)			(264	)			(34	)			-
Proceeds from issuance of warrants			26,574				3,406				-				-
Warrants issuance expenses paid			(3,281	)			(347	)			150				-
Proceeds from exercise of warrants			19,547				43				5,627				-
Repayment of lease liability			(188	)			(171	)			(108	)			(82	)
Interest paid			(15	)			(28	)			(4	)			(14	)
Net cash provided by (used in) financing activities			68,488				5,233				5,331				(96	)
Net increase (decrease) in cash and cash equivalents			6,801				(797	)			(51,823	)			1,622
Cash and cash equivalents at the beginning of the period			4,385				5,163				62,995				2,757
Effect of translation adjustments on cash and cash equivalents			61				19				75				6
Cash and cash equivalents at end of the period			11,247				4,385				11,247				4,385

Purple Biotech Ltd. Reconciliation of Non-IFRS Financial Results

Reconciliation of Adjusted Operating Loss

		For the year ended December 31,								For the six months ended December 31,
		2020				2019				2020				2019
		USD thousands				USD thousands				USD thousands				USD thousands
Operating loss for the year			12,612				7,156				8,310				3,593
Less ESOP expenses			(2,645	)			(1,273	)			(1,895	)			(773	)
			9,967				5,883				6,415				2,820

FAQ

What were the financial results of Purple Biotech for 2020?

Purple Biotech reported $1.0 million in revenues for 2020, an unchanged figure from 2019. The net loss was $28.1 million, or $2.44 per diluted share.

What clinical trials are currently underway for Purple Biotech's products?

Purple Biotech is advancing Phase 1/2 clinical studies for NT219 and plans to initiate Phase 1b/2 studies for CM24 imminently.

How much cash does Purple Biotech have as of December 31, 2020?

As of December 31, 2020, Purple Biotech had $60.8 million in cash, expected to support operations until 2024.

What are the key developments in Purple Biotech's product pipeline?

Key developments include the recruitment completion for NT219 trials and an expanded clinical trial for CM24 in combination with nivolumab and nab-paclitaxel.