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Progenity Provides Corporate Updates and Reports Fourth Quarter and Full-Year 2020 Financial Results

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Progenity reported approximately 82,000 tests in Q4 2020, generating $14.3 million in revenue, down from $25.9 million in Q3. The company raised $118 million in December 2020 through equity offerings and private placements. Despite reduced test volumes due to COVID-19, Progenity maintained its 2021 revenue guidance. The company achieved key milestones in its innovation pipeline, including validation for its Preecludia™ test. However, it faced a net loss of $75.5 million for the quarter and a gross margin of -50.1%. The management emphasized efforts to stabilize and grow its core testing business.

Positive
  • Raised $118 million in gross proceeds from equity offerings and private placements.
  • Achieved analytical and clinical verification for the Preecludia™ test.
  • Maintained 2021 revenue guidance despite challenges.
Negative
  • Revenue declined to $14.3 million in Q4 2020 from $25.9 million in Q3 2020.
  • Net loss increased to $75.5 million in Q4 2020 compared to $47.1 million in Q3 2020.
  • Gross margin was -50.1%, significantly down from 9.0% in Q3 2020.

Reports approximately 82,000 tests in the fourth quarter of 2020

Raised $118M gross proceeds in December 2020 from a concurrent secondary equity offering and issuance of convertible notes, and $25M in gross proceeds from a recent private placement with two leading healthcare-focused investment funds

Maintains 2021 revenue guidance range

Management will host conference call and webcast today at 4:30 p.m. ET/1:30 p.m. PT

SAN DIEGO, March 18, 2021 (GLOBE NEWSWIRE) -- Progenity, Inc. (Nasdaq: PROG), a biotechnology company with an established track record of success in developing and commercializing molecular testing products, today provided corporate updates and reported financial results for the fourth quarter and full-year ended December 31, 2020.

Progenity made significant progress during the fourth quarter, both with its revenue generating business and notably with its innovation pipeline programs. The company continued to transition its core molecular testing business towards growth, increased its in-network position by adding national and regional contracts, and saw additional commercial and government payors covering average risk NIPT.

Regarding its innovation pipeline programs, the company announced it successfully achieved the analytical and clinical verification milestone during the fourth quarter for its Preecludia™ preeclampsia rule-out test and has since initiated validation phase sample testing.

“We continue to make progress in establishing a strong foundation and stabilizing our core molecular testing business. We anticipate these efforts will translate into improved operating performance and near-term growth, consistent with our 2021 guidance. We also recently secured funding from leading healthcare-focused investment funds, allowing us to expand our investor base. We are particularly excited with the progress and potential of our R&D pipeline which includes completing our Preecludia™ test’s verification milestone and initiating the validation phase, advancing the Innatal 4 platform, and accelerating progress of our GI Precision Medicine programs,” said Harry Stylli, Ph.D., CEO, chairman of the board, and co-founder of Progenity.

Fourth Quarter 2020 Results and Other Corporate Highlights

  • Reported approximately 82,000 tests in the fourth quarter, including 56,000 core molecular tests and 26,000 COVID-19 tests.

  • Issued $168.5 million principal amount of 7.25% convertible senior notes due 2025 for gross proceeds of approximately $90.0 million and an additional $78.5 million principal amount of notes issued in exchange for the discharge of amounts outstanding under an existing credit and security agreement with entities affiliated with Athyrium Capital Management, LP.

  • Completed a concurrent underwritten secondary offering of common stock and issued approximately 8.8 million shares for gross proceeds of approximately $28.8 million.

  • In February 2021, raised approximately $25.0 million in gross proceeds from a private placement of approximately of 4.4 million shares of common stock and warrants to purchase an additional 4.4 million shares of common stock with two leading healthcare-focused investment funds.

  • Completed reduction in force, which resulted in the termination of approximately 9.5% of the Company’s employees, to enable the Company to control its costs and more effectively align resources to business priorities. 

  • Increased in-network covered lives by up to 60 million with the addition of the MultiPlan national contract and added 1 million lives from additional regional payors.

  • Initiated validation phase for its Preecludia™ preeclampsia test, after successfully completing analytical and clinical verification.

  • Announced encouraging preclinical data supporting the potential of the Company’s oral drug delivery system (DDS) using a proprietary autonomous localization technology designed to identify a key region of the GI tract for drug delivery.

  • Presented data from an award-winning abstract on a novel ingestible lab-in-a-capsule, PIL Dx, at the American College of Gastroenterology (ACG) 2020 Virtual Annual Meeting. The data in the presentation demonstrated the achievement of critical de-risking steps and Progenity’s progress toward novel approaches for the assessment, diagnosis, and future treatment of gastrointestinal diseases through ingestible capsule devices.

Fourth Quarter and Full-Year 2020 Financial Results

Comparison of Three Months Ended December 31, 2020 and September 30, 2020

Revenue was $14.3 million in the three months ended December 31, 2020, compared to $25.9 million in the three months ended September 30, 2020. The fourth quarter revenue includes a $10.7 million accrual as a reserve for potential payor settlements, as previously announced.

Total accessioned tests volume, which includes the company’s core molecular testing and COVID-19 testing, was 81,640 in the fourth quarter of 2020, a decrease of 3% compared to accessioned tests volume in the third quarter of 2020, which was 84,067 tests.

Gross margin was negative 50.1% for the three months ended December 31, 2020, as a result of accruals against revenue, compared to 9.0% for the three months ended September 30, 2020.

Operating expenses were $44.2 million for the three months ended December 31, 2020, compared to $46.9 million for the three months ended September 30, 2020.

Net loss attributable to common stockholders was $75.5 million for the three months ended December 31, 2020 and basic and diluted net loss per share was $1.53, compared to a net loss attributable to common stockholders of $47.1 million and a net loss per share of $1.01 for the three months ended September 30, 2020.

Comparison of Three Months Ended December 31, 2020 and 2019

Revenue was $14.3 million in the three months ended December 31, 2020, compared to $20.5 million in the three months ended December 31, 2019. The decrease in revenue was primarily attributable to a decrease in test volumes in 2020 as a result of the COVID-19 pandemic, partially offset by a decrease, as compared to the prior period, of $9.2 million in payor settlement reserves and accruals.

Gross margin was negative 50.1% for the three months ended December 31, 2020, as a result of accruals against revenue, compared to negative 21.9% for the three months ended December 31, 2019.

Operating expenses were $44.2 million for the three months ended December 31, 2020, compared to $44.5 million in the three months ended December 31, 2019.

Net loss attributable to common stockholders was $75.5 million for the three months ended December 31, 2020 and basic and diluted net loss per share was $1.53, compared to a net loss attributable to common stockholders of $86.8 million and a net loss per share of $17.46 for the three months ended December 31, 2019.

Comparison of Full-Year Ended December 31, 2020 and 2019

Revenue was $74.3 million in the year ended December 31, 2020, compared to $144.0 million in the year ended December 31, 2019. The decrease in revenues was largely attributable to a decrease in test volumes as a result of the COVID-19 pandemic during the second, third and fourth quarters of 2020, partially offset by a decrease, as compared to the prior period, of $6.2 million in payor settlement reserves and accruals.

Gross margin was negative 25.7% for the year ended December 31, 2020, compared to 30.2% for the year ended December 31, 2019.

Operating expenses were $176.1 million for the year ended December 31, 2020, compared to $183.6 million in the year ended December 31, 2019.

Net loss attributable to common stockholders was $192.8 million for the year ended December 31, 2020 and basic and diluted net loss per share was $7.01, compared to a net loss attributable to common stockholders of $228.8 million and a net loss per share of $46.87 for the year ended December 31, 2019.

Cash and cash equivalents were $92.1 million as of December 31, 2020. As of December 31, 2020, Progenity had 55.8 million shares outstanding, excluding shares issued in our recent private placement.

COVID-19 Update

Public health measures related to the novel coronavirus are greatly impacting healthcare practices. We have responded to the COVID-19 pandemic by implementing and maintaining robust response plans, seamlessly continuing laboratory operations and maintaining pre-pandemic turnaround times. We enhanced our digital sales and support capabilities, increased proactive test reporting and remote genetic counseling capabilities, and expanded our mobile phlebotomy services, assisting our customers to continue serving their patients with the same quality care.

Webcast and Conference Call Information

Progenity will host a webcast and conference call to discuss the second quarter financial results and answer investment community questions today, Thursday, March 18, 2021 at 4:30 p.m. ET / 1:30 p.m. PT. The live call may be accessed by dialing 833-519-1237 for domestic callers and 914-800-3810 for international callers and entering the conference code: 9677695. A live webcast and archive of the call will be available online from the investor relations section of the company website at www.progenity.com.

About Progenity

Progenity, Inc. is a biotechnology company with an established track record of success in developing and commercializing molecular testing products, as well as innovating in the field of precision medicine. Progenity provides in vitro molecular tests designed to improve lives by providing actionable information that helps guide patients and physicians in making medical decisions during key life stages. The company applies a multi-omics approach, combining genomics, epigenomics, proteomics, and metabolomics to its molecular testing products and to the development of a suite of investigational ingestible devices designed to provide precise diagnostic sampling and drug delivery solutions. Progenity’s vision is to transform healthcare to become more precise and personal by improving diagnoses of disease and improving patient outcomes through localized treatment with targeted therapies. For additional information about Progenity, please visit the company’s website at www.progenity.com.

Safe Harbor Statement or Forward-Looking Statements

This press release contains “forward-looking statements” within the meaning of the “safe harbor” provisions of the Private Securities Litigation Reform Act of 1995, which statements are subject to substantial risks and uncertainties and are based on estimates and assumptions. All statements, other than statements of historical facts included in this press release, including statements concerning the impact of the COVID-19 pandemic on our business, operations, financial results, and future performance, and the progress of our research and development efforts are forward-looking statements. In some cases, you can identify forward-looking statements by terms such as “may,” “might,” “will,” “objective,” “intend,” “should,” “could,” “can,” “would,” “expect,” “believe,” “design,” “estimate,” “predict,” “potential,” “plan” or the negative of these terms, and similar expressions intended to identify forward-looking statements. These statements reflect our plans, estimates, and expectations, as of the date of this press release. These statements involve known and unknown risks, uncertainties and other factors that could cause our actual results to differ materially from the forward-looking statements expressed or implied in this press release. Such risks, uncertainties, and other factors include, among others, the ongoing COVID-19 pandemic, our ability to develop and commercialize our testing products as well as innovate in the field of precision medicine, our ability to obtain and maintain regulatory approval or clearance of our products on expected timelines or at all, our plans to research, develop, and commercialize new products, the unpredictable relationship between preclinical study results and clinical study results, our expectations regarding future test volumes and revenues, our expectations regarding our in network position, anticipated capacity for our tests, and those risks described in “Risk Factors” and “Management’s Discussion and Analysis of Financial Condition and Results of Operations” in Progenity’s Annual Report on Form 10-K for the year ended December 31, 2020 to be filed with the SEC and other subsequent documents we file with the SEC.

Progenity expressly disclaims any obligation to update any forward-looking statements whether as a result of new information, future events or otherwise, except as required by law.

Investor Contact:
Robert Uhl
Managing Director, Westwicke ICR
ir@progenity.com
(619) 228-5886

Media Contact:
Kate Blom-Lowery
CG Life
kblomlowery@cglife.com
(858) 457-2436


Progenity, Inc.
Condensed Consolidated Statements of Operations
(Unaudited)
(In thousands, except share and per share amounts)

  Three Months Ended 
  December 31,
2020
  September 30,
2020
 
Revenues (1) $14,276  $25,943 
Cost of sales  21,427   23,601 
Gross profit (loss)  (7,151)  2,342 
Operating expenses:        
Research and development  11,226   13,043 
Selling and marketing  12,471   13,244 
General and administrative  20,523   20,626 
Total operating expenses  44,220   46,913 
Loss from operations  (51,371)  (44,571)
Interest expense  (2,699)  (2,476)
Interest and other income (expense), net  (21,294)  (18)
Loss before income taxes  (75,364)  (47,065)
Income tax expense  164    
Net loss  (75,528)  (47,065)
Dividend paid to preferred stockholders      
Net loss attributable to common stockholders $(75,528) $(47,065)
Net loss per share attributable to common stockholders, basic and diluted $(1.53) $(1.01)
Weighted average number of shares outstanding used in calculating net loss per share attributable to common stockholders, basic and diluted  49,288,579   46,632,043 

__________________

(1)Revenues for the three months ended December 31, 2020 reflect an accrual of $10.7 million recorded as a reserve for potential payor settlements.


Progenity, Inc.
Condensed Consolidated Statements of Operations
(Unaudited)
(In thousands, except share and per share amounts)

  Three Months Ended
December 31,
  Year Ended
December 31,
 
  2020  2019  2020  2019 
          (1)  (1) 
Revenues (2) $14,276  $20,476  $74,313  $143,985 
Cost of Sales  21,427   24,961   93,433   100,492 
Gross profit (loss)  (7,151)  (4,485)  (19,120)  43,493 
Operating Expenses:                
Research and development  11,226   14,609   47,743   63,400 
Selling and marketing  12,471   13,378   52,887   58,888 
General and administrative  20,523   16,501   75,438   61,324 
Total operating expenses  44,220   44,488   176,068   183,612 
Loss from operations  (51,371)  (48,973)  (195,188)  (140,119)
Interest expense  (2,699)  (2,327)  (9,984)  (9,199)
Interest and other income (expense), net  (21,294)  118   (24,888)  575 
Loss before income taxes  (75,364)  (51,182)  (230,060)  (148,743)
Income tax expense (benefit)  164   (706)  (37,532)  (706)
Net loss  (75,528)  (50,476)  (192,528)  (148,037)
Dividend paid to preferred shareholders        (268)  (3,652)
Stock dividend on exchange of Series A-1 to Series B Preferred Stock           (27,637)
Stock dividend on Series B Preferred Stock     (36,364)     (49,501)
Net loss attributable to common shareholders $(75,528) $(86,840) $(192,796) $(228,827)
Net loss per share attributable to common shareholders, basic and diluted $(1.53) $(17.46) $(7.01) $(46.87)
Weighted average number of shares outstanding used in calculating net loss per share, basic and diluted  49,288,579  4,974,825   27,512,876   4,882,662 

__________________

(1)The condensed consolidated statement of operations data for the year ended December 31, 2020 and 2019 has been derived from the audited consolidated financial statements.
  
(2)Revenues for the three months ended December 31, 2020 reflect a revenue reserve accrual of $10.7 million recorded for payor settlements. Revenues for the three months ended December 31, 2019 reflect an accrual of $19.9 million related to the settlements with the Department of Justice (DOJ) and the participating State Attorneys General (AGs).
  
 Revenues for the year ended December 31, 2020 reflect an aggregate revenue reserve accrual of $33.5 million related to the settlement with the DOJ and the participating State AGs and other payors settlements. Revenues for the year ended December 31, 2019 reflect a $39.7 million aggregate revenue reserve accrual related to the settlements with the DOJ and the participating State AGs and reimbursement claims and settlements with other payors.


Progenity, Inc.
Condensed Consolidated Balance Sheets
(Unaudited)
(In thousands)

  December 31,
2020
  December 31,
2019
 
  (1)  (1) 
Assets        
Current assets:        
Cash and cash equivalents $92,076  $33,042 
Accounts receivable, net  12,682   22,189 
Inventory  12,219   10,937 
Income tax receivable     634 
Prepaid expenses and other current assets  9,361   7,846 
Total current assets  126,338   74,648 
Property and equipment, net  17,842   15,891 
Goodwill and other intangible assets  10,062   10,990 
Other assets  198   198 
Total assets $154,440  $101,727 
Liabilities and Stockholders' Deficit        
Current liabilities:        
Accounts payable $17,410  $15,754 
Accrued expenses and other current liabilities  54,677   83,615 
Current portion of mortgages payable and capital lease obligations  583   968 
Total current liabilities  72,670   100,337 
Mortgages payable and capital lease obligations, net of current portion  2,841   3,439 
Convertible notes, net  158,886    
Note payable to related party, net     68,966 
Embedded derivative liability  18,370    
Other long-term liabilities  8,667   12,859 
Total liabilities $261,434  $185,601 
Stockholders' deficit:        
Common stock  59   9 
Series A Preferred Stock     4 
Series B Preferred Stock     102 
Additional paid-in capital  452,992   283,260 
Accumulated deficit  (541,274)  (348,478)
Treasury stock  (18,771)  (18,771)
Total stockholders' deficit  (106,994)  (83,874)
Total liabilities and stockholders' deficit $154,440  $101,727 

____________

(1)The condensed consolidated balance sheet data at December 31, 2020 and 2019 has been derived from the audited consolidated financial statements.

FAQ

What were the financial results for Progenity in Q4 2020?

Progenity reported $14.3 million in revenue for Q4 2020, down from $25.9 million in Q3 2020, with a net loss of $75.5 million.

How many tests did Progenity perform in the fourth quarter of 2020?

Progenity performed approximately 82,000 tests in Q4 2020, including 56,000 core molecular tests and 26,000 COVID-19 tests.

What is Progenity's revenue guidance for 2021?

Progenity has maintained its revenue guidance for 2021 despite the challenges faced in 2020.

What funding did Progenity secure in December 2020?

Progenity raised $118 million in gross proceeds from a concurrent secondary equity offering and the issuance of convertible notes.

What milestones has Progenity achieved in its innovation pipeline?

Progenity achieved the analytical and clinical verification milestone for its Preecludia™ test and initiated validation phase sample testing.

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