AnPac Bio Reports Strong First Quarter in 2021, with 137.2% Increase in Revenue and Record Number of Commercial Tests Completed

PHILADELPHIA, May 27, 2021 (GLOBE NEWSWIRE) — AnPac Bio-Medical Science Co., Ltd. (“AnPac Bio,” the “Company” or “we”) (NASDAQ: ANPC), a biotechnology company with operations in China and the United States, announced today its unaudited financial results for the first quarter ended March 31, 2021. The Company’s financial statements and related financial information for the quarter ended March 31, 2021 are unaudited or have not been reviewed by the Company’s independent registered accountant.  These financial results could differ materially if they were reviewed by the Company’s independent registered accountant.


Financial highlights for the First Quarter 2021

  • Total revenue was RMB2.2 million (US$0.3 million) for the first quarter of 2021, an increase of 137.2% from RMB0.9 million for the first quarter of 2020.

  • Gross profit margin was 58.4% for the first quarter of 2021, representing an increase of 25.7 % from 32.7% for the first quarter of 2020, primarily due to higher selling prices charged for CDA-based tests and improved operational efficiency as well as higher volume of CDA-based tests performed during the first quarter of 2021.

  • The average selling price (“ASP”) of CDA-based tests was RMB401.0(US$61.2) for the first quarter of 2021, an increase of RMB20.0, or 5.0% from RMB381.0 in the same period of 2020, primarily due to a broader product offering of more comprehensive multi-cancer detection tests at higher price points.

  • Net loss was RMB29.3 million (US$4.5 million) for the first quarter of 2021, compared to a net loss of RMB21.2 million for the first quarter of 2020. The net loss for the first quarter of 2021 was mainly attributable to RMB3.2 million (US$0.5 million) changes in the fair value of the convertible debts, RMB3.9 million (US$0.6 million) of selling and marketing expenses, RMB3.4 million (US$0.5 million) of research and development expenses and RMB 19.2 million (US$2.9 million) of general and administrative expenses.

  • Short-term debt was RMB22.4 million (US$3.4 million) as of March 31, 2021, an increase of 171.9% from RMB8.2 million at the end of last fiscal year (December 31, 2020). The increase in short-term debt was mainly due to issuance of additional convertible debentures with a fair value of USD$2.5 million.

    • As of March 31, 2021, the Company had cash and cash equivalents of RMB9.0 million (US$1.4 million), compared to RMB3.0 million as of December 31, 2020.


Business Highlights for the First Quarter of 2021

  • The Company reached a record high number of commercial CDA tests for the 1st Quarter versus any previous Q1 in the Company’s history.

  • The Company has developed and completed testing at the end of February 2021 of a new generation of multi-cancer detection sensor named CDA Pro Sensor (CDAPS) which is a technology breakthrough with improved performance over the previous generation cancer detection sensors in a number of areas, including detection signal stability, sensor device yield, and detection sensitivity and specificity. The Company expects that CDAPS will extend the competitiveness for AnPac in the space of cancer screening.

  • On January 25, 2021, the National Medical Products Administration (NMPA), the regulatory agent for medical products in China, approved the Company to start registration testing of AnPac Bio’s class III lung cancer auxiliary diagnosis medical device at its designated medical device testing laboratory, which is a major progress and step towards obtaining a Class III medical device registration certificate.

  • The Company continued to receive validation on the efficacy of CDA testing through follow-up studies. As of March 31, 2021, AnPac Bio had contacted 23,857 individuals tested using CDA packages in China and received substantive feedback regarding health conditions and disease development from 14,127 individuals.

  • As of March 31, 2021, the Company filed 237 patent applications globally, among which 142 patents had been granted, including 20 patents granted in the United States, 65 in greater China (including eight in Taiwan), and 57 in other countries and regions.

  • The Company continued to build a cancer risk assessment database, which totaled approximately 222,200 samples as of March 31, 2021, including approximately 178,300 samples from commercial CDA-based tests and approximately 43,900 samples from research studies.

Dr. Chris Yu, AnPac Bio’s Chairman and CEO commented: “We are very pleased with our strong Q1 performance results, including (1) a 137.2% in revenue increase over the same period last year, (2) development and final evaluations of our next generation of multi-cancer detection sensor technology which includes significant performance improvements, and (3) receiving approval from the National Medical Products Administration (NMPA) to start registration test of AnPac Bio’s class III lung cancer auxiliary diagnosis medical device.  We are going into Q2 with strong momentum.  Our continued focus in completing our Class III medical device registration and our new product development pipeline is showing great progress. We have also worked closely with our customers and commercial partners to achieve accelerated revenue growth.”


About AnPac Bio

AnPac Bio is a biotechnology company focused on early cancer screening and detection, with 142 issued patents as of March 31, 2021. With two certified clinical laboratories in China and one CLIA and CAP accredited clinical laboratory and one CLIA registered clinical laboratory in the United States, AnPac Bio performs a suite of cancer screening and detection tests, including CDA (Cancer Differentiation Analysis), bio-chemical, immunological, and genomics tests. According to Frost & Sullivan, AnPac Bio ranked third worldwide among companies offering next-generation early cancer screening and detection technologies in terms of the number of clinical samples for cancer screening and detection, based on approximately 41,700 clinical samples as of December 31, 2019. AnPac Bio’s CDA technology platform has been shown in retrospective validation studies to be able to detect the risk of over 20 different cancer types with high sensitivity and specificity.

For more information, please visit:


https://www.Anpacbio.com


.


For investor and media inquiries, please contact:


Company:


Phil Case, Marketing and Investor Relations

Phone: +1-267-810-6776 (US)

Email:


[email protected]


Investor Relations:


Ascent Investor Relations LLC

Tina Xiao, President

Phone: +1-917-609-0333 (US)

Email:


[email protected]


Safe Harbor Statement

This announcement contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934. These forward-looking statements are made under the “safe harbor” provisions of the Private Securities Litigation Reform Act of 1995 and are relating to the Company’s future financial and operating performance. The Company has attempted to identify forward-looking statements by terminologies including “believes,” “estimates,” “anticipates,” “expects,” “plans,” “projects,” “intends,” “potential,” “target,” “aim,” “predict,” “outlook,” “seek,” “goal” “objective,” “assume,” “contemplate,” “continue,” “positioned,” “forecast,” “likely,” “may,” “could,” “might,” “will,” “should,” “approximately” or other words that convey uncertainty of future events or outcomes to identify these forward-looking statements. These statements are based on current expectations, assumptions and uncertainties involving judgments about, among other things, future economic, competitive and market conditions and future business decisions, all of which are difficult or impossible to predict accurately and many of which are beyond the Company’s control. These statements also involve known and unknown risks, uncertainties and other factors that may cause the Company’s actual results to be materially different from those expressed or implied by any forward-looking statement. Known and unknown risks, uncertainties and other factors include, but are not limited to, the implementation of our business model and growth strategies; trends and competition in the cancer screening and detection market; our expectations regarding demand for and market acceptance of our cancer screening and detection tests and our ability to expand our customer base; our ability to obtain and maintain intellectual property protections for our CDA technology and our continued research and development to keep pace with technology developments; our ability to obtain and maintain regulatory approvals from the NMPA, the FDA and the relevant U.S. states and have our laboratories certified or accredited by authorities including the CLIA; our future business development, financial condition and results of operations and our ability to obtain financing cost-effectively; potential changes of government regulations; general economic and business conditions in China and elsewhere; our ability to hire and maintain key personnel; our relationship with our major business partners and customers; and the duration of the coronavirus outbreaks and their potential adverse impact on the economic conditions and financial markets and our business and financial performance, such as resulting from reduced commercial activities due to quarantines and travel restrictions instituted by China, the U.S. and many other countries around the world to contain the spread of the virus. Additionally, all forward-looking statements are subject to the “Risk Factors” detailed from time to time in the Company’s most recent Annual Report on Form 20-F and other filings with the U.S. Securities and Exchange Commission. Because of these and other risks, uncertainties and assumptions, undue reliance should not be placed on these forward-looking statements. In addition, these statements speak only as of the date of this press release and, except as may be required by law, the Company undertakes no obligation to revise or update publicly any forward-looking statements for any reason.


ANPAC BIO-MEDICAL SCIENCE CO., LTD.



UNAUDITED CONDENSED


CONSOLIDATED BALANCE SHEETS



(Amounts in thousands of Renminbi (“RMB”) and U.S. dollars (“US$”), except for number of shares and per share data)




December 31, 2020


March 31, 2021


March 31, 2021




RMB


RMB


US$


ASSETS
(Unaudited) (Unaudited)

Current assets:
Cash and cash equivalents 3,016 9,020 1,377
Advances to suppliers 5,588 5,295 808
Accounts receivable, net of allowance for doubtful accounts 7,792 4,443 678
Amounts due from related parties 1,277 3,773 576
Inventories 312 972 148
Other current assets 3,303 9,792 1,495
Total current assets 21,288 33,295 5,082
Property and equipment, net 19,267 19,183 2,928
Land use rights, net 1,166 1,159 177
Intangible assets, net 4,596 4,498 687
Goodwill 2,223 2,223 339
Long-term investments 883 805 123
Other assets 464 466 71

TOTAL ASSETS

.

49,887

61,629

9,407

LIABILITIES AND SHAREHOLDERS’ DEFICIT

Current liabilities:
Short-term debt 8,232 22,380 3,416
Accounts payable 2,127 687 105
Advance from customers 3,682 4,040 617
Amounts due to related parties 4,130 417 64
Accrued expenses and other current liabilities 25,353 22,192 3,387
Total current liabilities 43,524 49,716 7,589
Deferred tax liabilities 1,045 1,023 156
Other long-term liabilities 2,041 2,038 311

TOTAL LIABILITIES

.

46,610


52,777


8,056

Commitments and contingencies


Shareholders’ deficit:
Class A Ordinary shares ((US$0.01 par value per share; 70,000,000 shares authorized, 9,192,660 and 12,168,531 shares issued and outstanding as of December 31, 2020 and March 31, 2021, respectively) 618 811 124
Class B Ordinary shares ((US$0.01 par value per share; 30,000,000 authorized, 2,863,100 shares issued and outstanding as of December 31, 2020 and March 31, 2021) 191 191 29
Additional paid-in capital 354,295 390,527 59,606
Accumulated deficit (356,951 ) (385,980 ) (58,912 )
Accumulated other comprehensive income 4,795 3,191 487
Total AnPac Bio-Medical Science Co., Ltd. shareholders’ equity 2,948 8,740 1,334
Non-controlling interests 329 112 17

Total shareholders’ equity

3,277


8,852


1,351

TOTAL LIABILITIES AND SHAREHOLDERS’ EQUITY

49,887


61,629


9,407


ANPAC BIO-MEDICAL SCIENCE CO., LTD.



UNAUDITED CONDENSED CONSOLIDATED STATEMENTS OF COMPREHENSIVE LOSS



(Amounts in thousands of Renminbi (“RMB”) and U.S. dollars (“US$”), except for number of shares and per share data)






Three Months Ended March 31,




2020


2021


2021





RMB


RMB


US$
Revenues:
Cancer screening and detection tests 884 2,182 333
Physical checkup packages 37 3 0

Total revenues

921


2,185


333






Cost of revenues (620 ) (908 ) (139 )

Gross Profit

301


1,277


194
Operating expenses:
Selling and marketing expenses (3,596 ) (3,863 ) (590 )
Research and development expenses (2,937 ) (3,356 ) (512 )
General and administrative expenses (19,590 ) (19,226 ) (2,934 )
Impairment of long-term investments (820 )

Loss from operations

(26,642

)


(25,168

)


(3,842

)

Non-operating income and expenses:
Interest expense, net (266 ) (624 ) (95 )
Foreign exchange gain (loss), net 118 (139 ) (21 )
Share of net loss in equity method investments (21 ) (77 ) (12 )
Other income (expense), net 537 (45 ) (7 )
Change in fair value of convertible debt 5,041 (3,215 ) (491 )

Loss before income taxes

(21,233

)


(29,268

)


(4,468

)

Income tax benefit 22 22 3

Net loss

(21,211

)


(29,246

)


(4,465

)


Net loss attributable to non-controlling interests

(161

)


(217

)


(33

)


Net loss attributable to ordinary shareholders

(21,050

)


(29,029

)


(4,432

)


Loss per share

:
Class A and B Ordinary shares – basic and diluted (1.95 ) (2.43 ) (0.37 )

Weighted average shares outstanding used in calculating basic and diluted loss per share
Ordinary shares – basic and diluted 10,771,722 11,958,033 11,958,033

Other comprehensive income, net of tax

:
Fair value change relating to Company’s own credit risk on convertible loan (108 )
Foreign currency translation differences 2,717 (1,604 ) (245 )

Total comprehensive loss
(18,602 ) (30,850 ) (4,710 )
Total comprehensive loss attributable to non-controlling interests (161 ) (217 ) (33 )

Total comprehensive loss attributable to ordinary shareholders
(18,441 ) (30,633 ) (4,677 )



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