EX-99.1 2 exhibit_99-1.htm EXHIBIT 99.1

Exhibit 99.1


Check-Cap Reports Fourth Quarter and Full Year 2021 Financial Results

Company anticipates initiation of the first part of its U.S. pivotal study in April 2022

ISFIYA, Israel, April 7, 2022 -- Check-Cap Ltd. (the "Company" or "Check-Cap") (NASDAQ: CHEK), (NASDAQ: CHEKZ), a clinical stage medical diagnostics company advancing the development of C-Scan®, the first and only patient-friendly, preparation-free screening test to detect polyps before they may transform into colorectal cancer (CRC), today announced financial results for the fourth quarter and full year ended December 31, 2021.

2021 and Recent Highlights:

Clinical Progress: In February 2022, the U.S. Food and Drug Administration (FDA) approved the Company’s amended Investigational Device Exemption (IDE) application, enabling initiation of the U.S. pivotal study. The first part of the pivotal study will focus on device calibration and enhancement of C-Scan algorithms and is anticipated to begin in April 2022. The second part of the trial, anticipated to begin in Q4 2022, will compare performance of C-Scan to traditional colonoscopy. This second comparative portion of the study will be analyzed for statistical significance and will serve as the basis for the Company's filing of FDA approval in the U.S. The Company also continues patient enrollment and data collection at Israeli sites, to further enable optimization of C-Scan’s functionality and patient experience in parallel to the U.S. pivotal trial.

Strengthened Manufacturing Capacity: In 2021, the Company expanded the C-Scan manufacturing capacity and on-premise production line to ensure optimized execution of the U.S. pivotal study.

Expanded Clinical Team: In 2021, the Company strengthened its clinical team with the appointment of Dr. Hanit Brenner-Lavie as vice president of Clinical Affairs and of additional qualified clinical employees. Dr. Brenner-Lavie is leading the Company’s overall clinical strategy and its implementation, including the execution of the planned U.S. pivotal trial.

Strengthened the Balance Sheet: Cash and cash equivalents, restricted cash and short-term bank deposits as of December 31, 2021 were $51.9 million. In March 2022, the Company consummated a $10 million registered direct offering. The Company believes that it has sufficient capital to fund its ongoing operations and plans  into the first quarter of 2024.

Intellectual Property: In 2021, the Company was granted four new patents, including a new U.S. patent covering the C-Scan® proprietary tracking technology that enables real time tracking of the capsule and its activation only when it moves throughout the colon. This functionality allows for optimal scanning along the gastrointestinal (GI) tract while maintaining low energy consumption during the procedure. The patent also covers the capsule positioning data recording for the C-Scan analysis suite, which enables gastroenterologists to make a clinical decision and generate a report with their diagnosis and recommendations. This patent will expire in May 2034. Corresponding patents were issued in Japan and China and patents were approved for granting in Europe and Israel.


Breakthrough Device Designation: In early 2021, the FDA approved the Company's Breakthrough Device Designation, strengthening C-Scan's recognition as an alternative method to address the significant unmet need for patient-friendly CRC screening options.

Regulatory Renewals: In late 2021, the European Medical Device Regulation (MDR) issued a renewal of the Company's CE mark approval valid until December 1, 2026. This is a regulatory achievement for the Company, among the first medical device companies to comply with the strict requirements of this new advanced directive. The updated MDR CE approval not only permits Check-Cap to commercialize C-Scan in Europe but provides further external validation of the Company's quality systems. Additionally, the Company received renewal from the Israeli Ministry of Health, the Medical Device Division (AMAR) for marketing of C-Scan in Israel. While currently the Company remains focused primarily on the U.S. market, both renewals enable Check-Cap to continue to explore opportunities to launch C-Scan in multiple international markets.

“2021 was a productive year for Check-Cap as we made progress towards the initiation of the U.S. pivotal trial of C-Scan, including advancing the manufacturing process, optimizing our device, and expanding the clinical team in the past year”, said Alex Ovadia, chief executive officer of Check-Cap. “C-Scan aims to address issues associated with low adherence to preventive screenings with colonoscopies. We look forward to advancing the U.S. pivotal trial imminently to continue gathering clinical evidence of the potential of C-Scan to detect polyps before they may turn into cancer, through a more-patient friendly option. We believe C-Scan has the potential to redefine colorectal cancer screening in the future and we are excited to potentially bringing this option to the millions of people worldwide.”

Financial Results for the Fourth Quarter Ended December 31, 2021

Research and development expenses, net, were $4.1 million for the three months ended December 31, 2021 compared to $2.8 million for the same period in 2020.  The increase is primarily due to (i) an increase of approximately $0.5 million in salary and related expenses, mainly as a result of the expansion in employee head count and currency exchange rate fluctuation, (ii) an increase of approximately $0.4 million in other research and development expenses including clinical expenses, (iii) a $0.4 million increase in material expenses, and (iv) an increase of approximately $0.1 million in share-based compensation.
The increase in research and development expenses, net between 2021 and 2020 was offset in part by a $0.1 million grant from the Israel Innovation Authority (the “IIA”).

General and administrative expenses were $1.5 million for the three months ended December 31, 2021, compared to $1.1 million for the same period in 2020. The increase is primarily due to a $0.2 million increase in other general expenses, mainly associated with directors’ and officers’ liability insurance, a $0.1 million increase in salaries and related expenses and a $0.1 million increase in professional services.

Operating loss was $5.6 million for the three months ended December 31, 2021, compared to an operating loss of $3.9 million for the same period in 2020.

Net finance income was $101,000 for the three months ended December 31, 2021, compared to $24,000 for the same period in 2020.


Net loss was $5.5 million for the three months ended December 31, 2021, compared to $3.9 million for the same period in 2020.

Cash and cash equivalents, restricted cash and short-term bank deposits as of December 31, 2021 were $51.9 million as compared to $18.1 million as of December 31, 2020. On March 3, 2022, the Company consummated a registered direct offering for the sale of 20,000,000 of the Company's ordinary shares and accompanying warrants to purchase up to an aggregate of 15,000,000 of the Company's ordinary shares. The registered direct offering resulted in gross proceeds to the Company of $10.0 million or approximately $8.9 million net of offering expenses. The Company believes that it has sufficient capital to fund its ongoing operations and plans into the first quarter of 2024.

The number of outstanding ordinary shares as of December 31, 2021 was 96,411,949. As of April 6, 2022, the number of outstanding ordinary shares was 116,411,949.

Financial Results for the Twelve Months Ended December 31, 2021

Research and development expenses, net, were $12.3 million for the twelve months ended December 31, 2021, compared to $10.0 million for the same period in 2020. The increase in research and development, net expenses between 2021 and 2020 was primarily due to (i) an increase of approximately $1.3 million in salary and related expenses, mainly as a result of an expansion in employee head count and currency exchange rate fluctuation, (ii) a $1.2 million increase in material expenses, (iii) an increase of approximately $0.16 million in share-based compensation, and (iv) an increase of approximately $0.3 million in other research and development expenses including clinical expenses.  The increase in research and development expenses, net between 2021 and 2020 was offset in part by a $0.17 million decrease in subcontractor and consultants and a $0.43 million grant from the IIA.

General and administrative expenses were $5.0 million for the twelve months ended December 31, 2021, compared to $3.9 million for the same period in 2020. The increase in general and administrative expenses is primarily due to a $0.3 million increase in salaries and related expenses, a $0.1 million increase in professional services expenses and a $0.7 million increase in other general expenses, mainly associated with directors’ and officers’ liability insurance, offset in part by a $0.1 million decrease in share-based compensation expenses.

Operating loss was $17.3 million for the twelve months ended December 31, 2021, compared to $13.9 million for the same period in 2020.

Finance income, net, was $119,000 for the twelve months ended December 31, 2021, compared to $86,000 for the same period in 2020.

Net loss was $17.2 million for the twelve months ended December 31, 2021, compared to $13.8 million for the same period in 2020.

Net cash used in operating activities was $16.3 million for the twelve months ended December 31, 2021, compared to $13.1 million for the same period in 2020.


A copy of the Company’s annual report on Form 20-F for the year ended December 31, 2021 has been filed with the U.S. Securities and Exchange Commission at www.sec.gov and posted on the Company’s investor relations website at http://ir.check-cap.com/home. The Company will deliver a hard copy of its annual report, including its complete audited consolidated financial statements, free of charge, to its shareholders upon request to Mira Rosenzweig, chief financial officer, at mira.rosenzweig@check-cap.com.

About Check-Cap
Check-Cap is a clinical stage medical diagnostics company aiming to redefine colorectal cancer (CRC) screening through the introduction of C-Scan®, the first and only patient-friendly preparation-free screening test to detect polyps before they may transform into colorectal cancer and enable early intervention and cancer prevention. The Company’s disruptive capsule-based screening technology aims to help millions of people to stay healthy through preventive CRC screening. C-Scan uses an ultra-low dose X-ray capsule, an integrated positioning, control and recording system, as well as proprietary software to generate a 3D map of the inner lining of the colon as it travels naturally along the gastrointestinal tract. C-Scan is non-invasive and requires no sedation. It requires no bowel preparation, allowing the patients to continue their daily routine with no interruption. C-Scan is not intended to replace colonoscopy. A positive C-Scan result should be followed by colonoscopy.  C-Scan is an investigational device and is not available for sale in the United States.

Legal Notice Regarding Forward-Looking Statements
This press release contains "forward-looking statements" about the Company’s expectations, beliefs or intentions regarding, among other things, its product development efforts, business, financial condition, results of operations, strategies or prospects. Words such as "may," "should," "could," "would," "predicts," "potential," "continue," "expects," "anticipates," "future," "intends," "plans," "believes," "estimates," and similar expressions, as well as statements in future tense, often signify forward-looking statements. Forward-looking statements should not be read as a guarantee of future performance or results and may not be accurate indications of when such performance or results will be achieved. Forward-looking statements are based on information that the Company has when those statements are made or management's good faith belief as of that time with respect to future events, and are subject to risks and uncertainties that could cause actual performance or results to differ materially from those expressed in or suggested by the forward-looking statements. For a discussion of these and other risks that could cause such differences and that may affect the realization of forward-looking statements, please refer to the "Forward-looking Statements" and "Risk Factors" in the Company's Annual Report on Form 20-F for the year ended December 31, 2021 and other filings with the Securities and Exchange Commission (SEC). Investors and security holders are urged to read these documents free of charge on the SEC's web site at http://www.sec.gov. The Company assumes no obligation to publicly update or revise its forward-looking statements as a result of new information, future events or otherwise

Investor Contacts
Irina Koffler 
LifeSci Advisors, LLC 
646.970.4681
ikoffler@lifesciadvisors.com

Meirav Gomeh-Bauer
LifeSci Advisors, LLC 
+972(0)-54-476-4979
Meirav@lifesciadvisors.com

Media Contact
Mónica Rouco Molina
Account Supervisor - Europe
LifeSci Communications
mroucomolina@lifescicomms.com

CHECK CAP LTD.
CONSOLIDATED BALANCE SHEETS
 (U.S. dollars in thousands except share data)
 
   
December 31,
   
December 31,
 
   
2 0 2 1
   
2 0 2 0
 
Assets
           
Current assets
           
Cash and cash equivalents
 
$
26,457
   
$
7,703
 
Restricted cash
   
350
     
350
 
Short-term bank deposit
   
25,104
     
10,079
 
Prepaid expenses and other current assets
   
839
     
285
 
Total current assets
   
52,750
     
18,417
 
                 
Non-current assets
               
Property and equipment, net
   
1,793
     
823
 
Operating leases
   
1,116
     
398
 
Total non-current assets
   
2,909
     
1,221
 
Total assets
 
$
55,659
   
$
19,638
 
                 
Liabilities and shareholders' equity
               
Current liabilities
               
Accounts payable and accruals
               
Trade
 
$
1,050
   
$
862
 
Other
   
680
     
345
 
Employees and payroll accruals
   
1,961
     
1,510
 
Operating lease liabilities
   
350
     
264
 
Total current liabilities
   
4,041
     
2,981
 
 
               
Non-current liabilities
               
Royalties provision
   
132
     
154
 
Operating lease liabilities
   
795
     
125
 
Total non-current liabilities
   
927
     
279
 
                 
Shareholders' equity
               
Share capital, Ordinary shares, 2.4 NIS par value (360,000,000 authorized shares as of December 31
               
31, 2021 and 2020; 96,411,949 and 46,239,183 shares issued and
               
outstanding as of December 31, 2021 and 2020, respectively)
   
68,787
     
31,646
 
Additional paid-in capital
   
90,089
     
75,715
 
Accumulated deficit
   
(108,185
)
   
(90,983
)
Total shareholders' equity
   
50,691
     
16,378
 
                 
Total liabilities and shareholders' equity
 
$
55,659
   
$
19,638
 


CHECK CAP LTD.
CONSOLIDATED STATEMENTS OF OPERATIONS
 (U.S. dollars in thousands, except per share data)

   
Twelve months ended
December 31,
   
Three months ended
December 31,
 
   
2020
   
2021
   
2020
   
2021
 
Research and development expenses, net
 
$
12,349
   
$
10,008
   
$
4,126
   
$
2,831
 
General and administrative expenses
   
4,972
     
3,924
     
1,452
     
1,102
 
Operating loss
   
17,321
     
13,932
     
5,578
     
3,933
 
Finance Income, net
   
119
     
86
     
101
     
24
 
Net loss for the period
 
$
17,202
   
$
13,846
   
$
5,477
   
$
3,909
 
Loss per share:
                               
Net loss per ordinary share basic and diluted
   
0.21
     
0.46
     
0.06
     
0.08
 
                                 
Weighted average number of ordinary shares outstanding - basic and diluted
   
82,807,556
     
30,351,368
     
96,408,753
     
46,236,425
 



CHECK-CAP LTD.
CONSOLIDATED  STATEMENTS OF CASH FLOWS
  (U.S. dollars in thousands)

   
Year ended
   
Three months ended
 
   
December 31,
   
December 31,
 
   
2021
   
2020
   
2021
   
2020
 
CASH FLOWS FROM OPERATING ACTIVITIES
                       
Net loss
 
$
(17,202
)
 
$
(13,846
)
 
$
(5,477
)
 
$
(3,909
)
Adjustments required to reconcile net loss to net cash used in operating activities:
                               
Depreciation
   
205
     
148
     
66
     
41
 
Share-based compensation
   
491
     
408
     
223
     
91
 
Financial expense, net
   
-
     
7
     
47
     
34
 
Changes in assets and liabilities items:
                               
Decrease (increase) in prepaid and other current assets and non-current assets
   
(549
)
   
106
     
270
     
-
 
Increase (decrease) in trade accounts payable, accruals and other current liabilities
   
362
     
(317
)
   
119
     
(22
)
Increase in employees and payroll accruals
   
451
     
409
     
414
     
303
 
Decrease in royalties provision
   
(22
)
   
(28
)
   
(46
)
   
(34
)
Net cash used in operating activities
 
$
(16,264
)
 
$
(13,113
)
 
$
(4,384
)
 
$
(3,496
)
 
                               
CASH FLOWS FROM INVESTING ACTIVITIES
                               
Purchase of property and equipment
   
(1,006
)
   
(379
)
   
(263
)
   
(86
)
Proceeds from (Investment in) short-term bank and other deposits
   
(15,000
)
   
(10,072
)
   
(8,300
)
   
4,931
 
Net cash provided by (used in) investing activities
 
$
(16,006
)
 
$
(10,451
)
 
$
(8,563
)
 
$
4,845
 
                                 
CASH FLOWS FROM FINANCING ACTIVITIES
                               
Exercise of warrants into ordinary shares, net of issuance expenses
   
19,219
     
-
     
-
     
-
 
Issuance of ordinary shares in the registered direct offerings, net of issuance expenses
   
31,801
     
10,139
     
(207
)
   
-
 
Options exercise
   
4
     
-
     
4
     
-
 
Issuance of ordinary shares and warrants in the Warrant Exercise Transaction, net of issuance expenses
   
-
     
8,712
     
-
     
-
 
Issuance of ordinary shares in the private placement, net of issuance expenses
   
-
     
4,731
     
-
     
-
 
Net cash provided by financing activities
 
$
51,024
   
$
23,582
   
$
(203
)
 
$
-
 
Net increase (decrease) in cash, cash equivalents and restricted cash
   
18,754
     
18
     
(13,150
)
   
1,349
 
Cash, cash equivalents and restricted cash at the beginning of the period
   
8,053
     
8,035
     
39,957
     
6,704
 
Cash, cash equivalents and restricted cash at the end of the period
 
$
26,807
   
$
8,053
   
$
26,807
   
$
8,053