Conference call to be held today at 10:00 am Eastern Time; Focus on U.S. market for
ProSense® in breast cancer indication
CAESAREA, Israel, April 3,
2024 /PRNewswire/ -- IceCure Medical Ltd. (Nasdaq:
ICCM) ("IceCure" or the "Company"), developer of the ProSense®
System, a minimally-invasive cryoablation technology that destroys
tumors by freezing as an alternative to surgical tumor removal,
today reported sales as of and for the twelve months ended
December 31, 2023 increased 26%
compared to the twelve months ended December
31, 2022, as the Company continues to transition from a
research and development and clinical phase company to a commercial
phase company.
2023 Key Financial Highlights:
- Product sales globally rose 26%
- Product sales in the U.S. grew 24%
- Cash and cash equivalents of $11.1
million at December 31,
2023
- During the first quarter of 2024, the Company raised
$3 million in gross proceeds from the
sale of ordinary shares under its At-the-Market ("ATM") offering
facility, ending the quarter with cash and cash equivalents of
approximately $11 million, which the
Company believes provides the resources to execute its clinical,
regulatory and commercial objectives for 2024.
"We have achieved what we believe is the most significant
milestone in our company's history with the completion of the ICE3
breast cancer study and reporting of topline results," stated
IceCure's CEO, Eyal Shamir. "In the
next few weeks, we will be reporting full results and submitting
them to the FDA for review. We believe the data from ICE3 and
numerous independent studies of ProSense® in breast cancer support
our thesis that ProSense® can have a very meaningful positive
impact on the health and wellbeing of women with early-stage breast
cancer. Our U.S. commercial team is ready to launch marketing and
distribution of ProSense® for breast cancer as we await the U.S.
Food and Drug Administration's ("FDA") decision. Should the FDA
grant clearance, we believe this decision would further boost
commercial demand in global markets where ProSense® already has
approval for breast cancer."
"We are pleased that the ICE3 full data results will be
presented at the highly influential American Society of Breast
Surgeons ("ASBrS") 25th Annual Meeting by ICE3 Investigator Dr.
Richard Fine and by Dr. Michael Berry. Breast surgeons considering
ProSense® for their practice are eager to see the results, and we
are hopeful that they will be impressed by the data."
"Physician initiated studies in many other indications continue
to increase in Europe, the U.S.,
and Asia. The growing number of
independent studies, we believe, is a very strong indicator of
future adoption."
"As we increased our commercial activities through medical
conferences and added more distributors, we had a corresponding
growth in 2023 revenues, system, and probe sales. While total
revenues in 2023 were up slightly to $3.2
million, compared to $3.1
million in 2022, a more meaningful increase of 26% or
$0.6 million in ProSense® system and
disposable probe sales demonstrates continued increasing
demand."
2023 and Recent Significant Operating, Clinical, Regulatory
& Commercial Highlights:
Completed ICE3 Breast Cancer Study and Reported Topline
Results: IceCure successfully completed a 10-year long landmark
study, the largest controlled multicenter clinical trial ever
performed for liquid nitrogen (LN2) based cryoablation of low-risk,
early-stage malignant breast tumors. In the ICE3 study, 96.39% of
patients (187 out of 194 patients) were local recurrence-free with
no significant device-related adverse events or complications
reported. These results are in line with data from numerous
third-party studies conducted by physicians currently using
ProSense®.
Full ICE3 Data to be Submitted to FDA: The Company
plans to complete the analysis and evaluation of the full data set
and expects to submit the results to the FDA in April 2024. The FDA requested this data as part
of IceCure's De Novo Classification Request for Marketing
Authorization of ProSense® for the treatment of early-stage
low-risk breast cancer.
ICE3 Full Results to be Presented at ASBrS's 25th
Annual Meeting: Dr. Richard
Fine, ICE3 Investigator, will present the full ICE3 study
results at the ASBrS's annual meeting, the most prominent event in
the U.S. for breast surgeons, in a presentation titled
"Cryoablation Without Excision for Early-Stage Breast Cancer; ICE3
Trial 5 year follow up on Ipsilateral Breast Tumor Recurrence".
Additionally, ICE3 Investigator Dr. Michael
Berry will present a session titled "Cryoablation: Is It
Ready for Primetime?".
Regulatory Approval Received in Brazil, Canada, and China: ProSense® now has regulatory
approvals in 15 countries for a broad range of
indications.
Global Rollout Momentum with New Distribution and
Installations in Portugal,
India, and Brazil: IceCure entered a
non-exclusive distribution agreement with Medicinália Cormédica –
MC Medical, Lda., the largest distributor of third-party medical
devices in Portugal. The first
breast cryoablation procedure in India was performed in 2023 with ProSense® and
there has been strong interest in the country at medical
conferences where IceCure's cryoablation system was featured. In
Brazil, where ProSense® received
regulatory approval in 2023, IceCure's in-country distributor has
launched commercial activities and procedures have commenced.
Independent Investigator Initiated Studies Build Data to
Support Potential New Indications, Adoption, and
Reimbursement: Numerous third-party studies have been
initiated to evaluate ProSense® in various indications. Results
from completed studies have been presented at medical conferences
and published in peer-reviewed journals including studies from
Spain and Italy that demonstrated ProSense®'s efficacy
in early-stage breast cancer, with data similar to ICE3's topline
results. Two endometriosis studies in France revealed ProSense®'s potential in
treating a condition that afflicts 190 million women globally. With
current treatments only aiming to control symptoms and no curative
option available, endometriosis is an indication for which
ProSense® may deliver significant benefits to patients and payors
alike. Another study in France
reported a 92% disease-free survival rate in kidney cancer patients
treated with ProSense®. These data support further adoption and
reimbursement, particularly in countries where ProSense® has
already been approved for these indications. Elucidating
ProSense®'s efficacy in cancer, a study at Case Western Reserve University in the U.S.,
demonstrated that ProSense® boosts immune response against caner by
enhancing CD8+ T cell response.
IP Portfolio and Technology Pipeline Continue to Grow:
IceCure added three more patents to its expanding
cryoablation-focused IP portfolio. In March
2024, IceCure was issued a patent in Japan for a novel cryogen flow control system
to optimize patient outcomes. The U.S. and Japan both issued patents to IceCure for a
novel cryogenic pump for its next-generation cryoablation systems.
In April 2024, the Company filed a
510(k) submission with the FDA for its next-generation single probe
XSense™ System and cryoprobes for all the indications for which
ProSense® has already received the requisite FDA clearance.
Financial Results for the Twelve Months Ended December 31, 2023
Revenues for the twelve months ended December 31, 2023 were $3.2 million compared to $3.1 million for the twelve months ended
December 31, 2022. The minor increase
is due to the increase in ProSense® systems and disposables sales
which was offset by the decrease in revenue recognition from the
exclusive distribution rights agreement with Terumo Corporation in
Japan. For the twelve months
ended December 31, 2023, the Company reported a 26% increase
in ProSense® systems and disposable probes sales to $3 million, compared to $2.3 million for the twelve months ended
December 31, 2022, driven by higher
sales in the U.S. and other territories.
Gross profit was $1.3 million for the twelve months
ended December 31, 2023 compared to
$1.4 million for the twelve
months ended December 31, 2022. Gross
margin was 40% for the twelve months ended December 31, 2023, compared to 47% for the twelve
months ended December 31, 2022.
Non-GAAP gross profit and non-GAAP gross margin for the year
ended December 31, 2023, increased by
$0.3 million, or 47%, to $1 million, compared to $0.7 million for the year ended December 31, 2022. The increase in
non-GAAP gross profit and non-GAAP gross margin, without
taking into consideration revenue from the exclusive distribution
agreements, is attributable to the increase of 26% in revenue from
sales of ProSense® systems and probes while the increase in cost of
revenues was 18%.
Research and development expenses for the twelve months ended
December 31, 2023, were $8.3
million compared to $9.1 million for the twelve
months ended December 31, 2022. The
decrease was primarily due to the depreciation of NIS against the
USD on NIS-denominated expenses such as payroll and related
benefits, a reduction in our development expenses for the XSense™
System, and a decrease in clinical and regulatory costs.
In support of ongoing global commercial adoption and in
anticipation of increasing U.S. commercial efforts, sales and
marketing expenses for the twelve months ended December 31, 2023 were $4.4 million,
compared to $3.2 million for the twelve months ended
December 31, 2022. General and
administrative expenses for the twelve months ended December 31, 2023 decreased by 30% to $4.2
million, compared to $5.9 million the twelve months ended
December 31, 2022. A portion of the
decrease was due to a decrease in director and officer insurance
costs and the depreciation of NIS against USD on NIS denominated
expenses such as payroll and related benefits.
Total operating expenses for the twelve months ended
December 31, 2023 decreased
to $16.9 million, compared to $18.2 million for the
twelve months ended December 31,
2022. The decrease in operating expenses was attributable to
reductions in research and development expenses and general and
administrative expenses, which were partially offset by the
increase in sales and marketing expenses.
Net loss for the twelve months ended December 31, 2023 decreased by 14% to $14.7
million, or $0.32 per share, compared with a net loss
of $17.0 million, or $0.46 per share, for the same period
last year.
As of December 31, 2023, the Company had cash and cash
equivalents, including short-term deposits, of
approximately $11.1 million, compared to $23.7
million as of December 31, 2022. As of March 31,
2024, the Company had cash and cash equivalents, including
short-term deposits, of approximately $11 million. To ensure
the Company is in a position to achieve its near-term objectives,
IceCure has implemented an expense reduction plan that will reduce
its non-revenue generating and clinical efforts costs, lowering the
monthly cash utilization and ensuring it can meet its primary goals
in 2024.
Use of Non-U.S. GAAP Measures
In addition to disclosing financial results prepared in
accordance with accounting principles generally accepted in
the United States of America (U.S.
GAAP), this press release contains non-U.S. GAAP financial measures
that the Company uses as measures of its performance.
These measures may be different from non-GAAP financial measures
used by other companies. The Company calculates (i) non-GAAP
gross profit as gross profit, less revenue from exclusive
distribution agreements, as an indication of our gross profit from
sales of our systems and disposables; and (ii) non-GAAP gross
margin is a percentage of non-GAAP gross profit from revenues from
sales of systems and disposables which reflects the gross margins
on our systems and disposables sales. These non-GAAP financial
measures are included as a supplemental disclosure because they are
performance measures used by our management and board of directors
to determine the commercial performance of our business.
These non-GAAP measures should be viewed as a supplement to
and not a substitute for the Company's U.S. GAAP measures of
performance and financial results in accordance with U.S. GAAP and
reconciliations from these results should be carefully evaluated.
We have provided a reconciliation below of non-GAAP gross profit
and non-GAAP gross margin to the most directly comparable financial
measure calculated and presented in accordance with U.S. GAAP.
Conference call & webcast info:
Wednesday, April 3, 2024, at
10:00 am EDT
US: 1-888-407-2553
Israel/International:
+972-3-9180696
A live webcast will be available at:
https://veidan.activetrail.biz/IcecureQ4-2023
A recording of the webcast will be available at:
ir.icecure-medical.com/
About ProSense®
The ProSense® Cryoablation System provides a minimally invasive
treatment option to destroy tumors by freezing them. The system
uniquely harnesses the power of liquid nitrogen to create large
lethal zones for maximum efficacy in tumor destruction in benign
and cancerous lesions, including breast, kidney, lung, and
liver.
ProSense® enhances patient and provider value by accelerating
recovery, reducing pain, surgical risks, and complications. With
its easy, transportable design and liquid nitrogen utilization,
ProSense® opens that door to fast and convenient office-based
procedure for breast tumors.
About IceCure Medical
IceCure Medical (Nasdaq: ICCM) develops and markets ProSense®,
an advanced liquid-nitrogen-based cryoablation therapy for the
treatment of tumors (benign and cancerous) by freezing, with the
primary focus areas being breast, kidney, bone and lung cancer. Its
minimally invasive technology is a safe and effective alternative
to hospital surgical tumor removal that is easily performed in a
relatively short procedure. The system is marketed and sold
worldwide for the indications cleared and approved to date
including in the U.S., Europe, and
China.
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 and other Federal
securities laws. Words such as "expects," "anticipates," "intends,"
"plans," "believes," "seeks," "estimates" and similar expressions
or variations of such words are intended to identify
forward-looking statements. For example, IceCure is using forward
looking statements in this press release when it discusses: that
the Company will report and submit full results upon the completion
of the ICE3 breast cancer study, that the Company believes the data
from ICE3 and independent studies of ProSense® shows that ProSense®
can have a very meaningful positive impact on the health and
wellbeing of women with early-stage breast cancer, that prospective
FDA clearance would boost commercial demand for ProSense® where it
already has regulatory approval, and the belief that the growing
number of independent studies is a strong indicator of future
adoption. Historical results of scientific research and clinical
and preclinical trials do not guarantee that the conclusions of
future research or trials will suggest identical or even similar
conclusions. Important factors that could cause actual results,
developments and business decisions to differ materially from those
anticipated in these forward-looking statements include, among
others: the Company's planned level of revenues and capital
expenditures; the Company's available cash and its ability to
obtain additional funding; the Company's ability to market and sell
its products; legal and regulatory developments in the United States and other countries; the
Company's ability to maintain its relationships with suppliers,
distributors and other partners; the Company's ability to maintain
or protect the validity of its patents and other intellectual
property; the Company's ability to expose and educate medical
professionals about its products; political, economic and military
instability in the Middle East,
specifically in Israel; as well as
those factors set forth in the Risk Factors section of the
Company's Annual Report on Form 20-F for the year ended
December 31, 2023 filed with the U.S.
Securities and Exchange Commission (the "SEC") on April 3, 2024, and other documents filed with or
furnished to the SEC which are available on the SEC's website,
www.sec.gov. The Company undertakes no obligation to update these
statements for revisions or changes after the date of this release,
except as required by law.
IR Contact:
Email: investors@icecure-medical.com
Michael Polyviou
Phone: 732-232-6914
Todd Kehrli
Phone: 310-625-4462
|
CONSOLIDATED BALANCE
SHEETS
|
(U.S. dollars in
thousands, except share data and per share data)
|
|
|
As of
December 31,
|
As of
December 31,
|
|
2 0 2
3
|
2 0 2
2
|
ASSETS
|
|
|
|
|
|
CURRENT
ASSETS
|
|
|
Cash and cash
equivalents
|
10,533
|
23,659
|
Short-term
deposit
|
529
|
-
|
Restricted
deposit
|
-
|
296
|
Trade
receivables
|
103
|
78
|
Inventory
|
2,275
|
2,857
|
Prepaid expenses and
other receivables
|
744
|
1,240
|
Total current
assets
|
14,184
|
28,130
|
|
|
|
NON-CURRENT
ASSETS
|
|
|
|
|
|
Right of use
assets
|
679
|
668
|
Property and
equipment, net
|
1,513
|
1,356
|
Prepaid expenses and
other long-term assets
|
34
|
34
|
Total
non-current assets
|
2,226
|
2,058
|
|
|
|
TOTAL
ASSETS
|
16,410
|
30,188
|
|
|
|
LIABILITIES AND
SHAREHOLDERS' EQUITY
|
|
|
CURRENT
LIABILITIES
|
|
|
Trade
payables
|
502
|
714
|
Lease
liabilities
|
223
|
167
|
Other current
liabilities
|
3,146
|
3,455
|
Total current
liabilities
|
3,871
|
4,336
|
|
|
|
NON-CURRENT
LIABILITIES
|
|
|
Long term lease
liabilities
|
376
|
430
|
Total non-current
liabilities
|
376
|
430
|
|
|
|
Commitments and
contingencies
|
|
|
|
|
|
SHAREHOLDERS'
EQUITY
|
|
|
Ordinary shares, No
par value; Authorized
2,500,000,000 shares; Issued and outstanding:
45,729,684 shares and 45,623,434 shares as of
December 31, 2023 and December 31, 2022,
respectively
|
-
|
-
|
|
-
|
-
|
Additional paid-in
capital
|
102,224
|
100,831
|
Accumulated
deficit
|
(90,061)
|
(75,409)
|
Total shareholders'
equity
|
12,163
|
25,422
|
|
|
|
TOTAL LIABILITIES
AND SHAREHOLDERS' EQUITY
|
16,410
|
30,188
|
|
CONSOLIDATED
STATEMENTS OF COMPREHENSIVE LOSS
|
(U.S. dollars in
thousands, except share data and per share data)
|
|
|
Year ended
December 31,
|
Year ended
December 31,
|
|
2023
|
2022
|
|
|
|
Revenues
|
3,229
|
3,085
|
Cost of
revenues
|
1,929
|
1,640
|
Gross
profit
|
1,300
|
1,445
|
|
|
|
Research and
development expenses
|
8,273
|
9,123
|
Sales and marketing
expenses
|
4,437
|
3,204
|
General and
administrative expenses
|
4,166
|
5,857
|
Operating
loss
|
15,576
|
16,739
|
|
|
|
Financial expenses
(income), net
|
(924)
|
239
|
|
|
|
Net loss and
comprehensive loss
|
14,652
|
16,978
|
|
|
|
Basic and diluted
net loss per share
|
0.32
|
0.46
|
|
|
|
Weighted average
number of shares
outstanding used in computing basic
and diluted net loss per share
|
45,638,030
|
37,016,631
|
|
|
|
CONSOLIDATED
STATEMENTS OF CASH FLOWS
|
(U.S. dollars in
thousands, except share data and per share data)
|
|
|
Year ended
December 31,
|
Year ended
December 31,
|
|
2023
|
2022
|
Cash flows from
operating activities:
|
|
|
Net loss
|
(14,652)
|
(16,978)
|
Adjustments to
reconcile net loss to net cash used in operating
activities:
|
|
|
Depreciation
|
323
|
248
|
Share-based
compensation
|
1,310
|
1,865
|
Exchange rate
changes in cash and cash equivalents
and
deposit
|
(25)
|
359
|
Changes in assets
and liabilities:
|
|
|
Decrease (increase) in
trade receivables
|
(25)
|
378
|
Decrease (increase) in
inventory
|
582
|
(902)
|
Decrease
(increase) in prepaid expenses and other
receivables
|
496
|
1,050
|
Decrease (increase) in
right of use assets
|
182
|
245
|
Increase (decrease) in
trade payables
|
(212)
|
(167)
|
Increase (decrease) in
lease liabilities
|
(191)
|
(312)
|
Increase
(decrease) in other current liabilities
|
(309)
|
540
|
Increase (decrease) in
other long-term liabilities
|
-
|
(618)
|
Net cash used in
operating activities
|
(12,521)
|
(14,292)
|
|
|
|
Cash flows from
investing activities:
|
|
|
Realization of
(Investment in) deposits
|
(529)
|
-
|
Realization of
(investment in) restricted deposits
|
296
|
-
|
Purchase of property
and equipment
|
(480)
|
(891)
|
Net cash provided
by (used in) investing activities
|
(713)
|
(891)
|
|
|
|
Cash flows from
financing activities:
|
|
|
Issuance of ordinary
shares, net of issuance costs
|
-
|
13,569
|
Issuance of restricted
ordinary shares
|
-
|
6
|
Issuance of ordinary
shares and pre- funded
warrants, net of
issuance costs
|
-
|
-
|
Exercise of pre-
funded warrants
|
-
|
1
|
Exercise of options to
ordinary shares
|
83
|
1
|
Net cash provided
by financing activities
|
83
|
13,577
|
|
|
|
Increase (decrease)
in cash and cash equivalents
|
(13,151)
|
(1,606)
|
Cash and cash
equivalents beginning of the year
|
23,659
|
25,621
|
Effect of foreign
exchange rate on cash and cash equivalents
|
25
|
(356)
|
Cash and cash
equivalents end of the year
|
10,533
|
23,659
|
|
|
|
Non-cash
activities
|
|
|
Obtaining a
right-of-use asset in exchange for a lease liability
|
193
|
-
|
|
|
RECONCILIATIONS OF
US GAAP TO NON-US GAAP FINANCIAL MEASURES
|
|
|
|
|
|
Year Ended
December 31,
|
|
U.S. dollars in
thousands
|
|
2023
|
|
|
2022
|
|
GAAP
revenues
|
|
$
|
3,229
|
|
|
$
|
3,085
|
|
GAAP gross
profit
|
|
$
|
1,300
|
|
|
$
|
1,445
|
|
GAAP gross margin
%
|
|
|
40
|
%
|
|
|
47
|
%
|
|
|
|
|
|
|
|
|
|
Less:
|
|
|
|
|
|
|
|
|
Revenue from
exclusive distribution agreement
|
|
|
(274)
|
|
|
|
(747)
|
|
Revenues from sales
of systems and disposables
|
|
|
2,955
|
|
|
|
2,338
|
|
Non-GAAP gross
profit
|
|
|
1,026
|
|
|
|
698
|
|
Non-GAAP gross
margin %
|
|
|
35
|
%
|
|
|
30
|
%
|
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