Full Press Release Details
Reports First Quarter 2025 Financial Results
to host investor conference call today, May 9th, at 8:30am ET
FL - May 9, 2025 - InspireMD, Inc. (Nasdaq: NSPR), developer of the CGuard Prime carotid stent system for the
treatment of carotid artery disease and prevention of stroke, today announced financial and operating results for the first quarter ended
Slosman, CEO of InspireMD, commented: "In the first quarter we continued to drive commercial adoption of our technology in
our served markets, while laying a strong operational and strategic foundation for upcoming transformational milestones. With a clear roadmap for
commercial expansion and a disciplined focus on execution, we've built and trained a world-class commercial team-ready to
execute at scale upon potential FDA PMA approval. We're energized by the momentum and confident in the opportunities on the horizon."
continue to work interactively with the FDA and are optimistic for an anticipated approval of CGuard Prime in the third quarter of 2025.
Despite dynamics within the agency and the timing of our audit in February, we are confident the remaining items will be successfully
completed. I am excited about the transformative milestones ahead as we work to bring this innovative technology to patients in the U.S.
and drive the next chapter of InspireMD's growth," Mr. Slosman concluded.
Results for the First Quarter Ended March 31, 2025
the first quarter of 2025, total revenue increased by $18,000, or 1.2%, to $1,529,000 from
$1,511,000 during the first quarter of 2024. This increase was driven by continued adoption of our CGuard technology in existing markets,
offset by the impact of foreign exchange and distributors managing CGuard inventory levels in anticipation of CGuard Prime approval in
profit for the first quarter of 2025 remained constant at $292,000, compared to the gross profit of the first quarter of 2024.
operating expenses for the first quarter of 2025 were $11,752,000, an increase of $4,046,000, or 52.5% compared to $7,706,000 for the
first quarter of 2024. This increase was primarily due to higher salaries and share-based compensation tied to U.S. sales force expansion
ahead of FDA approval. Additional increases stemmed from CGuard Prime launch preparation, U.S. facility rent, and CFO recruitment fees.
income, net for the first quarter of 2025 was $294,000, a decrease of $88,000 or 23.0% compared to $382,000 for the first quarter of
2024. This decrease was primarily due to less interest income from investments in marketable securities and money market funds.
loss for the first quarter of 2025 totaled $11,166,000 or $0.22 per basic and diluted share, compared to a net loss of $7,032,000, or
$0.21 per basic and diluted share, for the same period in 2024.
of March 31, 2025, cash and cash equivalents and marketable securities were $26,086,000 compared to $34,637,000 as of December 31, 2024.
Call and Webcast Details
will host a conference call at 8:30 am ET today, May 9th, to review financial results and provide an update on corporate developments.
Following management's formal remarks, there will be a question-and-answer session.
May 9th at 8:30 a.m. ET
| Domestic: | 1-800-579-2543 | |
| International: | 1-785-424-1789 | |
| Conference ID: | IMD1Q25 | |
| Webcast: | Webcast Link - Click Here |
seeks to utilize its proprietary MicroNet technology to make its products the industry standard for carotid stenting by providing
outstanding acute results and durable, stroke-free, long-term outcomes. InspireMD's common stock is quoted on the Nasdaq under
the ticker symbol NSPR.
routinely post information that may be important to investors on our website. For more information, please visit www.inspiremd.com.
press release contains "forward-looking statements." Forward-looking statements include, but are not limited to, statements
regarding InspireMD or its management team's expectations, hopes, beliefs, intentions or strategies regarding future events, future
financial performance, strategies, expectations, competitive environment and regulation, including potential FDA approval and potential
U.S. commercial launch. Such statements may be preceded by the words "intends," "may," "will," "plans,"
"expects," "anticipates," "projects," "predicts," "estimates," "aims,"
"believes," "hopes," "potential", "scheduled" or similar words. Forward-looking statements
are not guarantees of future performance, are based on certain assumptions and are subject to various known and unknown risks and uncertainties,
many of which are beyond the company's control, and cannot be predicted or quantified and consequently, actual results may differ
materially from those expressed or implied by such forward-looking statements. Such risks and uncertainties include, without limitation,
risks and uncertainties associated with our history of recurring losses and negative cash flows from operating activities; substantial
doubt about our ability to continue as a going concern; significant future commitments and the uncertainty regarding the adequacy of
our liquidity to pursue our complete business objectives; our need to raise additional capital to meet our business requirements in the
future and such capital raising may be costly or difficult to obtain and could dilute out stockholders' ownership interests; market
acceptance of our products; an inability to secure and maintain regulatory approvals for the sale of our products; negative clinical
trial results or lengthy product delays in key markets; our ability to maintain compliance with the Nasdaq listing standards; our ability
to generate revenues from our products and obtain and maintain regulatory approvals for our products; our ability to adequately protect
our intellectual property; our dependence on a single manufacturing facility and our ability to comply with stringent manufacturing quality
standards and to increase production as necessary; the risk that the data collected from our current and planned clinical trials may
not be sufficient to demonstrate that our technology is an attractive alternative to other procedures and products; intense competition
in our industry, with competitors having substantially greater financial, technological, research and development, regulatory and clinical,
manufacturing, marketing and sales, distribution and personnel resources than we do; entry of new competitors and products and potential
technological obsolescence of our products; inability to carry out research, development and commercialization plans; loss of a key customer
or supplier; technical problems with our research and products and potential product liability claims; product malfunctions; price increases
for supplies and components; insufficient or inadequate reimbursement by governmental and other third-party payers for our products;
our efforts to successfully obtain and maintain intellectual property protection covering our products, which may not be successful;
adverse federal, state and local government regulation, in the United States, Europe or Israel and other foreign jurisdictions; the fact
that we conduct business in multiple foreign jurisdictions, exposing us to foreign currency exchange rate fluctuations, logistical and
communications challenges, burdens and costs of compliance with foreign laws and political and economic instability in each jurisdiction;
the escalation of hostilities in Israel, which could impair our ability to manufacture our products; and current or future unfavorable
economic and market conditions and adverse developments with respect to financial institutions and associated liquidity risk. More detailed
information about the Company and the risk factors that may affect the realization of forward-looking statements is set forth in the
Company's filings with the Securities and Exchange Commission (SEC), including the Company's Annual Report on Form 10-K and
its Quarterly Reports on Form 10-Q. 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.
CONSOLIDATED STATEMENTS OF OPERATIONS(1)
dollars in thousands, except share and per share data)
| Three months ended | ||||||||
| March 31, | ||||||||
| 2025 | 2024 | |||||||
| Revenues | $ | 1,529 | $ | 1,511 | ||||
| Cost of revenues | 1,237 | 1,219 | ||||||
| Gross Profit | 292 | 292 | ||||||
| Operating Expenses: | ||||||||
| Research and development | 4,059 | 2,625 | ||||||
| Selling and marketing | 2,750 | 1,237 | ||||||
| General and administrative | 4,943 | 3,844 | ||||||
| Total operating expenses | 11,752 | 7,706 | ||||||
| Loss from operations | (11,460 | ) | (7,414 | ) | ||||
| Financial Income, net | 294 | 382 | ||||||
| Net Loss | $ | (11,166 | ) | $ | (7,032 | ) | ||
| Net loss per share - basic and diluted | $ | (0.22 | ) | $ | (0.21 | ) | ||
| Weighted average number of shares of common stock used in computing net loss per share - basic and diluted | 49,993,509 | 34,242,976 |
CONSOLIDATED BALANCE SHEETS(2)
dollars in thousands, except share and per share data)
| March 31, | December 31, | |||||||
| 2025 | 2024 | |||||||
| ASSETS | ||||||||
| Current Assets: | ||||||||
| Cash and cash equivalents | $ | 12,383 | $ | 18,916 | ||||
| Marketable securities | 13,703 | 15,721 | ||||||
| Accounts receivable: | ||||||||
| Trade, net | 1,580 | 1,572 | ||||||
| Other | 763 | 682 | ||||||
| Prepaid expenses | 893 | 1,060 | ||||||
| Inventory | 2,822 | 2,570 | ||||||
| Total current assets | 32,144 | 40,521 | ||||||
| Non-current assets: | ||||||||
| Long term deposit | 430 | 426 | ||||||
| Property, plant and equipment, net | 2,736 | 2,371 | ||||||
| Operating lease right of use assets | 2,225 | 2,360 | ||||||
| Funds in respect of employee rights upon retirement | 1,137 | 1,129 | ||||||
| Total non-current assets | 6,528 | 6,286 | ||||||
| Total assets | $ | 38,672 | $ | 46,807 |
| March 31, | December 31, | |||||||
| 2025 | 2024 | |||||||
| LIABILITIES AND EQUITY | ||||||||
| Current liabilities: | ||||||||
| Accounts payable and accruals: | ||||||||
| Trade | $ | 1,727 | $ | 1,254 | ||||
| Other | 5,640 | 6,424 | ||||||
| Total current liabilities | 7,367 | 7,678 | ||||||
| Long-term liabilities: | ||||||||
| Operating lease liabilities net of current maturities | 1,639 | 1,796 | ||||||
| Liability for employee rights upon retirement and others | 1,321 | 1,247 | ||||||
| Total long-term liabilities | 2,960 | 3,043 | ||||||
| Total liabilities | $ | 10,327 | $ | 10,721 | ||||
| Equity: | ||||||||
| Common stock, par value $0.0001 per share; 150,000,000 shares authorized at March 31, 2025 and December 31, 2024; 29,752,661 and 26,611,033 shares issued and outstanding at March 31, 2025 and December 31, 2024, respectively | 3 | 3 | ||||||
| Preferred C shares, par value $0.0001 per share; 1,172,000 shares authorized at March 31, 2025 and December 31, 2024; 1,718 shares issued and outstanding at March 31, 2025 and December 31, 2024, respectively | * | * | ||||||
| Additional paid-in capital | 293,014 | 289,589 | ||||||
| Accumulated deficit | (264,672 | ) | (253,506 | ) | ||||
| Total equity | 28,345 | 36,086 | ||||||
| Total liabilities and equity | $ | 38,672 | $ | 46,807 |
All 2025 financial information is derived from the Company's 2025 unaudited financial statements, as disclosed in the Company's
Quarterly Report on Form 10-Q, filed with the Securities and Exchange Commission; all 2024 financial information is derived from the
Company's 2024 unaudited financial statements, as disclosed in the Company's Quarterly Report on Form 10-Q, filed with the
Securities and Exchange Commission.
All March 31, 2025financial information is derived from the Company's 2025 unaudited financial statements, as disclosed in the
Company's Quarterly Report on Form 10-Q, filed with the Securities and Exchange Commission. All December 31, 2024 financial information
is derived from the Company's 2024 audited financial statements as disclosed in the Company's Annual Report on Form 10-K,
for the twelve months ended December 31, 2024 filed with the Securities and Exchange Commission.