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8-K

PAVmed Inc. (PAVM)

8-K 2024-11-14 For: 2024-11-14
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Added on April 07, 2026

UNITED

STATES

SECURITIES

AND EXCHANGE COMMISSION

WASHINGTON,

DC 20549


FORM

8-K


CURRENT

REPORT

PURSUANT

TO SECTION 13 OR 15(d) OF THE

SECURITIES

EXCHANGE ACT OF 1934


Date of Report (Date of earliest event reported): November 14, 2024

PAVMED INC.
(Exact<br> Name of Registrant as Specified in Charter)
Delaware 001-37685 47-1214177
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(State<br> or Other Jurisdiction <br><br> of Incorporation) (Commission<br> <br><br> File Number) (IRS<br> Employer <br><br> Identification No.)
360 Madison Avenue, 25th Floor, New York, New York 10017
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(Address<br> of Principal Executive Offices) (Zip<br> Code)

Registrant’s telephone number, including area code: (917) 813-1828

N/A
(Former<br> Name or Former Address, if Changed Since Last Report)

Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions (see General Instruction A.2. below):

Written<br> communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425).
Soliciting<br> material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12).
Pre-commencement<br> communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b)).
Pre-commencement<br> communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c)).

Securities registered pursuant to Section 12(b) of the Act:

Title of each class Trading Symbol(s) Name of each exchange on which registered
Common<br> Stock, Par Value $0.001 Per Share PAVM The<br> Nasdaq Stock Market LLC
Series<br> Z Warrants to Purchase Common Stock PAVMZ The<br> Nasdaq Stock Market LLC

Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).

Emerging growth company ☐

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐

Item2.02. Results of Operations and Financial Condition.

On November 14, 2024, PAVmed Inc. (the “Company”) issued a press release announcing financial results for its fiscal quarter ended September 30, 2024 and providing a business update. A copy of the press release is attached to this report as Exhibit 99.1 and is incorporated herein by reference.

Item7.01. Regulation FD Disclosure.

The disclosure set forth under Item 2.02 is incorporated herein by reference.

The information furnished under Items 2.02 and 7.01, including the exhibit related thereto, shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, nor shall it be deemed incorporated by reference in any disclosure document of the Company, except as shall be expressly set forth by specific reference in such document.

Item9.01. Financial Statements and Exhibits.

(d) Exhibits:

Exhibit<br> No. Description
99.1 Press release.
104 Cover<br> Page Interactive Data File (embedded within the Inline XBRL document).

SIGNATURE

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.

Dated:<br> November 14, 2024 PAVMED<br> INC.
By: /s/ Dennis McGrath
Dennis<br> McGrath
President<br> and Chief Financial Officer

Exhibit99.1


PAVmedProvides Business Update and Third Quarter 2024 Financial Results

Lucidreports record quarterly EsoGuard^®^revenue and completes clinical evidence package for imminent submission to formallyseek Medicare coverage

VerisHealth completes pilot program with The Ohio State’s James Cancer Hospital and continues pursuit of financing to relaunch developmentof implantable monitor

Ongoinginitiatives position PAVmed to preserve Nasdaq listing

Conferencecall and webcast to be held today, November 14^th^ at 8:30 AM EST

NEWYORK, November 14, 2024 - PAVmed Inc. (NASDAQ: PAVM, PAVMZ) (“PAVmed” or the “Company”), a diversified commercial-stage medical technology company, operating in the medical device, diagnostics, and digital health sectors, today provided a business update for the Company and its subsidiaries, Lucid Diagnostics Inc. (NASDAQ: LUCD) (“Lucid”) and Veris Health Inc. (“Veris”), and presented financial results for the Company for the three months ended September 30, 2024.

ConferenceCall and Webcast

The webcast will take place on Thursday, November 14, 2024, at 8:30 AM and is accessible in the investor relations section of the Company’s website at pavmed.com. Alternatively, to access the conference call by telephone, U.S.-based callers should dial 1-800-836-8184 and international listeners should dial 1-646-357-8785. All listeners should provide the operator with the conference call name “PAVmed Business Update” to join.

Following the conclusion of the conference call, a replay will be available for 30 days on the investor relations section of the Company’s website at pavmed.com.

BusinessUpdate Highlights


“During the third quarter and in recent weeks, we have taken important transformational steps to solidify and stabilize PAVmed as a sustainable and diversified commercial life sciences company with multiple independently-financed subsidiaries, consistent with the updated business strategy we laid out earlier this year,” said Lishan Aklog, M.D., PAVmed’s Chairman and Chief Executive Officer. “We have completed the deconsolidation and are in the final stages of a debt restructuring necessary for us to regain compliance with the Nasdaq listing requirements. Lucid continues to make significant strides, both commercially and clinically, and is now ready to submit its complete clinical evidence package to formally seek Medicare coverage of EsoGuard. Our other subsidiaries, Veris Health and the PMX incubator, also continue to execute their strategic plans. In light of these developments, I am optimistic about what the future holds for PAVmed and its subsidiaries.”

Highlightsfrom the third quarter and recent weeks:

Lucid<br> reported that 3Q24 EsoGuard^®^ Esophageal DNA Test revenue was $1.2M, which represents a single-quarter record<br> and 20 percent increase sequentially from 2Q24.
Lucid<br> performed 2,787 commercial EsoGuard tests in 3Q24. Additionally, in October the lab performed a single-month record of more than<br> 1,400 tests, contributing to the largest three-month total in the Company’s history.
Lucid’s<br> ESOGUARD BE-1 clinical validation study accepted for peer-reviewed publication completing the clinical evidence package for<br> submission to formally seek Medicare coverage of EsoGuard.
Lucid<br> is now leveraging this clinical evidence to expand its direct contracting initiative with multiple programs focused on driving<br> near-term revenue growth, including a shift to fully-contracted #CYFT Precancer Testing Events, broadening employer markets activity,<br> and a new foray into the concierge medicine sector.
Veris<br> completed pilot program with The Ohio State’s James Cancer Hospital and is now in active discussions on long-term commercial<br> and strategic partnerships.
Veris<br> awarded a $1.8 million National Institutes of Health (NIH) grant to further optimize Veris Cancer Care Platform in partnership<br> with an academic cancer center.
Veris<br> continuing to pursue financing to relaunch the development of its implantable monitor.
As<br> part of PAVmed’s efforts to regain compliance with the Nasdaq listing standards by increasing its stockholders’ equity<br> above the minimum required, the Company completed the deconsolidation of Lucid from its balance sheet on September 10, and reached<br> an agreement in principle with its convertible debt holder (the structure of which was presented to the Nasdaq hearing panel) regarding<br> the terms on which $25 million of PAVmed’s convertible debt would be exchanged into preferred equity of an equivalent value.<br> Nasdaq has granted PAVmed until January 31, 2025 to regain compliance through this exchange transaction, which remains subject to<br> the Company’s accounting advisors completing their analysis of the transaction structure and stockholder approval.

FinancialResults:

For<br> the three months ended September 30, 2024, EsoGuard related revenues were $1.0 million, net of the deconsolidation. Operating expenses<br> were approximately $12.6 million which include stock-based compensation expenses of $1.9 million. GAAP net income attributable to<br> common stockholders was approximately $64.3 million, or $1.44 per common share on a diluted basis.
As<br> shown below and for the purpose of illustrating the effect of stock-based compensation and other non-cash income and expenses on<br> the Company’s financial results, the Company’s non-GAAP adjusted loss was approximately $5.4 million or $(0.54) per common<br> share.
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PAVmed<br> had cash and cash equivalents of $0.8 million as of September 30, 2024, compared to $19.6 million as of December 31, 2023.
PAVmed’s<br> Equity method investment (Lucid Diagnostics) fair value at September 30, 2024 was $25.5 Million. In accordance with GAAP, the comparable<br> periods before deconsolidation of Lucid are not reflected on PAVmed’s balance sheets prior to September 10, 2024.
The<br> unaudited financial results for the three months ended September 30, 2024 were filed with the SEC on Form 10-Q on November 13, 2024,<br> and are available at www.pavmed.com or www.sec.gov.

PAVmedNon-GAAP Measures

To<br> supplement our financial results presented in accordance with U.S. generally accepted accounting principles (GAAP), management provides<br> certain non-GAAP financial measures of the Company’s financial results. These non-GAAP financial measures include net loss<br> before interest, taxes, depreciation, and amortization (EBITDA) and non-GAAP adjusted loss, which further adjusts EBITDA for stock-based<br> compensation expense, loss on the issuance or modification of convertible securities, the periodic change in fair value of convertible<br> securities, and loss on debt extinguishment. The foregoing non-GAAP financial measures of EBITDA and non-GAAP adjusted loss are not<br> recognized terms under U.S. GAAP.
Non-GAAP<br> financial measures are presented with the intent of providing greater transparency to the information used by us in our financial<br> performance analysis and operational decision-making. We believe these non-GAAP financial measures provide meaningful information<br> to assist investors, shareholders, and other readers of our financial statements in making comparisons to our historical financial<br> results and analyzing the underlying performance of our results of operations. These non-GAAP financial measures are not intended<br> to be, and should not be, a substitute for, considered superior to, considered separately from, or as an alternative to, the most<br> directly comparable GAAP financial measures.
Non-GAAP<br> financial measures are provided to enhance readers’ overall understanding of our current financial results and to provide further<br> information for comparative purposes. Management believes the non-GAAP financial measures provide useful information to management<br> and investors by isolating certain expenses, gains, and losses that may not be indicative of our core operating results and business<br> outlook. Specifically, the non-GAAP financial measures include non-GAAP adjusted loss, and its presentation is intended to help the<br> reader understand the effect of the loss on the issuance or modification of convertible securities, the periodic change in fair value<br> of convertible securities, the loss on debt extinguishment and the corresponding accounting for non-cash charges on financial performance.<br> In addition, management believes non-GAAP financial measures enhance the comparability of results against prior periods.
A<br> reconciliation to the most directly comparable GAAP measure of all non-GAAP financial measures included in this press release for<br> the three and nine months ended September 30, 2024 and 2023 are as follows:
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CondensedConsolidated Statement of Operations (Unaudited)

For the three months ended <br>September 30, For the nine months ended <br>September 30,
2024 2023 2024 2023
(in thousands except per-share amounts)
Revenue $ 996 $ 791 $ 2,985 $ 1,403
Operating expenses 12,574 16,319 42,285 53,815
Other (Income) Expense (72,289 ) 6,222 (66,585 ) 9,443
Net (Income) Loss (60,711 ) 21,750 (27,285 ) 61,855
Net income (loss) attributable to common stockholders 64,316 (17,748 ) 30,620 (50,365 )
Preferred Stock dividends and deemed dividends 83 77 7,740 226
Net income (loss) as reported 64,399 (17,671 ) 38,360 (50,139 )
Adjustments:
Depreciation and amortization expense^1^ 238 733 1,129 2,207
Interest expense, net^2^ (58 ) 35 (214 ) 162
NCI ownership share of Interest and Depreciation adjustments (43 ) (213 ) (229 ) (627 )
EBITDA 64,536 (17,116 ) 39,046 (48,397 )
Other non-cash or financing related expenses:
Stock-based compensation expense^3^ 1,931 2,245 5,716 9,171
ResearchDx acquisition/settlement paid in stock^1^ 713
Operating expenses issued in stock^1^ 285 625 448 625
Gain on deconsolidation of subsidiary (72,287 ) (72,287 )
Change in FV equity method investments (407 ) (407 )
Change in FV convertible debt^2^ (240 ) 4,392 2,488 5,772
Offering costs convertible debt^2^ 1,186
Loss on debt extinguishment^2^ 1,403 1,764 2,535 3,032
Debt modification expense 2,000
Other non-cash charges
NCI ownership share of non-GAAP adjustments (660 ) (1,453 ) (1,262 ) (3,645 )
Non-GAAP adjusted (loss) $ (5,439 ) $ (9,543 ) $ (21,723 ) $ (31,543 )
Non-GAAP shares outstanding, basic and diluted 10,005 7,463 9,287 6,968
Non-GAAP adjusted (loss) income per share, basic and diluted $ (0.54 ) $ (1.28 ) $ (2.34 ) $ (4.53 )

**^1^**Included in general and administrative expenses in the financial statements.

^2^Included in other income and expenses.

^3^Stock-based compensation (“SBC”) expense included in operating expenses is detailed as follows in the table below by category within operating expenses for the non-GAAP Net operating expenses:

Reconciliationof GAAP Operating Expenses to Non-GAAP Net Operating Expenses

(in thousands except per-share amounts) For the three months ended <br>September 30, For the nine months ended <br>September 30,
2024 2023 2024 2023
Cost of revenue $ 1,381 $ 1,779 $ 4,792 $ 4,809
Stock-based compensation expense^3^ (32 ) (32 ) (112 ) (86 )
Net cost of revenue 1,349 1,747 4,680 4,723
Amortization of acquired intangible assets 82 505 559 1,516
Sales and marketing 2,920 4,016 11,472 12,893
Stock-based compensation expense^3^ (292 ) (403 ) (1,082 ) (1,302 )
Net sales and marketing 2,628 3,613 10,390 11,591
General and administrative 6,649 6,858 20,337 23,916
Depreciation expense (156 ) (228 ) (570 ) (691 )
ResearchDx acquisition/settlement paid in stock (713 )
Operating expenses issued in stock (285 ) (625 ) (448 ) (625 )
Stock-based compensation expense^3^ (1,426 ) (1,499 ) (3,717 ) (6,761 )
Net general and administrative 4,782 4,506 15,602 15,126
Research and development 1,542 3,161 5,125 10,681
Stock-based compensation expense^3^ (181 ) (311 ) (805 ) (1,022 )
Net research and development 1,361 2,850 4,320 9,659
Total operating expenses 12,574 16,319 42,285 53,815
Depreciation and amortization expense (238 ) (733 ) (1,129 ) (2,207 )
ResearchDx acquisition/settlement paid in stock (713 )
Operating expenses issued in stock (285 ) (625 ) (448 ) (625 )
Stock-based compensation expense^3^ (1,931 ) (2,245 ) (5,716 ) (9,171 )
Net operating expenses $ 10,120 $ 12,716 $ 34,992 $ 41,099

AboutPAVmed and its Subsidiaries

PAVmed Inc. is a diversified commercial-stage medical technology company operating in the medical device, diagnostics, and digital health sectors. Its subsidiary, Lucid Diagnostics Inc. (NASDAQ: LUCD), is a commercial-stage cancer prevention medical diagnostics company that markets the EsoGuard^®^ Esophageal DNA Test and EsoCheck^®^ Esophageal Cell Collection Device—the first and only commercial tools for widespread early detection of esophageal precancer to mitigate the risks of esophageal cancer deaths. Its other subsidiary, Veris Health Inc., is a digital health company focused on enhanced personalized cancer care through remote patient monitoring using implantable biologic sensors with wireless communication along with a custom suite of connected external devices. Veris is concurrently developing an implantable physiological monitor, designed to be implanted alongside a chemotherapy port, which will interface with the Veris Cancer Care Platform.

For more and for more information about PAVmed, please visit pavmed.com.

For more information about Lucid Diagnostics, please visit luciddx.com.

For more information about Veris Health, please visit verishealth.com.

Forward-LookingStatements

This press release includes forward-looking statements that involve risks and uncertainties. Forward-looking statements are any statements that are not historical facts. Such forward-looking statements, which are based upon the current beliefs and expectations of PAVmed’s and Lucid’s management, are subject to risks and uncertainties, which could cause actual results to differ from the forward-looking statements. Risks and uncertainties that may cause such differences include, among other things, volatility in the price of PAVmed’s and Lucid’s common stock; PAVmed’s Series Z warrants; general economic and market conditions; the uncertainties inherent in research and development, including the cost and time required to advance PAVmed’s and Lucid’s products to regulatory submission; whether regulatory authorities will be satisfied with the design of and results from PAVmed’s and Lucid’s clinical and preclinical studies; whether and when PAVmed’s and Lucid’s products are cleared by regulatory authorities; market acceptance of PAVmed’s and Lucid’s products once cleared and commercialized; PAVmed’s and Lucid’s ability to raise additional funding as needed; and other competitive developments. In addition, new risks and uncertainties may arise from time to time and are difficult to predict. For a further list and description of these and other important risks and uncertainties that may affect PAVmed’s and Lucid’s future operations, see Part I, Item 1A, “Risk Factors,” in PAVmed’s and Lucid’s most recent Annual Report on Form 10-K filed with the Securities and Exchange Commission, as the same may be updated in Part II, Item 1A, “Risk Factors” in any Quarterly Report on Form 10-Q filed by PAVmed or Lucid after its most recent Annual Report. PAVmed and Lucid disclaim any intention or obligation to publicly update or revise any forward-looking statement to reflect any change in its expectations or in events, conditions, or circumstances on which those expectations may be based, or that may affect the likelihood that actual results will differ from those contained in the forward-looking statements.

Investorand Media Contact

Matt Riley

PAVmed and Lucid Diagnostics

mjr@pavmed.com