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UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 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):
August 14, 2024
Longeveron Inc.
(Exact name of registrant as specified in its
charter)
Delaware |
|
001-40060 |
|
47-2174146 |
(State or Other Jurisdiction
of Incorporation) |
|
(Commission File Number) |
|
(IRS Employer
Identification No.) |
1951 NW 7th Avenue, Suite 520
Miami, Florida 33136
(Address of Principal Executive Offices)
Registrant’s Telephone Number, Including
Area Code: (305) 909-0840
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:
☐ |
Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425) |
☐ |
Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12) |
☐ |
Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b)) |
☐ |
Pre-commencement 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 |
Class A Common Stock, $0.001 par value per share |
|
LGVN |
|
The Nasdaq Capital Market |
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.
Item 2.02. Other Events
On August 14, 2024, Longeveron Inc. (the “Company”)
announced financial and operating results for the three and six months ended June 30, 2024. The full text of the press release issued
in connection with the announcement is attached as Exhibit 99.1 to this Current Report on Form 8-K and incorporated by reference herein.
The information provided under this Form 8-K (including
Exhibit 99.1) shall not be deemed “filed” for any purposes of Section 18 of the Securities Exchange Act of 1934 (the “Exchange
Act”) or otherwise subject to the liabilities of that section, nor shall it be deemed incorporated by reference in any filing under
the Securities Act of 1933, as amended, or the Exchange Act, except as expressly set forth by specific reference in such a filing.
Item 9.01. Financial Statements and Exhibits.
(d) Exhibits.
The exhibits listed in the following Exhibit Index are filed as part
of this Current Report on Form 8-K.
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.
|
LONGEVERON INC. |
|
|
Date: August 14, 2024 |
/s/ Wa’el Hashad |
|
Name: |
Wa’el Hashad |
|
Title: |
Chief Executive Officer |
Exhibit 99.1
![](https://www.sec.gov/Archives/edgar/data/1721484/000121390024069029/ex99-1_001.jpg)
Longeveron Announces Second Quarter 2024 Financial
Results and Provides Business Update
| ● | Positive data from the Phase 2a clinical trial (CLEAR MIND ) evaluating Lomecel-BTM
in Alzheimer’s disease presented in Featured Research Oral Presentation at Alzheimer’s Association International Conference®
(AAIC) |
| ● | U.S. FDA granted Lomecel-B™ both Regenerative Medicine Advanced Therapy
(RMAT) designation and Fast Track designation for the treatment of mild Alzheimer’s disease |
| ● | Phase 2b clinical trial (ELPIS II) evaluating Lomecel-BTM in rare
pediatric disease HLHS has achieved 70% enrollment with completion of enrollment targeted for the end of 2024 |
| ● | Strengthened Board of Directors with election of 3 experienced industry veterans
at Annual Meeting |
| ● | Focused expenditure management reduced first half Total Operating Expenses
22% year-over-year |
| ● | Financing transaction and warrant exercises in July raised gross proceeds
of $15.3 million to fund continued clinical development, and current cash and cash equivalents are expected to be sufficient to fund Company
through the fourth quarter of 2025 |
| ● | Company to host conference call and webcast today at 4:30 p.m. ET |
MIAMI, August 14, 2024 -- Longeveron Inc. (NASDAQ:
LGVN), a clinical stage regenerative medicine biotechnology company developing cellular therapies for life-threatening and chronic aging-related
conditions, today reported financial results for the quarter ended June 30, 2024 and provided a business update.
“In the second quarter, we continued to
make strong progress advancing our investigational cellular therapy candidate, Lomecel-BTM, as a potential treatment for both
Alzheimer’s disease and Hypoplastic Left Heart Syndrome (HLHS),” said Wa’el Hashad, Chief Executive Officer of Longeveron.
“Based on the clinical data generated thus far, which in our view has been impressive, the U.S. FDA granted Lomecel-B™ Regenerative
Medicine Advanced Therapy (RMAT) designation and Fast Track designation for the treatment of mild Alzheimer’s disease. With these
designations, and the positive CLEAR MIND Phase 2a clinical trial data recently presented at AAIC, we believe there is strong evidence
supporting the therapeutic potential of Lomecel-BTM in the treatment of mild Alzheimer’s disease. Similarly, we were
delighted to see the level of interest and support at our June investigator meeting for the HLHS ELPIS II Phase 2b clinical trial, which
recently achieved 70% enrollment and for which we are targeting completion of enrollment by the end of this year. Lastly, with the capital
we have recently raised from warrant exercises and equity transactions, including participation from certain board members and insiders
of the Company in one of those transactions, we believe we have capital sufficient to fund the Company through the fourth quarter of 2025.”
Development Programs Update
Longeveron’s
lead investigational therapeutic candidate is Lomecel-BTM,
a proprietary, scalable, allogeneic cellular therapy being evaluated in multiple indications.
Hypoplastic Left Heart Syndrome (HLHS)
– a rare pediatric congenital heart birth defect in which the left ventricle (one of the pumping chambers of the heart) is either
severely underdeveloped or missing.
| ● | On-going Phase 2b clinical trial (ELPIS II) enrolling
38 pediatric patients, with enrollment completion currently targeted for year-end 2024. Given their smaller populations, clinical trial
timing for rare diseases is difficult to predict. |
| ● | In June, the Company hosted a successful ELPIS
II investigator meeting, bringing together principal investigators and site staff from premier infant and children’s treatment institutions
across the country |
| ● | ELPIS II is being conducted in collaboration
with the National Heart, Lung, and Blood Institute (NHLBI) through grants from the National Institutes of Health (NIH) |
| ● | ELPIS II builds on the positive clinical results
of ELPIS I, in which children in the trial experienced 100% transplant-free survival up to five years of age after receiving Lomecel-BTM
compared to approximate 20% mortality rate observed from historical control data |
| ● | ELPIS I five-year post-treatment completion data
anticipated in Q3 2024 |
| ● | The FDA has granted Lomecel-BTM Orphan
Drug designation, Fast Track designation, and Rare Pediatric Disease designation for the treatment of HLHS |
| ● | The Company anticipates feedback from a Type
C meeting with the U.S. Food and Drug Administration (FDA) before year-end on development strategy for HLHS and expectations for the potential
Biologics License Application (BLA) approval |
Alzheimer’s disease (AD) –
a neurodegenerative disorder that leads to progressive memory loss and death and currently has very limited therapeutic options.
| ● | Full results from the Phase 2a clinical trial
(CLEAR MIND) were presented in a featured research oral presentation at the 2024 Alzheimer's Association International Conference (AAIC) |
| o | In the clinical trial, Lomecel-B™ treated patients showed an overall slowing/prevention of disease
worsening compared to placebo |
| o | The trial achieved the primary safety and secondary efficacy endpoints and showed statistically significant
improvements in pre-specified clinical and biomarker endpoints in specific Lomecel-B™ groups compared to placebo |
| o | The established safety profile of Lomecel-B™ for single and multiple dosing regimens was demonstrated in study data that showed
no incidence of hypersensitivity, infusion-related reactions, and no cases of amyloid-related imaging abnormalities (ARIA) |
| o | Administration of Lomecel-B™ was associated with slowing cognitive and functional decline as demonstrated by statistically significant
results in the Montreal Cognitive Assessment and statistical trending improvements compared to placebo in CDR-SB and MMSE |
| o | There was a statistically significant improvement relative to placebo observed in the Alzheimer’s
Disease Cooperative Study Activities of Daily Living (ADCS-ADL) |
| o | Brain MRI results demonstrated a 49% reduction in brain volume loss and improvement in cerebral blood
flow |
| o | These results support the therapeutic potential of Lomecel-BTM in the treatment of mild Alzheimer’s
disease and provided evidence-based support for further clinical development |
| ● | The FDA has granted Lomecel-B™ both Regenerative
Medicine Advanced Therapy (RMAT) designation and Fast Track designation for the treatment of mild Alzheimer’s disease |
| ● | The Company anticipates meeting with the FDA
before year-end to review future clinical and regulatory strategy |
Recent Corporate Highlights
| ● | As part of the planned Board of Directors refreshment
process, with a focus on bringing in new, relevant, experienced leaders over time to add to the knowledge base and experience provided
by current and departing members, three new members were elected to the Company’s Board of Directors at the Company’s annual
meeting of stockholders on July 2, 2024: |
| o | Richard Kender, retired SVP of Business Development and Corporate Licensing for Merck & Co., Inc., |
| o | Roger Hajjar, M.D., gene therapy pioneer and Director of the Gene and Cell Therapy Institute at Mass General
Brigham, |
| o | Neha Motwani, senior healthcare investment banker |
| ● | Launch of contract development and manufacturing
business, which the Company believes has the potential to generate approximately $4-5 million in annual revenues once it is up and running
fully |
Year to Date 2024 Summary Financial Results
| ● | Revenues, Cost of Revenues
and Gross Profit: Revenues for the six months ended June 30, 2024 and 2023 were $1.0 million and $0.5 million, respectively.
2024 revenues increased $0.5 million, or 105%, when compared to the same period in 2023 mainly as a result of increased participant demand
for our investigational Frailty and Cognitive Impairment registry trial in the Bahamas (the “Bahamas Registry Trial”). Clinical
trial revenue, which is derived from the Bahamas Registry Trial, for the six months ended June 30, 2024 and 2023, was $0.8 million and
$0.5 million, respectively. Clinical trial revenue for the six months ended June 30, 2024 increased by $0.3 million, or 76%, when compared
to the same period in 2023 as a result of increased participant demand. Contract manufacturing revenue for the six months ended June 30,
2024 was $0.2 million from our first manufacturing services contract with Secretome Therapeutics. |
| ● | Related cost of revenues:
Cost of revenues was $0.3 million for the six-month periods ended June 30, 2024 and 2023. This resulted in a gross profit of
approximately $0.7 million for the six months ended June 30, 2024, an increase of $0.5 million, or greater than 100%, when compared with
a gross profit of $0.2 million for 2023. This increase is driven by higher Clinical trial revenue and the new manufacturing services contract
revenue. |
| ● | General and Administrative
Expenses: General and administrative expenses for the six months ended June 30, 2024 decreased to approximately $4.3 million compared
to $5.5 million for the same period in 2023. The decrease of approximately $1.2 million, or 22%, was primarily related to a decrease in
personnel expenses as a result of lower severance and stock compensation costs in 2024. |
| ● | Research and Development
Expenses: Research and development expenses for the six months ended June 30, 2024 decreased to approximately $3.9 million from
approximately $5.1 million for the same period in 2023. The decrease of $1.2 million, or 22%, was primarily due to a decrease of $1.3
million in research and development expenses being incurred for the completed Phase 2a (CLEAR MIND) Alzheimer’s disease clinical
trial and reduced costs for the aging-related frailty clinical trial following our decision to discontinue trial activities in Japan,
reduced cost of supplies of $0.4 million and $0.1 million of lower equity-based compensation expenses allocated to research and development
expenses. These reductions were partially offset by $0.6 million of higher compensation and benefit costs. |
| ● | Other Income, net: Other
income for the six months ended June 30, 2024 was $0.1 million. Other income consisted of $0.1 million from interest earned on money market
funds and marketable securities. Other income for the six months ended June 30, 2023 was $0.1 million as result of gains from marketable
securities. |
| ● | Net Loss: Net loss
decreased to approximately $7.5 million for the six months ended June 30, 2024 from a net loss of $10.3 million for the same period in
2023. The decrease in the net loss of $2.8 million, or 27%, was for the reasons outlined above. |
| ● | Cash and cash equivalents
and marketable securities: as of June 30, 2024 were $12.4 million. Following capital raises and warrant exercises in April and June
2024 resulting in gross proceeds of $17.6 million, in July 2024, the Company completed a Registered Direct Offering which resulted in
gross proceeds of $9.0 million. Additionally, certain warrant holders exercised their existing warrants in July, generating gross proceeds
of $6.3 million. The Company believes its existing cash and cash equivalents will enable it to fund its operating expenses and capital
expenditure requirements through the fourth quarter of 2025. These estimates are based on assumptions that may prove to be imprecise,
and the Company could utilize its available capital resources sooner than it expects. |
Conference Call and Webcast
The Company will host a conference call and webcast
today at 4:30 p.m. ET.
Conference Call Number: |
|
1.877.407.0789 |
Conference ID: |
|
13747923 |
Call meTM Feature: |
|
Click Here |
Webcast: |
|
Click Here |
An archived replay of the webcast will be available
on the “Events & Presentations” section of the Company’s website following the conference.
About
Longeveron Inc.
Longeveron is a clinical stage biotechnology company
developing regenerative medicines to address unmet medical needs. The Company’s lead investigational product is Lomecel-B™,
an allogeneic medicinal signaling cell (MSC) therapy product isolated from the bone marrow of young, healthy adult donors. Lomecel-B™
has multiple potential mechanisms of action encompassing pro-vascular, pro-regenerative, anti-inflammatory, and tissue repair and healing
effects with broad potential applications across a spectrum of disease areas. Longeveron is currently pursuing three pipeline indications:
hypoplastic left heart syndrome (HLHS), Alzheimer’s disease, and Aging-related Frailty. Lomecel-BTM development programs
have received five distinct and important FDA designations: for the HLHS program - Orphan Drug designation, Fast Track designation, and
Rare Pediatric Disease designation; and, for the AD program - Regenerative Medicine Advanced Therapy (RMAT) designation and Fast Track
designation. For more information, visit www.longeveron.com or follow Longeveron on LinkedIn, X, and Instagram.
Forward-Looking Statements
Certain statements in this press release that
are not historical facts are forward-looking statements made pursuant to the safe harbor provisions of the Private Securities Litigation
Reform Act of 1995, which reflect management’s current expectations, assumptions, and estimates of future operations, performance
and economic conditions, and involve risks and uncertainties that could cause actual results to differ materially from those anticipated
by the statements made herein. Forward-looking statements are generally identifiable by the use of forward-looking terminology such as
“believe,” “expects,” “may,” “looks to,” “will,” “should,” “plan,”
“intend,” “on condition,” “target,” “see,” “potential,” “estimates,”
“preliminary,” or “anticipates” or the negative thereof or comparable terminology, or by discussion of strategy
or goals or other future events, circumstances, or effects and include, but are not limited to, the anticipated use of proceeds from recent
offerings. Factors that could cause actual results to differ materially from those expressed or implied in any forward-looking statements
in this release include, but are not limited to, market and other conditions, our limited operating history and lack of products approved
for commercial sale; adverse global conditions, including macroeconomic uncertainty; inability to raise additional capital necessary to
continue as a going concern; our history of losses and inability to achieve profitability going forward; the absence of FDA-approved allogenic,
cell-based therapies for Aging-related Frailty, Alzheimer’s disease, or other aging-related conditions, or for HLHS or other cardiac-related
indications; ethical and other concerns surrounding the use of stem cell therapy or human tissue; our exposure to product liability claims
arising from the use of our product candidates or future products in individuals, for which we may not be able to obtain adequate product
liability insurance; the adequacy of our trade secret and patent position to protect our product candidates and their uses: others could
compete against us more directly, which could harm our business and have a material adverse effect on our business, financial condition,
and results of operations; if certain license agreements are terminated, our ability to continue clinical trials and commercially market
products could be adversely affected; the inability to protect the confidentiality of our proprietary information, trade secrets, and
know-how; third-party claims of intellectual property infringement may prevent or delay our product development efforts; intellectual
property rights do not necessarily address all potential threats to our competitive advantage; the inability to successfully develop and
commercialize our product candidates and obtain the necessary regulatory approvals; we cannot market and sell our product candidates in
the U.S. or in other countries if we fail to obtain the necessary regulatory approvals; final marketing approval of our product candidates
by the FDA or other regulatory authorities for commercial use may be delayed, limited, or denied, any of which could adversely affect
our ability to generate operating revenues; we may not be able to secure and maintain research institutions to conduct our clinical trials;
ongoing healthcare legislative and regulatory reform measures may have a material adverse effect on our business and results of operations;
if we receive regulatory approval of Lomecel-B™ or any of our other product candidates, we will be subject to ongoing regulatory
requirements and continued regulatory review, which may result in significant additional expense; being subject to penalties if we fail
to comply with regulatory requirements or experience unanticipated problems with our therapeutic candidates; reliance on third parties
to conduct certain aspects of our preclinical studies and clinical trials; interim, “topline” and preliminary data from our
clinical trials that we announce or publish from time to time may change as more data become available and are subject to audit and verification
procedures that could result in material changes in the final data; the volatility of the price of our Class A common stock; we could
lose our listing on the Nasdaq Capital Market; provisions in our certificate of incorporation and bylaws and Delaware law might discourage,
delay or prevent a change in control of our company or changes in our management and, therefore, depress the market price of our Class
A common stock; we have never commercialized a product candidate before and may lack the necessary expertise, personnel and resources
to successfully commercialize any products on our own or together with suitable collaborators; and in order to successfully implement
our plans and strategies, we will need to grow our organization, and we may experience difficulties in managing this growth. Further information
relating to factors that may impact the Company’s results and forward-looking statements are disclosed in the Company’s filings
with the Securities and Exchange Commission, including Longeveron’s Annual Report on Form 10-K for the year ended December 31, 2023,
filed with the Securities and Exchange Commission on February 27, 2024, as amended by the Annual Report on Form 10-K/A filed March 11,
2024, its Quarterly Reports on Form 10-Q, and its Current Reports on Form 8-K. The forward-looking statements contained in this press
release are made as of the date of this press release, and the Company disclaims any intention or obligation, other than imposed by law,
to update or revise any forward-looking statements, whether as a result of new information, future events, or otherwise.
Investor and Media Contact:
Derek Cole
Investor Relations Advisory Solutions
derek.cole@iradvisory.com
---tables follow---
Longeveron Inc.
Condensed Balance Sheets
(In thousands, except share and per share data)
| |
June 30, 2024 | | |
December 31, 2023 | |
| |
(Unaudited) | | |
| |
Assets | |
| | |
| |
Current assets: | |
| | |
| |
Cash and cash equivalents | |
$ | 12,375 | | |
$ | 4,949 | |
Marketable securities | |
| - | | |
| 412 | |
Prepaid expenses and other current assets | |
| 817 | | |
| 376 | |
Accounts and grants receivable | |
| 218 | | |
| 111 | |
Total current assets | |
| 13,410 | | |
| 5,848 | |
Property and equipment, net | |
| 2,371 | | |
| 2,529 | |
Intangible assets, net | |
| 2,353 | | |
| 2,287 | |
Operating lease asset | |
| 1,055 | | |
| 1,221 | |
Other assets | |
| 204 | | |
| 193 | |
Total assets | |
$ | 19,393 | | |
$ | 12,078 | |
Liabilities and stockholders’ equity | |
| | | |
| | |
Current liabilities: | |
| | | |
| | |
Accounts payable | |
$ | 600 | | |
$ | 638 | |
Accrued expenses | |
| 1,605 | | |
| 2,152 | |
Current portion of lease liability | |
| 608 | | |
| 593 | |
Deferred revenue | |
| 397 | | |
| 506 | |
Total current liabilities | |
| 3,210 | | |
| 3,889 | |
Long-term liabilities: | |
| | | |
| | |
Lease liability | |
| 1,140 | | |
| 1,448 | |
Other liabilities | |
| 132 | | |
| - | |
Total long-term liabilities | |
| 1,272 | | |
| 1,448 | |
Total liabilities | |
| 4,482 | | |
| 5,337 | |
Commitments and contingencies (Note 9) | |
| | | |
| | |
Stockholders’ equity: | |
| | | |
| | |
Preferred stock, $0.001 par value per share, 5,000,000 shares authorized, no shares issued and outstanding at June 30, 2024, and December 31, 2023 | |
| - | | |
| - | |
Class A common stock, $0.001 par value per share, 84,295,000 shares authorized, 8,116,909 shares issued and outstanding at June 30, 2024; 1,025,183 issued and outstanding at December 31, 2023 | |
| 8 | | |
| 1 | |
Class B common stock, $0.001 par value per share, 15,705,000 shares authorized, 1,484,005 shares issued and outstanding at June 30, 2024; 1,485,560 issued and outstanding at December 31, 2023 | |
| 1 | | |
| 1 | |
Additional paid-in capital | |
| 115,859 | | |
| 91,823 | |
Stock subscription receivable | |
| - | | |
| (100 | ) |
Accumulated deficit | |
| (100,956 | ) | |
| (84,984 | ) |
Accumulated other comprehensive loss | |
| (1 | ) | |
| - | |
Total stockholders’ equity | |
| 14,911 | | |
| 6,741 | |
Total liabilities and stockholders’ equity | |
$ | 19,393 | | |
$ | 12,078 | |
See accompanying notes to unaudited condensed
financial statements.
Longeveron Inc.
Condensed Statements of Operations
(In thousands, except per share data)
(Unaudited)
| |
Three months ended June 30, | | |
Six months ended June 30, | |
| |
2024 | | |
2023 | | |
2024 | | |
2023 | |
Revenues | |
| | |
| | |
| | |
| |
Clinical trial revenue | |
$ | 287 | | |
$ | 217 | | |
$ | 802 | | |
$ | 455 | |
Contract manufacturing revenue | |
| 181 | | |
| - | | |
| 214 | | |
| - | |
Grant revenue | |
| - | | |
| - | | |
| - | | |
| 41 | |
Total revenues | |
| 468 | | |
| 217 | | |
| 1,016 | | |
| 496 | |
Cost of revenues | |
| 124 | | |
| 124 | | |
| 343 | | |
| 327 | |
Gross profit | |
| 344 | | |
| 93 | | |
| 673 | | |
| 169 | |
| |
| | | |
| | | |
| | | |
| | |
Operating expenses | |
| | | |
| | | |
| | | |
| | |
General and administrative | |
| 2,122 | | |
| 3,518 | | |
| 4,322 | | |
| 5,530 | |
Research and development | |
| 1,722 | | |
| 2,287 | | |
| 3,941 | | |
| 5,067 | |
Total operating expenses | |
| 3,844 | | |
| 5,805 | | |
| 8,263 | | |
| 10,597 | |
Loss from operations | |
| (3,500 | ) | |
| (5,712 | ) | |
| (7,590 | ) | |
| (10,428 | ) |
Other income and (expenses) | |
| | | |
| | | |
| | | |
| | |
Other income, net | |
| 87 | | |
| 80 | | |
| 119 | | |
| 149 | |
Total other income, net | |
| 87 | | |
| 80 | | |
| 119 | | |
| 149 | |
Net loss | |
$ | (3,413 | ) | |
$ | (5,632 | ) | |
$ | (7,471 | ) | |
$ | (10,279 | ) |
Deemed dividend – warrant inducement offers | |
| (8,501 | ) | |
| - | | |
| (8,501 | ) | |
| - | |
Net loss attributable to common stockholders | |
$ | (11,914 | ) | |
$ | (5,632 | ) | |
$ | (15,972 | ) | |
$ | (10,279 | ) |
Basic and diluted net loss per share | |
$ | (1.83 | ) | |
$ | (2.67 | ) | |
$ | (3.54 | ) | |
$ | (4.88 | ) |
Basic and diluted weighted average common shares outstanding | |
| 6,509,881 | | |
| 2,110,544 | | |
| 4,511,734 | | |
| 2,106,973 | |
See accompanying notes to unaudited condensed
financial statements.
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Longeveron (NASDAQ:LGVNR)
過去 株価チャート
から 7 2024 まで 8 2024
Longeveron (NASDAQ:LGVNR)
過去 株価チャート
から 8 2023 まで 8 2024