STOCK TITAN

[8-K] LISATA THERAPEUTICS, INC. Reports Material Event

LISATA THERAPEUTICS, INC.

(Very High)
(Neutral)
Form Type
8-K

Rhea-AI Filing Summary

LISATA THERAPEUTICS, INC. (symbol: LSTA) is the issuer of record for a Form 8-K filing submitted to the SEC.

Positive

  • None.

Negative

  • None.

Insights

Analyzing...

Item 1.01 Entry into a Material Definitive Agreement Business
The company signed a significant contract such as a merger agreement, credit facility, or major partnership.
Item 2.01 Completion of Acquisition or Disposition of Assets Financial
The company completed a significant acquisition or sale of business assets.
Item 3.02 Unregistered Sales of Equity Securities Securities
The company sold equity securities in a private placement or other unregistered transaction.
Item 5.02 Departure of Directors or Certain Officers; Election of Directors; Appointment of Certain Officers Governance
Key personnel changes including departures, elections, or appointments of directors and executive officers.
Item 5.03 Amendments to Articles of Incorporation or Bylaws; Change in Fiscal Year Governance
The company amended its charter documents, bylaws, or changed its fiscal year.
Item 7.01 Regulation FD Disclosure Disclosure
Material non-public information disclosed under Regulation Fair Disclosure, often investor presentations or guidance.
Item 9.01 Financial Statements and Exhibits Exhibits
Financial statements, pro forma financial information, or exhibit attachments filed with this report.

AI-generated analysis. How Rhea-AI works. Not financial advice.

See more from StockTitan in Google Search and AI answers. Adds StockTitan as a preferred source · opens Google
Add on Google
Learn about SEC filing dates

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): September 17, 2026

LISATA THERAPEUTICS, INC.
(Exact name of registrant as specified in its charter)



Delaware
001-33650
22-2343568
(State or other jurisdiction of incorporation)
(Commission File Number)
(IRS Employer Identification No.)

P.O. Box 173 Liberty Corner, NJ 07938
(Address of principal executive offices, including zip code)

(908) 842-0100
(Registrant’s telephone number, including area code)

Not Applicable
(Former 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:


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
 
Trade
Symbol(s)
 
Name of each exchange
on which registered
Common Stock, $0.001 par value per share
 
LSTA
 
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 1.01 Entry into a Material Definitive Agreement.

Agreement and Plan of Merger
 
On September 17, 2026, Lisata Therapeutics, Inc., a Delaware corporation (the “Company” or “Lisata”), acquired Marea Therapeutics, Inc., a Delaware corporation (“Marea”), in accordance with the terms of the Agreement and Plan of Merger, dated September 17, 2026 (the “Merger Agreement”), by and among the Company, Mariner Merger Sub I, Inc., a Delaware corporation and a wholly owned subsidiary of the Company (“First Merger Sub”), Mariner Merger Sub II, LLC, a Delaware limited liability company and wholly owned subsidiary of the Company (“Second Merger Sub”), and Marea. Pursuant to the Merger Agreement, First Merger Sub merged with and into Marea, pursuant to which Marea was the surviving corporation and became a wholly owned subsidiary of the Company (the “First Merger”). Immediately following the First Merger, Marea merged with and into Second Merger Sub, pursuant to which Second Merger Sub was the surviving entity (together with the First Merger, the “Merger”). The Merger is intended to qualify as a tax-free reorganization for U.S. federal income tax purposes.
 
Under the terms of the Merger Agreement, upon the closing of the Merger (the “Closing”), the Company issued to the stockholders of Marea (i) 1,793,129.0 shares of the common stock of the Company, par value $0.001 per share (the “Common Stock”), and (ii) 211,365.213 shares of Series C Non-Voting Convertible Preferred Stock of the Company, par value $0.01 per share (the “Series C Preferred Stock”), each share of which is convertible into 1,000 shares of Common Stock, subject to approval by the stockholders of the Company of the Conversion Proposal (as defined below). The powers, preferences, rights, qualifications, limitations and restrictions applicable to the Series C Preferred Stock are set forth in the Certificate of Designation (as defined below).
 
Reference is made to the discussion of the Series C Preferred Stock in Item 5.03 of this Current Report on Form 8-K, which is incorporated into this Item 1.01 by reference.
 
Shares of Common Stock held by holders thereof immediately prior to the First Effective Time (as defined in the Merger Agreement) remain outstanding and were unaffected by the Merger. Immediately following the consummation of the Merger but prior to giving effect to the Financing (as defined below), assuming the conversion of shares of Series C Preferred Stock issued pursuant to the Merger Agreement into shares of Common Stock (without giving effect to any beneficial ownership limitations), pre-transaction equityholders of the Company held approximately 3.87% of the issued and outstanding shares of Common Stock and former equityholders of Marea held approximately 96.13% of the issued and outstanding shares of Common Stock, in each case, calculated on a fully-diluted basis and based on the implied equity values of the Company and Marea. Following the consummation of the Financing (as defined below), assuming the conversion of the PIPE Securities (as defined below) and shares of Series C Preferred Stock issued pursuant to the Merger Agreement into shares of Common Stock (in each case, without giving effect to any beneficial ownership limitations), pre-transaction stockholders of the Company hold approximately 2.39% of the issued and outstanding shares of Common Stock, former equityholders of Marea hold approximately 59.54% of the issued and outstanding shares of Common Stock and the Investors (as defined below) hold approximately 38.07% of the issued and outstanding shares of Common Stock, in each case, calculated on a fully-diluted basis and based on the implied equity values of the Company and Marea.
 
Pursuant to the terms of the Merger Agreement, each option to purchase Marea common stock was assumed by the Company and converted into an option to purchase Series C Preferred Stock (each, a “Parent Assumed Option”), which options are subject to exercise restrictions prior to obtaining the approval of the Parent Stockholder Matters (as defined below).
 
Pursuant to the Merger Agreement and the Purchase Agreement (as defined below), the Company has agreed to hold a stockholders’ meeting (the “Stockholders’ Meeting”) to submit the following matters to its stockholders for their consideration: (i) the approval of the conversion of the Series C Preferred Stock into shares of Common Stock in accordance with certain of the rules of the Nasdaq Stock Market LLC (the “Conversion Proposal”), (ii) the approval of a “change of control” under Nasdaq Listing Rules 5110 and 5635(b) (the “Change in Control Proposal”), (iii) to the extent deemed necessary or advisable by Company and/or Marea, the approval of an amendment to the certificate of incorporation of the Company to authorize sufficient shares of Common Stock for the conversion of the Series C Preferred Stock issued pursuant to the Merger Agreement and the Purchase Agreement (as described below) and/or to effectuate a reverse stock split of all outstanding shares of Common Stock at a reverse stock split ratio to be reasonably determined by the Company for the purpose of maintaining compliance with Nasdaq listing standards (the “Charter Amendment Proposal”), (iv) to the extent deemed necessary or advisable by the Company and/or Marea, the approval of (A) an equity incentive plan and (B) an employee stock purchase plan, in each case as approved by the Board (as defined below), and (v) such additional matters as may be mutually agreed between the Company and Marea to facilitate approval of the Conversion Proposal (the matters contemplated by clauses (i)–(v) collectively, the “Parent Stockholder Matters”). In connection with these matters, the Company intends to file with the Securities and Exchange Commission (the “SEC”) a proxy statement and other relevant materials. Holders of shares of Common Stock issued pursuant to the Merger Agreement and Parent Assumed Options (as defined in the Merger Agreement) will not be entitled to vote such shares in connection with the Conversion Proposal in accordance with Rule 5635 of the listing rules of Nasdaq and as provided in the Merger Agreement.
 
The Board of Directors of the Company (the “Board”) unanimously approved the Merger Agreement and the related transactions, and the consummation of the Merger did not require the approval of the Company stockholders.


The foregoing description of the Merger and the Merger Agreement does not purport to be complete and is qualified in its entirety by reference to the Merger Agreement, which is filed as Exhibit 2.1 to this Current Report on Form 8-K and is incorporated herein by reference.
 
The Merger Agreement has been included to provide investors and security holders with information regarding its terms. It is not intended to provide any other factual information about the Company or Marea. The Merger Agreement contains representations, warranties and covenants that the Company and Marea made to each other as of specific dates. The assertions embodied in those representations, warranties and covenants were made solely for purposes of the Merger Agreement between the Company and Marea and may be subject to important qualifications and limitations agreed to by the Company and Marea in connection with negotiating its terms, including being qualified by confidential disclosures exchanged between the parties in connection with the execution of the Merger Agreement. Moreover, the representations and warranties may be subject to a contractual standard of materiality that may be different from what may be viewed as material to investors or securityholders, or may have been used for the purpose of allocating risk between the Company and Marea rather than establishing matters as facts. Moreover, information concerning the subject matter of the representations and warranties may change after the date of the Merger Agreement, which subsequent information may or may not be fully reflected in the Company’s public disclosures. For the foregoing reasons, no person should rely on the representations and warranties as statements of factual information at the time they were made or otherwise.

Marea Stockholders Registration Rights Agreement

In connection with the execution of the Merger Agreement, the Company entered into a Registration Rights Agreement (the “Marea Stockholders Registration Rights Agreement”) pursuant to which as promptly as practicable following the date of the Closing (and in any event not later than the later of (i) 45 days following the Financing Closing Date (as defined below) and (ii) the date upon which the Company shall have filed a current report on Form 8-K/A containing the financial statements of Marea and pro forma financial information required to be filed with the SEC in connection with the Merger (which Form 8-K/A shall be filed in any event no later than November 12, 2026) (such date in clause (ii), the “Form 8-K/A Filing Date”)), the Company has agreed to prepare and file with the SEC a Registration Statement on Form S-3 (or, if Form S-3 is not then available to the Company, on such form of registration statement as is then available) to register the resale of (i) the shares of Common Stock issued pursuant to the Merger Agreement and (ii) the shares of Common Stock underlying the Series C Preferred Stock issued pursuant to the Merger Agreement.
 
The foregoing summary of the Marea Stockholders Registration Rights Agreement does not purport to be complete and is qualified in its entirety by reference to the form of Marea Stockholders Registration Rights Agreement, which is filed as Exhibit 10.1 to this Current Report on Form 8-K and incorporated herein by reference.

Support Agreements

In connection with the execution of the Merger Agreement, the Company and Marea entered into stockholder support agreements (the “Support Agreements”) with the Company’s officers and directors (together with affiliated entities), solely in their capacity as stockholders of the Company, and representing approximately 4.3% of the pre-transaction shares of Common Stock outstanding. The Support Agreements provide that, among other things, each of the parties thereto has agreed to vote or cause to be voted all of the shares of Common Stock owned by such stockholder in favor of the Parent Stockholder Matters at the Stockholders’ Meeting to be held in connection therewith, subject to and in accordance with the terms of the Support Agreements.
 
The foregoing description of the Support Agreements does not purport to be complete and is qualified in its entirety by reference to the form of the Support Agreement, which is provided as Exhibit E to the Merger Agreement, which is filed as Exhibit 2.1 to this Current Report on Form 8-K and incorporated herein by reference.

Lock-up Agreements

Concurrently and in connection with the execution of the Merger Agreement, certain officers, directors and stockholders of Marea as of immediately prior to the Merger, and the Company’s directors and officers (together with affiliated entities) as of immediately prior to the Merger entered into lock-up agreements (the “Lock-up Agreements”) with the Company and Marea, pursuant to which each such stockholder will be subject to a 180-day lockup on the sale or transfer of shares of Common Stock, Series C Preferred Stock and any securities convertible into Common Stock held by each such stockholder at the Closing, including those shares received by Marea stockholders in the Merger.
 
The foregoing description of the Lock-up Agreements does not purport to be complete and is qualified in its entirety by reference to the form of the Lock-up Agreement, which is provided as Exhibit B to the Merger Agreement, which is filed as Exhibit 2.1 to this Current Report on Form 8-K and incorporated herein by reference.

Private Placement and Securities Purchase Agreement
 
On September 17, 2026, the Company entered into a Securities Purchase Agreement (the “Purchase Agreement”) with the purchasers named therein (the “Investors”).
 
Pursuant to the Purchase Agreement, the Company agreed to sell an aggregate of 150,867.995 shares of Series C Preferred Stock (the “PIPE Securities”) for an aggregate purchase price of approximately $225 million (the “Financing”). Each share of Series C Preferred Stock is convertible into 1,000 shares of Common Stock, as described below. The powers, preferences, rights, qualifications, limitations and restrictions applicable to the Series C Preferred Stock are set forth in the Certificate of Designation (as defined below).
 

The closing of the Financing is expected to occur on September 18, 2026 (the “Financing Closing Date”), subject to the satisfaction of customary conditions to closing.

The Financing is exempt from registration pursuant to Section 4(a)(2) of the Securities Act of 1933, as amended (the “Securities Act”), as a transaction by an issuer not involving a public offering. The Investors acquired the securities for investment only and not with a view to or for resale in connection with any public sale or distribution thereof, and appropriate legends have been affixed to the securities issued in this transaction.

The foregoing summary of the Purchase Agreement does not purport to be complete and is qualified in its entirety by reference to the Purchase Agreement, which is filed as Exhibit 10.2 to this Current Report on Form 8-K and incorporated herein by reference.

Registration Rights Agreement
 
In connection with the closing of the Financing, the Company will enter into a Registration Rights Agreement (the “Registration Rights Agreement”) with the Investors. Pursuant to the Registration Rights Agreement, the Company is required to prepare and file a resale registration statement with the SEC by the later of (i) 45 days following the Financing Closing Date and (ii) the Form 8-K/A Filing Date. The Company shall use its commercially reasonable efforts to cause this registration statement to be declared effective by the SEC within five business days of the date the Company is notified by the SEC that the registration statement will not be reviewed (or within 60 calendar days if the SEC reviews the registration statement).
 
The Company has also agreed to, among other things, indemnify the Investors, their officers, directors, members, employees, partners, managers, stockholders, affiliates, investment advisors and agents under the registration statement from certain liabilities and pay all fees and expenses (excluding any legal fees of the selling holder(s), and any underwriting discounts and selling commissions) incident to the Company’s obligations under the Registration Rights Agreement.
 
The foregoing summary of the Registration Rights Agreement does not purport to be complete and is qualified in its entirety by reference to the form of Registration Rights Agreement, which is filed as Exhibit 10.3 to this Current Report on Form 8-K and incorporated herein by reference.

Item 2.01 Completion of Acquisition or Disposition of Assets.

On September 17, 2026, the Company completed its acquisition of Marea pursuant to the Merger Agreement. The information contained in Item 1.01 of this Current Report on Form 8-K is incorporated by reference into this Item 2.01.

Item 3.02 Unregistered Sales of Equity Securities.

The information contained in Item 1.01 of this Current Report on Form 8-K is incorporated by reference into this Item 3.02. The PIPE Securities were offered and sold in transactions exempt from registration under the Securities Act in reliance on Section 4(a)(2) thereof. Each of the Investors represented that it was an “accredited investor,” as defined in Regulation D, and is acquiring the PIPE Securities for investment only and not with a view towards, or for resale in connection with, the public sale or distribution thereof. The PIPE Securities have not been registered under the Securities Act and may not be offered or sold in the United States absent registration or an exemption from registration under the Securities Act and any applicable state securities laws.

Pursuant to the Merger Agreement, the Company issued shares of Common Stock and Series C Preferred Stock. The information contained in Item 1.01 of this Current Report on Form 8-K is incorporated by reference into this Item 3.02. Such issuances were exempt from registration pursuant to Section 4(a)(2) of the Securities Act and Regulation D promulgated thereunder.
 
Neither this Current Report on Form 8-K nor any of the exhibits attached hereto is an offer to sell or the solicitation of an offer to buy shares of Common Stock or any other securities of the Company.

Item 5.02 – Departure of Directors or Certain Officers; Election of Directors; Appointment of Certain Officers; Compensatory Arrangements of Certain Officers.
 
Appointment of Director
 
In accordance with the Merger Agreement, on September 17, 2026, effective immediately after the First Effective Time, Ted W. Love, M.D. was appointed to the Board as a director.


Ted W. Love, M.D. (Age 67).  Prior to the Merger, Dr. Love served as the Chairman of the board of directors of Marea since May 2023. Since June 2025, Dr. Love has served as the Immediate Past Chairman of the board of directors of the Biotechnology Innovation Organization, a trade association representing biotechnology companies, academic institutions, state biotechnology centers and related organizations across the United States and in more than 30 other countries. From June 2014 to October 2022, Dr. Love was the President and Chief Executive Officer of Global Blood Therapeutics, Inc. (formerly Nasdaq: GBT, a publicly traded biopharmaceutical company acquired by Pfizer, Inc.), where he led the company from a pre-clinical startup through its growth to a global commercial company with a pipeline of innovative therapies focused on sickle cell disease. Previously, he was Executive Vice President, Research and Development and Technical Operations at Onyx Pharmaceuticals, Inc. He also served as President, Chief Executive Officer and Chairman of Nuvelo, Inc., and Senior Vice President, Development at Theravance Biopharma, Inc. (Nasdaq:TBPH). He began his biotech career at Genentech, Inc., where he held several senior management positions in clinical science and product development, and ultimately as chair of Genentech’s Product Development Committee. Prior to Genentech, Dr. Love served as a consultant in medicine in the Department of Cardiology at the Massachusetts General Hospital. Dr. Love has served on the boards of directors of Jazz Pharmaceutics plc (Nasdaq: JAZZ) since December 2025, Gilead Sciences, Inc. (Nasdaq: GILD) as Chairman since 2024, Royalty Pharma plc (Nasdaq: RPRX) as Lead Independent Director since July 2020, and Structure Therapeutics Inc. (Nasdaq: GPCR) since August 2023. He previously served on the boards of directors of Seagen Inc. from 2020 to 2023, Global Blood Therapeutics from 2013 to 2022, Portola Pharmaceuticals, Inc. from 2019 to 2020, and Amicus Therapeutics, Inc. (Nasdaq: FOLD) from 2012 to 2020. He received his B.A. in Molecular Biology from Haverford College and his M.D. from Yale School of Medicine.
 
We believe that Dr. Love is qualified to serve on our board of directors based on his leadership as Marea’s Chairman of the board of directors and extensive experience as a leader in the biopharmaceutical industry, including as a board member of multiple publicly traded biotechnology and biopharmaceutical companies.
 
Dr. Love has no family relationships with any of the executive officers or directors of the Company. Except as described in the Merger Agreement, there are no arrangements or understandings between Dr. Love and any other person pursuant to which he was appointed as a director of the Company. Except as described below, Dr. Love is not a party to any transaction required to be disclosed pursuant to Item 404(a) of Regulation S-K.

Appointment of Executive Officer
 
In accordance with the Merger Agreement, on September 17, 2026, effective immediately after the First Effective Time, Josh Lehrer, M.D., M.Phil., FACC was appointed as the President and Chief Operating Officer of the Company. Immediately prior to such appointment, David J. Mazzo, Ph.D. resigned solely from the office of President, but he retained his position as Chief Executive Officer of the Company.
 
Josh Lehrer, M.D., M.Phil., FACC. (Age 53) Prior to the Merger, Dr. Lehrer served as the Chief Executive Officer of Marea since October 2023. Previously, Dr. Lehrer served as president and chief executive officer and as a member of the board of directors of Graphite Bio, Inc. (subsequently merged with LENZ Therapeutics, Inc.), a publicly traded clinical-stage biotechnology company, from April 2020 until September 2023. From October 2013 to April 2020, Dr. Lehrer held various leadership roles at Global Blood Therapeutics, Inc., including Chief Medical Officer where he oversaw the development and approval of Oxbryta® (voxelotor) for the treatment of sickle cell disease. From September 2009 to October 2013, Dr. Lehrer served in leadership roles at Genentech, Inc. in clinical development and business development. Dr. Lehrer has also held attending physician roles at Stanford University Medical Center and the Palo Alto Veteran’s Affairs Health System. Dr. Lehrer has served on the board of directors of Fulcrum Therapeutics, Inc. (Nasdaq: FULC) since April 2026. He holds an A.B. in Biochemical Sciences from Harvard University and a Master of Philosophy in Biological Sciences from the University of Cambridge. Dr. Lehrer earned his Doctor of Medicine at the University of California, San Francisco (UCSF), School of Medicine and completed his residency at UCSF in Internal Medicine. Dr. Lehrer served as a Clinical and Postdoctoral Fellow in cardiovascular medicine at Stanford University and attended the Institute for Entrepreneurship at the Stanford Graduate School of Business.

Dr. Lehrer has no family relationships with any of the executive officers or directors of the Company. Except as described in the Merger Agreement, there are no arrangements or understandings between Dr. Lehrer and any other person pursuant to which he was appointed as Chief Operating Officer of the Company. Except as described below, Dr. Lehrer is not a party to any transaction required to be disclosed pursuant to Item 404(a) of Regulation S-K.

In connection with the Closing, the Board approved certain compensation-related matters effective as of the First Effective Time, for Josh Lehrer, as described below, and consistent with his previous compensation as Chief Executive Officer of Marea as described in the Offer Letter, dated October 11, 2023, by and between Dr. Lehrer and Marea (the “Lehrer-Marea Offer Letter”).
 
Effective as of the Closing, Dr. Lehrer’s will receive an annual base salary of $475,000, subject to applicable deductions and withholdings and periodic review and adjustment at the Board’s discretion. Dr. Lehrer is eligible to receive an annual cash performance bonus targeted at 40% of his base salary, with the actual bonus amount being discretionary and subject to his continued employment through the applicable payment date. In the event Dr. Lehrer’s employment is terminated without Cause (as defined in the Lehrer-Marea Offer Letter) or he resigns for Good Reason (as defined in the Lehrer-Marea Offer Letter) outside of a Change in Control Period (as defined in the Lehrer-Marea Offer Letter), he will be entitled to receive a severance amount equal to 12 months of his base salary in addition to reimbursement of premiums for continued health coverage pursuant to the Consolidated Omnibus Budget Reconciliation Act of 1985, as amended (“COBRA”), for up to 12 months following termination, in each case subject to his execution of a separation agreement and release. In the event Dr. Lehrer’s employment is terminated without Cause or he resigns for Good Reason within a Change in Control Period, he will be entitled to receive the severance pay and benefits described above plus his annual target bonus for the 12 months following such termination, and all of his time-based equity awards will immediately accelerate and become fully vested.


The foregoing description of the Lehrer-Marea Offer Letter is not complete and is qualified in its entirety by the full text of the Lehrer-Marea Offer Letter, a copy of which the Company intends to file with the SEC as an exhibit to the Company’s Quarterly Report on Form 10-Q for the quarter ending September 30, 2026.
 
Effective as of the Closing, Dr. Lehrer is also entitled to receive other customary benefits provided to the Company’s other executive officers pursuant to 2018 Equity Incentive Compensation Plan, as amended (the “Equity Incentive Plan”), which is filed as Exhibit 10.2 to the Company’s Annual Report on Form 10-K for the fiscal year ended December 31, 2025.

Indemnification Agreements
 
Each of Dr. Love and Dr. Lehrer will enter into the Company’s standard form of indemnification agreement, a copy of which was filed as Exhibit 10.2 to the Company’s Current Report on Form 8-K, filed with the SEC on September 15, 2022.

Item 5.03 – Amendments to Articles of Incorporation or Bylaws; Change in Fiscal Year.
 
On September 17, 2026, the Company filed with the Secretary of State of the State of Delaware a Certificate of Designation of Preferences, Rights and Limitations of the Series C Preferred Stock (the “Certificate of Designation”) in connection with the Merger and the Financing referenced in Item 1.01 above. The Certificate of Designation provides for the issuance of shares of the Company’s Series C Preferred Stock.
 
Holders of Series C Preferred Stock are entitled to receive dividends on shares of Series C Preferred Stock, equal to, on an as-if-converted-to-Common-Stock basis, and in the same form as dividends actually paid on shares of the Common Stock. Except as otherwise required by law, the Series C Preferred Stock does not have voting rights. However, as long as any shares of Series C Preferred Stock are outstanding, the Company will not, without the affirmative vote of the holders of a majority of the then outstanding shares of Series C Preferred Stock, (a) alter or change adversely the powers, preferences or rights given to the Series C Preferred Stock, (b) alter or amend the Certificate of Designation, (c) amend its certificate of incorporation or other charter documents in any manner that adversely affects any rights of the holders of Series C Preferred Stock, (d) issue additional shares of Series C Preferred Stock or increase or decrease (other than by conversion) the number of authorized shares of Series C Preferred Stock, (e) prior to the automatic conversion of the Series C Preferred Stock, consummate a Fundamental Transaction (as defined in the Certificate of Designation) or a Change of Control Transaction (as defined in the Certificate of Designation), (f) prior to the automatic conversion of the Series C Preferred Stock, authorize or issue any class or series of stock that is senior to the Series C Preferred Stock, (g) amend, waive or modify the Merger Agreement in a manner that would be reasonably likely to prevent, impede or materially delay the obtainment of stockholder approval of the Conversion Proposal or the automatic conversion of the Series C Preferred Stock or (h) enter into any agreement with respect to any of the foregoing. The Series C Preferred Stock ranks senior to the Common Stock upon any liquidation, dissolution or winding-up of the Company solely to the extent of a nominal liquidation amount of $0.01 per share, and on parity with the Common Stock in all other respects.
 
Following stockholder approval of the Conversion Proposal, each share of Series C Preferred Stock will automatically convert into 1,000 shares of Common Stock, subject to certain limitations, including that a holder of Series C Preferred Stock is prohibited from converting shares of Series C Preferred Stock into shares of Common Stock if, as a result of such conversion, such holder, together with its affiliates, would beneficially own more than a specified percentage (to be established by the holder between 4.99% and 19.99%, with a default of 9.99%) of the total number of shares of Common Stock issued and outstanding immediately after giving effect to such conversion.
 
If at any time after the earlier of (i) the Stockholder Approval or (ii) six months after the initial issuance of the Series C Preferred Stock, the Company fails to deliver to the holder of the Series C Preferred Stock shares of Common Stock underlying such shares of Series C Preferred Stock, then (other than in certain circumstances set forth in the Certificate of Designation), the Company will pay, at the request of such holder, an amount of cash by wire transfer of immediately available funds equal to the Fair Value (as defined in the Certificate of Designation) of such undelivered shares, provided that the Company has funds legally available for such payment.
 
The foregoing description of the Series C Preferred Stock does not purport to be complete and is qualified in its entirety by reference to the Certificate of Designation, a copy of which is filed as Exhibit 3.1 to this Current Report on Form 8-K and is incorporated herein by reference.

Item 7.01 – Regulation FD Disclosure.
 
On September 17, 2026, the Company issued a press release related to the Merger and the Financing, and made available a presentation used with Investors to discuss the Merger and the Financing. Copies of the press release and presentation are furnished as Exhibit 99.1 and Exhibit 99.2, respectively, to this Current Report on Form 8-K.


The information in Item 7.01 of this Current Report on Form 8-K, including the information in the press release attached as Exhibit 99.1 and the presentation attached as Exhibit 99.2 to this Current Report on Form 8-K, is furnished pursuant to Item 7.01 of Form 8-K and shall not be deemed “filed” for the purposes of Section 18 of the Securities Exchange Act of 1934, as amended, or otherwise subject to the liabilities of that section. Furthermore, the information in Item 7.01 of this Current Report on Form 8-K, including Exhibit 99.1 and Exhibit 99.2 to this Current Report on Form 8-K, shall not be deemed to be incorporated by reference in the filings of the Company under the Securities Act.

Forward Looking Statements
 
This Current Report on Form 8-K contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, including, but not limited to, statements regarding: stockholder approval of the Parent Stockholder Matters and the subsequent automatic conversion of the Series C Preferred Stock following stockholder approval of the Conversion Proposal, the filing of one or more resale registration statement(s) pursuant to the Marea Stockholders Registration Rights Agreement and the Registration Rights Agreement and the timing thereof, and the closing of the Financing, if at all. The use of words such as, but not limited to, “anticipate,” “believe,” “continue,” “could,” “estimate,” “expect,” “intend,” “may,” “might,” “plan,” “potential,” “predict,” “project,” “should,” “target,” “will,” or “would” and similar words expressions are intended to identify forward-looking statements. Forward-looking statements are neither historical facts nor assurances of future performance. Instead, they are based on the Company’s current beliefs, expectations and assumptions regarding the future of its business, future plans and strategies, its clinical results and other future conditions. New risks and uncertainties may emerge from time to time, and it is not possible to predict all risks and uncertainties. No representations or warranties (expressed or implied) are made about the accuracy of any such forward-looking statements. The Company may not actually achieve the forecasts disclosed in our forward-looking statements, and you should not place undue reliance on forward-looking statements. Such forward-looking statements are subject to a number of material risks and uncertainties including but not limited to those set forth under the caption “Risk Factors” in the Company’s most recent Annual Report on Form 10-K filed with the SEC, as supplemented by its Quarterly Reports on Form 10-Q, as well as discussions of potential risks, uncertainties, and other important factors in the Company’s subsequent filings with the SEC. Any forward-looking statement speaks only as of the date on which it was made. Neither the Company, nor its affiliates, advisors or representatives, undertake any obligation to publicly update or revise any forward-looking statement, whether as result of new information, future events or otherwise, except as required by law. These forward-looking statements should not be relied upon as representing the Company’s views as of any date subsequent to the date hereof.

Item 9.01 – Financial Statements and Exhibits.

(a)
Financial Statements of Business Acquired

The financial statements required by this Item 9.01(a) are not included in this Current Report on Form 8-K. The Company intends to include such financial statements by amendment to this Current Report on Form 8-K no later than 71 calendar days after the date this Current Report on Form 8-K is required to be filed.

(b)
Pro Forma Financial Information

The pro forma financial information required by this Item 9.01(b) is not included in this Current Report on Form 8-K. The Company intends to include such pro forma financial information by amendment to this Current Report on Form 8-K no later than 71 calendar days after the date this Current Report on Form 8-K is required to be filed.

(d)
Exhibits

Exhibit
Number
 
 
Description
     
2.1(1)
 
Agreement and Plan of Merger, dated September 17, 2026, by and among Lisata Therapeutics, Inc., Mariner Merger Sub I, Inc., Mariner Merger Sub II, LLC and Marea Therapeutics, Inc.
     
3.1
 
Certificate of Designation of Series C Non-Voting Convertible Preferred Stock
     
10.1
 
Form of Marea Stockholders Registration Rights Agreement, by and among Lisata Therapeutics, Inc. and certain Marea stockholders
 
10.2(1)
 
Form of Securities Purchase Agreement, dated as of September 17, 2026, by and among Lisata Therapeutics, Inc. and each investor listed on Exhibit A thereto
     
10.3
 
Form of Registration Rights Agreement, by and among Lisata Therapeutics, Inc. and certain investors signatory thereto
 
99.1
 
Press Release issued on September 17, 2026
     
99.2
 
Presentation made available to the Investors by Lisata Therapeutics, Inc. and Marea Therapeutics, Inc. on September 17, 2026
     
104
 
Cover Page Interactive Data File (embedded within the Inline XBRL document)

(1) Certain schedules and attachments have been omitted pursuant to Item 601(a)(5) of Regulation S-K. The Company agrees to provide, on a supplemental basis, a copy of any omitted schedules and attachments to the Securities and Exchange Commission or its staff upon request.


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.

 
Lisata Therapeutics, Inc.
     
Date: September 17, 2026
By:
/s/ David J. Mazzo, Ph.D.
   
David J. Mazzo, Ph.D.
   
Chief Executive Officer




Exhibit 99.1

Lisata Therapeutics Announces Acquisition of Marea Therapeutics and $225 Million Concurrent Private Placement
 
Combined company to focus on developing first-in-class next-generation medicines for cardioendocrine diseases
 
Marea has multiple late-stage clinical product candidates: MAR001/005 for severe hypertriglyceridemia (sHTG) currently in Phase 2b and MAR002 for the treatment of acromegaly which is advancing to a Phase 2 study
 
Concurrent financing of $225 million from leading life sciences investors and other institutional investors projected to fund operations into 2028
 
Liberty Corner, N.J., September 17, 2026 – Lisata Therapeutics, Inc. (Nasdaq: LSTA) (“Lisata”), a clinical-stage pharmaceutical company, today announced that it has acquired Marea Therapeutics, Inc. (“Marea”), a clinical-stage biotechnology company harnessing the latest advances in human genetics to develop first-in-class, next-generation medicines for cardioendocrine diseases.
 
Concurrent with the acquisition, Lisata entered into a definitive purchase agreement for the sale of Series C non-voting convertible preferred stock in a private placement financing, which is expected to result in gross proceeds to Lisata of approximately $225 million before deducting placement agent and other offering expenses. The oversubscribed financing included participation from leading life sciences investors including RA Capital Management, Forbion, Third Rock Ventures, Alpha Wave, Perceptive Advisors, Sofinnova Investments, Omega Funds, Surveyor Capital (a Citadel company), Columbia Threadneedle Investments, Nantahala Capital, Affinity Asset Advisors, LLC, venBio, Rock Springs Capital and other institutional investors.
 
Lisata plans to use the net proceeds primarily to advance MAR001/005 and MAR002 through key clinical milestones, including the completion of an ongoing Phase 2b trial in patients with severe hypertriglyceridemia, as well as a Phase 2 trial in patients with acromegaly.  Both studies are expected to report topline data in the fourth quarter of 2027.  Remaining proceeds will be used for general corporate purposes.
 
“After a thorough review of strategic alternatives, the acquisition of Marea marks a significant milestone for Lisata as we broaden our focus toward advancing Marea’s product candidate portfolio, which addresses significant unmet need across a range of cardioendocrine diseases,” said Dr. David J. Mazzo, CEO of Lisata. “This pipeline, led by MAR001, is designed to overcome the limitations of current treatment paradigms and has the potential to establish a new standard of care in the treatment of severe hypertriglyceridemia (sHTG). With a strong balance sheet, we believe that we are well-positioned to drive these programs through their next stages of development and ultimately deliver meaningful benefit to patients. We believe that this acquisition, in combination with our parallel efforts to evaluate possible next steps in the development of certepetide, can provide long-term value to our shareholders.”
 

“This transaction provides the combined company with the resources to advance our two clinical stage drug candidates through pivotal milestones, including MAR001 topline Phase 2b data in severe hypertriglyceridemia and MAR002 Phase 2 proof of concept data in patients with acromegaly next year, as well as initiation of Phase 3 registrational studies for both programs,” said Dr. Josh Lehrer, newly appointed Chief Operating Officer and President of Lisata Therapeutics and Chief Executive Officer of Marea. “Joining with Lisata gives our first-in-class antibody programs a faster path to patients who today have limited options for these serious cardioendocrine diseases, and we’re grateful for the continued confidence of our new and existing investors.”
 
About the Transactions
The acquisition of Marea was structured as a stock-for-stock transaction pursuant to which all of Marea’s outstanding equity interests were exchanged based on a fixed exchange ratio for a combination of 1,793,129 shares of Lisata common stock and 211,365.213 shares of Series C non-voting convertible preferred stock (representing in the aggregate 213,158,342 shares of Lisata common stock on an as-converted-to-common stock basis), in each case, calculated on a fully-diluted basis (and without giving effect to any beneficial ownership limitations). Concurrently with the acquisition of Marea, Lisata entered into a definitive purchase agreement for a private placement financing with leading life sciences investors and other institutional investors to raise $225 million in which the investors will be issued an aggregate of 150,867.995 shares of Series C non-voting convertible preferred stock (or 150,867,995 shares of Lisata common stock on an as-converted-to-common stock basis and without giving effect to any beneficial ownership limitations) at a price of approximately $1,491.37 per share (or approximately $1.4914 per share of common stock on an as-converted-to-common stock basis). Subject to Lisata stockholder approval, each share of Series C non-voting convertible preferred stock will automatically convert into 1,000 shares of common stock, subject to certain beneficial ownership limitations set by each holder. As a result of the transactions, equity holders of Lisata immediately prior to the acquisition will own approximately 2.39% of Lisata’s common stock, equity holders of Marea immediately prior to the acquisition will own approximately 59.54% of Lisata’s common stock and investors in the private placement financing will own approximately 38.07% of Lisata’s common stock, in each case, calculated on a fully-diluted, as-converted-to-common-basis (and without giving effect to any beneficial ownership limitations) using the treasury stock method and based on the implied equity values of Lisata and Marea.
 
The acquisition was approved by the Board of Directors of Lisata and the Board of Directors and stockholders of Marea. The acquisition and private placement financing were not subject to the approval of Lisata’s stockholders. The approval of Lisata’s stockholders is required under the terms of the Series C non-voting convertible preferred stock in order for the Series C non-voting convertible preferred stock to be converted into shares of Lisata common stock, and Lisata is required to hold a stockholder meeting for such vote. On an as-converted basis and after accounting for these transactions (and without giving effect to any beneficial ownership limitations), the total number of shares of Lisata common stock (including shares underlying the Series C non-voting convertible preferred stock) will be approximately 396,315,542.
 

H.C. Wainwright is serving as financial advisor to LisataMintz, Levin, Cohn, Ferris, Glovsky and Popeo, P.C. is serving as legal counsel to LisataLeerink Partners is serving as financial advisor to Marea. Jefferies, Leerink Partners, Guggenheim Securities, Cantor and LifeSci Capital are acting as placement agents for the concurrent private placement financing. Goodwin Procter LLP is serving as legal counsel to Marea. Cooley LLP is serving as legal counsel to the placement agents.
 
About Lisata Therapeutics

Lisata Therapeutics is a clinical-stage pharmaceutical company dedicated to the discovery, development and commercialization of innovative therapies for the treatment of advanced solid tumors and other major diseases. Lisata’s cyclic peptide product candidate, certepetide, is an investigational drug designed to activate a novel uptake pathway that allows co-administered or tethered anti-cancer drugs to selectively target and penetrate solid tumors more effectively. Lisata has established noteworthy partnerships based on its CendR Platform® technology. For a comprehensive overview of certepetide’s mechanism of action, please view our informative short film.
 
About Marea Therapeutics

Marea Therapeutics is a clinical-stage biotechnology company harnessing the latest advances in human genetics to develop first-in-class, next-generation medicines for cardioendocrine diseases. The company’s lead product candidate, MAR001, is in Phase 2b clinical development for the treatment of severe hypertriglyceridemia (sHTG), a condition characterized by very high triglyceride levels. The company is also advancing MAR002 for the treatment of acromegaly.
 
About MAR001/005

MAR001 is a potential first-in-class monoclonal antibody in clinical development that targets ANGPTL4, a protein that is highly expressed in adipose tissue. By inhibiting ANGPTL4 and thereby augmenting lipoprotein lipase (LPL) activity, MAR001 is designed to lower triglycerides and improve adipose tissue function. Human genetic data has identified ANGPTL4 as a highly promising therapeutic target because loss of function alleles lead to lower triglyceride levels, improved adipose distribution, better insulin sensitivity, and protection from cardiovascular disease and type 2 diabetes.
 
MAR005, a half-life-extended version of MAR001 with an improved pharmacokinetic profile, is Marea’s planned Phase 3 candidate and is in clinical development for the treatment of severe hypertriglyceridemia (sHTG), a condition characterized by very high triglyceride levels. Preclinical models with MAR001 demonstrated reduction in triglycerides, remnant cholesterol and ectopic fat, and improved insulin sensitivity. MAR001 has demonstrated strong Phase 1a and 2a results and is in Phase 2b clinical development.
 
About Severe Hypertriglyceridemia (sHTG)

Severe hypertriglyceridemia (sHTG) is a serious and often under-recognized metabolic condition marked by triglyceride levels high enough to place patients at significant risk of acute pancreatitis, a painful and potentially life-threatening complication that frequently results in hospitalization. Patients with sHTG also commonly present with a broader burden of cardiometabolic comorbidities, including insulin resistance, type 2 diabetes, and cardiovascular disease, compounding the overall health risks associated with the condition. Despite the availability of lifestyle modification and existing lipid-lowering therapies, many patients with sHTG continue to experience dangerously elevated triglycerides and recurrent pancreatitis events, underscoring a persistent gap in disease management.
 

About MAR002

MAR002 is a potent and selective half-life-extended, allosteric, human monoclonal growth hormone receptor antagonist (GHRA) antibody being developed for the treatment of acromegaly. The in vivo PK and PD properties of MAR002 are predictable and typical of a half-life extended human antibody, showing a long duration of action compatible with infrequent subcutaneous dose administration in humans. These characteristics support its potential to offer an effective and convenient treatment for patients with acromegaly.  In a Phase 1 study in healthy volunteers, MAR002 achieved proof-of-concept dose-dependent suppression of IGF-1, and was generally well tolerated with no serious adverse events. Marea is currently evaluating MAR002 in a Phase 2 trial of patients with acromegaly.
 
About Acromegaly

Acromegaly is an orphan disease characterized by the excess secretion of growth hormone (GH) from a benign pituitary adenoma. Acromegaly affects approximately 30,000 patients in the U.S. If left untreated, acromegaly is highly morbid, leading to significant comorbidities such as GH-induced insulin resistance and diabetes, and serious cardiovascular pathology. The median lifespan of patients can be shortened by 10 years without effective therapy, and incomplete IGF-1 normalization is associated with increased mortality. Despite its severity, acromegaly is often under or misdiagnosed, with an average time from symptom onset to diagnosis of approximately eight years.
 
The current treatment paradigm for acromegaly often involves surgery, performed in over 90% of patients, which achieves remission in about 50% of cases, though this can degrade over time. Medical therapy is required for approximately 65% (around 20,000 in the U.S.) of patients during their disease journey. Current medical treatments include somatostatin receptor ligands (SRLs) and GHRA pegvisomant. However, most patients do not achieve biochemical control with existing therapies.
 

Cautionary Note Regarding Forward-Looking Statements

Certain statements in this press release, other than purely historical information, may constitute “forward-looking statements” within the meaning of the federal securities laws, including for purposes of the safe harbor provisions under the United States Private Securities Litigation Reform Act of 1995, concerning Lisata, Marea, the concurrent private placement financing and the acquisition of Marea by Lisata (the “Transactions”) and other matters. These forward-looking statements include, but are not limited to, express or implied statements relating to the company’s expectations, hopes, beliefs, intentions or strategies regarding the future including, without limitation, statements regarding: the Transactions, including the closing of the concurrent private placement financing, and the expected effects, perceived benefits or opportunities and related timing with respect thereto; expectations regarding or plans for Marea’s pipeline, including its ongoing clinical trials, research and development programs and the expected timing for key milestones, including the release of clinical data; the potential benefits of MAR001/005 and MAR002; and expectations regarding the use of proceeds from the concurrent private placement financing and cash runway expectations therefrom, including such proceeds funding the company through key clinical milestones. In addition, any statements that refer to projections, forecasts or other characterizations of future events or circumstances, including any underlying assumptions, are forward-looking statements. The words “opportunity,” “potential,” “milestones,” “pipeline,” “can,” “goal,” “aim,” “strategy,” “target,” “seek,” “anticipate,” “achieve,” “believe,” “contemplate,” “continue,” “could,” “estimate,” “expect,” “intends,” “may,” “might,” “plan,” “possible,” “predict,” “project,” “should,” “will,” “would” and similar expressions (including the negatives of these terms or variations of them) may identify forward-looking statements, but the absence of these words does not mean that a statement is not forward-looking. These forward-looking statements are based on current expectations and beliefs concerning future developments and their potential effects. There can be no assurance that future developments affecting the company or the Transactions will be those that have been anticipated. These forward-looking statements involve a number of risks, uncertainties (some of which are beyond the company’s control) or other assumptions that may cause actual results or performance to be materially different from those expressed or implied by these forward-looking statements. These risks and uncertainties include, but are not limited to those uncertainties and factors described under the heading “Risk Factors” and in the company’s most recent Annual Report on Form 10-K for the year ended December 31, 2025, filed with the Securities and Exchange Commission (the “SEC”) on March 12, 2026, as well as discussions of potential risks, uncertainties, and other important factors included in other filings by the company from time to time, as well as risk factors associated with companies, such as Marea, that operate in the biotechnology industry. Should one or more of these risks or uncertainties materialize, or should any of the company’s assumptions prove incorrect, actual results may vary in material respects from those projected in these forward-looking statements. Nothing in this press release should be regarded as a representation by any person that the forward-looking statements set forth herein will be achieved or that any of the contemplated results of such forward-looking statements will be achieved. You should not place undue reliance on forward-looking statements in this press release, which speak only as of the date they are made and are qualified in their entirety by reference to the cautionary statements herein. The company does not undertake or accept any duty to release publicly any updates or revisions to any forward-looking statements. This press release does not purport to summarize all of the conditions, risks and other attributes of an investment in the company.
 
Contacts:

Lisata:

Investors and Media:
John Menditto
jmenditto@lisata.com

Marea:

Media:
1AB


Katie Engleman
katie@1abmedia.com  

Investors:
Meru Advisors
Lauren Glaser
lglaser@meruadvisors.com




Exhibit 99.2

 Marea TherapeuticsTransformative cardioendocrine therapies  Confidential 
 

 Forward Looking Statements & Disclaimers  Confidential  This presentation has been prepared by the Company based on information and data which the Company considers reliable, but no reliance shall be placed on, and no representation or warranty, express or implied, whatsoever is or will be given by the Company or any of its affiliates, directors, officers, employees or advisers or any other person as to the truth, accuracy, completeness, fairness, and reasonableness of the contents of this presentation. This presentation may not be all-inclusive and does not purport to contain all of the information that may be required to evaluate a possible investment decision with respect to the Company. The recipient agrees and acknowledges that (i) this presentation is not intended to form the basis of any investment decision by the recipient and does not constitute investment, tax or legal advice, and (ii) the information contained in this presentation is subject to change, and any such changes may be material. Any liability in respect of the contents of or any omission from this presentation is expressly excluded.  Forward-Looking Statements  This presentation contains forward-looking statements. Such statements include, but are not limited to, statements regarding our research, preclinical and clinical development activities, plans and projected timelines for our product candidates, plans regarding regulatory filings, our expectations regarding the relative benefits of our product candidates versus competitive therapies, our expectations regarding the therapeutics and commercial potential of our product candidates, our expectations regarding the completion of the Private Placement and the anticipated use of proceeds from the Private Placement. The words “believe,” “may,” should,” “will,” “estimate,” “promise,” “plan,” “continue,” “anticipate,” “intend,” “expect,” “potential” and similar expressions including the negative thereof) are intended to identify forward-looking statements. Because such statements are subject to risks and uncertainties, actual results may differ materially from those expressed or implied by such forward-looking statements. Risks that contribute to the uncertain nature of the forward-looking statements include: our preclinical studies and clinical trials may not be successful; the U.S. Food and Drug Administration may not agree with our interpretation of the data from clinical trials of our product candidates; we may experience delays in the commencement, enrollment, completion or analysis of clinical testing for our product candidates, or in the reporting of data from such clinical testing; significant issues regarding the adequacy of our clinical trial designs or the execution of our clinical trials may arise, which could result in increased costs and delays, or limit our ability to obtain regulatory approval; our product candidates may not receive regulatory approval or be successfully commercialized; unexpected adverse side effects or inadequate therapeutic efficacy of our product candidates could delay or prevent regulatory approval or commercialization; and we may not be able to obtain additional financing. Additional risks and uncertainties may emerge from time to time, and it is not possible for our management to predict all risks and uncertainties.  All forward-looking statements contained in this presentation speak only as of the date on which they were made. We undertake no obligation to update such statements to reflect events that occur or circumstances that exist after the date on which they were made.  Use of Trademarks, Trade Names and other Marks  All service marks, trademarks and trade names appearing in this presentation are the property of their respective owners. Solely for convenience, the trademarks and trade names referred to in this presentation appear without the ® and TM symbols, but those references are not intended to indicate, in any way, that we will assert, to the fullest extent under applicable law, our rights, or the right of the applicable licensor to these trademarks and trade names. The information herein is for informational purposes only and represents the current view of Marea as of the date of this presentation (or as of an earlier date if specifically noted).  Disclaimers  This presentation is strictly confidential and being made to you solely as a prospective investor in the proposed private placement (the “Private Placement") of securities of Lisata Therapeutics, Inc. in connection with their contemplated merger transaction with Marea Therapeutics, Inc. ("we," "us," "our" or the "Company"). The securities have not been and will not be registered under the U.S. Securities Act of 1933 (as amended, the "Securities Act") or any state securities laws or the laws of any foreign jurisdiction. The securities are being offered only to persons in reliance upon the exemption from securities registration for transactions not involving any public offering afforded by Section 4(a)(2) of the Securities Act. The securities have not been approved or disapproved by the United States Securities and Exchange Commission, or any other securities regulating body or agency, nor has any such authority, commission, or body passed on the accuracy or adequacy of this presentation. Any representation to the contrary is a criminal offense. By accepting this presentation, you will be deemed to represent that you are an accredited investor, have the capacity to protect your own interests in connection with the Private Placement, and have sufficient knowledge and experience in investing in investments similar to the securities to properly evaluate the merits and risks of the investment in the securities. This presentation is meant only for the intended recipient based on its representations regarding such qualifications.   This presentation shall not constitute an offer to sell or the solicitation of an offer to buy, nor shall there be any sale of these securities in any state or other jurisdiction in which such offer, solicitation or sale would be unlawful prior to registration or qualification under the securities laws of any such state or other jurisdiction. This presentation is for informational purposes only and only a summary of certain information related to the Company. It does not purport to be complete and does not contain all information that an investor may need to consider in making an investment decision. You may not take away, reproduce, or distribute this presentation, in whole or in part, and you may not disclose any of the contents of this presentation to any other person. Acceptance of this presentation constitutes an agreement to be bound by the terms set forth herein. The information contained herein does not constitute investment, legal, accounting, regulatory, taxation or other advice, and the information does not take into account your investment objectives or legal, accounting, regulatory, taxation or financial situation or particular needs. Investors must conduct their own investigation of the investment opportunity and evaluate the risks of acquiring the securities based solely upon such investor's independent examination and judgment as to the prospects of the Company as determined from information in the possession of such investor or obtained by such investor from the Company, including the merits and risks involved.   Statements in this presentation are made as of the date hereof unless stated otherwise herein, and neither the delivery of this presentation at any time, nor any sale of securities, shall under any circumstances create an implication that the information contained herein is correct as of any time subsequent to such date. The Company is under no obligation to update or keep current the information contained in this document. No representation or warranty, express or implied, is made as to, and no reliance should be placed on, the fairness, accuracy, completeness or correctness of the information or opinions contained herein, and any reliance you place on them will be at your sole risk. The Company, its affiliates and advisors do not accept any liability whatsoever for any loss howsoever arising, directly or indirectly, from the use of this document or its contents, or otherwise arising in connection with the Private Placement. 
 

 Transaction Summary  Transaction Structure  Proposed sign-and-close merger whereby Lisata Therapeutics would acquire 100% of the outstanding equity interests of Marea Therapeutics in exchange for a combination of common stock and Series C non-voting convertible preferred stock of Lisata, as well as Lisata options exercisable for Series C non-voting convertible preferred stock.  Financing  Concurrent with the acquisition of Marea, Lisata executed a definitive agreement for an oversubscribed private placement of approximately $225 million in gross proceeds.  The financing included participation from RA Capital Management, Forbion, Third Rock Ventures, Alpha Wave Global, Perceptive Advisors, Sofinnova Investments, Omega Funds, Surveyor Capital (a Citadel company), Columbia Threadneedle Investments, Nantahala Capital, Affinity Asset Advisors, LLC, venBio, Rock Springs Capital and other institutional investors.  Management and BOD  Continuing leadership includes Josh Lehrer, newly appointed President and Chief Operating Officer of Lisata Therapeutics and Chief Executive Officer of Marea.   Use of Proceeds  The net proceeds from the private placement are primarily to advance MAR001/005 and MAR002 through key clinical milestones, including completion of an ongoing Phase 2b trial in patients with severe hypertriglyceridemia and a Phase 2 trial in patients with acromegaly. Both studies are expected to report topline data in the fourth quarter of 2027. Remaining proceeds will be used for general corporate purposes.  Confidential 
 

 Capitalization  Lisata issued shares of common stock and Series C non-voting convertible preferred stock to Marea security holders and options exercisable for Series C non-voting convertible preferred stock to Marea option holders, in exchange for all of Marea’s outstanding equity interest.  Shares of Series C non-voting convertible preferred stock are issuable to investors upon the closing of the $225 million private placement.  Shares of Series C non-voting convertible preferred stock will automatically convert into 1,000 shares of common stock, subject to certain beneficial ownership limitations set by each holder and approval by Lisata’s stockholders.  Please refer to Lisata’s SEC filings for additional information.  1. Includes 178,673 restricted stock awards.   2. Calculated using the treasury stock method.  3. Common stock consideration is capped at 19.9% of pre-acquisition Lisata common stock outstanding and reflects certificate-level rounding.   4. Represents shares of Series C non-voting convertible preferred stock issuable upon exercise of Lisata Options issued in exchange for outstanding Marea options. Included on a fully diluted basis and equivalent to 22,801,406 shares of Lisata common stock on an as-converted basis.   5. Represents shares of Series C non-voting convertible preferred stock issuable upon the closing of the concurrent financing.  6. Calculated on an as-converted-to-common-stock basis.   7. Represents Lisata’s pre-acquisition common stock outstanding and equity awards, parent common stock and Series C non-voting preferred stock issued to Marea security holders, Series C non-voting preferred stock underlying Lisata options issued in exchange for outstanding Marea options, and Series C non-voting preferred stock issued in the concurrent financing, calculated on an as-converted basis.  8. Market Cap at Deal Price calculated using treasury stock method equals to $580,734,913.  Confidential  8 
 

 Rapid Path to Value Creation  1. Christian JB, et al., Am J Cardiol. 2011;107(6):891–897; 2. Zafrir B, et al. J Clin Lipidol 2018;12(4):928-936; 3. Marea data on file; 4. Burton T et al. Pituitary 2016;19(3):262-267; 5. EvaluatePharma, ClearView market research, company press releases  Abbreviations: GHR: growth hormone receptor; sHTG: Severe Hypertriglyceridemia; SRL: somatostatin receptor ligand *MAR001 is parent antibody; MAR005 formerly known as MAR001-HLE  Two potentially first-in-class assets with best-in-disease potential in large addressable markets  Confidential  Severe Hypertriglyceridemia  Potent sHTG candidate with a clean metabolic profile  >3M US patients¹  At risk of acute pancreatitis; APOC3 drugs worsen diabetes / liver fat  ~70% TG reduction3  Phase 2b sHTG POC (subgroup with baseline TG>500, n=7)  TG lowering in Phase 2 similar to approved APOC3s  >$10B market opportunity5  First choice for >1.8M2 diabetics with sHTG  Clean metabolic profile  No HbA1c increase or liver-fat penalty to date – potentially differentiated from approved APOCs  MAR002  Acromegaly  First long-acting GHR antagonist candidate for acromegaly  ~30K US patients4  Highly morbid; >70% uncontrolled  Potential Best-in-class anti-GHR mAb  Target profile: Best-in-class efficacy, safety and biweekly dosing  Phase 1 proof of mechanism  Promising IGF-1 suppression (approvable endpoint)  >$1B in SRL sales5  Potential to address 3x more patients than SRLs 
 

 Molecule  Target  Indication  Disc  IND-E  Ph1  Ph2  Ph3  Anticipated Near-term Milestones  MAR001  (parent mAb)  ANGPTL4  sHTG  MAR005  (half-life extended MAR001)  ANGPTL4  sHTG  MAR002  Growth hormone receptor  Acromegaly  Advancing a Late-Stage Cardioendocrine Pipeline Toward Potential 2026-27 Value Inflections  MAR001 Phase 2b TYDAL (mHTG/sHTG)  Abbreviations: NHV: normal healthy volunteer; sHTG: Severe Hypertriglyceridemia  Q2 2026  Phase 2/2b 12-week data  H2 2026  Phase 2/2b 24-week data  H2 2027  Phase 2 extension (sHTG) topline data  Q1 2026  Phase 1 (NHV) topline data  Mid-2026  Initiate Phase 2 study  Mid-2027  Interim Phase 2 data  Q4 2027  Phase 2 topline data  H1 2028  Phase 3 FPI  MAR001 Phase 2 Mechanistic Study  Endocrine     Cardiometabolic  Mid-2027  Phase 3 MAR005 dose selection including additional TG efficacy/PD  H2 2027  Phase 3 FPI     MAR001 Phase 2b extension (sHTG)     MAR001 has established POC in Phase 2. MAR005 is our Phase 3 candidate- it is an improved version of MAR001 with half-life extension and improved PK. The FDA agreed to PK bridging to Phase 3.  Marea also has developed a SiRNA platform and is developing adipose tissue targeted SiRNAs  Confidential 
 

 MAR005 for sHTG  Potent sHTG candidate with a clean metabolic profile  Section IV  Confidential 
 

 Recurrent Pancreatitis in sHTG: A Life-Altering Condition with Limited Options  >3 million Americans; $9B in healthcare costs, no approved prevention therapies until recently  The Unmet Need  Limited Generic Options  The Critical Gap  Inadequate TG lowering  ~30% reduction leaves most sHTG patients above the AP risk threshold  No evidence for AP prevention  Poor tolerability  1. Marston, NA, et al., N Engl J Med 2025;394:429-441; 2. Gurevitz, C et al., JACC: Advances 2024;3(5) 3. Lee PJ,. Nat Rev Gastroenterol Hepatol. 2019;16(8):479-496; 4. Lu J, et al., BMC Gastroenterology. 2025;25:374. Abbreviations: SOC: standard-of-care; AP: acute pancreatitis; MI: myocardial infarction; CAD: coronary artery disease. 4. Marea claims data analysis  Until Recently: Limited Options  >3M Americans with sHTG face recurrent AP attacks  Up to 20% mortality per episode4   Cumulative attacks cause irreversible pancreatic destruction, chronic pain, and secondary diabetes   60% T2DM1, 30% CAD1, 70% fatty liver 2 : a high-risk population with >$9B annual cost burden3  30% have poorly controlled T2DM (HbA1c>9%)4  Fibrates  Omega-3 Fatty Acids  Confidential 
 

 APOC3 Inhibition: New Treatments Driving a Potential Multi-Billion Dollar Opportunity  Sources: Marston, NA, et al., N Engl J Med 2025;394:429-441; Ionis AHA 2025 press release; Arrowhead July 2026 press release; Overall NNT=20; ClearView market research; AP: acute pancreatitis; SOC: standard of care  First class of medications to demonstrate acute pancreatitis (AP) event reduction  Next-Gen Rx sHTG Opportunity  60-80%  TG reduction — dramatically superior to fibrates or omega-3 fish oil  78-85%  Reduction in AP events first proven AP reduction in sHTG  >80%  Patients reaching TG <500 mg/dL vs. 35% placebo — bringing most patients below the AP-risk threshold at 12 months  Clinical benefit supports premium list pricing at $40–45k  PROJECTED US MARKET  >$10B  Olezarsen (Ionis): >$3B projected peak sales  Plozasiran (Arrowhead): $3–4B projected peak sales  “What patients really look for is not going through [AP] again. If you can reduce it to almost zero, that’s what patients care about most.”  — Endocrinologist  “It’s more effective than 6 or 9 fish oil pills and a fibrate every day, forever … one shot at home, every four weeks. I have no trouble convincing somebody.”  — PCP  Confidential 
 

 HbA1c +0.3 despite Rx; Hyperglycemia AEs were most common Plozasiran AE1,4; Plozasiran excluded HBA1c>9  Population  Drug / Study  TG Reduction  Adverse Effects on Glycemic Control (in T2DM)  Source  mHTG  Plozasiran — MUIR Ph2b, Wk 24  58% (56% pbo corrected) – 25mg  +0.36% (25mg) absolute vs. placebo  Ballantyne, NEJM 2024  sHTG  Plozasiran — SHASTA-2 Ph2b, Wk 24  70% (53% pbo-corrected) - 25mg  Worsening glycemic control TEAE 16.4% (25 mg) vs 11.5% pbo  Gaudet, JAMA Cardiol 2024  sHTG + mHTG  Plozasiran — SHASTA-2 + MUIR OLE, 24 mo  −83% (SHASTA-2 OLE) – 25mg  −67% (MUIR OLE) – 25mg  9.6% T2DM / 6.7% DM / 4.1% "HbA1c increased" as TEAEs; glycemic terms drove 69% of drug d/c  Ballantyne, Am J Prev Cardiol 2026  sHTG  Plozasiran — SHASTA-3/4  79-81% (52-54% pbo-corrected*) – 25mg, 12 mo  +0.2-0.3% in overall population at 6 months (T2DM subgroup not yet reported); 14% glycemic AEs vs 8.7% pbo despite active protocol- mandated management  Watts GF, ESC Congress 2026  sHTG  Olezarsen — CORE/CORE2 Ph3  63% (49-63% pbo corrected) – 50mg, 6 mo  68-73% (55-72 pbo corrected) – 80mg, 6 mo  +0.34% (50mg) / +0.25% (80mg) pbo-adj. at 12 mo, both p<0.05  Marston, NEJM 2025  sHTG  Olezarsen – approved sHTG label  As above  Hepatic fat in Warnings & Precautions   Increase in glucose, worse in diabetics (clinical trial section of label)  FDA-approved USPI  FCS  Plozasiran — PALISADE, 10 mo  80% (59% pbo corrected) – 25mg  +0.36% HbA1c (25mg); FPG +9 mg/dL (diabetic+nondiabetic); hyperglycemia 40% (nondiabetic) vs 20% placebo  Redemplo USPI, Nov 2025  FCS  Olezarsen — approved FCS label  30% (43% pbo corrected) – 80mg  Hyperglycemia 52% (nondiabetic) vs 35% placebo  Tryngolza USPI  Summary: APOC3 class effect; 2 molecules, 3 populations (mHTG, sHTG, FCS); 5+ independent studies and 2 FDA labels all show the same ~0.3–0.4% HbA1c signal despite antidiabetic meds  1. Ballantyne et al., NEJM 2024 & Am J Prev Cardiol 2026; 2. Marston et al., NEJM 2025; 3. Gaudet et al., JAMA Cardiol 2024; 4. Tryngolza & Redemplo USP; 5. Watts GF, et al. SHASTA-3/SHASTA-4. ESC Congress 2026  *Placebo correction calculated by Marea  APOC3 Class Comes at a Cost:Deterioration in Glycemia / Exclusion of the 30% Patients with Poorly Controlled T2DM  Confidential  Cross-trial comparisons are subject to inherent limitations and should be interpreted with caution; no head-to-head studies were conducted 
 

 Biology and Genetics Support Inhibition of ANGPTL4 as Potential Best-in-Disease Profile  The first physiologic sink for excess triglycerides  Genetics predict differentiated impact on glycemic control*  APOC3 Inhibition (Olezarsen/Plozasiran)  ANGPTL4 Inhibition (MAR001/5)  Abbreviations: LPL: lipoprotein lipase; HFF: hepatic fat fraction;* https://academic.oup.com/ehjopen/article/4/3/oeae035/7659859; https://doi. org/10.1186/s12933-026-03209-w; https://doi.org/10.1038/s41467-018-04611-z  A potential mechanism with no observed metabolic penalty  Forced hepatic TG clearance  HbA1c increases in patients with T2DM  HFF increases   Physiological adipose TG clearance  No hepatic fat loading  TG lowering scales with disease severity  APOC3  ANGPTL4  T2DM risk  Glucose  Confidential 
 

 TYDAL-TIMI 78 Phase 2b: Establishing a Potential Best in Disease Profile  >60% T2DM/pre-DM informs metabolic safety profile; sHTG subgroup informs clinical activity  Pre-read  1. Participants are randomized 3:1 MAR001 to placebo (~59 participants per arm); TG: triglycerides; RC: remnant cholesterol; TD2M: Type-2 diabetes mellitus; https://timi.org/tydal-timi-78; 2. 12-week efficacy data available for 23 patients; efficacy numbers are median change to 12 weeks  Day 1  Randomization  Week 12:  Primary Endpoint  300 mg  450 mg  900 mg  Placebo  MAR001  Active  Treatment  Arms  (Q4W)  Week 24  Confidential  Study Population (N=235)  Key Inclusion Criteria:  TG ≥ 150 to < 880 mg/dL  Baseline characteristics  ~61% pre-DM/T2DM  ≥400 mg/dL subgroup (n=252): baseline TG = 495 mg/dL  ≥500 mg/dL subgroup (n=12): baseline TG = 606 mg/dL  Key Endpoints:  Primary (at 12 weeks):   % Reduction in TG  % Reduction in RC  Other secondary and exploratory endpoints  HbA1c  Lipids at Week 12 and 24  Key 12-week Topline Data  Approx 40% TG lowering overall  TG lowering scales with baseline TG  >65% in TG≥400 mg/dL group (n=15; MAR001 pooled)  ~70% in TG≥500 mg/dL group (n=7; MAR001 pooled)  Consistent effects at 24 weeks  Safety profile consistent with placebo (overall TEAES < pbo)  No increase in HbA1c (numeric reduction)  No liver enzyme elevation signal (numeric reductions)  Injection site reactions similar to placebo  PK/PD supports go-forward MAR005 dose of 300mg monthly for Phase 3 
 

 MAR001: Emerging Clinical Data Supports Potential Best-in-Disease Profile  1. Marston, NA, et al. N Engl J Med 2025;394:429-441; 2. Gaudet D, et al. JAMA Cardiol. 2024;9(7):620-630; 3. Cummings, B, et al. The Lancet. 2025;405(10493):1923-1934; 4. Ballantyne C, et al. N Engl J Med 2024;391(10):899-912; (the SHASTA-2 study did not report HbA1c in T2DM, this data is from the MUIR study of Plozasiran in mixed dyslipidemia); 5. Marea data on file from MAR-102 and MAR-104; 6. Lepor N, et al. WCIRDC 2025; Poster #0034; 7. Watts GF, et al. SHASTA-3/SHASTA-4. ESC Congress 2026  Confidential  MAR001/005  Olezarsen1  Plozasiran2,4,6, 7  TG Lowering  HbA1c  Hepatic Fat  Dosing  -70% +  Phase 2b, pooled 450/900 mg dose; >500 mg/dL subgroup; median TG 606 mg/dL at baseline  -63 to -73%  Phase 3 efficacy; median TG 793 mg/dL at baseline  -79 to -81%  -27% pbo  Phase 3 efficacy; median TG 677 mg/dL at baseline  -0.2%  Decrease in Phase 2b vs. pbo (prelim. & not significant)  +0.25 to +0.34%  Increase in T2D subgroup in Phase 3 vs. pbo  +0.36%  Increase in T2D subgroup in Phase 2b vs. pbo; up to 20% diabetes AEs  0%  No hepatic fat increase3, 5  +2 to +4%  Absolute increase in hepatic fat fraction  +1.5%  Absolute increase in hepatic fat fraction vs pbo in Phase 3 (NS, p=0.70)  Q4W–Q12W  SC dosing with MAR005  Q4W  SC dosing  Q12W  SC dosing  Cross-trial comparisons are subject to inherent limitations and should be interpreted with caution; no head-to-head studies were conducted 
 

 +0.3 HbA1c difference could be clinically meaningful  Even small, sustained HbA1c increases carry independent cardiovascular risk1  +0.3 HbA1c increase is estimated to lead to ~6% higher risk of diabetes-related death and ~11% higher risk of microvascular complications2  HbA1c drives physician choice in sHTG  HbA1c stabilization #1 physician weighted attribute for new sHTG drugs in T2DM patients3  Potential for 1/3 or more of a $10B market  Driven by uptake in the 1.8 M patients with sHTG+T2DM where at least 50% have uncontrolled glucose4 and where competitors excluded poorly controlled T2DM (30% of sHTG patients)  “Any new starts would probably go to the ANGPTL4 inhibitor … a much cleaner profile without the hepatic-fat increase, and you don’t see an A1C increase.”  — Endocrinologist  “The main difference is in the safety category, which I put at the top … there’s no hepatic-fat issue, there’s no A1C issue.”  — Cardiologist  1. Luo S, et al. Diabetologia 2021;64(11):2502–2510; 2. Stratton IM, et al. BMJ 2000;321(7258):405–412. Data above are an illustrative linear scaling of this relationship to a 0.3-point change and are not a direct finding from APOC3 clinical trials.  3. Market research conducted by ClearView Healthcare Partners (Q1 2026): quantitative physician survey (N=151: 75 endocrinologists, 70 cardiologists, 6 lipidologists) plus N=15 in-depth qualitative interviews incorporating a blinded discrete-choice/conjoint exercise to isolate the relative importance of individual product attributes (efficacy, safety, dosing) on treatment share; 4. "Trends in Diabetes Treatment and Control in U.S. Adults, 1999–2018," N Engl J Med 2021;384:2219–2228  “I would target the use of [MAR005] for patients who have diabetes or prediabetes, or I think are at high risk for developing diabetes”  -Cardiologist  Confidential  MAR001/5 Profile: Highly Differentiated; Compelling to Physicians; Represents Large Potential Opportunity 
 

 As Predicted by Biology: ANGPTL4 Inhibition Overperforms in sHTG vs. mHTG  TG lowering scales with baseline TGs: MAR001 is competitive with APOC3 inhibitors in severe patients  Notes: Clinical Data from MAR001 and APOC3 Programs; data extrapolation and curve fitting are based on the following:  Olezarsen data are from four trials (BRIDGE-TIMI 73a, ESSENCE-TIMI 73b, CORE-TIMI 72a, CORE2-TIMI 72b) at both the 50mg and 80mg Q4W doses, with overall trial populations at Month 6.  Plozasiran data are from the MUIR trial (25mg Q12W, overall population, Week 24) and the SHASTA-2 trial (25mg Q12W, overall population, Week 24). Phase 3 plozasiran data pending  MAR001 data are from three studies: the Phase 1 single-dose study (450mg, overall populations from Parts IA, IB, and IC at Day 15), the Phase 1b/2a multidose study (MAR-102; 450mg Q2W, overall population, Week 12), and TYDAL-TIMI 78 (MAR-103; 900mg Q4W, overall population and baseline TG subgroups ≥300, ≥400, and ≥500 mg/dL, Week 12).   Confidential  APOC3: (Olezarsen, Plozasiran)  MAR001  Cross-trial comparisons are subject to inherent limitations and should be interpreted with caution; no head-to-head studies were conducted 
 

 MAR-104 Study: Potential Best-in-Class Suppression of Postprandial TGs  MAR001 flattens the post-prandial TG surge, the key driver of AP risk  Participants are randomized 2:1 MAR001 to placebo (~21 participants in MAR001 arm and 10 patients in placebo arm) TG: triglycerides; AP; acute pancreatitis, iAUC is AUC corrected for baseline fasting TGs  Kraaijenhof JM et al. "Plasma reduction of apolipoprotein C-III with olezarsen leads to significant reductions in postprandial triglyceride levels: results from a randomized trial." Eur J Prev Cardiol 2025; Estimate from figure 1D  Post-prandial TG suppression similar to or greater than results with Olezarsan (↓50% AUC, 28% iAUC)2  Study Population (N=31)  Key Inclusion Criteria  TG ≥ 175 to < 500 mg/dL   HbA1c: 5.5 to 9%  Key Baseline Characteristics  % Pts with Pre-DM/T2DM: 87%  Mean TG: 261 mg/dL  Key Endpoints  Post-prandial TG at week 12 and 24  Day 1  Randomization  Week 12:  Primary Endpoint  MAR001 900 mg Q4W   Placebo Q4W  Week 24  Key 12-week topline data  42% reduction in TG AUC at 12 weeks for MAR001 vs. Pbo  40% reduction in TG iAUC at 12 weeks vs pbo  Confidential  mixed meal challenge  TG (mg/dL)  Hours Post-Meal 
 

 MAR002 for Acromegaly  First long-acting GHR antagonist candidate for acromegaly  Section IV  Confidential 
 

 Acromegaly: Serious Disease with Inadequate Options for Medical Therapy  ~30K patients US   caused by excess GH production from benign pituitary adenoma.  Early Mortality and High Morbidity  Bone/organ overgrowth, cardiovascular & metabolic disease.  Median lifespan shortened by ~10 years without effective therapy.  Medical Therapy Goals:  Decrease tumor volume (some patients)  Normalize IGF-1 levels (all patients)  >70% of patients are addressable: Approx 9K US patients need a better GH antagonist to achieve IGF-1 normalization  Efficient Development Path: IGF-1 is an established clinical and regulatory endpoint.  Abbreviations: GH: Growth Hormone; GHR; Growth Hormone Receptor; SRL: Somatostatin Receptor Ligand  Sources: UpToDate; Holdaway et al., Eur J Endo, 2008; Moustaki et al, Endocrine, 2023; van der Lely et al., Lancet, 2001  The Burden & Opportunity  Pituitary Gland  Liver  Body Tissue  Excess IGF-1  Somatic Growth & Metabolic Dysfunction  Inhibit Secretion (e.g., SRLs)  Acts on pituitary to reduce GH release  Can also shrink tumor  1  x  Block Action (e.g., Somavert)  Blocks GH receptor signaling.  2  Two Approaches to Medical Therapy  Confidential 
 

 Medical Therapy Treatment Guidelines: Direct Growth Hormone Antagonists Critical for >70% of Patients  IGF-1 > ULN after surgery  T2DM, unfavorable tumor histology  lower IGF-1, favorable tumor histology, tumor mass concerns  Direct GHRA (somavert)  SRL or Dopamine Agonists  IGF-1 uncontrolled  add GHRA  IGF-1 and glucose uncontrolled, no tumor mass concerns  switch to GHRA  IGF-1 uncontrolled + tumor mass concerns  ~80%  ~10-20%  >70%  SRLs often initiated first for tumor volume control  Role for first line GHRA in ~10-20% of patients  70% of patients prescribed SRLs require second-line GHRA  First Line  Second Line  Sources: Melmed & Giustina, Nat Rev Endocrinol, 2025; Fleseriu et al., J Endocr Soc, 2023; Moustaki et al., Endocrine, 2023; Carmichael et al., J Clin Endocrinol Metab, 2014; Colao et al., J Clin Endocrinol Metab, 2014.   Abbreviations: GHRA: growth hormone receptor antagonist; SRL: somatostatin receptor ligand.  Confidential 
 

 The Marea Opportunity  Most patients are not fully controlled or cannot tolerate current therapies  MAR002 (anti-GHR mAb)  A Potential Optimal Direct GHRA  SRLs: First line, but limited control  Somatostatin receptor ligands: <30% disease control  SRL class causes GI intolerance and hyperglycemia  Often used first-line for tumor mass control  A $1B US market despite addressing only 30% of patients  The most effective drug class is underused  Direct GHRA: 81% disease2 control  The only approved GHRA has poor PK, tolerability  1-2 daily painful injections, LFTs  Real-world efficacy is only 50% (low compliance)  $300M global sales despite severe limitations  Strong drive to treat patients to IGF-1 Goal  2.5x mortality rate in patients who do not achieve IGF-1 normalization1  Guidelines mandate medical therapy to control  1. Holdaway IM, et al. Eur J Endocrinol 2008;159(2):89–95; 2. Trainer PJ, et al. N Engl J Med 2000;342(16):1171–1177; 3. Marea data on file; 4. Cross-trial comparisons are subject to inherent limitations and should be interpreted with caution. MAR002: Marea data on file (single 900 mg SC dose, n=8); Pegvisomant (Somavert) comparator estimated from Thorner MO, et al. J Clin Endocrinol Metab 1999;84(6):2098–2103, Fig 6 (single 1.0 mg/kg SC dose, n=6); *SRL projected market opportunity; Abbreviations: GHRA: growth hormone receptor antagonist  IGF-1 max suppression3  >60%  >10x  Longer duration of >45% IGF-1 suppression vs. Somavert in healthy volunteers4  >$1B*  Potential to address 3x more patients than SRLs  “I loved how I felt on GHR-antagonist therapy, but the daily injections were hard to sustain. Having that same level of clinical control without the daily burden would be life-changing. MAR002 isn’t just a new drug; it’s a chance to get our lives back.”  Jill Sisco, President, Acromegaly Community  This drug could improve control in most patients, either alone or in combination with an SRL.   leading U.S. KOL  Confidential 
 

 An Optimal Direct GHRA Could Address 3-4x More Patients than the SRL Class  A better GHRA than Somavert is needed to address >9K patients  Sources: Crinetics, FDA Pegvisomant and Paltusotine labelling; https://www.accessdata.fda.gov/drugsatfda_docs/label/2025/219070s000lbl.pdf; https://labeling.pfizer.com/ShowLabeling.aspx?id=3213   SRLs: <30% Disease Control in   Treatment-naïve patients  (Paltusotine)   GH Antagonist: >90% Disease Control  (Somavert)   Treatment-naive subgroup (n=22) analysis from Phase 3 Pathfinder-2 Study  Safety: mechanism-related hyperglycemia (74% of treated participants developed at least 1 incident) and GI AEs  Limitations: daily, painful injections, LFT elevations related to pegylation, poor access   IGF > normal  (uncontrolled,   2.5x mortality)  77%   IGF normal  (controlled)  Naïve to GHRA treatment  18%  23%   82%   Phase 3  The Marea opportunity  Mono-and combination with SRLs  TAM 3-4x SRL class  Confidential 
 

 MAR002: Allosteric Mechanism, Potential for greater Efficacy than Somavert  Maintains Potent GHR Antagonism at High GH Levels (Preclinical Data)  Confidential  Somavert: loses efficacy at high GH concentrations  MAR002: maintains reduction at high GH concentrations  Increasing growth hormone levels  Growth hormone signaling  No drug: increasing GH leads to increased signaling   Source: Kurylo K, et al. Development and characterization of a long-acting allosteric GHRA for acromegaly. Endocrinology 2026 
 

 Phase 1 Healthy Volunteer Study Established Potential Best-in-Class Profile  Potential best-in-disease suppression; 300 mg Q2W predicted clinical dose  1. Cross-trial comparison, not a head-to-head study. MAR002: Marea data on file (single 900 mg SC dose, n=8); Pegvisomant (Somavert) comparator estimated from Thorner MO, et al. J Clin Endocrinol Metab 1999;84(6):2098–2103, Fig 6 (single 1.0 mg/kg SC dose, n=6); 2. Tiberg F et al. Br J Clin Pharmacol 2015;80(3):460–472. 3. Madan A et al. Pituitary 2022;25(2):328–339; Abbreviations: FIH: first-inhuman; POM: proof-of-mechanism; SAD: single ascending dose; BL: baseline; SC: subcutaneous; all cohorts N = 8 (6:2); All doses of MAR002 were a single dose except for 900mgx3  Confidential  Phase 1 Study Design  Healthy men (n=45), baseline IGF-1 > 100 ng/ml  MAR002 Safety Summary to Date  Generally well tolerated  No serious AEs  All doses tolerated  No related signals  Somavert (49%)1  SRLs (37-40%)2,3  Somavert  (<4 days) 
 

 MAR002: Emerging Clinical Data Supports Potential Best-in-Class Profile  Confidential  MAR002  Somavert  Peak IGF-1 Suppression in HV  In vitro potency with excess GH  IGF-1 Normalization  PK/Dosing  -64%  -49%1  90% suppression  24% suppression2  competitive peptide  Expected > Somavert  81% IGF-1 normalization in patients3 (Phase 3)  Q2W SC  Qday dosing4  Painful injections  Vial and syringe  Allosteric mAb  Tolerability  No signals to date  Significant LFTs, ISRs4  1. Thorner MO, et al. J Clin Endocrinol Metab 1999;84:2098–2103 (single 1.0 mg/kg SC, day 5, n=6); 2. Kurylo K, et al. Development and characterization of a long-acting allosteric GHRA for acromegaly. Endocrinology 2026; 3. Trainer PJ, et al. N Engl J Med 2000;342:1171–1177 (15 mg/day, week 12, n=112); 4. SOMAVERT (pegvisomant) US Prescribing Information, rev. 7/2023, §§2.1, 5.2, 6.1, 16.  Cross-trial comparisons are subject to inherent limitations and should be interpreted with caution; no head-to-head studies were conducted 
 

 Efficient Development to POC to Evaluate 1st and 2nd Line Label  Phase 2 study population supports 1) first line monotherapy 2) second line combination therapy 3) second line monotherapy  Week 10:  Primary Endpoint  150 mg Q2W  300 mg Q2W  600 mg Q2W  Placebo  + Open Label Extension  MAR002  Active  Treatment  Arms  Study Population  (N~72)  All-Comers  Untreated   Controlled on peg therapy – washout   Uncontrolled on stable medical therapy - add on  IGF-1 > 1.3x ULN  1st dose: 900 mg loading dose  Key week-10 Topline Data  Assess the effect on serum insulin-like growth factor 1 (IGF-1) response  Explore effects on acromegaly symptoms  Assess safety and tolerability  Confidential 
 

 Molecule  Target  Indication  Disc  IND-E  Ph1  Ph2  Ph3  Anticipated Near-term Milestones  MAR001  (parent mAb)  ANGPTL4  sHTG  MAR005  (half-life extended MAR001)  ANGPTL4  sHTG  MAR002  Growth hormone receptor  Acromegaly  Advancing a Late-Stage Cardioendocrine Pipeline Toward Potential 2026-27 Value Inflections  MAR001 Phase 2b TYDAL (mHTG/sHTG)  Abbreviations: NHV: normal healthy volunteer; sHTG: Severe Hypertriglyceridemia  Q2 2026  Phase 2/2b 12-week data  H2 2026  Phase 2/2b 24-week data  H2 2027  Phase 2 extension (sHTG) topline data  Q1 2026  Phase 1 (NHV) topline data  Mid-2026  Initiate Phase 2 study  Mid-2027  Interim Phase 2 data  Q4 2027  Phase 2 topline data  H1 2028  Phase 3 FPI  MAR001 Phase 2 Mechanistic Study  Endocrine     Cardiometabolic  Mid-2027  Phase 3 MAR005 dose selection including additional TG efficacy/PD  H2 2027  Phase 3 FPI     MAR001 Phase 2b extension (sHTG)     MAR001 has established POC in Phase 2. MAR005 is our Phase 3 candidate- it is an improved version of MAR001 with half-life extension and improved PK. The FDA agreed to PK bridging to Phase 3.  Marea also has developed a SiRNA platform and is developing adipose tissue targeted SiRNAs  Confidential 
 

 Experienced Team; Strong Investor Base  MANAGEMENT TEAM  Josh Lehrer, MD  CEO  Caitlin Murray, Esq  Fractional GC  Ian Clements, PhD  CFO  Ethan Weiss, MD  CSO, Scientific Founder  Shishir Gadam, PhD  CTO  Max Zeiberg  SVP, Corp Dev  Rebecca Juliano, PhD  CDO  SCIENTIFIC FOUNDERS  Joshua Rabinowitz, MD, PhD  Professor of Chemistry,                  Princeton University  Sir Stephen O’Rahilly, MD, FRS  Professor of Clinical Biochemistry & Medicine, University of Cambridge  Charles Homcy, MD  Founder: Myokardia, GBT, BridgeBio, Portola, Maze, Pliant  INVESTORS  Confidential 
 

 ©2026 Marea Therapeutics, Inc. All rights reserved.   Confidential 
 



Filing Exhibits & Attachments

10 documents

Keep reading