STOCK TITAN

AIM ImmunoTech (AIM) inks $1.5M manufacturing pact for Ampligen

(Moderate)
(Neutral)
Form Type
8-K

Rhea-AI Filing Summary

AIM ImmunoTech Inc. entered into a Proposal Agreement with Sterling Pharma Solutions on July 31, 2026. Under this arrangement, Sterling will manufacture additional batches of the polynucleotide drug substances PolyI and Poly C12U and transfer associated test methods at its Dudley, UK facility. These materials serve as polymer precursors for producing the drug Ampligen.

The estimated cost to AIM is approximately $1.5 million, payable over 12 months. AIM plans to use the manufactured product in ongoing and future clinical trials, including potentially a Phase 3 clinical trial for metastatic pancreatic cancer.

AIM also outlined timing requirements for stockholders wishing to nominate directors or bring other business at the 2026 annual meeting outside Rule 14a-8. Notices must be received between August 18, 2026 and 5:00 p.m. local time on September 17, 2026, with a separate Rule 14a-19 universal proxy notice due by October 19, 2026.

Positive

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Negative

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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 5.08 Shareholder Director Nominations Governance
Shareholder nominations for board of directors under proxy access rules. Rarely used -- the underlying SEC rule was vacated.
Item 9.01 Financial Statements and Exhibits Exhibits
Financial statements, pro forma financial information, and exhibit attachments filed with this report.
Proposal Agreement estimated cost $1.5 million Estimated cost to AIM under the Proposal Agreement, payable over 12 months
Payment period 12 months Period over which the approximately $1.5 million is to be paid
Nomination notice opening date August 18, 2026 Earliest date stockholder notices for the 2026 annual meeting may be received
Nomination notice deadline 5:00 p.m. local time on September 17, 2026 Latest time for stockholder notices for the 2026 annual meeting
Universal proxy notice deadline October 19, 2026 Deadline to provide Rule 14a-19 notice for alternative director nominees
Agreement date July 31, 2026 Date AIM and Sterling Pharma Solutions entered into the Proposal Agreement
Material Definitive Agreement regulatory
"Item 1.01 Entry into a Material Definitive Agreement."
A material definitive agreement is a legally binding contract that creates major, long‑term obligations or rights for a company, such as loans, asset sales, mergers, or supplier deals. Think of it like a mortgage or lease for a business: it can change future cash flow, risk and control, so investors watch these agreements closely because they can materially affect a company’s value, financial health and stock price.
Master Service Agreement regulatory
"related to the Master Service Agreement and a Quality Agreement entered into"
A master service agreement (MSA) is a framework contract that sets standard terms—such as pricing rules, responsibilities, liability limits and dispute processes—for all future work between two parties, so individual projects only need a short statement of work. For investors, an MSA matters because it creates predictable revenue procedures, reduces deal-making friction, clarifies risk exposure and can speed sales cycles, improving the company’s ability to win and deliver repeat business.
Quality Agreement regulatory
"related to the Master Service Agreement and a Quality Agreement entered into"
universal proxy rules regulatory
"In addition to satisfying the foregoing requirements, to comply with the universal proxy rules"
Universal proxy rules require that when shareholders vote to elect directors in a contested election, the proxy card mailed to investors can include candidates nominated by both the company and dissident shareholders, letting investors mix and match their choices on a single ballot. This matters to investors because it makes their vote more flexible and easier to use, like replacing separate lists with one common ballot, which can influence who controls the board and the company’s future direction.
Rule 14a-19 regulatory
"must provide notice that sets forth the information required by Rule 14a-19 under the Exchange Act"
Rule 14a-19 is a U.S. Securities and Exchange Commission rule that governs how independent proxy advisory firms produce and distribute voting recommendations for shareholders. It requires these advisers to provide companies with notice of their recommendations and a chance to respond, and to disclose certain conflicts; think of it as a referee ensuring both sides see a game plan before fans cast votes. Investors care because proxy advisers influence voting outcomes and corporate governance, so the rule affects transparency, potential bias, and the reliability of guidance that many investors rely on when voting shares.
metastatic pancreatic cancer medical
"including potentially a Phase 3 clinical trial for metastatic pancreatic cancer."
A serious form of cancer that began in the pancreas and has spread to other parts of the body, such as the liver or lungs; think of it like a fire that started in one room and has moved through the house. It matters to investors because metastatic disease usually signals advanced illness with limited treatment options, influencing the commercial prospects of therapies, clinical trial success, healthcare costs, and the financial outlook for companies working on diagnostics or treatments.

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FAQ

What material agreement did AIM (AIM) enter into on July 31, 2026?

AIM ImmunoTech entered a Proposal Agreement with Sterling Pharma Solutions. Sterling will manufacture PolyI and Poly C12U and transfer test methods at its Dudley, UK site to support Ampligen production for clinical trials.

What is the value and duration of AIM’s new manufacturing arrangement (AIM)?

The estimated cost to AIM under the Proposal Agreement is approximately $1.5 million, payable over a period of 12 months. Payment timing and milestones are described in more detail in the Proposal Agreement itself.

How will AIM (AIM) use the products from the Sterling Pharma Proposal Agreement?

AIM anticipates using the manufactured PolyI and Poly C12U to produce Ampligen for ongoing and future clinical trials, including potentially a Phase 3 metastatic pancreatic cancer trial, subject to clinical and regulatory progress.

What are the 2026 director nomination deadlines for AIM (AIM) stockholders?

To nominate directors or bring other business at the 2026 annual meeting outside Rule 14a-8, stockholders must deliver notice between August 18, 2026 and 5:00 p.m. local time on September 17, 2026 to AIM’s Secretary.

What is the universal proxy notice deadline for AIM (AIM) stockholders?

Stockholders planning to solicit proxies for director nominees other than AIM’s nominees must provide a Rule 14a-19 universal proxy notice by October 19, 2026. The notice must include the information specified by Rule 14a-19 under the Exchange Act.

Which drug substances are covered by AIM’s (AIM) new Proposal Agreement?

The Proposal Agreement covers manufacturing further batches of PolyI and Poly C12U and transferring associated test methods. These are polynucleotide drug substances used as polymer precursors in the manufacture of the drug Ampligen.
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UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

 

FORM 8-K

 

CURRENT REPORT

 

Pursuant to Section 13 OR 15(d) of The

Securities Exchange Act of 1934

 

Date of Report (Date of earliest event reported): July 31, 2026

 

AIM IMMUNOTECH INC.

(Exact name of registrant as specified in its charter)

 

Delaware   001-27072   52-0845822
(state or other jurisdiction   (Commission   (IRS Employer
of incorporation)   File Number)   Identification No.)

 

2117 SW Highway 484, Ocala, FL   34473
(Address of principal executive offices)   (Zip Code)

 

Registrant’s telephone number, including area code: (352) 448-7797

 

 

(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 (see General Instruction A.2. below):

 

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

 

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

 

Title of each class   Trading Symbol   Name of each exchange on which registered
Common Stock, par value $0.001 per share   AIM   NYSE American

 

Indicate by check mark whether the registrant is an emerging growth company as defined in 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.

 

On July 31, 2026, AIM ImmunoTech Inc. (the “Company”) entered into a proposal (the “Proposal Agreement”) with Sterling Pharma Solutions (the “Manufacturer”) that is related to the Master Service Agreement and a Quality Agreement entered into between the Company and the Manufacturer in 2022. Pursuant to the Proposal Agreement, the Manufacturer agreed to manufacture further batches of the polynucleotide drug substances PolyI and Poly C12U and transfer of associated test methods at the Manufacturer’s Dudley, UK location to produce the polymer precursors to manufacture the drug Ampligen. The estimated cost to the Company under the Proposal Agreement is approximately $1.5 million to be paid over a period of 12 months, as set forth in more detail in the Proposal Agreement. The Company anticipates using the manufactured product for ongoing and future clinical trials, including potentially a Phase 3 clinical trial for metastatic pancreatic cancer.

 

The foregoing summary of the Proposal Agreement does not purport to be complete and is qualified in its entirety by reference to the full text of the Proposal Agreement, which is attached as Exhibit 10.1 to this Current Report on Form 8-K and incorporated herein by reference.

 

Item 5.08 Shareholder Director Nominations.

 

Stockholders who wish to nominate a director at the Company’s 2026 annual meeting of stockholders (the “2026 Annual Meeting”), or to bring any other proposal before the 2026 Annual Meeting, that is not to be included in this year’s proxy materials pursuant to Rule 14a-8, must do so in accordance with the Company’s Restated and Amended Bylaws, which require notice be received by the Secretary at the Company’s principal executive offices not later than 5:00 p.m. local time on September 17, 2026 and not earlier than August 18, 2026.

 

In addition to satisfying the foregoing requirements, to comply with the universal proxy rules, stockholders who intend to solicit proxies in support of director nominees other than the Company’s nominees must provide notice that sets forth the information required by Rule 14a-19 under the Exchange Act no later than October 19, 2026.

 

Item 9.01 Financial Statements and Exhibits.

 

(d) Exhibits

 

Exhibit No.   Description
10.1   Proposal Agreement between the Company and the Manufacturer, dated July 31, 2026.
104   Cover Page Interactive Data File (embedded within the Inline XBRL document).

 

Cautionary Note Regarding Forward-Looking Statements

 

This Current Report on Form 8-K contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended (the “Securities Act”), and Section 21E of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), including with respect to the anticipated use of the manufactured products and any future clinical trial. These statements are subject to risks and uncertainties that could cause actual results to differ materially, including but not limited to risks related to NYSE compliance, clinical development, regulatory approval, and other factors described in the Company’s filings with the U.S. Securities and Exchange Commission, including its most recent Annual Report on Form 10-K and subsequent Quarterly Reports on Form 10-Q. The Company undertakes no obligation to update any forward-looking statements.

 

 

 

 

SIGNATURES

 

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.

 

  AIM IMMUNOTECH INC.
     
Date: August 6, 2026 By: /s/ Thomas K. Equels
    Thomas K. Equels, CEO

 

 

Filing Exhibits & Attachments

11 documents