STOCK TITAN

Notifications

Limited Time Offer! Get Platinum at the Gold price until January 31, 2026!

Sign up now and unlock all premium features at an incredible discount.

Read more on the Pricing page

[8-K] HCW Biologics Inc. Reports Material Event

Filing Impact
(Neutral)
Filing Sentiment
(Neutral)
Form Type
8-K
Rhea-AI Filing Summary

HCW Biologics Inc. entered into an Amended and Restated License, Research and Co-Development Agreement with Beijing Trimmune Biotech covering the HCW11-006 molecule for in vivo applications. The deal restructures an earlier license so Trimmune pays a $7.0 million upfront fee, split into $3.5 million in cash at closing and $3.5 million in transferable equity in Trimmune valued from its current equity financing round. The agreement also gives Trimmune an option to license HCW9302 for in vivo use in China or Asia and sets a 90-day window from signing to close the transaction.

HCW Biologics keeps a payment-free, milestone-free, and royalty-free option to recapture rights to develop and commercialize HCW11-006 for in vivo applications in the United States, Canada, Central America, and South America after Phase 1 clinical trials. Trimmune will be financially responsible for research, development, manufacturing, clinical work, regulatory approvals, and commercialization in its territory. If the closing does not occur within 90 days of execution, all intellectual property and rights to HCW11-006 revert to HCW Biologics.

Positive
  • None.
Negative
  • None.

Insights

HCW Biologics restructures HCW11-006 rights with Trimmune, securing a mixed cash and equity upfront payment and retaining a key opt-in option.

The agreement gives HCW Biologics a restructured pathway to monetize HCW11-006 for in vivo applications while leaning on Beijing Trimmune Biotech to fund development in its territory. The upfront consideration is $7.0M, split into $3.5M cash at closing and $3.5M in transferable Trimmune equity valued from its current equity financing. This combines immediate cash with potential upside from Trimmune’s valuation.

Operationally, Trimmune assumes financial responsibility for research and development, manufacturing, clinical trials, regulatory approvals, and commercialization in its territory, which can limit HCW Biologics’ cash outlay for HCW11-006 outside the Americas. The structure also includes an option for Trimmune to license HCW9302 for in vivo use in China or Asia, which could expand collaboration scope if exercised.

A notable feature is HCW Biologics’ payment-free, milestone-free, and royalty-free option to recapture all rights for HCW11-006 in the United States, Canada, Central America, and South America after completion of a Phase 1 clinical trial. This preserves strategic flexibility should early data be favorable. However, the transaction must close within 90 days of execution, by January 16, 2026; otherwise, all HCW11-006 intellectual property and rights automatically return to HCW Biologics, so the practical impact depends on achieving a timely closing.

false000182867300018286732025-11-172025-11-17

 

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): November 17, 2025

 

 

HCW Biologics Inc.

(Exact name of Registrant as Specified in Its Charter)

 

 

Delaware

001-40591

82-5024477

(State or Other Jurisdiction
of Incorporation)

(Commission File Number)

(IRS Employer
Identification No.)

 

 

 

 

 

2929 N. Commerce Parkway

 

Miramar, Florida

 

33025

(Address of Principal Executive Offices)

 

(Zip Code)

 

Registrant’s Telephone Number, Including Area Code: 954 842-2024

 

 

(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

 

Trading
Symbol(s)

 


Name of each exchange on which registered

Common Stock, par value $0.0001 per share

 

HCWB

 

The Nasdaq Stock Market LLC

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

Emerging growth company

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

 


Item 1.01 Entry into a Material Definitive Agreement.

On November 17, 2025, HCW Biologics Inc. (the “Company”) and Beijing Trimmune Biotech Co., Ltd. (“Trimmune”) entered into an Amended and Restated License, Research and Co-Development Agreement (“A&R License”) following the assignment of the original License, Research and Co-Development Agreement, which includes an exclusive license to HCW11-006 for in vivo applications (“WY Biotech License”) from WY Biotech Co., Ltd. to Trimmune. The parties restructured the terms of the original WY Biotech License to include the assignment of rights to Trimmune, payment of half of the $7.0M upfront license fee (i.e., $3.5M) in cash at closing and the other half in transferable equity in Trimmune (valued based on its current round of equity financing), an option to license HCW9302 for in vivo applications in China or Asia, and a 90-day period to close the deal from execution of the A&R License. Pursuant to the terms of the A&R License, the Company will retain its payment-free, milestone-free, and royalty-free option to recapture all rights to the development and commercialization of the licensed molecule for in vivo applications in the United States, Canada, Central America, and South America (Opt-in Territory) after the conclusion of the Phase 1 clinical trial. Trimmume is financially responsible for all costs associated with research and development, manufacturing, clinical development, regulatory approval, and commercialization for the molecule in its territory. If the closing under the A&R License Agreement does not occur within 90 days of execution (i.e., by January 16, 2026), all intellectual property and rights with respect to HCW11-006 will be returned to the Company.

 


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.

 

 

 

HCW BIOLOGICS INC.

 

 

 

 

Date:

November 18, 2025

By:

 /s/ Hing C. Wong

 

 

 

Hing C. Wong, Founder and Chief Executive Officer

 


FAQ

What agreement did HCW Biologics (HCWB) announce with Beijing Trimmune Biotech?

HCW Biologics entered into an Amended and Restated License, Research and Co-Development Agreement with Beijing Trimmune Biotech for HCW11-006 in vivo applications, replacing and restructuring an earlier license that had been assigned to Trimmune.

How much is the upfront payment Trimmune will provide to HCW Biologics for HCW11-006?

The deal includes a $7.0M upfront license fee, with $3.5M paid in cash at closing and $3.5M paid in transferable equity in Trimmune valued from its current equity financing round.

What rights does HCW Biologics retain under the new Trimmune license agreement?

HCW Biologics retains a payment-free, milestone-free, and royalty-free option to recapture all rights to develop and commercialize HCW11-006 for in vivo applications in the United States, Canada, Central America, and South America after completion of the Phase 1 clinical trial.

Who is responsible for development and commercialization costs for HCW11-006 under the Trimmune deal?

Trimmune is financially responsible for all costs related to research and development, manufacturing, clinical development, regulatory approval, and commercialization of HCW11-006 in its territory.

Is there an option related to HCW9302 in the HCW Biologics and Trimmune agreement?

Yes. The restructured agreement includes an option for Trimmune to license HCW9302 for in vivo applications in China or Asia, adding potential future scope to the collaboration.

What happens if the HCW Biologics–Trimmune deal does not close by January 16, 2026?

If closing under the Amended and Restated License agreement does not occur within 90 days of execution, i.e., by January 16, 2026, all intellectual property and rights related to HCW11-006 will be returned to HCW Biologics.

Hcw Biologics Inc.

NASDAQ:HCWB

HCWB Rankings

HCWB Latest News

HCWB Latest SEC Filings

HCWB Stock Data

5.20M
2.11M
27.3%
1%
11.41%
Biotechnology
Pharmaceutical Preparations
Link
United States
MIRAMAR