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