PRESS RELEASE · Development Update
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TFA Reports Progress in Antcin A Drug Development for Companion Animals
Canine osteoarthritis toxicology studies advance; TFA reports a technical breakthrough in ongoing injectable nanoformulation development

PINGTUNG, Taiwan, October 1, 2026 — TFA Therapeutics, Inc. presented progress in its Antcin A drug development program for companion animals on September 29 at the Graduate Institute of Animal Vaccine Technology, National Pingtung University of Science and Technology (NPUST). Toxicology studies for the initial indication, canine osteoarthritis, are progressing smoothly, and the company reported a technical breakthrough in ongoing injectable nanoformulation development. The seminar also covered research progress in feline stomatitis, the second indication under development, as well as HPF strain-fusion technology and production capacity improvements.
Toxicology studies advance, with the injectable nanoformulation intended for subsequent studies
TFA is continuing toxicology research related to canine osteoarthritis while developing an injectable nanoformulation of Antcin A. Once formulation development is complete, the formulation will be supplied for use in toxicology studies in target animals and subsequent clinical trials, supporting the progression from safety studies to clinical evaluation.
Nanoformulation development focuses on biological activity and dose optimization
Nanoformulation development was a key part of the progress presented at the seminar. Its rationale includes improving the utilization of the active compound and optimizing biological activity at the cellular level. Further research will assess whether nanoformulated Antcin A can enhance efficacy and explore the possibility of reducing the dose needed to achieve the intended effect.
Dr. Wei-Yu Chen of NPUST’s Functional Materials and Analytical Technology Laboratory presented research on nanomaterial design and biomedical applications. He outlined the use of appropriate processing techniques to enhance the biological activity of naturally derived active molecules and shared findings from sepsis experiments in his nanomaterial research, along with related patent work. These studies provide a research reference for further development of the Antcin A nanoformulation.
If subsequent studies confirm that nanoformulated Antcin A can achieve comparable or greater efficacy at a lower dose, the amount of raw material needed to achieve the intended effect could be reduced, creating an opportunity to improve costs. Actual cost benefits will be assessed alongside nanoformulation manufacturing costs, quality consistency, and study results to inform process scale-up and commercialization planning.
Efficacy optimization
Evaluate the potential to enhance biological activity at the cellular level
Dose optimization
Explore whether a lower dose can achieve the intended effect
Cost improvement
Assess potential raw material savings alongside nanoformulation manufacturing costs
Research progress in feline stomatitis, the second indication under development
Professor Hsian-Yu Wang of NPUST’s Graduate Institute of Animal Vaccine Technology gave the opening presentation, outlining the research plan and current progress for Antcin A in feline stomatitis, the second indication under development. The research will continue to evaluate its potential in feline stomatitis as TFA expands its companion-animal drug development program to additional indications.
Raw material supply and nanoformulation development strengthen technical differentiation
TFA Chief Technology Officer Vincent Liu presented “Antcin A: From a Scarce Compound to a Stable Supply.” He reported on experimental progress with HPF strain-fusion technology and current production capacity improvements to support the preparation of research materials and further formulation development.
Obtaining, preparing, and reliably supplying Antcin A already involves technical barriers. Building on this foundation through nanoformulation development, TFA is developing capabilities across raw material supply and dosage-form design to strengthen product differentiation and support further drug development and future market competition.
The seminar focused on progress in Antcin A formulation optimization and pharmacological research.



These programs remain in drug development. Safety, efficacy, and the specific benefits of nanoformulation will be assessed through subsequent studies.
About TFA
TFA Therapeutics, Inc. (OTCQB: RAJAF) is developing TFA-01, an Antcin A-based drug candidate, with canine osteoarthritis as its initial target indication. The program includes source material and formulation development, as well as safety and efficacy evaluation.
Forward-looking statements: The development plans described in this release may change in response to study results, regulatory requirements, and funding arrangements. Actual progress and outcomes may differ from current expectations.