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Ainos Completes VELDONA Data Delivery, Triggers $600,000 Initial Payment
Ainos has completed the required data delivery and technology transfer under its VELDONA license agreement, triggering a $600,000 initial license payment. The licensing partner confirmed completion in writing on September 29. Payment is due within 15 business days under the agreement. The delivery includes clinical and regulatory materials for Sjogren's disease and thrombocytopenia, providing a foundation for the partner's continued development work in autoimmune and hematologic diseases. The initial payment is part of the previously announced potential $10M licensing framework, which also includes conditional payments tied to the first sublicense and licenses for 15 additional indications. Ainos is separately entitled to 25% of net sublicensing revenue, as defined in the agreement.
Ainos Completes Delivery of 1,400 AI Nose Systems to ASE
Ainos has completed delivery of all 1,400 AI Nose systems to ASE Technology Holding under the announced $2.1M, three-year agreement. The completed delivery marks a major commercial milestone for Ainos' Chemical Intelligence platform in advanced back-end semiconductor manufacturing. Management expects the delivery to contribute to revenue beginning in the third-quarter 2026 revenue, advancing the Company's previously communicated second-half commercialization outlook. ASE's experience deploying the first-phase systems across different locations, primarily in advanced packaging processes, has helped identify the need for broader coverage. Ainos has begun discussion for a larger scale, second-phase deployment based on the companies' existing memorandum of understanding. A separate agreement is currently under negotiation to cover that phase.
Ainos VELDONA License Agreement Initial Fee of $600,000
Ainos detailed the financial and strategic benefits of the VELDONA License Agreement announced on September 24. Ainos expects to complete the agreed contractual delivery shortly, with an initial license fee of $600,000 payable within 15 business days after the applicable payment conditions are satisfied. This payment does not depend on completion of future clinical trials or receipt of marketing approval. The pharmaceutical development partner identified in the September 24 announcement will fund and execute the clinical and regulatory activities assigned to it for the two initial globally licensed indications, Sjogren's disease and thrombocytopenia. This structure reduces Ainos' need to independently finance subsequent development, expand specialist teams and devote additional management resources to pharmaceutical execution, supporting the Company's priority investment in Chemical Intelligence. Ainos is also entitled to 25% of applicable net sublicensing revenue. Qualifying transactions may generate upfront payments, option fees and development or regulatory milestones during clinical development, creating opportunities for payments to Ainos before a product reaches the market. The Agreement provides distinct sources of potential consideration: Initial license fee: $600,000 payable under the contractual delivery and payment provisions. Sublicensing participation: 25% of applicable net sublicensing revenue, which may include upfront payments, option fees, milestones, royalties and other consideration covered by the Agreement. First-sublicense fee: A separate, one-time fee payable within 30 days after the first third-party sublicense takes effect, without reducing or offsetting Ainos' applicable revenue share. Additional indication licenses: A pathway for 15 additional VELDONA indications, subject to applicable contractual rights, separate definitive agreements and payment. Product supply: Opportunities under separately negotiated agreements and accepted purchase orders. The potential $10M framework comprises the initial license fee, conditional additional-indication consideration and the first-sublicense fee. Partner-funded development expenditures, applicable sublicensing revenue participation and potential product supply revenue are additional to that framework. Where additional indication licenses carry forward the 25% net sublicensing participation, that share would be additional to the corresponding license fees. Accordingly, $10M is not a ceiling on Ainos' total economic participation. Further value will depend on completed licenses, qualifying sublicensing transactions and supply arrangements. Neither party is obligated to complete all 15 additional licenses, and the framework represents neither guaranteed revenue nor a platform valuation. The 25% share applies to the defined net sublicensing revenue base, subject to permitted deductions and other applicable terms. Payments depend on qualifying transactions, receipt of consideration and contractual payment provisions; clinical activity alone does not trigger a payment. License fees, the first-sublicense fee and separate supply payments are independent of that percentage calculation. Ainos may also negotiate direct licenses for available indications with other third parties, subject to the licensee's applicable contractual priority rights. Consideration contemplated under this Agreement does not set a ceiling on those separately negotiated transactions.
Ainos Enters VELDONA License Agreement with BioPhoenix, Potential Value of $10M
Ainos entered into a VELDONA License Agreement with BioPhoenix, establishing a collaboration framework with a potential aggregate value of $10M. The framework comprises an initial license fee, conditional consideration for licenses covering 15 additional indications, and a one-time fee upon the first sublicense. The agreement marks a significant milestone for VELDONA by establishing a partner-funded development model. BioPhoenix will assume primary funding and execution responsibilities for the clinical and regulatory development activities allocated to it under the agreement for the two initial licensed indications, while Ainos retains core platform ownership and long-term commercial interests. Development expenditures funded by BioPhoenix, potential product supply revenue and downstream revenue sharing are separate from, and are not included in, the $10M collaboration framework.Under the agreement, BioPhoenix receives an exclusive worldwide license to VELDONA for two initial indications-Sjogren's disease and thrombocytopenia-to conduct research, development, manufacturing, marketing authorization activities and commercialization within the agreed scope. The collaboration framework includes: An initial license fee for the two initial indications, payable in accordance with the agreement. Potential license consideration for 15 additional indications under the BioPhoenix agreement, assuming all 15 licenses are completed on the contemplated terms, subject to the execution of separate license agreements and payment of the applicable consideration. A one-time fee upon the first sublicense, payable by BioPhoenix within 30 days after the effective date of its first sublicense to a third party under the agreement. This fee is payable only once under the entire agreement, regardless of which indication is covered by the first sublicense. Subsequent sublicenses, whether involving the same or different indications or additional third parties, do not trigger another first-sublicense fee. Each additional indication requires a separate license agreement and payment. Neither party is obligated to complete all 15 licenses, and there can be no assurance that all will be completed. Accordingly, the $10 million collaboration framework is conditional and does not represent guaranteed revenue or a valuation of the VELDONA platform.
Ainos Launches Second-Gen AI Nose Platform, Secures Initial Orders
Ainos announced that its second-generation AI Nose platform is advancing into commercial deployment in front-end semiconductor manufacturing, building on validation activities initiated earlier this year involving approximately 200 AI Nose systems. Ainos is receiving initial commercial orders from a front-end semiconductor company.
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