TransCode Therapeutics Secures Up to $20M Financing Agreement
TransCode Therapeutics has entered into an agreement with an institutional healthcare investor for financing of up to $20M. The arrangement comprises pre-paid advances of up to $6M and a three-year Standby Equity Purchase Agreement , or SEPA, providing the company the right to sell up to $14M of its common stock to the investor, subject to certain conditions. TTX-MC138 is a first-in-class therapeutic candidate designed to inhibit microRNA-10b, or miR-10b, a microRNA widely believed to be critical to the emergence and progression of many metastatic cancers. TransCode's Phase 0 clinical trial produced evidence of delivery of a radiolabeled version of TTX-MC138 to metastatic lesions and pharmacodynamic activity, even at a microdose of the drug candidate, suggesting a broad therapeutic window for TTX-MC138. In the company's Phase 1a clinical trial, TTX-MC138 met its safety endpoint and was well tolerated by patients. A Phase 2a clinical trial with TTX-MC138 is expected to begin in Q2. The pre-paid advance will be evidenced by convertible promissory notes priced at 95% of face value. TransCode will issue a $1M principal amount note concurrently with its Annual Report for 2025, and, subject to certain closing conditions, will issue an additional $5M principal amount note upon shareholder approval of the transaction. The advance will accrue interest at a simple annual rate of 5% and may be converted into TransCode's common stock.
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- Financing Agreement: TransCode Therapeutics has entered into a financing agreement with an institutional investor for up to $20 million, which includes $6 million in pre-paid advances and a three-year Standby Equity Purchase Agreement, ensuring operational flexibility during the Phase 2a trial of TTX-MC138.
- Clinical Trial Progress: TTX-MC138, a first-in-class therapeutic candidate targeting miR-10b, has shown effective delivery and pharmacodynamic activity in its Phase 0 trial, with the Phase 2a trial expected to commence in Q2 2026, further advancing the company's strategic positioning in cancer treatment.
- Convertible Note Issuance: The financing will be executed through convertible promissory notes priced at 95% of face value, with an initial issuance of a $1 million note and an additional $5 million note upon shareholder approval, accruing interest at 5% annually, providing crucial funding support for the company.
- Strategic Collaboration Outlook: The financing agreement not only secures funding for TransCode but also lays the groundwork for exploring strategic collaborations, aiming to leverage the therapeutic potential of TTX-MC138 to enhance the company's position in the competitive cancer treatment market.
- Financing Agreement Details: TransCode Therapeutics has entered into a financing agreement with an institutional investor for up to $20 million, which includes $6 million in prepaid advances and a three-year Standby Equity Purchase Agreement, ensuring financial flexibility as the company conducts its Phase 2a trial for TTX-MC138.
- Clinical Trial Progress: TTX-MC138, a first-in-class therapeutic candidate targeting microRNA-10b, has shown efficacy against metastatic lesions in its Phase 0 trial, with the Phase 2a trial expected to commence in Q2 2026, further validating its therapeutic potential.
- Convertible Note Issuance: The prepaid financing will be evidenced by convertible promissory notes priced at 95% of face value, accruing interest at 5% annually, providing TransCode with additional funding to support its clinical research and operations.
- Strategic Collaboration Outlook: Following the completion of the Phase 2a trial, the company plans to explore strategic collaborations with other institutions to advance the development of TTX-MC138, enhancing its competitive position in the cancer treatment market.
- Exclusive License Agreement: TransCode Therapeutics has signed an exclusive, worldwide, fully paid-up royalty-free license agreement with Unleash Immuno Oncolytics, acquiring rights to develop three drug candidates, UIO-524, UIO-525, and UIO-526, marking a strategic expansion in the field of immuno-oncology.
- Equity Payment Structure: Under the agreement, Unleash will receive 1,136,364 shares of a new series of non-voting convertible preferred stock, equivalent to 6.8% of TransCode's common stock upon conversion, enhancing Unleash's shareholder position while providing TransCode with funding to advance its R&D efforts.
- Market Opportunity: UIO-524, as a next-generation biology-driven oncolytic immunotherapy, aims to address muscle-invasive bladder cancer, a high unmet medical need, potentially opening up a multi-billion-dollar market opportunity for TransCode and strengthening its competitive position in cancer treatment.
- Clinical Trial Progress: TransCode's lead candidate, TTX-MC138, is advancing into a Phase 2a clinical trial, and the introduction of UIO-524 will further enrich its oncology pipeline, enhancing the company's market positioning and therapeutic capabilities in more aggressive disease settings.
- Innovative Immunotherapy: TransCode Therapeutics' published research introduces a novel tumor-selective immunotherapy that activates innate immune signaling within cancer cells, significantly enhancing non-invasive imaging capabilities for drug delivery, potentially transforming cancer treatment paradigms.
- Collaborative Research Findings: Conducted in collaboration with Dr. Anna Moore from Michigan State University, the study utilizes overexpressed oncogenic microRNAs as intracellular assembly templates, successfully addressing challenges associated with RIG-I agonists, including off-target immune activation and inefficient systemic delivery.
- Clinical Trial Progress: TransCode's TTX delivery platform is currently under evaluation in clinical trials, underscoring the translational feasibility of this immunotherapy approach, which may provide new treatment options for patients with high-risk and advanced cancers.
- Market Potential: TransCode's lead therapeutic candidate, TTX-MC138, targets metastatic tumors that overexpress microRNA-10b, highlighting its unique market positioning and potential commercial value in the tumor immunotherapy landscape.
- Research Publication: TransCode Therapeutics, in collaboration with Michigan State University, published preclinical research on TTX-MC138 for glioblastoma treatment, demonstrating significant survival improvements, marking a crucial advancement in addressing treatment-resistant cancers.
- Efficacy Validation: The study showed that TTX-MC138 effectively delivered to human glioblastoma in murine models, inducing a five-fold increase in apoptotic activity, further validating its potential to overcome drug delivery barriers.
- Clinical Trial Progress: TTX-MC138 has completed IND studies and toxicity testing, showing good safety in Phase I trials for non-CNS cancers, with a Phase II trial anticipated to begin in the first half of 2026, advancing its clinical application.
- Strategic Implications: This research not only provides robust biological support for TransCode's RNA therapeutic platform but also showcases its broad potential in treating metastatic tumors, potentially transforming the treatment landscape for glioblastoma.

- Survival Extension: TTX-MC138 successfully delivered via intravenous injection in glioblastoma mouse models significantly extends survival, indicating its potential in treating this highly aggressive cancer.
- Target Mechanism Validation: The study demonstrates that TTX-MC138 effectively suppresses miR-10b, resulting in a five-fold increase in apoptotic activity in tumors, thereby enhancing therapeutic efficacy and supporting its clinical development.
- Preclinical Research Findings: Conducted in collaboration with Michigan State University and published in the Journal of Functional Biomaterials, this study lays the groundwork for the clinical application of TTX-MC138, which is expected to drive future clinical trials.
- Future Clinical Trial Plans: Currently undergoing Phase 1 clinical trials, TTX-MC138 is anticipated to enter Phase 2 trials in the first half of 2026, further validating its potential application in metastatic diseases.








