SEED Therapeutics Closes $6M Series A-3 Funding, Advances to Clinical Stage

Meta description: SEED Therapeutics completes $6M Series A-3 funding, backed by major pharma partners, and moves toward first clinical trials in 2026.

SEED Therapeutics has secured $6 million in its latest Series A-3 financing round, marking a significant step in its growth trajectory. The raise positions the biotech firm to advance its lead program into first-in-human trials in early 2026, following recent FDA clearance. Investors and industry stakeholders will note the strong institutional support behind this move, including partnerships with Eli Lilly and Eisai.

In this article:

What are the funding details?

The Series A-3 round closed with an additional $6 million in proceeds from the sale of preferred shares. This is the second close of a planned $30 million total, indicating staged capital deployment to match development milestones. The fresh funding comes shortly after SEED Therapeutics received regulatory approval from the Food and Drug Administration to proceed with clinical testing of its flagship candidate, ST-01156, which targets RBM39.

By completing this tranche, the company gains financial runway to initiate first-in-human clinical trials in the first quarter of 2026. Strategic allocation will likely cover trial preparation, early-stage patient enrollment, and advancement of the firm’s molecular glue degrader platform.

Who are the key investors?

Strong financial backing in this round comes from established pharmaceutical players, notably Eli Lilly and Eisai. These partnerships do more than supply capital. They provide industry expertise, validation of technology potential, and possible routes for collaboration in commercialization. Such support is critical for a company transitioning from preclinical research to active patient trials.

Backing from industry leaders suggests that SEED’s approach to targeting previously undruggable proteins resonates with partners looking to diversify therapeutic portfolios. The investor participation in multiple closes of the Series A-3 round indicates sustained confidence in the business model.

What does this mean for growth?

The funding, combined with regulatory clearance, transforms SEED Therapeutics into a clinical-stage entity. This milestone changes the scope of operations, adding regulatory compliance burdens, clinical recruitment needs, and data management for trial results.

The RITE3 platform’s application across oncology, neurodegeneration, immunology, and virology offers multiple paths for long-term growth. Successful early trials for ST-01156 could open doors for accelerated development of other pipeline candidates. The $72.19 million current market capitalization provides a benchmark for investors monitoring valuation changes as trials progress.

Beyondspring, through its connection to SEED, remains under close scrutiny by market analysts. Despite technical indicators showing short-term momentum, broader financial metrics continue to highlight operational challenges such as zero revenue and negative margins.

FAQ

  1. How much funding did SEED Therapeutics secure in the recent round?
    SEED Therapeutics raised $6 million in the latest closing of its Series A-3 round.
  2. What is the total planned size of the Series A-3 financing?
    The total Series A-3 financing is planned at $30 million, with the recent close representing part of this target.
  3. What is the lead program advancing to trials?
    ST-01156, targeting RBM39, is the lead program expected to start first-in-human clinical trials in Q1 2026.
  4. Who are the major investors in this round?
    Eli Lilly and Eisai are notable participants providing both funding and strategic support.

Conclusion

SEED Therapeutics’ $6 million funding close aligns with its entry into the clinical stage, supported by key pharmaceutical investors. The transition sets up the company for trial initiation in 2026 and signals confidence in its molecular glue degrader technology. Founders and investors watching the biotech sector should note the blend of capital infusion and strategic partnerships in this case as a model for scaling from preclinical to clinical phases.

Disclaimer

This content is provided for informational purposes only and does not constitute financial advice. Readers should conduct their own due diligence before making investment decisions.

This article is based on publicly available financial information.