SanegeneBio, a biotechnology company specializing in RNAi therapeutics, today announced a global research collaboration and licensing agreement with Eli Lilly (NYSE: LLY). The two parties will jointly leverage SanegeneBio’s proprietary LEAD platform to accelerate the discovery and development of RNAi candidates that target metabolic disorders.
Partnership Highlights
- Technology – SanegeneBio will employ the LEAD platform to screen and identify the most potent RNAi active molecules for the collaboration.
- Drug Development Pathway – Eli Lilly will lead all Investigational New Drug (IND) enabling studies, clinical development, and eventual commercialization of the compounds.
- Financial Terms – SanegeneBio receives an upfront payment and an equity injection, with the potential for up to USD 1.2 billion in milestone payments and tiered royalties on commercial sales.
Strategic Rationale
- For SanegeneBio – Access to Eli Lilly’s global R&D, regulatory, and commercial platforms, thereby accelerating the path from bench to bedside.
- For Eli Lilly – Integration of a cutting‑edge RNAi discovery platform within its expanding metabolic disease program, broadening its therapeutic portfolio.
- Industry Impact – The alliance underscores the growing momentum of RNAi as a viable modality for complex metabolic conditions such as type 2 diabetes, non‑alcoholic fatty liver disease, and dyslipidemia.
Timeline & Next Steps
| Milestone | Target Date | Owner |
|---|---|---|
| IND filing preparation | Q3 2025 | Eli Lilly |
| Phase I clinical safety studies | Q1 2026 | Eli Lilly |
| Commercial launch (targeted) | 2028 | Eli Lilly |
Forward‑Looking Statements
This release contains forward‑looking statements regarding future milestones, regulatory approvals, and commercial prospects. Actual results may differ materially from those expressed herein.-Fineline Info & Tech
