| Valuation method | Value, € | Upside, % |
|---|---|---|
| Artificial intelligence (AI) | 44.95 | 13358 |
| Intrinsic value (DCF) | 2.61 | 681 |
| Graham-Dodd Method | n/a | |
| Graham Formula | n/a |
Poxel S.A. (POXEL.PA) is a clinical-stage biopharmaceutical company headquartered in Lyon, France, specializing in innovative treatments for metabolic disorders, including type 2 diabetes and liver diseases such as non-alcoholic steatohepatitis (NASH). The company's lead candidate, Imeglimin, is an oral therapy that has completed Phase III trials in Japan and is advancing in Phase III in the U.S. and Europe, targeting type 2 diabetes by improving pancreatic beta cell function and reducing insulin resistance. Poxel also develops PXL770, a Phase 2a-stage AMPK activator for metabolic and liver diseases, and PXL065, a mitochondrial pyruvate carrier inhibitor in Phase I for NASH. Additionally, Poxel has strategic partnerships, including a licensing agreement with Enyo Pharma for PXL007 (EYP001), an FXR agonist in Phase II for hepatitis B and NASH. With a focus on addressing unmet medical needs in metabolic diseases, Poxel leverages its expertise in drug development to position itself as a key player in the global biotech sector.
Poxel S.A. presents a high-risk, high-reward investment opportunity due to its clinical-stage pipeline targeting large and growing markets like type 2 diabetes and NASH. The company's lead candidate, Imeglimin, shows promise with its unique mechanism of action, but regulatory approvals and commercialization risks remain. Financially, Poxel operates at a loss (net income of -€35.09M in FY 2023) with limited revenue (€1.98M) and high debt (€47.03M), relying heavily on funding for clinical trials. The stock's high beta (1.845) indicates significant volatility, making it suitable for speculative investors comfortable with biotech sector risks. Success in late-stage trials or partnerships could drive upside, but failure could exacerbate financial strain.
Poxel competes in the crowded metabolic and liver disease therapeutics market, where differentiation is critical. Its lead candidate, Imeglimin, stands out by targeting multiple pathways in type 2 diabetes (beta cell function, insulin resistance), unlike most diabetes drugs that focus on single mechanisms. However, it faces competition from established players like Novo Nordisk (semaglutide) and Eli Lilly (tirzepatide), which dominate the GLP-1 and dual-agonist markets. In NASH, Poxel's PXL770 and PXL065 compete with Madrigal Pharmaceuticals' resmetirom (first FDA-approved NASH drug) and Intercept Pharmaceuticals' obeticholic acid. Poxel's small size and limited resources (€2.34M cash vs. €47.03M debt) constrain its ability to commercialize independently, making partnerships vital. Its competitive edge lies in novel mechanisms and strategic collaborations, but scalability and funding remain challenges compared to larger rivals with deeper pipelines and commercialization capabilities.