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25/03/2026 21:58
Inside Information / News release on accounts, resultsProjet strictement confidentiel Poxel confirms the drawdown under the additional Tranche D PDR bond issue as part of the continuation plan
LYON, France 25 March 2026– POXEL SA (Euronext: POXEL - FR0012432516), a clinical-stage biopharmaceutical company that has developed innovative treatments for serious chronic diseases with metabolic pathophysiology, including metabolic dysfunction-associated steatohepatitis (MASH) and rare metabolic diseases (the "Company"), announces that it has signed, on March 25, 2026, the new Tranche D PDR subscription agreement with IPF Partners ("IPF"), for €3.75 million as part of the continuation plan approved by the Lyon Commercial Court (Tribunal des activités économiques de Lyon) on January 22, 2026 Poxel has already issued €0.5 million of Tranche D PDR bonds on February 16, 2026, and plans to issue an additional €0.5 million on March 26, 2026. Key terms of the Tranche D PDRAs a reminder, Tranche D PDR results from a contractual amendment to Tranche D of the IPF bond financing entered into in September 2024, as amended in September 2025 to finance the observation period, and is intended to secure the Company's operations as part of the continuation plan approved by the Lyon Commercial Court (Tribunal des activités économiques de Lyon) on January 22, 20262. In particular, it provides for the following stipulations as validated by the Lyon Commercial Court:
In addition, the Company has committed to submit resolutions to Poxel's next general meeting to authorize the issuance of share subscription warrants. Prospects and security of financingThe purpose of the Tranche D PDR is to secure the financing of the Company's operations as well as the settlement of its liabilities over the duration of the plan, in addition to the other financing operations and cost reductions envisaged, in particular:
About Poxel SAPoxel is a clinical stage biopharmaceutical Company developing innovative treatments for chronic serious diseases with metabolic pathophysiology, including metabolic dysfunction-associated steatohepatitis (MASH) and rare disorders. For the treatment of MASH, PXL065 (deuterium-stabilised Rpioglitazone) met its primary endpoint in a streamlined Phase 2 trial (DESTINY-1). In rare diseases, development of PXL770, a first-in-class direct adenos Source : Webdisclosure.com |
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