• Nanexa's NEX-22, a once-monthly liraglutide formulation for type 2 diabetes, demonstrated a favorable pharmacokinetic profile and safety in a Phase I study.
• The trial met all primary and secondary endpoints, showing dose linearity and no significant adverse events, positioning NEX-22 as a potential alternative to daily GLP-1 injections.
• Nanexa is actively seeking licensing partners to advance NEX-22 to Phase Ib/II studies, with plans to compare it directly to Victoza and explore a 505(b)(2) regulatory pathway in the US.
• With secured funding into 2026, Nanexa aims to initiate Phase Ib/II trials before the end of the year and is also progressing in its development project with Novo Nordisk.