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Lipigon Pharmaceuticals (LPGO) investor relations material

Lipigon Pharmaceuticals Study Result summary

Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.
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Study Result summary4 Dec, 2025

Study design and objectives

  • Phase II randomized, placebo-controlled trial included 23 patients with moderate to severe hypertriglyceridemia.

  • Patients received four weekly doses and were followed for 12 weeks, with a 6-month long-term follow-up planned.

  • Primary objective was to assess safety and tolerability; secondary objectives included effects on triglycerides, remnant cholesterol, and insulin resistance.

Key results and findings

  • Lipisense® was found to be safe and well tolerated, with no serious treatment-related adverse events.

  • No clinically relevant reduction in triglyceride or remnant cholesterol levels was observed compared to placebo.

  • A trend toward decreased insulin resistance was noted in the treatment group.

  • No statistically significant efficacy signals for lipid markers were detected.

Next steps and future outlook

  • Detailed analysis of the results is ongoing to determine the future direction of the development project.

  • Complete results, including long-term follow-up data, are expected in 2026.

  • The company aims to establish a global licensing agreement for Lipisense®.

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Q4 202518 Feb, 2026
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Frequently asked questions

Lipigon Pharmaceuticals AB specializes in developing therapeutics for lipid-related disorders. The company focuses on creating drugs with unique mechanisms of action to treat diseases resulting from disruptions in the body's lipid metabolism. Their projects include treatments for severe hypertriglyceridemia, familial chylomicronemia syndrome, lipodystrophy, dyslipidemia, and acute respiratory distress syndrome. The company is headquartered in Umeå, Sweden, and its shares are listed on the OMX Stockholm.

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