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Zealand Pharma (ZEAL) investor relations material
Zealand Pharma CMD 2025 summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Strategic vision and market opportunity
Aims to become a generational biotech shaping obesity and metabolic health, leveraging 25+ years of peptide expertise, AI-driven innovation, and a robust culture of accountability and patient-centricity.
Sees obesity as a civilization-scale crisis, with projections that half the global population will be overweight or obese by 2030, and only 3% of eligible U.S. patients currently treated with GLP-1s.
Metabolic Frontier 2030 strategy targets five product launches and over ten clinical programs by 2030, aiming for industry-leading cycle times and world-class pipeline.
Commercial strategy targets both prescriber-driven and consumer-driven segments, focusing on patient experience, tolerability, and long-term adherence.
Expanding R&D capabilities in Copenhagen and Boston, integrating AI, automation, and next-generation molecule creation.
Pipeline and clinical development
Survodutide, a GLP-1/glucagon dual agonist, is in Phase 3 for obesity and MASH, showing up to 18.7% weight loss and breakthrough liver fibrosis improvement, with pivotal data expected in 2026.
Petrelintide, a long-acting amylin analog, demonstrates strong weight loss and tolerability in early trials, with Phase 2 data expected in Q1 2026 and Phase 3 initiation in H2 2026.
Fixed-dose combinations (petrelintide + CT388) and multi-hormone approaches are in development to optimize efficacy and minimize adverse effects, with combination trials starting in H1 2026.
Early pipeline includes next-generation peptides, oral and long-acting amylin analogs, weight-independent insulin sensitizers, and assets for congenital hyperinsulinism and short bowel syndrome.
More than ten drug candidates have entered clinical development, with two products on the market and three in late-stage development.
Market and unmet needs
Obesity is projected to affect 50% of adults globally by 2030, with current therapies facing challenges in persistence, tolerability, and real-world efficacy.
Amylin analogs like petrelintide offer potential for durable weight loss, improved tolerability, and restoration of leptin sensitivity.
MASH remains a major unmet need, with survodutide showing best-in-disease potential in Phase 2 trials.
Strategy includes multiple waves of innovation to surpass current medicine adherence rates and deliver a world-class pipeline.
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