Orion's ODM-212 granted orphan designation for malignant mesothelioma
The European Commission granted the designation based on EMA recommendation, following FDA's prior orphan drug designation.
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Finnish pharmaceutical company
orionpharma.comLast updated
In short: Orion reported strong 2025 financial growth, advanced its oncology pipeline with ODM-212 trials, and achieved carbon-neutral production in Turku.
The European Commission granted the designation based on EMA recommendation, following FDA's prior orphan drug designation.
The target covers Scopes 1&2 and relies on energy efficiency, electrification, and carbon-free sources.
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Orion Corporation (Orion Pharma) today announced that its investigational drug ODM-212 has received Orphan Designation from the European Commission, based on the recommendation from the...
Orion Pharma is a Finnish pharmaceutical company – a builder of well-being that operates globally. We develop, manufacture and market human and veterinary pharmaceuticals and active pharmaceutical ingredients. Our operations combine a solid...
Orion Oyj presented first-in-human Phase 1 data for its pan-TEAD inhibitor ODM-212 at the 2026 ASCO Annual Meeting. The trial targets advanced solid tumours, including...
The results showed ODM-212 was well tolerated, with no dose-limiting toxicities and no maximum tolerated dose reached.
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