Idorsia
IDIA.SWIDIA.SW · Stock Price
Historical price data
Overview
Idorsia's mission is to discover, develop, and commercialize innovative medicines, building on a legacy of scientific excellence from its Actelion origins. Its key achievement is the global commercialization of QUVIVIQ (daridorexant), a dual orexin receptor antagonist for insomnia, alongside the recent approval of TRYVIO/JERAYGO (aprocitentan) for resistant hypertension. The company's strategy is centered on unlocking the full value of its commercial assets, expanding strategic partnerships, advancing a prioritized pipeline, and maintaining financial discipline, all supported by a highly skilled team of approximately 500 employees.
Technology Platform
A specialized small-molecule drug discovery engine leveraging medicinal chemistry and computational design, complemented by a novel glycoconjugate vaccine platform for synthetic antigen development.
Pipeline
105| Drug | Indication | Stage | Watch |
|---|---|---|---|
| Daridorexant + Placebo | Insomnia Disorder | Approved | |
| Daridorexant 50 mg + Placebo | Alzheimer Disease | Approved | |
| Lucerastat | Fabry Disease | Phase 3 | |
| Clazosentan + Placebo | Aneurysmal Subarachnoid Hemorrhage | Phase 3 | |
| Daridorexant 25 mg + Daridorexant 50 mg | Insomnia Disorder | Phase 3 |
FDA Approved Drugs
2Opportunities
Risk Factors
Competitive Landscape
Idorsia faces intense competition in all core areas: against other DORAs and generics in insomnia, and within complex treatment regimens for hypertension and autoimmune disease. Its competitive edge lies in differentiated mechanisms (e.g., dual orexin/endothelin receptor antagonism), first-mover status in specific indications, and a deep, pragmatic discovery culture that can generate novel compounds.
Company Timeline
Founded in Allschwil, Switzerland
FDA Approval: QUVIVIQ
FDA Approval: TRYVIO