Idorsia

Idorsia

IDIA.SWApproved
Allschwil, SwitzerlandFounded 2017idorsia.com

Idorsia is a public Swiss biotech company that emerged from the demerger of Actelion following its acquisition by Johnson & Johnson in 2017. It has built a balanced portfolio with one commercial product (QUVIVIQ for insomnia) and several late-stage clinical assets, including TRYVIO/JERAYGO for resistant hypertension. The company's strategy focuses on unlocking the value of its commercial product, expanding strategic partnerships, advancing its differentiated pipeline, and maintaining financial discipline.

Market Cap
$1.0B
Founded
2017
Employees
~500
Focus
Small Molecules

IDIA.SW · Stock Price

USD 3.1514.55 (-82.20%)

Historical price data

AI Company Overview

Idorsia is a public Swiss biotech company that emerged from the demerger of Actelion following its acquisition by Johnson & Johnson in 2017. It has built a balanced portfolio with one commercial product (QUVIVIQ for insomnia) and several late-stage clinical assets, including TRYVIO/JERAYGO for resistant hypertension. The company's strategy focuses on unlocking the value of its commercial product, expanding strategic partnerships, advancing its differentiated pipeline, and maintaining financial discipline.

Technology Platform

Specialized small-molecule drug discovery engine and a glycoconjugate vaccine platform utilizing synthetic antigenic glycan molecules.

Pipeline Snapshot

105

105 drugs in pipeline, 14 in Phase 3

DrugIndicationStage
Daridorexant 50 mg + PlaceboAlzheimer DiseaseApproved
Daridorexant + PlaceboInsomnia DisorderApproved
Daridorexant 25 mg + Daridorexant 50 mgInsomnia DisorderPhase 3
Daridorexant 10 mg + Daridorexant 25 mg + Daridorexant 50 mg + PlaceboInsomnia DisorderPhase 3
Clazosentan + PlaceboAneurysmal Subarachnoid HemorrhagePhase 3

FDA Approved Drugs

2
TRYVIONDAMar 19, 2024
QUVIVIQNDAJan 7, 2022

Opportunities

Significant growth opportunity from the global expansion of QUVIVIQ in the large insomnia market.
Near-term pipeline catalysts in 2026 from Phase 3 readouts for cenerimod and selatogrel could create substantial value.
The company's partnership model provides non-dilutive funding and de-risks development while retaining economic interest.

Risk Factors

Heavy reliance on the commercial success of QUVIVIQ.
Clinical failure of late-stage assets (cenerimod, selatogrel) would be a major setback.
The company is not yet profitable from operations and faces ongoing financial sustainability challenges.
Leadership transition with the search for a permanent CEO adds uncertainty.

Competitive Landscape

Competes in insomnia with other orexin antagonists (Belsomra, Dayvigo) and generics. TRYVIO is first-in-class for resistant hypertension but competes with entrenched drug classes. Pipeline assets face competition in crowded markets (SLE biologics, AMI antiplatelets). Idorsia's differentiation lies in its specialized discovery engine targeting novel mechanisms and its strategic use of partnerships.

Publications
19
Patents
20
Pipeline
105
FDA Approvals
2

Company Info

TypeTherapeutics
Founded2017
Employees~500
LocationAllschwil, Switzerland
StageApproved
RevenueRevenue Generating

Trading

TickerIDIA.SW
ExchangeSIX Swiss Exchange

Contact

idorsia.com+41 58 844 00 00

Therapeutic Areas

CNSCardiovascularImmunological DisordersOrphan Diseases

Partners

Johnson & Johnson Innovative Medicine (Janssen)ViatrisNxera PharmaSimcereUS Department of Defense (DOD)PharmalinkSanthera
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