Cereno Scientific
CRNO-B.STPhase 2Cereno Scientific is a Swedish clinical-stage biotech company developing first-in-class epigenetic therapies targeting the root causes of rare cardiovascular and pulmonary diseases. The company's lead program, CS1, has demonstrated disease-modifying potential in a Phase IIa trial for PAH and holds FDA Fast Track designation, while its broader HDACi portfolio and preclinical prostacyclin receptor agonist CS585 address significant unmet medical needs. With a strengthened focus on rare diseases, Cereno aims to deliver high treatment value through a business model characterized by relatively shorter development timelines and reduced capital requirements.
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AI Company Overview
Cereno Scientific is a Swedish clinical-stage biotech company developing first-in-class epigenetic therapies targeting the root causes of rare cardiovascular and pulmonary diseases. The company's lead program, CS1, has demonstrated disease-modifying potential in a Phase IIa trial for PAH and holds FDA Fast Track designation, while its broader HDACi portfolio and preclinical prostacyclin receptor agonist CS585 address significant unmet medical needs. With a strengthened focus on rare diseases, Cereno aims to deliver high treatment value through a business model characterized by relatively shorter development timelines and reduced capital requirements.
Technology Platform
Cereno's core technology platform focuses on epigenetic modulation through histone deacetylase inhibitors (HDACi) that regulate gene expression to reverse pathological vascular remodeling and fibrosis, complemented by a novel prostacyclin (IP) receptor agonist platform for thrombosis prevention without increased bleeding risk.
Pipeline
3| Drug | Indication | Stage | Watch |
|---|---|---|---|
| CS1 Administration | Pulmonary Arterial Hypertension | Phase 2 | |
| CS1-Sodium Valproate | Thrombosis | Phase 1 | |
| CS1 | Pulmonary Arterial Hypertension | Pre-clinical |
Funding History
3Opportunities
Risk Factors
Competitive Landscape
Cereno faces competition from established PAH therapies that primarily provide symptomatic relief (J&J's Uptravi, Bayer's Adempas) but differentiates through disease-modifying potential. In the HDAC inhibitor space for cardiovascular diseases, competition is limited as most development focuses on oncology. For CS585, traditional anticoagulants and existing IP receptor agonists represent competition, but CS585's proposed bleeding safety advantage could provide significant differentiation.