Cyclerion Therapeutics Inc - ESG Rating & Company Profile powered by AI
Other companies in the rating industry group for Cyclerion Therapeutics Inc are shown. This assessment of Cyclerion Therapeutics Inc uses intelligence from across the web and also from available documents by Cyclerion Therapeutics Inc. The analysis of Cyclerion Therapeutics Inc is assembled by All Street Sevva using leading Cognitive Robots.
Cyclerion Therapeutics Inc in the Pharmaceuticals industry gained a UN SDG ESG Transparency Score of 1.9; made up of an environmental score of 0.0, social score of 1.6 and governance score of 4.0.
1.9
Low ImpactEnvironmental
Social
Governance
Peer Group Comparison
Rank | Company | SDG Transparency Score ⓘ | Performance |
---|---|---|---|
1 | Caladrius Biosciences Inc | 8.0 | High |
1 | Can Fite Biopharma Ltd | 8.0 | High |
... | ... | ... | |
1608 | Agios Pharmaceuticals Inc | 2.0 | Medium |
1608 | Unrivaled Brands Inc | 2.0 | Medium |
... | ... | ... | |
1617 | Cyclerion Therapeutics Inc | 1.9 | Low |
1617 | Celsion Corp | 1.9 | Low |
1617 | Ainos Inc | 1.9 | Low |
1970 | Zyden Gentec Ltd | 0.0 | Low |
1970 | iNtRON Biotechnology Inc | 0.0 | Low |
... | ... | ... |
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Potential Risks for Cyclerion Therapeutics Inc
These potential risks are based on the size, segment and geographies of the company.
Cyclerion Therapeutics, Inc., a clinical-stage biopharmaceutical company, engages in the discovering, development, and commercialization of medicines for serious central nervous system (CNS) diseases. Its lead product candidate is CY6463, a CNS-penetrant, soluble guanylate cyclase (sGC) stimulator that is in Phase IIa trials for the treatment of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes, as well as Alzheimer's disease with vascular pathology; and Phase 1 trials diagnosed with schizophrenia in adults. It is also developing Praliciguat, an orally administered systemic sGC stimulator, which is in Phase II studies to treat resistant hypertension and diabetic nephropathy; Olinciguat, an orally administered vascular sGC stimulator that is in Phase II studies for the sickle cell disease; and CY3018 for the treatment of disorders of the CNS. It has license agreement with Akebia Therapeutics, Inc. for the development, manufacture, medical affairs, and commercialization of pharmaceutical products, including pharmaceutical compound, and other related products and forms. The company was incorporated in 2018 and is headquartered in Cambridge, Massachusetts.