Cyclerion Therapeutics IncCyclerion Therapeutics Inc - ESG Rating & Company Profile powered by AI

Industry Group:Pharmaceuticals

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.

SDG Transparency Score for Cyclerion Therapeutics Inc 

1.9

Low Impact
0 - 3
Medium
4 - 6
High
7 - 10
Last Score Update: 2024-05-01
What drives the score for Cyclerion Therapeutics Inc 
0.0

Environmental

1.6

Social

4.0

Governance

Detailed ESG Breakdown
SEVVA Platform offers unique drill down to the underlying sources powering the ratings. Break down your ESG analysis by 17 UN SDGs and 8 additional governance factors.

Peer Group Comparison

RankCompanySDG Transparency Score Performance
1Caladrius Biosciences Inc
8.0
High
1Can Fite Biopharma Ltd
8.0
High
.........
1608Agios Pharmaceuticals Inc
2.0
Medium
1608Unrivaled Brands Inc
2.0
Medium
.........
1617Cyclerion Therapeutics Inc
1.9
Low
1617Celsion Corp
1.9
Low
1617Ainos Inc
1.9
Low
1970Zyden Gentec Ltd
0.0
Low
1970iNtRON Biotechnology Inc
0.0
Low
.........
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Peer Companies Benchmark
SEVVA Platform benchmarks each company against a peer group. View the full score distribution for peers by logging into SEVVA

Frequently Asked Questions

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Does Cyclerion Therapeutics Inc disclose current and / or historical scope 1 emissions?

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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.

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