Cyclacel Pharmaceuticals Inc - ESG Rating & Company Profile powered by AI
The analysis of Cyclacel Pharmaceuticals Inc was prepared by All Street Sevva using advanced Cognitive Robots. The Disclosure rating includes seventeen United Nations SDGs including: 'Gender Equality', 'Climate Action' and 'Life below Water'. The SDG rating for Cyclacel Pharmaceuticals Inc represents the company's reporting of the United Nations Sustainable Development Goals.
Cyclacel Pharmaceuticals Inc in the Pharmaceuticals industry gained a UN SDG ESG Transparency Score of 2.7; made up of an environmental score of 0.0, social score of 2.7 and governance score of 5.3.
2.7
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 |
... | ... | ... | |
1393 | Vaccinex Inc | 2.8 | Medium |
1393 | YSP Southeast Asia Holding Bhd | 2.8 | Medium |
1437 | Cyclacel Pharmaceuticals Inc | 2.7 | Medium |
1437 | CanadaBis Capital Inc | 2.7 | Medium |
1437 | Cannabics Pharmaceuticals Inc | 2.7 | Medium |
... | ... | ... | |
1970 | Zyden Gentec Ltd | 0.0 | Low |
1970 | iNtRON Biotechnology Inc | 0.0 | Low |
... | ... | ... |
Frequently Asked Questions
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Potential Risks for Cyclacel Pharmaceuticals Inc
These potential risks are based on the size, segment and geographies of the company.
Cyclacel Pharmaceuticals, Inc., a clinical-stage biopharmaceutical company, develops medicines for the treatment of cancer and other proliferative diseases. The company's development programs include fadraciclib, a cyclin dependent kinase Inhibitors (CDK) that is in Phase 1/2 clinical trial for the treatment of solid tumors, as well as in combination with venetoclax to treat relapsed or refractory chronic lymphocytic leukemia; and CYC140, a polo-like kinase inhibitor program, which is in Phase 1/2 clinical trial for the treatment of advanced leukemias and solid tumors. Its development programs also comprise Sapacitabine, a novel nucleoside analog that is orally available prodrug of CNDAC, which is in Phase 1/2 clinical trials to treat acute myeloid leukemia and myelodysplastic syndrome; and seliciclib, a CDK inhibitor that is in Phase 2 investigator-sponsored trials (IST) for Cushing's disease, as well as in Phase 1/2 IST for the treatment for advanced rheumatoid arthritis. The company has a clinical collaboration agreement with the University of Texas MD Anderson Cancer Center to clinically evaluate the safety and efficacy of three cyclacel medicines in patients with hematological malignancies, including chronic lymphocytic leukemias, acute myeloid leukemias, myelodysplastic syndromes, and other advanced leukemias. Cyclacel Pharmaceuticals, Inc. is headquartered in Berkeley Heights, New Jersey.