Adagene Inc - ESG Rating & Company Profile powered by AI
The analysis of Adagene Inc incorporates data from across the web as well as from available disclosures by Adagene Inc. This SDG score for Adagene Inc indicates its reporting of the United Nations SDGs. The page is a zero-cost ESG assessment for Adagene Inc.
Adagene Inc in the Pharmaceuticals industry gained a UN SDG ESG Transparency Score of 1.8; made up of an environmental score of 1.6, social score of 3.2 and governance score of 0.0.
1.8
Low ImpactEnvironmental
Social
Governance
Peer Group Comparison
Rank | Company | SDG Transparency Score ⓘ | Performance |
---|---|---|---|
1 | Novartis AG | 9.2 | High |
2 | Daiichi Sankyo Co Ltd | 8.9 | High |
... | ... | ... | |
2215 | Wyeth Pakistan Ltd | 1.9 | Low |
2215 | WSI Co Ltd | 1.9 | Low |
2277 | Adagene Inc | 1.8 | Low |
2277 | Apeloa Pharmaceutical Co Ltd | 1.8 | Low |
2277 | Betta Pharmaceuticals Co Ltd | 1.8 | Low |
2749 | Xynomic Pharmaceuticals Holdings Inc | 0.0 | Low |
2749 | Zyden Gentec Ltd | 0.0 | Low |
... | ... | ... |
Frequently Asked Questions
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Potential Risks for Adagene Inc
These potential risks are based on the size, segment and geographies of the company.
Adagene Inc., a clinical stage biopharmaceutical company, engages in the research, development, and production of monoclonal antibody drugs for cancers. The company's product candidates include ADG106, a human ligand-blocking agonistic anti-CD137 monoclonal antibodies (mAbs) that is in Phase 1b/2 clinical trials for the treatment advanced solid tumors and non-Hodgkin's lymphoma; ADG126, a fully-human anti-CTLA-4 mAb that is in Phase 1 clinical trial for the treatment advanced/metastatic solid tumors; and ADG116, a human ligand-blocking anti-CTLA-4 mAb, which is in Phase I clinical trial for the treatment of advanced metastatic solid tumors. It also offers ADG104, an anti-PD-L1 mAb that is in Phase 2 clinical development; ADG125, a novel anti-CSF-1R mAb, which is in Phase I clinical trial; ADG206, a masked, Fc engineered anti-CD137 agonistic POWERbody, which is in preclinical; ADG153, a masked anti-CD47 IgG1 SAFEbody, which is in preclinical stage for the treatment hematologic and solid tumors; ADG138, novel HER2xCD3 POWERbody, which is in preclinical for the treatment HER2-expressing solid tumors; and ADG152, a CD20xCD3 POWERbody, which is in preclinical stage for the treatment off-tumor toxicities. The company was incorporated in 2011 and is headquartered in Suzhou, China.