Akebia Therapeutics Inc - ESG Rating & Company Profile powered by AI
The page is a zero-cost Sustainability report covering Akebia Therapeutics Inc. The Disclosure score includes seventeen United Nations SDGs including: 'Zero Hunger', 'Climate Action' and 'Partnerships for the Goals'. Comprehensive Sustainability assessment of Akebia Therapeutics Inc are reached by signing in.
Akebia Therapeutics Inc in the Pharmaceuticals industry gained a UN SDG ESG Transparency Score of 4.5; made up of an environmental score of 1.6, social score of 3.2 and governance score of 8.0.
4.5
Medium 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 |
| 1199 | Tianda Pharmaceuticals Ltd | 4.6 | High |
| 1199 | Zai Lab Ltd | 4.6 | High |
| 1252 | Akebia Therapeutics Inc | 4.5 | High |
| 1252 | Amicus Therapeutics Inc | 4.5 | High |
| 1252 | Aldeyra Therapeutics Inc | 4.5 | High |
| ... | ... | ... | |
| 2749 | Xynomic Pharmaceuticals Holdings Inc | 0.0 | Low |
| 2749 | Zyden Gentec Ltd | 0.0 | Low |
| ... | ... | ... |
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Potential Risks for Akebia Therapeutics Inc
These potential risks are based on the size, segment and geographies of the company.
Akebia Therapeutics, Inc., a biopharmaceutical company, focuses on the development and commercialization of renal therapeutics for patients with kidney diseases. The company's lead product investigational product candidate is vadadustat, an oral therapy, which is in Phase III development for the treatment of anemia due to chronic kidney disease (CKD) in dialysis-dependent and non-dialysis dependent adult patients. It also offers Auryxia, a ferric citrate that is used to control the serum phosphorus levels in adult patients with CKD on dialysis; and the treatment of iron deficiency anemia in adult patients with CKD not on dialysis. Akebia Therapeutics, Inc. has collaboration agreements with Otsuka Pharmaceutical Co. Ltd. for the development and commercialization of vadadustat in the United States, the European Union, Russia, China, Australia, Canada, the Middle East, and other countries; and Mitsubishi Tanabe Pharma Corporation for the development and commercialization of vadadustat in Japan and other Asian countries, as well as research and license agreement with Janssen Pharmaceutica NV for the development and commercialization of hypoxia-inducible factor prolyl hydroxylase targeted compounds worldwide. The company was incorporated in 2007 and is headquartered in Cambridge, Massachusetts.