Akebia Therapeutics
AKBAAKBA · Stock Price
Historical price data
Overview
Akebia Therapeutics is a commercial-stage biopharma with a mission to better the lives of those impacted by kidney disease through innovative therapeutics. The company has achieved significant milestones, including the FDA approval and commercialization of two oral HIF-PHI products, vadadustat and Auryxia, establishing it as a trusted leader in nephrology. Its strategy centers on maximizing the value of its commercial portfolio, advancing its late-stage pipeline in kidney disease complications, and leveraging its fully integrated operational model and deep renal community expertise for sustainable growth.
Technology Platform
Proprietary hypoxia-inducible factor prolyl hydroxylase inhibitor (HIF-PHI) platform, leveraging Nobel Prize-winning science to develop oral small-molecule therapeutics that mimic the body's physiological response to low oxygen.
Pipeline
40| Drug | Indication | Stage | Watch |
|---|---|---|---|
| Ferric Citrate 1 gram Oral Tablet + Standard of care phospha... | Hyperphosphatemia | Approved | |
| Vadadustat + Darbepoetin alfa | Anemia | Phase 3 | |
| Vadadustat + Darbepoetin alfa | Anemia | Phase 3 | |
| Vadadustat | Anemia of Chronic Kidney Disease | Phase 3 | |
| Vadadustat + Darbepoetin alfa | Anemia | Phase 3 |
Funding History
4FDA Approved Drugs
2Opportunities
Risk Factors
Competitive Landscape
Akebia competes directly with injectable ESAs (Amgen, J&J) and other oral HIF-PHIs like GSK's daprodustat in the anemia market. In hyperphosphatemia, Auryxia faces competition from multiple phosphate binders. Success depends on commercial execution and differentiation of its oral therapies.
Company Timeline
Founded in Cambridge, United States
Series B: $48.0M
Series C: $78.0M
IPO — $108.0M
FDA Approval: AURYXIA
FDA Approval: VAFSEO