Akebia Therapeutics

Akebia Therapeutics

AKBA
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AKBA · Stock Price

USD 1.18-1.37 (-53.73%)
Market Cap: $309.8M

Historical price data

Market Cap: $309.8MPipeline: 40 drugs (13 Phase 3)Patents: 20Founded: 2007HQ: Cambridge, United States

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.

RenalMetabolic

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
40 drugs in pipeline13 in Phase 3
DrugIndicationStageWatch
Ferric Citrate 1 gram Oral Tablet + Standard of care phospha...HyperphosphatemiaApproved
Vadadustat + Darbepoetin alfaAnemiaPhase 3
Vadadustat + Darbepoetin alfaAnemiaPhase 3
VadadustatAnemia of Chronic Kidney DiseasePhase 3
Vadadustat + Darbepoetin alfaAnemiaPhase 3

Funding History

4
Total raised:$269M
IPO$108M
Series C$78M
Series B$48M
Series A$35M

FDA Approved Drugs

2
VAFSEONDAMar 27, 2024
AURYXIANDASep 5, 2014

Opportunities

The primary opportunity is displacing the multi-billion dollar injectable ESA market with oral vadadustat, offering a more physiological treatment for CKD anemia.
Additionally, leveraging the HIF platform to address other serious complications of kidney disease represents a significant long-term value creation avenue.

Risk Factors

Key risks include intense commercial competition from established injectables and other oral HIF-PHIs, potential challenges achieving profitability amid launch costs, and pipeline concentration on two core products.
Regulatory and clinical risks persist for future pipeline expansion.

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

2007Founded

Founded in Cambridge, United States

2009Series B

Series B: $48.0M

2011Series C

Series C: $78.0M

2014IPO

IPO — $108.0M

2014FDA Approval

FDA Approval: AURYXIA

2024FDA Approval

FDA Approval: VAFSEO