Akebia Therapeutics/$AKBA

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About Akebia Therapeutics

Akebia Therapeutics Inc is a fully integrated biopharmaceutical company. The Company's operating segment is the business of developing and commercializing novel therapeutics for people with kidney disease. The current portfolio of the company includes Auryxia (ferric citrate), a medicine approved and marketed in the United States for the control of serum phosphorus levels in adult patients with dialysis-dependent chronic kidney disease and the treatment of iron deficiency anemia, in adult patients with non-dialysis-dependent chronic kidney disease, Vafseo (vadadustat), an oral hypoxia-inducible factor prolyl hydroxylase, inhibitor approved in Japan for the treatment of anemia due to chronic kidney disease, in adult patients, HIF-PH inhibitors in preclinical development.

Ticker

$AKBA
Sector
Primary listing

Employees

181

AKBA Metrics

BasicAdvanced
$541M
-
-$0.16
0.68
-

What the Analysts think about AKBA

Analyst ratings (Buy, Hold, Sell) for Akebia Therapeutics stock.

Bulls say / Bears say

Total Q2 2025 revenues climbed 43% year-over-year to $62.5 million, driven by $13.3 million in Vafseo sales and $47.2 million in Auryxia sales, marking the company’s strongest quarter ever (Akebia IR).
Vafseo secured commercial supply agreements covering almost all U.S. dialysis patients, began shipping January 9, 2025, and registered prescriptions from over 725 prescribers with an 80% refill rate in Q2, demonstrating strong initial uptake (Akebia IR).
Akebia ended Q1 2025 with $113.4 million in cash and cash equivalents, reinforced by a $50 million public offering, providing funding to support commercial expansion and pipeline trials through at least 2027 (Akebia IR).
Auryxia lost U.S. exclusivity on March 20, 2025, exposing its $47.2 million Q2 revenue stream to generic competition that could significantly reduce sales once generics are approved (Akebia IR).
Broad adoption of Vafseo depends on large dialysis providers implementing prescribing protocols—currently, only a pilot program with DaVita started in Q3—pushing meaningful revenue contributions to late 2025 (Akebia IR).
Key post-marketing data from VOICE will not be available until early 2027 and the VALOR trial for non-dialysis CKD patients is only set to begin mid-to-late 2025, delaying prospects for label expansion into a multi-billion dollar market (Akebia IR).
Data summarised monthly by Lightyear AI. Last updated on 8 Nov 2025.

AKBA Financial Performance

Revenues and expenses
QuarterlyAnnual
Q3 24
QoQ growth
Revenue
$37B
-39.75%
Net income
$45B
107.52%
Profit margin
37.65%
6.78%

AKBA Earnings Performance

Company profitability
QuarterlyAnnual
Q4 23
Q1 24
Q2 24
Q3 24
Q4 24
Actual
$3.69
$2.85
$2.45
$2.42
-
Expected
$3.55
$2.61
$2.05
$2.31
$3.94
Surprise
3.94%
9.20%
19.51%
4.63%
-
Data displayed above is indicative only and its accuracy or completeness is not guaranteed. Actual execution price may vary. Past performance is not indicative of future results. Your return may be affected by currency fluctuations and applicable fees and charges. Capital at risk.
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