Akero Therapeutics/$AKRO
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About Akero Therapeutics
Akero Therapeutics Inc is a clinical-stage biotechnology company focused on developing and commercializing transformative treatments for serious metabolic diseases with high unmet medical needs. Its focus is nonalcoholic steatohepatitis (MASH), or NASH, a disease without any approved therapies. The company's product candidate efruxifermin is an FGF21 analog with properties that have the potential to address the core processes underlying NASH pathogenesis.
Ticker
$AKRO
Sector
Primary listing
Employees
67
Headquarters
Website
AKRO Metrics
BasicAdvanced
$3.5B
-
-$3.78
-0.28
-
Price and volume
Market cap
$3.5B
Beta
-0.28
52-week high
$58.40
52-week low
$21.34
Average daily volume
966K
Financial strength
Current ratio
12.659
Quick ratio
12.29
Long term debt to equity
2.196
Total debt to equity
3.543
Interest coverage (TTM)
-67.37%
Profitability
EBITDA (TTM)
-321.458
Management effectiveness
Return on assets (TTM)
-20.36%
Return on equity (TTM)
-31.14%
Valuation
Price to book
3.43
Price to tangible book (TTM)
3.43
Price to free cash flow (TTM)
-13.051
Free cash flow yield (TTM)
-7.66%
Free cash flow per share (TTM)
-3.374
Growth
Earnings per share change (TTM)
11.00%
3-year earnings per share growth (CAGR)
6.30%
What the Analysts think about AKRO
Analyst ratings (Buy, Hold, Sell) for Akero Therapeutics stock.
Bulls say / Bears say
The peer-reviewed Phase 2b SYMMETRY trial published in the New England Journal of Medicine on May 9, 2025 showed that 29% of patients receiving EFX 50 mg achieved at least a 1-stage improvement in fibrosis at Week 96 without MASH worsening versus 11% for placebo in the ITT analysis (p=0.031), representing the first significant evidence of cirrhosis reversal in MASH.
Akero’s cash, cash equivalents, and marketable securities totaled $1,086.2 million as of June 30, 2025, which provides funding through 2028 to support its Phase 3 SYNCHRONY program.
At the EASL Congress 2025, new analyses from the Phase 2b HARMONY trial showed that over 50% of pre-cirrhotic (F2-F3) patients treated with 50 mg EFX were responders by all three measures—qFibrosis® AI, ELF score, and FibroScan®—compared to less than 5% of placebo patients, underscoring strong anti-fibrotic effects.
The Phase 2b SYMMETRY study failed to meet its primary endpoint at Week 36, with EFX groups showing numerical but not statistically significant fibrosis improvement compared to placebo, raising concerns about the reliability of early surrogate endpoints.
Akero will not report its first Phase 3 efficacy results until the first half of 2026 from the SYNCHRONY Real-World study, so clinical and regulatory prospects remain dependent on upcoming trial performance.
Research and development expenses increased 25% year-over-year to $69.3 million in Q2 2025, driven by rising costs from late-stage trials and higher operating expenses, while Akero still has no approved products generating revenue.
Data summarised monthly by Lightyear AI. Last updated on 5 Sept 2025.
AKRO Financial Performance
Revenues and expenses
AKRO Earnings Performance
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FAQs
What’s the current market cap for Akero Therapeutics stock?
Akero Therapeutics (AKRO) has a market cap of $3.5B as of September 05, 2025.
What is the P/E ratio for Akero Therapeutics stock?
The price to earnings (P/E) ratio for Akero Therapeutics (AKRO) stock is 0 as of September 05, 2025.
Does Akero Therapeutics stock pay dividends?
No, Akero Therapeutics (AKRO) stock does not pay dividends to its shareholders as of September 05, 2025.
When is the next Akero Therapeutics dividend payment date?
Akero Therapeutics (AKRO) stock does not pay dividends to its shareholders.
What is the beta indicator for Akero Therapeutics?
Akero Therapeutics (AKRO) has a beta rating of -0.28. This means that it has an inverse relation to market volatility.