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Jun 30, 2024

Akero Q2 2024 Earnings Report

Akero Therapeutics reported financial results and provided a business update, highlighting the initiation of the Phase 3 SYNCHRONY Outcomes trial of Efruxifermin (EFX) and expansion of the leadership team.

Key Takeaways

Akero Therapeutics reported second quarter financial results, including cash, cash equivalents and marketable securities of $848.3 million as of June 30, 2024. The company believes its current resources will fund Phase 3 SYNCHRONY studies through primary endpoint readouts and its operating plan into the second half of 2027.

Initiated Phase 3 SYNCHRONY Outcomes trial of Efruxifermin (EFX) in patients with compensated cirrhosis (F4) due to MASH.

Presented poster and late-breaking oral presentation on EFX at the EASL Congress 2024.

Expanded leadership team with the addition of Scott Gangloff as Chief Technical Officer.

Cash, cash equivalents and short and long-term marketable securities totaled $848.3 million as of June 30, 2024.

Total Revenue
$0
EPS
-$0.81
Previous year: -$0.6
+35.0%
Gross Profit
-$1K
Cash and Equivalents
$760M
Previous year: $639M
+18.9%
Free Cash Flow
-$57.5M
Total Assets
$865M
Previous year: $664M
+30.3%

Akero

Akero

Forward Guidance

Akero believes that its current cash, cash equivalents, and short- and long-term marketable securities will be sufficient to fund its Phase 3 SYNCHRONY Histology and Real-World studies through readout of their respective primary endpoints and Akero’s current operating plan into the second half of 2027.

Positive Outlook

  • Current cash, cash equivalents, and short- and long-term marketable securities are projected to be sufficient to fund Phase 3 SYNCHRONY Histology and Real-World studies through readout of their respective primary endpoints.
  • Current resources are expected to fund Akero’s current operating plan into the second half of 2027.
  • Ongoing Phase 3 SYNCHRONY clinical trial program consists of three global, randomized, placebo-controlled trials to support marketing applications.
  • Patients are using the LyoJect 3S dual chamber syringe, a pre-filled device designed for self-administration and intended for commercial use.
  • Scott’s extensive knowledge and experience of establishing and optimizing supply chains will support a robust manufacturing capability for EFX at launch.

Challenges Ahead

  • The success, cost, and timing of Akero’s product candidate development activities and planned clinical trials.
  • Akero’s ability to execute on its strategy.
  • Positive results from a clinical study may not necessarily be predictive of the results of future or ongoing clinical studies.
  • Regulatory developments in the United States and foreign countries.
  • Akero’s ability to fund operations.