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Sep 30, 2022

Adverum Q3 2022 Earnings Report

Adverum Biotechnologies reported financial results for the third quarter ended September 30, 2022, and dosed the first subject in its Phase 2 LUNA trial with Ixo-vec.

Key Takeaways

Adverum Biotechnologies reported a net loss of $40.1 million for the third quarter of 2022. The company's cash, cash equivalents, and short-term investments were $203.3 million as of September 30, 2022, which is expected to fund operations into 2025. The first subject was dosed in the Phase 2 LUNA trial with Ixo-vec.

Dosed first subject in Phase 2 LUNA trial with Ixo-vec and anticipate preliminary data throughout 2023.

Cash runway into 2025 prioritizing Ixo-vec clinical development in wet AMD.

Presented two-year data from OPTIC trial, indicating a single IVT injection of Ixo-vec was generally well tolerated and can maintain or improve vision.

Data demonstrated that a single intravitreal injection of Ixo-vec can lead to stable and persistent aflibercept protein levels through three years.

Total Revenue
$0
0
EPS
-$4
Previous year: -$3.9
+2.6%
Cash and Equivalents
$203M
Previous year: $333M
-38.9%
Free Cash Flow
-$32.6M
Previous year: -$31.5M
+3.5%
Total Assets
$332M
Previous year: $491M
-32.3%

Adverum

Adverum

Forward Guidance

Adverum expects the September 30, 2022 cash position to fund operations into 2025 and anticipates preliminary data from the LUNA trial throughout 2023.

Positive Outlook

  • Cash runway into 2025.
  • Advancing Phase 2 LUNA trial of Ixo-vec in wet AMD.
  • Ixo-vec has the potential to transform the treatment paradigm for patients with wet age-related macular degeneration.
  • Ixo-vec can meaningfully reduce the burden of frequent anti-VEGF injections.
  • Data demonstrating that a single intravitreal injection of Ixo-vec can lead to stable and persistent aflibercept protein levels through three years.

Challenges Ahead

  • Novel technology makes it difficult to predict the timing of commencement and completion of clinical trials
  • Regulatory uncertainties
  • Enrollment uncertainties
  • The results of early clinical trials not always being predictive of future clinical trials and results
  • Potential for future complications or side effects in connection with use of Ixo-vec