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Jun 30, 2024

Atai Q2 2024 Earnings Report

Atai reported positive Phase 1b results for VLS-01 and announced clinical development plans for EMP-01, with cash runway extended into 2026.

Key Takeaways

Atai Life Sciences reported its Q2 2024 financial results, highlighting advancements in its pipeline with positive Phase 1b results for VLS-01 and progress in EMP-01 clinical development. The company's cash, marketable securities, and committed term loan funding are expected to fund operations into 2026. R&D expenses decreased compared to the same period last year, while G&A expenses also saw a reduction. Net loss attributable to stockholders was $57.3 million, compared to $33.0 million for the same period in 2023.

atai reported positive Phase 1b results for VLS-01 (buccal film DMT) and expects to initiate a Phase 2 study in treatment-resistant depression patients around year-end 2024.

The company announced clinical development plans for EMP-01 (oral R-MDMA) and anticipates initiating a Phase 2 study in social anxiety disorder patients around year-end 2024.

atai's cash, marketable securities, and committed term loan funding are expected to fund operations into 2026.

Net loss attributable to stockholders for the quarter was $57.3 million.

Total Revenue
$273K
Previous year: $172K
+58.7%
EPS
-$0.36
Previous year: -$0.21
+71.4%
Gross Profit
$191K
Previous year: -$23K
-930.4%
Cash and Equivalents
$19.3M
Previous year: $141M
-86.3%
Free Cash Flow
-$16.2M
Previous year: -$22.6M
-28.1%
Total Assets
$216M
Previous year: $254M
-14.9%

Atai

Atai

Atai Revenue by Segment

Forward Guidance

atai anticipates several R&D catalysts in the near term, including the initiation of Phase 2 studies for VLS-01 in TRD and EMP-01 in SAD around year-end 2024, as well as topline data readouts for other programs in H2 2024 and 2025.

Positive Outlook

  • Initiation of VLS-01 Phase 2 study in TRD around year-end 2024.
  • Initiation of EMP-01 Phase 2 study in SAD around year-end 2024.
  • Initiation of IBX-210 Phase 1b/2a study in opioid use disorder.
  • Completion of patient enrollment for BPL-003 Phase 2b study in TRD.
  • Topline open-label data for BPL-003 Phase 2a study in alcohol use disorder.

Challenges Ahead

  • Potential delays or setbacks in clinical trials.
  • Uncertainties in regulatory approvals.
  • Risks associated with drug development and commercialization.
  • Dependence on third-party collaborations and partnerships.
  • Market competition and changing industry dynamics.