Atai Life Sciences reported a net loss of $26.3 million for the third quarter of 2024. The company's cash, cash equivalents, and short-term securities totaled $101.0 million as of September 30, 2024, expected to fund operations into 2026.
FDA cleared the investigational new drug application for VLS-01 (buccal film DMT).
Atai expects to initiate a Phase 2 study in treatment-resistant depression patients around YE’24.
Remain on track to initiate a Phase 2 study of EMP-01 (oral R-MDMA) in social anxiety disorder patients around YE’24.
Cash, marketable securities, and committed term loan funding expected to fund operations into 2026.
Atai Life Sciences anticipates several R&D catalysts in the near term, including the initiation of Phase 2 trials for VLS-01 and EMP-01 around year-end 2024, and topline data readouts for multiple programs in 2025.