Atai Beckley reported peer-reviewed Phase 2a Cohort 1 results for BPL-003 (mebufotenin benzoate nasal spray) in 12 patients with moderate-to-severe treatment-resistant depression who were not taking concomitant antidepressants. In this 12-week open-label trial, a single 10 mg intranasal dose reduced mean MADRS total score by 12.6 points by Day 2 and the mean score was 14.5 at Day 85. The response rate (≥50% MADRS reduction) was 54.5% from the day after dosing through Day 85, and 63.6% of patients achieved remission (MADRS ≤10) at one or more timepoints. The company said its Phase 3 program remains on track to initiate in Q2 2026, and initial data from a Part 4 cohort evaluating a two-dose induction regimen (8 mg + 8 mg) are expected in Q4 2026.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Atai Beckley Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: 202603170600PRIMZONEFULLFEED9672793) on March 17, 2026, and is solely responsible for the information contained therein.