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(State or other jurisdiction of incorporation)
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(Commission File Number)
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(IRS Employer Identification No.)
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(Address of principal executive offices)
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(Zip Code)
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Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)
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Soliciting material pursuant to Rule 14a‑12 under the Exchange Act (17 CFR 240.14a‑12)
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Pre‑commencement communications pursuant to Rule 14d‑2(b) under the Exchange Act (17 CFR 240.14d‑2(b))
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Pre‑commencement communications pursuant to Rule 13e‑4(c) under the Exchange Act (17 CFR 240.13e‑4(c))
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Title of each class
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Trading
Symbol(s)
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Name of each exchange
on which registered
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(Nasdaq Global Market)
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Item 5.02
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Departure of Directors or Certain Officers; Election of Directors; Appointment of
Certain Officers; Compensatory Arrangements of Certain Officers.
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| Item 7.01 |
Regulation FD Disclosure.
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| Item 9.01 |
Financial Statements and Exhibits.
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(d)
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Exhibits.
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Exhibit
No.
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Description
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Press Release, dated January 8, 2026 (furnished herewith).
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104
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Cover Page Interactive Data File (embedded within the Inline
XBRL document).
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Date: January 8, 2026
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AtaiBeckley Inc.
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By:
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/s/ Ryan Barrett
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Name:
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Ryan Barrett
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Title:
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Chief Legal and Business Officer
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•
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Reported positive topline data from the eight-week, quadruple-masked, dose-finding, core stage of the Phase 2b
clinical trial evaluating the efficacy and safety of a single dose of BPL-003 in patients with treatment-resistant depression (TRD) in July 2025. The study met its primary and all key secondary endpoints, and BPL-003 demonstrated
rapid, robust and durable antidepressant effects with a single dose. Both 8 mg and 12 mg single doses of BPL-003 showed statistically significant and clinically meaningful reductions in depressive symptoms at all time points of the
study compared to a 0.3 mg low-dose active control out to Week 8.
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•
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Reported positive topline data from the eight-week open-label extension (OLE) study of the Phase 2b clinical
trial of BPL-003 in patients with TRD in November 2025. The findings showed that a 12 mg dose of BPL-003, administered eight weeks after an initial dose, was generally well-tolerated and produced additional clinically meaningful
antidepressant effects that were sustained for up to two months.
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•
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Company anticipates providing guidance on the BPL-003 Phase 3 clinical program in Q1’26 with Phase 3 trial initiation in Q2’26, pending outcome of the scheduled
End-of-Phase 2 meeting with the U.S. Food and Drug Administration (FDA).
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•
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Initiation of an additional cohort in an open-label Phase 2a study of BPL-003 in patients with TRD planned in Q1’26, with initial data expected in Q4’26. The study will
evaluate a two-dose induction regimen of BPL-003, where patients who are also taking defined antidepressants will be given an 8 mg dose of BPL-003 followed by a second 8 mg dose two weeks later, and then followed for a further 10 weeks.
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•
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Company anticipates topline data from Elumina, the Phase 2, multicenter, double-blind, randomized, placebo-controlled trial of repeated doses of VLS-01 in 142 patients with
TRD in H2’26
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•
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•
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Last patient last visit in the exploratory Phase 2a study of EMP-01 (oral R-MDMA) in approximately 70 adults with social anxiety disorder occurred in Q4 ‘25, with topline data
expected in Q1’26.
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•
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Completed the redomiciliation of Atai Beckley N.V. from the Netherlands to the United States (via Luxembourg) in December 2025. All issued and outstanding ordinary shares of Atai Beckley N.V. were
exchanged on a one-for-one basis for newly issued shares of common stock of the Delaware company, AtaiBeckley Inc. The former shareholders of Atai Beckley N.V. are now the stockholders of the Delaware company. AtaiBeckley Inc’s common
stock will continue to trade on NASDAQ under the trading symbol “ATAI”. The Company expects the redomiciliation to save costs,
create alignment with its U.S. listing and shareholder base, simplify its corporate structure, streamline reporting requirements, and reduce the associated administrative burden for the Company and investors.
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•
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Announced that AtaiBeckley Inc’s common stock had been added to the NASDAQ biotechnology index (NBI) in December 2025.
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