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|
|
(State or other jurisdiction of incorporation or organization)
|
(Commission File Number)
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(I.R.S. Employer Identification No.)
|
Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)
|
Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)
|
Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))
|
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
|
Trading
Symbol(s)
|
Name of each exchange
on which registered
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||
|
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(Nasdaq Global Market)
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Item 2.02. |
Results of Operations and Financial Condition.
|
Item 9.01. |
Financial Statements and Exhibits.
|
Exhibit
No.
|
Description
|
|
Press Release of ATAI Life Sciences N.V., dated August 13, 2024.
|
||
104
|
Cover Page Interactive Data File (embedded within the inline XBRL document).
|
*
|
Furnished herewith.
|
ATAI LIFE SCIENCES N.V.
|
||
Date: August 13, 2024
|
By:
|
/s/ Florian Brand
|
Name:
|
Florian Brand
|
|
Title:
|
Co-Chief Executive Officer
|
|
By:
|
/s/ Srinivas Rao
|
|
Name:
|
Srinivas Rao, M.D.
|
|
Title:
|
Co-Chief Executive Officer
|
- |
Reported positive Phase 1b results of VLS-01 (buccal film DMT); expect to initiate a Phase 2 study in treatment-resistant depression patients around YE’24
|
- |
Announced clinical development plans for EMP-01 (oral R-MDMA); expect to initiate a Phase 2 study of EMP-01 in social anxiety disorder patients around YE’24
|
- |
Cash, marketable securities, and committed term loan funding expected to fund operations into 2026
|
• |
VLS-01 is a proprietary oral transmucosal film formulation of DMT applied to the buccal surface designed to fit within a two-hour in-clinic treatment paradigm.
|
• |
Recently, atai announced positive topline data from the Phase 1b trial of VLS-01 buccal film in 17 healthy participants. Peak plasma concentration of VLS-01 occurred within
30-45 minutes. VLS-01 was shown to induce a short psychedelic experience, with subjective effects generally resolving within 90-120 minutes.
|
• |
VLS-01 demonstrated a favorable safety profile and was well tolerated, with all adverse events classified as either mild or moderate, most resolving on the day of dosing, and none related to blood
pressure, heart rate, or suicidality.
|
|
• |
The Company expects to initiate a randomized, double-blind, placebo-controlled Phase 2 study to assess the safety, efficacy and durability of response of repeated doses of VLS-01 buccal film in
patients with TRD around year-end 2024.
|
• |
EMP-01 is an oral formulation of R-MDMA that demonstrated a unique, dose-dependent subjective effect profile in a Phase 1 trial that was generally found to be more similar to
classical psychedelics than to racemic MDMA.
|
• |
atai expects to initiate an exploratory, randomized, double-blind, placebo-controlled Phase 2 study to assess the safety, tolerability and efficacy of EMP-01 in adults with SAD around year-end
2024.
|
• |
SAD is an area of high unmet medical need with approximately 18 million people in the U.S. diagnosed in the past year and no novel molecules approved in over two decades.
|
• |
H2’24
|
o |
VLS-01 TRD: Phase 2 initiation (around YE’24)
|
o |
EMP-01 SAD: Phase 2 initiation (around YE’24)
|
o |
IBX-210 opioid use disorder (OUD): Phase 1b/2a initiation
|
o |
BPL-003 TRD: Phase 2b complete patient enrollment
|
o |
BPL-003 alcohol use disorder (AUD): Phase 2a topline open-label data
|
o |
ELE-101 major depressive disorder (MDD): Phase 2a topline open-label data
|
o |
COMP360 TRD: Phase 3 Pivotal Trial 1 topline data
|
• |
2025
|
o |
RL-007 cognitive impairment associated with schizophrenia (CIAS): Phase 2b topline data (mid’25)
|
o |
COMP360 TRD: Phase 3 Pivotal Trial 2 topline data (mid’25)
|
|
|
|
Three Months Ended
|
Six Months Ended
|
|||||||||||||||
June 30,
|
June 30,
|
|||||||||||||||
2024
|
2023
|
2024
|
2023
|
|||||||||||||
(unaudited)
|
(unaudited)
|
|||||||||||||||
License revenue
|
$
|
273
|
$
|
172
|
$
|
273
|
$
|
209
|
||||||||
Operating expenses:
|
||||||||||||||||
Research and development
|
12,605
|
15,476
|
24,136
|
34,757
|
||||||||||||
General and administrative
|
13,397
|
16,558
|
25,952
|
30,529
|
||||||||||||
Total operating expenses
|
26,002
|
32,034
|
50,088
|
65,286
|
||||||||||||
Loss from operations
|
(25,729
|
)
|
(31,862
|
)
|
(49,815
|
)
|
(65,077
|
)
|
||||||||
Other income (expense), net
|
(31,348
|
)
|
204
|
(32,943
|
)
|
263
|
||||||||||
Loss before income taxes
|
(57,077
|
)
|
(31,658
|
)
|
(82,758
|
)
|
(64,814
|
)
|
||||||||
Provision for income taxes
|
(19
|
)
|
(185
|
)
|
(15
|
)
|
(351
|
)
|
||||||||
Losses from investments in equity method investees, net of tax
|
(273
|
)
|
(1,928
|
)
|
(1,974
|
)
|
(2,961
|
)
|
||||||||
Net loss
|
(57,369
|
)
|
(33,771
|
)
|
(84,747
|
)
|
(68,126
|
)
|
||||||||
Net loss attributable to noncontrolling interests
|
(57
|
)
|
(729
|
)
|
(722
|
)
|
(1,948
|
)
|
||||||||
Net loss attributable to ATAI Life Sciences N.V. stockholders
|
$
|
(57,312
|
)
|
$
|
(33,042
|
)
|
$
|
(84,025
|
)
|
$
|
(66,178
|
)
|
||||
Net loss per share attributable to ATAI Life Sciences N.V.
stockholders — basic and diluted |
$
|
(0.36
|
)
|
$
|
(0.21
|
)
|
$
|
(0.53
|
)
|
$
|
(0.42
|
)
|
||||
Weighted average common shares outstanding attributable to
ATAI Life Sciences N.V. stockholders — basic and diluted |
160,387,701
|
155,792,490
|
159,643,518
|
155,793,323
|
|
June 30,
|
December 31,
|
|||||||
2024
|
2023
|
|||||||
(unaudited)
|
(1)
|
|
||||||
Assets
|
||||||||
Cash and cash equivalents
|
$
|
19,333
|
$
|
45,034
|
||||
Securities carried at fair value
|
69,013
|
109,223
|
||||||
Short term restricted cash for other investments
|
15,000
|
-
|
||||||
Committed investment funds
|
-
|
25,000
|
||||||
Prepaid expenses and other current assets
|
4,690
|
5,830
|
||||||
Short term convertible notes receivable - related party
|
7,976
|
-
|
||||||
Short term notes receivable - related party, net
|
1,896
|
505
|
||||||
Property and equipment, net
|
873
|
981
|
||||||
Operating lease right-of-use asset, net
|
1,043
|
1,223
|
||||||
Other investments held at fair value
|
61,141
|
89,825
|
||||||
Other investments
|
32,381
|
1,838
|
||||||
Long term notes receivable - related party, net
|
-
|
97
|
||||||
Convertible notes receivable - related party
|
-
|
11,202
|
||||||
Other assets
|
2,432
|
2,720
|
||||||
Total assets
|
$
|
215,778
|
$
|
293,478
|
||||
Liabilities and Stockholders' Equity
|
||||||||
Accounts payable
|
3,814
|
4,589
|
||||||
Accrued liabilities
|
12,911
|
15,256
|
||||||
Current portion of lease liability
|
239
|
275
|
||||||
Other current liability
|
680
|
—
|
||||||
Contingent consideration liability - related parties
|
580
|
620
|
||||||
Contingent consideration liability
|
1,373
|
1,637
|
||||||
Noncurrent portion of lease liability
|
838
|
990
|
||||||
Convertible promissory notes and derivative liability - related party
|
1,270
|
164
|
||||||
Convertible promissory notes and derivative liability
|
2,049
|
2,666
|
||||||
Long term debt, net
|
15,236
|
15,047
|
||||||
Other liabilities
|
8,255
|
7,918
|
||||||
Total stockholders' equity attributable to ATAI Life Sciences N.V. stockholders
|
167,890
|
242,962
|
||||||
Noncontrolling interests
|
643
|
1,354
|
||||||
Total liabilities and stockholders' equity
|
$
|
215,778
|
$
|
293,478
|