• |
First participant dosed in Phase 1b trial of VLS-01 with data expected in 2H’24; Phase 2 study in TRD patients anticipated to initiate around YE’24
|
• |
Beckley Psytech’s Phase 2a study of BPL-003 in TRD patients showed rapid and durable antidepressant effects; Phase 2b topline data expected in 2H’24
|
• |
Compass Pathways’ Phase 2 study of COMP360 in PTSD patients demonstrated durable improvement in symptoms; Phase 3 data of COMP360 in TRD patients expected in 4Q’24
|
• |
Co-Founder Florian Brand to step down as CEO as part of a planned transition by YE’24 and to be succeeded by Co-Founder and current Chief Scientific Officer Srinivas Rao, M.D.,
Ph.D.
|
• |
Cash, marketable securities, and committed term loan funding expected to fund operations into 2026
|
• |
Florian Brand, Co-Founder and current CEO of atai, will assume the role of Co-CEO effective June 1, 2024 and will step down as CEO by the end of this year.
|
• |
Co-Founder Srinivas Rao, currently the Chief Scientific Officer of atai, will be promoted to Co-CEO effective June 1, 2024, and intends to assume the role of CEO by the end of the year subject to
appointment as required by local law.
|
• |
VLS-01 is an oral transmucosal film (OTF) formulation of DMT designed to fit within the two-hour in-clinic treatment paradigm successfully established by Spravato®
|
• |
In March 2024, we announced the initiation of dosing in a Phase 1b study that is designed to evaluate the relative safety, tolerability, pharmacokinetics (PK) and pharmacodynamics (PD) of an
optimized OTF formulation of VLS-01, compared to intravenous (IV) DMT.
|
• |
Results of the Phase 1b study are anticipated in 2H 2024.
|
• |
The Company plans to initiate a randomized, placebo-controlled Phase 2 trial of VLS-01 in TRD patients around YE’24.
|
• |
Beckley Psytech’s BPL-003 is an intranasal formulation of 5-methoxy-N,N-dimethyltryptamine (5-MeO-DMT) designed to fit
within an approximately two hour in-clinic treatment paradigm.
|
• |
In March 2024, Part 1 of a Phase 2a open-label (OL) study showed that a single administration of BPL-003 resulted in rapid and durable antidepressant effects, with 45% of patients in remission
three months after dosing. Acute effects resolved on average in less than two hours, and BPL-003 was found to be well-tolerated, with no serious adverse events reported.
|
• |
In April 2024, Part 2 of the Phase 2a OL study initiated to investigate BPL-003 as an adjunctive therapy to Selective Serotonin Reuptake Inhibitors in TRD patients.
|
• |
A randomized, controlled Phase 2b study of BPL-003 in TRD patients is underway with topline data expected in 2H 2024.
|
• |
Compass Pathways’ COMP360 is an oral formulation of synthetic psilocybin that is currently being evaluated in multiple clinical studies.
|
• |
In May 2024, results from an OL Phase 2 study in 22 patients with PTSD showed that COMP360 met its primary safety endpoint and was well tolerated, with no serious adverse events. COMP360
demonstrated a rapid and durable improvement in PTSD symptoms.
|
o |
Week 4 and 12 reductions in the CAPS-5 total score of 29.9 and 29.5, respectively, were observed.
|
o |
The response rate, as defined by patients experiencing a ≥ 15-point improvement on CAPS-5 score, was 81.8% at week 4 and 77.3% at week 12.
|
o |
The remission rate, as defined by CAPS-5 total score of ≤ 20, was 63.6% at week 4 and 54.5% at week 12.
|
• |
The Phase 3 program of COMP360 in TRD patients is composed of two pivotal trials, each with a long-term follow-up component. Pivotal Trial 1 (COMP005) topline data is expected in the fourth quarter
of 2024 and Pivotal Trial 2 (COMP006) topline data is anticipated mid-2025.
|
• |
1H’24
|
o |
ELE-101 MDD Phase 1/2a initial data
|
• |
2H’24
|
o |
VLS-01 Phase 1b topline data
|
o |
BPL-003 AUD Phase 2a OL data (mid’24)
|
o |
COMP360 TRD Phase 3 Pivotal Trial 1 topline data
|
o |
BPL-003 TRD Phase 2b data
|
o |
IBX-210 OUD Phase 1/2a initiation
|
o |
VLS-01 TRD Phase 2 initiation (around YE’24)
|
• |
2025
|
o |
RL-007 CIAS Phase 2b topline data (mid’25)
|
o |
COMP360 TRD Phase 3 Pivotal Trial 2 topline data (mid’25)
|
Three Months Ended
|
||||||||
March 31,
|
||||||||
2024
|
2023
|
|||||||
(unaudited)
|
||||||||
License revenue
|
$
|
—
|
$
|
37
|
||||
Operating expenses:
|
||||||||
Research and development
|
11,530
|
19,281
|
||||||
General and administrative
|
12,555
|
13,970
|
||||||
Total operating expenses
|
24,085
|
33,251
|
||||||
Loss from operations
|
(24,085
|
)
|
(33,214
|
)
|
||||
Other income (expense), net
|
(1,596
|
)
|
58
|
|||||
Loss before income taxes
|
(25,681
|
)
|
(33,156
|
)
|
||||
Benefit from (provision for) income taxes
|
4
|
(165
|
)
|
|||||
Losses from investments in equity method investees, net of tax
|
(1,701
|
)
|
(1,033
|
)
|
||||
Net loss
|
(27,378
|
)
|
(34,354
|
)
|
||||
Net loss attributable to noncontrolling interests
|
(665
|
)
|
(1,219
|
)
|
||||
Net loss attributable to ATAI Life Sciences N.V. stockholders
|
$
|
(26,713
|
)
|
$
|
(33,135
|
)
|
||
Net loss per share attributable to ATAI Life Sciences N.V. stockholders — basic and diluted
|
$
|
(0.17
|
)
|
$
|
(0.21
|
)
|
||
Weighted average common shares outstanding attributable to ATAI Life Sciences N.V. stockholders — basic and diluted
|
158,891,067
|
155,792,490
|
March 31,
2024
|
December 31,
2023
|
|||||||
Assets
|
||||||||
Cash and cash equivalents
|
$
|
18,867
|
$
|
45,034
|
||||
Short term restricted cash for other investments
|
5,000
|
-
|
||||||
Securities carried at fair value
|
87,379
|
109,223
|
||||||
Committed Investment Funds
|
-
|
25,000
|
||||||
Prepaid expenses and other current assets
|
5,732
|
5,830
|
||||||
Short term notes receivable - related party, net
|
522
|
505
|
||||||
Long term restricted cash for other investments
|
10,000
|
-
|
||||||
Property and equipment, net
|
920
|
981
|
||||||
Operating lease right-of-use asset, net
|
1,115
|
1,223
|
||||||
Other investments held at fair value
|
90,205
|
89,825
|
||||||
Other investments
|
32,807
|
1,838
|
||||||
Long term notes receivable - related parties, net
|
98
|
97
|
||||||
Convertible notes receivable - related party
|
13,902
|
11,202
|
||||||
Other assets
|
2,574
|
2,720
|
||||||
Total assets
|
$
|
269,121
|
$
|
293,478
|
||||
Liabilities and Stockholders' Equity
|
||||||||
Accounts payable
|
3,843
|
4,589
|
||||||
Accrued liabilities
|
10,926
|
15,256
|
||||||
Current portion of lease liability
|
244
|
275
|
||||||
Contingent consideration liability - related parties
|
607
|
620
|
||||||
Contingent consideration liability
|
1,406
|
1,637
|
||||||
Noncurrent portion of lease liability
|
907
|
990
|
||||||
Convertible promissory notes - related parties
|
417
|
164
|
||||||
Convertible promissory notes and derivative liability
|
4,099
|
2,666
|
||||||
Long term debt, net
|
15,140
|
15,047
|
||||||
Other liabilities
|
8,275
|
7,918
|
||||||
Total stockholders' equity attributable to ATAI Life Sciences N.V. stockholders
|
222,544
|
242,962
|
||||||
Noncontrolling interests
|
713
|
1,354
|
||||||
Total liabilities and stockholders' equity
|
269,121
|
293,478
|