Company expects to report results from
Phase 2b study of NYX-2925 in fibromyalgia in August
Data from Phase 2 study of NYX-458 in cognitive
impairment expected in 1Q 2023
IND cleared for NIH grant-funded evaluation of
NYX-783 in opioid use disorder
$85 million cash balance provides operational
runway into 2024 and enables readouts from multiple Phase 2
studies
Management to host conference call today at
5:00 p.m. ET
Aptinyx Inc. (Nasdaq: APTX), a clinical-stage biopharmaceutical
company developing transformative therapies for the treatment of
brain and nervous system disorders, today reported financial
results for the second quarter of 2022 and provided key business
updates across the company’s clinical-stage pipeline of novel NMDA
receptor modulators.
“We have made great progress advancing our clinical development
programs and remain on track to deliver multiple near-term data
readouts,” said Andy Kidd, M.D., president and chief executive
officer of Aptinyx. “Our Phase 2b study of NYX-2925 in fibromyalgia
will report data in August and represents a significant opportunity
to bring a novel therapy to millions of underserved patients living
with this centralized pain disorder. I am also very pleased with
the strong execution of enrollment in our Phase 2 study of NYX-458
in cognitive impairment associated with Parkinson’s disease and
dementia with Lewy bodies. We are on track to complete enrollment
in the coming weeks and expect to report data in the first quarter
of 2023. With financial runway into 2024, we are equipped to
continue executing across our full slate of ongoing R&D
programs as we approach several major milestones.”
Pipeline Updates
- NYX-2925 for the treatment of fibromyalgia
- The company’s Phase 2b study enrolled 305 patients with
fibromyalgia randomized to receive oral doses of NYX-2925 50 mg,
NYX-2925 100 mg, or placebo once daily over a 12-week treatment
period.
- The primary endpoint in the study is the change from baseline
in average daily pain scores as reported on the zero-to-ten numeric
rating scale (NRS). Multiple secondary endpoints related to pain,
fatigue, cognitive performance, and patient quality of life are
also evaluated.
- The company expects to report data from the Phase 2b study in
August 2022.
- NYX-458 for the treatment of cognitive impairment
- The company’s ongoing exploratory Phase 2 study will enroll
approximately 100 patients with cognitive impairment associated
with Parkinson’s disease related Dementia or mild Cognitive
Impairment or Dementia with Lewy bodies randomized to receive oral
doses of NYX-458 30 mg or placebo once daily over a 12-week
treatment period.
- The primary endpoint in the study is overall safety and
tolerability of NYX-458. Additional endpoints will evaluate a
battery of neurocognitive assessments focused on attention, memory,
and executive function.
- Enrollment is nearing completion and the company expects to
report data from the Phase 2 study in the first quarter of
2023.
- NYX-783 for the treatment of post-traumatic stress disorder
(PTSD)
- The company’s ongoing Phase 2b study will enroll approximately
300 patients with PTSD randomized to receive oral doses of NYX-783
50 mg or placebo once daily over a 10-week treatment period.
- The primary endpoint in the study is the change from baseline
in the Clinician-Administered PTSD Scale for the DSM-5 (CAPS-5)
total score. Key secondary endpoints include various measures of
global impression of severity and improvement (CGI-S, CGI-I, PGI-S,
PGI-I).
- Enrollment is progressing and the company expects to report
data from the Phase 2b study in the second half of 2023.
Second Quarter 2022 and Recent Highlights
- Investigational New Drug (IND) application cleared for NIH
grant-funded evaluation of NYX-783 in opioid use disorder (OUD)
– In June, the U.S. Food and Drug Administration (FDA) indicated
the company’s IND application to evaluate NYX-783 in opioid use
disorder was cleared to proceed. Preclinical research and expected
clinical development of NYX-783 in OUD is funded by a
multimillion-dollar grant under the National Institutes of Health
(NIH) Helping to End Addiction Long-term (HEAL) Initiative,
administered by the National Institute on Drug Abuse (NIDA) and
awarded to researchers at Yale University School of Medicine, who
are conducting the studies.
- Presented preclinical data on NYX-783 in models of
PTSD at the 2022 American Psychiatric Association annual
meeting – In May, the company delivered a poster presentation
at the 2022 American Psychiatric Association annual meeting
highlighting data from preclinical studies showing that NYX-783
builds long-lasting fear-inhibitory memories in PTSD-relevant
models, ultimately leading to reduced spontaneous recovery (i.e.,
return) of fear.
Anticipated Upcoming Milestones
- Results from Phase 2b study of NYX-2925 in patients with
fibromyalgia (expected in August 2022)
- Results from exploratory Phase 2 study of NYX-458 in patients
with cognitive impairment (expected in 1Q 2023)
- Results from Phase 2b study of NYX-783 in patients with PTSD
(expected in 2H 2023)
Second Quarter 2022 Financial Results
Cash Position: Cash and cash equivalents were $85.3
million at June 30, 2022, compared to $106.1 million at December
31, 2021. Aptinyx expects its current cash balance to fund readouts
from each of the company’s Phase 2 clinical development programs
and support anticipated operations into 2024.
Research and Development (R&D) Expenses: Research and
development expenses were $11.9 million for the three months ended
June 30, 2022, compared to $14.8 million for the three months ended
June 30, 2021. The decrease in R&D expenses was primarily
driven by the completion of enrollment in the company’s Phase 2b
studies of NYX-2925 in painful diabetic peripheral neuropathy and
fibromyalgia.
General and Administrative (G&A) Expenses: General
and administrative expenses were $5.2 million for the three months
ended June 30, 2022, compared to $5.1 million for the same period
in 2021.
Net Loss: Net loss was $17.7 million for the second
quarter of 2022, compared to a net loss of $19.8 million for the
second quarter of 2021.
Conference Call
The Aptinyx management team will host a conference call and
webcast today at 5:00 p.m. ET to review its financial results and
highlights for the second quarter of 2022 and subsequent period. To
access the live conference call, please dial (888) 660-6390
(domestic) or (929) 203-1902 (international) and refer to
conference ID 4855909. A live audio webcast of the event will be
available on the Investors & Media section of Aptinyx’s website
at https://ir.aptinyx.com. A replay of the webcast will be archived
on Aptinyx’s website for 30 days following the event.
About Aptinyx
Aptinyx Inc. is a clinical-stage biopharmaceutical company
focused on the discovery, development, and commercialization of
proprietary synthetic small molecules for the treatment of brain
and nervous system disorders. Aptinyx has a platform for discovery
of novel compounds that work through a unique mechanism to
modulate—rather than block or over-activate—NMDA receptors and
enhance synaptic plasticity, the foundation of neural cell
communication. The company has three product candidates in clinical
development in central nervous system indications, including
fibromyalgia cognitive impairment, and post-traumatic stress
disorder. Aptinyx is also advancing additional compounds from its
proprietary discovery platform, which continues to generate a rich
and diverse pipeline of small-molecule NMDA receptor modulators
with the potential to treat an array of neurologic disorders. For
more information, visit www.aptinyx.com or follow Aptinyx on
Twitter @Aptinyx.
Forward-Looking Statements
Statements contained in this press release regarding matters
that are not historical facts are “forward-looking statements”
within the meaning of the Private Securities Litigation Reform Act
of 1995. Because such statements are subject to risks and
uncertainties, actual results may differ materially from those
expressed or implied by such forward-looking statements. Such
statements include, but are not limited to, statements regarding
the company’s business plans and objectives, including future plans
or expectations for NYX-2925, NYX-783, or NYX-458, the potential
therapeutic effects of the company’s product candidates and
discovery platform, expectations regarding the design,
implementation, timing, and success of its current and planned
clinical studies, the timing for the company’s receipt and
announcement of data from its clinical studies, and the company’s
expectations regarding its uses and sufficiency of capital,
including the operational runway of its current cash balance. Risks
that contribute to the uncertain nature of the forward-looking
statements include: the effect of the COVID-19 pandemic on the
company’s business and financial results, including with respect to
disruptions to the company’s clinical studies, business operations,
and ability to raise additional capital; the success, cost, and
timing of the company’s product candidate development activities
and planned clinical studies; the company’s ability to execute on
its strategy; positive results from a clinical study may not
necessarily be predictive of the results of future or ongoing
clinical studies; regulatory developments in the United States and
foreign countries; the company’s estimates regarding expenses,
future revenue, and capital requirements; the company’s ability to
fund operations into 2023; as well as those risks and uncertainties
set forth in the company’s most recent annual report on Form 10-K
and subsequent filings with the Securities and Exchange Commission,
including the company’s upcoming Quarterly Report on Form 10-Q for
the period ended June 30, 2022. All forward-looking statements
contained in this press release speak only as of the date on which
they were made. Aptinyx undertakes no obligation to update such
statements to reflect events that occur or circumstances that exist
after the date on which they were made.
APTINYX INC.
CONDENSED BALANCE
SHEETS
(in thousands)
(unaudited)
Assets
June 30, 2022
December 31, 2021
Current Assets:
Cash and cash equivalents
$
85,269
$
106,124
Restricted cash
105
197
Prepaid expenses and other current
assets
6,766
8,422
Total current assets
92,140
114,743
Property and equipment, net and other
long-term assets
166
185
Total assets
$
92,306
$
114,928
Liabilities and stockholders’
equity
Current Liabilities:
Accounts payable
$
2,106
$
622
Accrued expenses and other current
liabilities
3,576
5,064
Total current liabilities
5,682
5,686
Term loan, non-current
24,498
14,155
Other long-term liabilities
27
331
Total liabilities
30,207
20,172
Stockholders’ equity
62,099
94,756
Total liabilities and stockholders’
equity
$
92,306
$
114,928
APTINYX INC.
CONDENSED STATEMENTS OF
OPERATIONS
(in thousands, except per
share data)
(Unaudited)
Three Months Ended
June 30,
Six Months Ended
June 30,
2022
2021
2022
2021
Revenues
Collaboration revenue
$
—
$
—
$
—
$
1,000
Operating expenses
Research and development
11,909
14,796
25,511
25,110
General and administrative
5,196
5,070
10,973
10,046
Total operating expenses
17,105
19,866
36,484
35,156
Loss from operations
(17,105
)
(19,866
)
(36,484
)
(34,156
)
Other (income) expense, net
(195
)
(47
)
(224
)
(111
)
Interest Expense
757
—
1,234
—
Net loss and comprehensive loss
$
(17,667
)
$
(19,819
)
$
(37,494
)
$
(34,045
)
Net loss per share - basic and diluted
$
(0.26
)
$
(0.29
)
$
(0.55
)
$
(0.51
)
Weighted average shares outstanding -
basic and diluted
67,716
67,381
67,716
66,716
Source: Aptinyx Inc.
View source
version on businesswire.com: https://www.businesswire.com/news/home/20220804005945/en/
Investor & Media Contact: Patrick Flavin Aptinyx Inc.
ir@aptinyx.com or corporate@aptinyx.com 847-871-0377
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