Aptinyx Reports on Fourth Quarter and Full Year 2022 Results and Highlights and Review of Strategic Alternatives
Aptinyx Inc. (Nasdaq: APTX) announced significant business updates and financial results for Q4 and full year 2022. The company halted its Phase 2b study of NYX-783 for PTSD due to insufficient effectiveness, prompting a workforce reduction of approximately 60% to lower operational costs. Total cash stood at $56.2 million, down from $106.1 million in 2021. No collaboration revenue was reported for 2022, and R&D expenses decreased to $42.7 million from $55.4 million. The company's net loss improved to $64.8 million for 2022 compared to $74.9 million in the previous year, reflecting a net loss per share of $0.96.
- Net loss reduced from $74.9 million in 2021 to $64.8 million in 2022, indicating improved financial performance.
- R&D expenses decreased significantly, from $55.4 million in 2021 to $42.7 million in 2022, suggesting enhanced cost management.
- Phase 2b study of NYX-783 was halted due to insufficient primary endpoint improvement, limiting further development.
- Workforce reduction by approximately 60% indicates financial distress and operational challenges.
- No collaboration revenue generated in 2022 compared to $1 million in 2021, highlighting a decline in revenue generation.
Recent Business Updates
-
In March,
Aptinyx completed an analysis of the data from the first 100 patients enrolled in its Phase 2b clinical study of NYX-783 50 mg in patients with post-traumatic stress disorder (PTSD). The study was halted in February prior to its completion in support of the company’s preservation of capital. In the analysis, NYX-783 did not demonstrate sufficient improvement on the study’s primary endpoint to support continued advancement of the development program byAptinyx . -
In March,
Aptinyx engagedLadenburg Thalmann as its exclusive financial advisor to assist in the company’s exploration and evaluation of strategic alternatives. -
In March,
Aptinyx announced a reduction in its workforce by approximately60% to reduce the company’s operating costs and better align its workforce with the needs of its business as the company assesses strategic alternatives. -
In February,
Aptinyx announced results from its Phase 2 clinical study of NYX-458 in patients with cognitive impairment associated with Parkinson’s disease and dementia with Lewy bodies. Across the overall study population, NYX-458 did not demonstrate clinically meaningful improvements over placebo on the study’s efficacy endpoints. The results do not support further advancement of the development program by the company. -
Aptinyx’s NMDA receptor positive allosteric modulator, NYX-783, is under development as a treatment for opioid use disorder (OUD), supported by a
grant issued to researchers at$5.6 million Yale University School of Medicine . The grant was awarded under theNational Institutes of Health (NIH) Helping to End Addiction Long-term (HEAL) Initiative, administered by theNational Institute on Drug Abuse (NIDA), and funds the research and development of NYX-783 for the treatment of OUD. A Phase 1 drug-drug interaction study is ongoing and is being administered by the Yale Interdisciplinary Stress Center through a research collaboration withAptinyx .
Fourth Quarter and Full Year 2022 Financial Results
Cash Position: Cash and cash equivalents were
Collaboration Revenue: Revenue was
Research and Development (R&D) Expenses: R&D expenses were
General and Administrative (G&A) Expenses: G&A expenses were
Net Loss: Net loss was
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, the company’s ongoing evaluation of strategic alternatives, including future plans or expectations for NYX-783 and NYX-458, the safety, therapeutic effects, and stage of development of the company’s product candidates and discovery platform, expectations regarding the design, implementation, timing, and success of its current and planned clinical studies, including providing updated guidance with respect thereto, the timing for the company’s receipt and announcement of data from its clinical studies, the timing and outcome of discussions with FDA and other regulatory agencies, expectations regarding its preclinical development activities, expectations regarding its uses and sufficiency of capital, the company’s growth and the anticipated contribution of its executive officers and management to its operations and progress, and its expectations regarding its uses of capital and expenses, and the effect of the COVID-19 pandemic on the foregoing. Risks that contribute to the uncertain nature of the forward-looking statements include: the effect of the COVID-19 pandemic on our business and financial results, including with respect to disruptions to our clinical trials, business operations, and ability to raise additional capital; the success, cost, and timing of the company’s product candidate development activities and clinical studies; the company’s ability to execute on its strategy; including its ongoing strategic evaluation; the company’s estimates regarding expenses, future revenue, and capital requirements; as well as those risks and uncertainties set forth in the company’s most recent quarterly report on Form 10-Q and subsequent filings with the
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Assets |
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Current Assets: |
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Cash and cash equivalents |
|
$ |
56,205 |
|
$ |
106,124 |
Restricted cash |
|
179 |
|
197 |
||
Prepaid expenses and other current assets |
|
7,646 |
|
8,422 |
||
Total current assets |
|
64,030 |
|
114,743 |
||
Property and equipment and other long-term assets |
|
2,654 |
|
185 |
||
Total assets |
|
$ |
66,684 |
|
$ |
114,928 |
|
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Liabilities and stockholders’ equity |
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Current Liabilities: |
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Accounts payable |
|
$ |
724 |
|
$ |
622 |
Accrued expenses and other current liabilities |
|
2,772 |
|
5,064 |
||
Term loan, current |
|
2,795 |
|
---- |
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Total current liabilities |
|
6,291 |
|
5,686 |
||
Other long-term liabilities |
|
22,108 |
|
14,486 |
||
Total liabilities |
|
28,399 |
|
20,172 |
||
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|
|
|
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Stockholders’ equity |
|
38,285 |
|
94,756 |
||
Total liabilities and stockholders’ equity |
|
$ |
66,684 |
|
$ |
114,928 |
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Three Months Ended
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Year Ended
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2022 |
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2021 |
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2022 |
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2021 |
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Collaboration revenue |
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$ |
— |
|
|
$ |
— |
|
|
$ |
— |
|
|
$ |
1,000 |
|
|
|
|
|
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|
|
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Operating expenses |
|
|
|
|
|
|
|
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Research and development |
|
7,230 |
|
|
14,056 |
|
|
42,748 |
|
|
55,444 |
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General and administrative |
|
4,196 |
|
|
5,116 |
|
|
19,819 |
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|
20,090 |
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Total operating expenses |
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11,426 |
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|
19,172 |
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|
62,567 |
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|
75,534 |
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Loss from operations |
|
(11,426 |
) |
|
(19,172 |
) |
|
(62,567 |
) |
|
(74,534 |
) |
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Other income (expense) |
|
(627 |
) |
|
(438 |
) |
|
(2,282 |
) |
|
(352 |
) |
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Net loss and comprehensive loss |
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$ |
(12,053 |
) |
|
$ |
(19,610 |
) |
|
$ |
(64,849 |
) |
|
$ |
(74,886 |
) |
Net loss per share - basic and diluted |
|
$ |
(0.18 |
) |
|
$ |
(0.29 |
) |
|
$ |
(0.96 |
) |
|
$ |
(1.11 |
) |
Weighted average shares outstanding - basic and diluted |
|
67,716 |
|
|
67,716 |
|
|
67,716 |
|
|
67,220 |
|
Source:
View source version on businesswire.com: https://www.businesswire.com/news/home/20230330005712/en/
Investor & Media Contact:
ir@aptinyx.com or corporate@aptinyx.com
847-871-0377
Source:
FAQ
What were Aptinyx's financial results for Q4 2022?
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What major strategic changes did Aptinyx announce in March 2023?
Did Aptinyx generate any collaboration revenue in 2022?