Aptinyx Completes Enrollment in Phase 2 Study of NYX-458 in Cognitive Impairment Associated with Parkinson’s Disease and Dementia with Lewy Bodies
Aptinyx Inc. (NASDAQ: APTX) has completed the enrollment of 99 patients in its Phase 2 study of NYX-458, targeting cognitive impairment associated with Parkinson’s disease and dementia with Lewy bodies. The 12-week treatment period has commenced, followed by a 30-day safety follow-up. Results are anticipated in 1Q 2023. NYX-458 acts as a positive allosteric modulator of NMDA receptors, potentially addressing cognitive deficits in affected patients. Current treatment options are limited, highlighting the significance of this study.
- Completion of enrollment in Phase 2 study of NYX-458 is a significant milestone.
- NYX-458 has shown potential to address NMDA receptor hypofunction related to cognitive impairment.
- None.
Results from the Phase 2 study are expected in 1Q 2023
"The completion of enrollment in our Phase 2 study of NYX-458 is a significant milestone for Aptinyx,” said
The Phase 2 study is a randomized, double-blind, parallel-design, placebo-controlled study to evaluate the safety and potential cognitive benefits of NYX-458 in 99 patients with mild cognitive impairment or mild dementia associated with Parkinson’s disease or dementia with Lewy bodies. The study evaluates daily oral dosing of a 30 mg dose level of NYX-458 compared to placebo over a 12-week period. The study assesses the overall safety and tolerability of NYX-458 in patients, as well as its effects across multiple neurocognitive endpoints focused on attention, memory, and executive function. More information about this study can be found on clinicaltrials.gov (NCT04148391).
About Cognitive Impairment Associated with Parkinson’s Disease and Dementia with Lewy Bodies
Cognitive impairment associated with Parkinson’s disease and dementia with Lewy bodies is characterized by a broad range of deficits related to attention, memory, and executive function. A common disease pathology—elevated levels of alpha synuclein—is implicated in these conditions. Alpha synuclein has been shown to contribute to a decrease in NMDA receptor expression and activity, leading to a decline in cognitive and functional abilities. It is estimated that approximately 1.4 million people in
About NYX-458
NYX-458 is a novel oral NMDA receptor positive allosteric modulator currently in clinical development for the treatment of cognitive impairment associated with Parkinson’s disease and dementia with Lewy bodies. NYX-458 has been shown to reverse cognitive deficits in non-human primates in a model that is highly translatable to Parkinson’s disease in humans. NYX-458 has also been shown to improve cognitive performance across various other preclinical models of neurodegeneration. In a Phase 1 clinical study, NYX-458 exhibited a favorable safety and tolerability profile across a wide dose range and achieved CNS exposures consistent with exposures observed at efficacious preclinical dose levels.
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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-458 and potential therapeutic effects of NYX-458, expectations regarding the design, implementation, timing, and success of the company’s current and potential clinical studies of NYX-458, and the timing for the company’s receipt and announcement of data from its Phase 2 study of NYX-458. Risks that contribute to the uncertain nature of the forward-looking statements include: the effect of COVID-19 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 planned clinical studies; the company’s ability to execute on its strategy; 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
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