Aptinyx Highlights Key Goals and Anticipated Development Milestones for 2022
Aptinyx Inc. (APTX) has announced significant developments for 2022, focusing on their Phase 2 studies for chronic pain, cognitive impairment, and PTSD. Key milestones include data readouts for NYX-2925 in chronic pain and NYX-458 for cognitive issues expected in mid-2022 and the second half of the year, respectively. The company has a strong financial position with approximately $106 million in cash, sufficient to fund ongoing studies and operations through 2023. Aptinyx aims to establish itself as a leading neuroscience firm with transformative therapies for serious nervous system disorders.
- Upcoming Phase 2 readouts for NYX-2925 and NYX-458 could enhance market perception.
- Strong cash position of approximately $106 million supports ongoing studies and operations through 2023.
- Diverse pipeline of NMDA receptor modulators targeting various neurological disorders.
- None.
Catalyst-rich year with data readouts expected from three Phase 2 studies across chronic pain and cognitive impairment development programs
Advancing PTSD development program with initiation of Phase 2b studies
Strong balance sheet expected to fund Phase 2 readouts from each ongoing development program
Company will host Portfolio Review Event on
“Following a year of extraordinary execution,
Clinical Programs and Anticipated 2022 Milestones
NYX-2925 for chronic pain – Phase 2b readouts expected in 2Q and mid-year 2022: NYX-2925 is a novel oral NMDA receptor positive allosteric modulator currently in Phase 2b clinical development for the treatment of painful DPN and fibromyalgia.
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In late
October 2021 ,Aptinyx announced the completion of enrollment in its Phase 2b study of NYX-2925 in 229 patients with painful diabetic peripheral neuropathy (DPN). The company anticipates reporting results from the study in early to mid second quarter 2022. - The company’s Phase 2b study of NYX-2925 in 300 patients with fibromyalgia is on track to report results in mid 2022.
NYX-458 for cognitive impairment – Phase 2 readout expected in 2H 2022: NYX-458 is a novel oral NMDA receptor positive allosteric modulator currently in Phase 2 clinical development for the treatment of cognitive impairment associated with Parkinson’s disease and dementia with Lewy bodies.
- Enrollment is progressing in an exploratory Phase 2 study of NYX-458 in 100 patients with cognitive impairment associated with Parkinson’s disease and dementia with Lewy bodies. The company anticipates reporting data from the study in the second half of 2022.
NYX-783 for PTSD – Phase 2b readout expected in 2023: NYX-783 is a novel, oral NMDA receptor positive allosteric modulator currently in Phase 2b clinical development for the treatment of post-traumatic stress disorder (PTSD).
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In
December 2021 ,Aptinyx initiated a Phase 2b study evaluating 50 mg QD of NYX-783 in 300 patients with PTSD. The company anticipates reporting data from the study in the second half of 2023. - A Phase 2b study evaluating a higher 150 mg QD dose level of NYX-783 in 300 patients with PTSD is on track for initiation in the first quarter of 2022.
Cash Position and Financial Guidance
Upcoming Q1 2022 Presentations and Discussions
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January 10, 2022 – Virtual Presentation at the H.C. Wainwright 2022BioConnect Conference -
January 13, 2022 – Virtual presentation at the 40th AnnualJ.P. Morgan Healthcare Conference -
February 9, 2022 – Aptinyx Portfolio Review Event, featuring Dr.Richard Rauck , board certified physician in pain medicine and anesthesiology atCarolinas Pain Institute and medical director forThe Center for Clinical Research based in Winston-Salem -
February 14-15, 2022 – Virtual fireside chat at the 11th AnnualSVB Leerink Global Healthcare Conference -
March 7-9, 2022 – Neuropysch panel discussion at the 42nd AnnualCowen Health Care Conference
About NYX-2925
NYX-2925 is a novel oral NMDA receptor positive allosteric modulator currently in Phase 2 clinical development for the treatment of chronic pain. In clinical studies, NYX-2925 has demonstrated activity that affects central pain processing, resulting in alleviation of pain and other symptoms associated with chronic pain conditions. NYX-2925 has also exhibited a favorable safety and tolerability profile across a wide dose range in clinical studies to date. The
About NYX-783
NYX-783 is a novel oral NMDA receptor positive allosteric modulator currently in Phase 2 clinical development for the treatment of post-traumatic stress disorder (PTSD). In preclinical studies of NYX-783, therapeutically relevant enhancement of extinction learning has been observed in models of conditioned fear and substance abuse. In an exploratory Phase 2 clinical study, administration of NYX-783 resulted in clinically meaningful improvements on PTSD symptoms. NYX-783 has also exhibited a favorable safety and tolerability profile across a wide dose range in clinical studies to date. The
About NYX-458
NYX-458 is a novel oral NMDA receptor positive allosteric modulator currently in Phase 2 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.
About
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, expectations, and potential therapeutic effects of its development candidates, expectations regarding the design, implementation, timing, and success of its current and potential clinical studies, the timing for the company’s receipt and announcement of data, the company’s belief in the potential for upcoming catalysts and milestones to be transformational and to support our mission, the company’s views as to the potential profile and benefit of our product candidates, and expectations regarding the company’s cash runway. 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; delays of any current preclinical studies; 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 annual report on Form 10-K and subsequent filings with the
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FAQ
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