Aptinyx Announces Publication in Molecular Psychiatry Demonstrating Reduction of Spontaneous Recovery of Fear with NYX-783
Aptinyx Inc. (Nasdaq: APTX) announced significant preclinical data on NYX-783, a drug candidate for treating post-traumatic stress disorder (PTSD). Published in Molecular Psychiatry, the findings indicate NYX-783 effectively reduces fear recovery in animal models, suggesting its potential for human therapy. The Phase 2b study is ongoing, aiming to leverage NYX-783's NMDA receptor modulation to improve emotional control. Approximately 15 million adults in the U.S. suffer from PTSD, highlighting the need for effective treatments.
- NYX-783 shows promise in reducing spontaneous fear recovery in PTSD models.
- Positive results in preclinical studies published in a reputable journal.
- Ongoing Phase 2b study supports further clinical development.
- FDA granted Fast Track designation for NYX-783's development.
- Limited therapeutic options exist for PTSD, indicating competition is high.
- The efficacy of NYX-783 has yet to be confirmed in human trials.
Preclinical data support the continued clinical development of NYX-783 as a novel mechanistic approach for treating post-traumatic stress disorder (PTSD)
NYX-783 is currently under evaluation in a Phase 2b study in patients with PTSD
The publication, entitled "Positive modulation of N-methyl-D-aspartate receptors in the mPFC reduces the spontaneous recovery of fear," details the ability of NYX-783 to reduce fear-based behaviors in animal models of PTSD by measuring enhanced fear extinction and reduced spontaneous recovery (i.e., return) of fear. NYX-783 significantly reduced spontaneous recovery of fear in mice in the conventional auditory fear-conditioning model. NYX-783 also reduced spontaneous recovery in the single-prolonged stress model of PTSD. These data suggest NYX-783 can inhibit the spontaneous recovery of learned fear even after exposure to an additional significant stressor.
The inhibition of spontaneous recovery of learned fear by NYX-783 results from increased NMDAR2B-mediated activity of neurons in the infralimbic medial prefrontal cortex. These results elucidate the cellular targets of NYX-783 and the molecular mechanisms underlying the inhibition of spontaneous recovery.
These preclinical findings indicate NYX-783 may be particularly useful for inhibiting spontaneous recovery of fear and provide further support for the drug candidate’s therapeutic potential as a treatment for PTSD.
The study was led by
“We are very excited by these data as they underscore the potential of NYX-783 to treat the dysfunction of emotional control in post-traumatic stress disorder,” said
About Post-Traumatic Stress Disorder
Approximately fifteen million adults in
About NYX-783
NYX-783 is a novel, oral, positive allosteric modulator of NMDA receptors currently in Phase 2 development for the treatment of post-traumatic stress disorder (PTSD). In preclinical studies of NYX-783, particularly strong results were observed in psychiatric models, models of fear extinction, and models of substance abuse. In a Phase 1 clinical study of NYX-783, ample central nervous system exposure was observed and the product candidate demonstrated a favorable adverse event and tolerability profile, with no serious adverse effects, across a wide dose range. In an exploratory Phase 2a study in patients with PTSD, patients receiving a 50 mg dose level of NYX-783 showed meaningful symptom improvements and rates of response. The
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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-783, therapeutic effects of the company’s product candidates, expectations regarding the design, implementation, timing, and success of its current and planned clinical trials, expectations regarding its preclinical development activities, and expectations regarding its uses and sufficiency of capital. Risks that contribute to the uncertain nature of the forward-looking statements include: 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; regulatory developments in
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