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Praxis Precision Medicines Announces Publication of Preclinical Data Highlighting Differentiated and Potent Antiepileptic Activity of PRAX-562PRAX-562 demonstrated robust preclinical antiseizure activity and exhibited an improved preclinical tolerability profile compared to standard-of-care Praxis expects to initiate a Phase 2 trial in the first half of 2022 to explore the potential for PRAX-562 to treat rare DEEs BOSTON, Jan. 18, 2022 (GLOBE NEWSWIRE) -- Praxis Precision Medicines, Inc. (NASDAQ: PRAX), a clinical-stage biopharmaceutical company translating genetic insights into the development of therapies for central nervous system (CNS) disorders characterized by neuronal excitation-inhibition imbalance, today announced the publication of data in the journal Epilepsia from a preclinical study of PRAX-562, a preferential persistent sodium channel blocker currently in development for the potential treatment of rare adult cephalgias and Developmental and Epileptic Encephalopathies (DEEs). This preclinical study investigated the effects of PRAX-562 on intrinsic neuronal excitability and protection from induced seizures as compared to sodium channel blockers used as standard-of-care antiepileptic treatments. In the study, PRAX-562 demonstrated robust preclinical antiseizure activity and significantly improved preclinical tolerability, with improved or comparable efficacy when evaluated against currently used sodium channel blockers. The data demonstrate that by preferentially blocking persistent sodium current, PRAX-562 may represent a differentiated treatment option for disorders of hyperexcitability, such as DEEs, where standard sodium channel blockers are effective but poorly tolerated. “Sodium channel blockers are a fundamental component of epilepsy management, but dose-limiting characteristics must be addressed for patients to realize their full benefits,” said Steven Petrou, Ph.D., co-founder and chief scientific officer of Praxis. “This study supports the potential for PRAX-562, a persistent sodium channel blocker with a favorable therapeutic window, to improve tolerability relative to marketed therapies while achieving potent antiseizure activity.” DEEs are a group of disorders characterized by intractable seizures and other co-morbidities. Mutations in voltage-gated sodium channel (NaV) genes are the most common causes of DEEs. Given the number of NaV-targeting antiepileptic drugs (AEDs), and the well understood role of sodium channels in governing brain excitability, it is clear that mutations and other causes of sodium channel dysregulation contribute to the pathology of DEEs and other, more common, forms of epilepsy.1 “As a company deeply committed to delivering new treatment options for people suffering from complex brain disorders, we are pleased that the data highlight the potential for PRAX-562 to be a therapeutic option for people living with epilepsy,” said Marcio Souza, president and chief executive officer of Praxis. “A lot has been learned about neuronal modulation and physiology in recent years, and we are excited to initiate a study for the treatment of EEs in the first half of this year with PRAX-562.” Additional data supporting clinical investigation of PRAX-562 were presented at the American Epilepsy Society 2021 Annual Meeting in December. About PRAX-562 About Praxis Forward-Looking Statements The express or implied forward-looking statements included in this press release are only predictions and are subject to a number of risks, uncertainties and assumptions, including, without limitation: uncertainties inherent in clinical trials; the expected timing of submissions for regulatory approval or review by governmental authorities; regulatory approvals to conduct trials; risks, uncertainties and assumptions regarding the impact of the continuing COVID-19 pandemic on Praxis’ business, operations, strategy, goals and anticipated timelines, Praxis’ ongoing and planned preclinical activities, Praxis’ ability to initiate, enroll, conduct or complete ongoing and planned clinical trials and Praxis’ timelines for regulatory submissions; and other risks concerning Praxis’ programs and operations are described in additional detail in its Annual Report on Form 10-K for the year ended December 31, 2020, its Quarterly Reports on Form 10-Q and its other subsequent filings made with the Securities and Exchange Commission. Although Praxis’ forward-looking statements reflect the good faith judgment of its management, these statements are based only on information and factors currently known by Praxis. As a result, you are cautioned not to rely on these forward-looking statements. Any forward-looking statement made in this press release speaks only as of the date on which it is made. Praxis undertakes no obligation to publicly update or revise any forward-looking statement, whether as a result of new information, future developments or otherwise. Investor Contact: Media Contact: 1 Brunklaus A, Lal D. Sodium channel epilepsies and neurodevelopmental disorders: from disease mechanisms to clinical application. Dev Med Child Neurol. 2020 Jul;62(7):784-792. doi: 10.1111/dmcn.14519. Epub 2020 Mar 30. PMID: 32227486. |