Axsome Therapeutics Presents Data From Multiple Programs at Sleep Europe 2024
Axsome Therapeutics Presents Data From Multiple Programs at Sleep Europe 2024
Seven presentations highlight the Company's growing CNS portfolio and commitment to improving treatment outcomes for patients with sleep disorders
七個演講突出了公司不斷增長的中樞神經系統投資組合,並致力於改善睡眠障礙患者的治療結果
NEW YORK, Sept. 24, 2024 (GLOBE NEWSWIRE) -- Axsome Therapeutics, Inc. (NASDAQ: AXSM), a biopharmaceutical company developing and delivering novel therapies for the management of central nervous system (CNS) disorders, today announced seven presentations on AXS-12 and solriamfetol at Sleep Europe 2024, the 27th Congress of the European Sleep Research Society, being held September 24-27, 2024, in Seville, Spain. Featured presentations include data from the SYMPHONY Phase 3 trial of AXS-12 in narcolepsy, findings from the CRESCENDO patient survey underscoring the unmet needs of patients with type 1 narcolepsy, and previously reported data on solriamfetol demonstrating improvement in cognitive function in patients with excessive daytime sleepiness (EDS) associated with OSA and narcolepsy.
紐約,2024年9月24日(環球新聞社)-axsome therapeutics,Inc.(納斯達克: AXSM)是一家生物製藥公司,致力於開發並提供新穎的治療方案,用於治療中樞神經系統(CNS)疾病,今天宣佈將在2024年歐洲睡眠大會上舉辦關於AXS-12和solriamfetol的七場演講,該大會是歐洲睡眠研究協會第27屆大會,於2024年9月24日至27日在西班牙塞維利亞舉行。重點演講包括AXS-12在嗜睡症中的SYMPHONY第3期臨床試驗數據,CRESCENDO患者調查的發現凸顯了1型嗜睡症患者的未滿足需求,以及此前報告的solriamfetol數據,顯示solriamfetol在與OSA和嗜睡症相關的白天過度嗜睡(EDS)患者中改善認知功能。
Details for the presentations are as follows:
演講詳情如下:
AXS-12:
AXS-12:
Title: AXS-12 for the Treatment of Narcolepsy: Topline Results from the Phase 3 SYMPHONY Trial
Poster Presentation Date and Time: Wednesday, September 25, 12:15 - 1:15 p.m. and 4:00 - 5:45 p.m. CEST
Lead Author: Michael Thorpy, MD, Director of the Sleep-Wake Disorders Center at the Montefiore Medical Center and Professor of Neurology at Albert Einstein College of Medicine, New York, NY, USA
Poster Number: P254
標題: AXS-12用於嗜睡症的治療:SYMPHONY第3期臨床試驗頂線結果
海報展示日期和時間: 中歐時間9月25日星期三,12:15 - 1:15 下午和4:00 - 5:45 下午
主要作者:Michael Thorpy, MD,Montefiore醫學中心睡眠-覺醒障礙中心主任,紐約愛因斯坦醫學院神經學教授,美國紐約
海報編號: P254
Title: CRESCENDO: Results from a Survey of Symptom Burden and Quality of Life in Patients with Narcolepsy Type 1
Poster Presentation Date and Time: Wednesday, September 25, 12:15 - 1:15 p.m. and 4:00 - 5:45 p.m. CEST
Lead Author: Michael Thorpy, MD, Director of the Sleep-Wake Disorders Center at the Montefiore Medical Center and Professor of Neurology at Albert Einstein College of Medicine, New York, NY, USA
Poster Number: P265
標題: CRESCENDO:關於1型嗜睡症患者症狀負擔和生活質量調查的結果
海報展示日期和時間: 中歐時間9月25日星期三,12:15 - 1:15 下午和4:00 - 5:45 下午
主要作者:Michael Thorpy, MD,Montefiore醫學中心睡眠-覺醒障礙中心主任,紐約愛因斯坦醫學院神經學教授,美國紐約
海報編號: P265
Solriamfetol:
Solriamfetol:
Title: Solriamfetol and Maintenance of Wakefulness Outcomes in Patients with Narcolepsy and Obstructive Sleep Apnea
Oral Presentation Date and Time: Tuesday, September 24, 9:55 - 10:01 a.m. CEST
Poster Presentation Date and Time: Wednesday, September 25, 12:15 - 1:15 p.m. and 4:00 - 5:45 p.m. CEST
Lead Author: Michael Thorpy, MD, Director of the Sleep-Wake Disorders Center at the Montefiore Medical Center and Professor of Neurology at Albert Einstein College of Medicine, New York, NY, USA
Poster Number: P475
標題:Solriamfetol對嗜睡症和阻塞性睡眠呼吸暫停症患者的清醒維持結果的影響。
口頭報告日期和時間:週二,9月24日,上午9:55 - 10:01 CEST
海報展示日期和時間: 中歐時間9月25日星期三,12:15 - 1:15 下午和4:00 - 5:45 下午
主要作者:Michael Thorpy, MD,Montefiore醫學中心睡眠-覺醒障礙中心主任,紐約愛因斯坦醫學院神經學教授,美國紐約
海報編號:P475
Title: Effects of Solriamfetol on Cognition in Patients with Excessive Daytime Sleepiness Associated with Narcolepsy
Poster Presentation Date and Time: Wednesday, September 25, 12:15 - 1:15 p.m. and 4:00 - 5:45 p.m. CEST
Lead Author: Yaroslav Winter, MD, Mainz Comprehensive Epilepsy and Sleep Medicine Center, Department of Neurology, Johannes Gutenberg-University, Mainz, Germany
Poster Number: P197
標題: Solriamfetol對嗜睡症合併過度白天嗜睡患者認知功能的影響
海報展示日期和時間: 中歐時間9月25日星期三,12:15 - 1:15 下午和4:00 - 5:45 下午
主要作者:Yaroslav Winter博士,Mainz綜合癲癇和睡眠醫學中心,神經病學系,Johannes Gutenberg大學,Mainz,德國。
海報編號: P197
Title: Real-world Use of Solriamfetol for Excessive Daytime Sleepiness in Patients Reporting Anxiety or Depression
Poster Presentation Date and Time: Friday, September 27, 10:45 a.m. - 1:30 p.m. CEST
Lead Author: Yaroslav Winter, MD, Mainz Comprehensive Epilepsy and Sleep Medicine Center, Department of Neurology, Johannes Gutenberg-University, Mainz, Germany
Poster Number: P198
標題:報道焦慮、抑鬱症患者在現實中使用Solriamfetol緩解日間過度嗜睡的情況
海報展示日期和時間: 9月27日,星期五,上午10:45 - 下午1:30,中歐製造時區
主要作者:Yaroslav Winter博士,緬因茨大學神經內科,緬茨綜合癲癇和睡眠醫學中心,德國約翰內斯·古騰堡大學
海報編號:P198
Title: SURWEY: Treatment of Excessive Daytime Sleepiness with Solriamfetol: Initiation, Titration, and Outcome
Poster Presentation Date and Time: Thursday, September 26, 12:00 - 1:30 p.m. and 5:30 – 6:45 p.m. CEST
Lead Author: Samantha Floam, DMD, Axsome Therapeutics
Poster Number: P799
標題:SURWEY:使用Solriamfetol治療過度白天嗜睡:起始、逐步加量和結果
海報展示日期和時間:CEST時間,9月26日星期四,12:00 - 1:30下午和5:30 - 6:45下午
主要作者:Samantha Floam,DMD,Axsome Therapeutics。
海報編號:P799
Title: Effects of Solriamfetol on Cognition in Obstructive Sleep Apnea with Excessive Daytime Sleepiness and Impaired Cognition
Poster Presentation Date and Time: Friday, September 27, 10:45 a.m. - 1:30 p.m. CEST
Lead Author: Hans Van Dongen, PhD, Professor at Washington State University
Poster Number: P1248
標題: Solriamfetol對合並白天過度嗜睡和認知障礙的阻塞性睡眠呼吸暫停症的影響
海報展示日期和時間: 9月27日,星期五,上午10:45 - 下午1:30,中歐製造時區
主要作者: Hans Van Dongen,華盛頓州立大學教授,博士
海報編號: P1248
About Axsome Therapeutics
關於axsome therapeutics
Axsome Therapeutics, Inc. is a biopharmaceutical company developing and delivering novel therapies for central nervous system (CNS) conditions that have limited treatment options. Through development of therapeutic options with novel mechanisms of action, we are transforming the approach to treating CNS conditions. At Axsome, we are committed to developing products that meaningfully improve the lives of patients and provide new therapeutic options for physicians. For more information, please visit the Company's website at .
Axsome Therapeutics, Inc.是一家生物製藥公司,致力於開發和提供中樞神經系統(CNS)疾病的新療法,這些疾病的治療選擇有限。通過開發具有新型作用機制的治療選擇,我們正在改變治療CNS疾病的方法。在axsome,我們致力於開發可以顯著改善患者生活併爲醫生提供新療法選擇的產品。欲了解更多信息,請訪問公司網站。
Forward Looking Statements
前瞻性聲明
Certain matters discussed in this press release are "forward-looking statements". The Company may, in some cases, use terms such as "predicts," "believes," "potential," "continue," "estimates," "anticipates," "expects," "plans," "intends," "may," "could," "might," "will," "should" or other words that convey uncertainty of future events or outcomes to identify these forward-looking statements. In particular, the Company's statements regarding trends and potential future results are examples of such forward-looking statements. The forward-looking statements include risks and uncertainties, including, but not limited to, the continued commercial success of the Company's Sunosi and Auvelity products and the success of the Company's efforts to obtain any additional indication(s) with respect to solriamfetol and/or AXS-05; the Company's ability to maintain and expand payer coverage; the success, timing and cost of the Company's ongoing clinical trials and anticipated clinical trials for the Company's current product candidates, including statements regarding the timing of initiation, pace of enrollment and completion of the trials (including the Company's ability to fully fund the Company's disclosed clinical trials, which assumes no material changes to the Company's currently projected revenues or expenses), futility analyses and receipt of interim results, which are not necessarily indicative of the final results of the Company's ongoing clinical trials, and/or data readouts, and the number or type of studies or nature of results necessary to support the filing of a new drug application ("NDA") for any of the Company's current product candidates; the Company's ability to fund additional clinical trials to continue the advancement of the Company's product candidates; the timing of and the Company's ability to obtain and maintain U.S. Food and Drug Administration ("FDA") or other regulatory authority approval of, or other action with respect to, the Company's product candidates, including statements regarding the timing of any NDA submission; whether issues identified by FDA in the complete response letter may impact the potential approvability of the Company's NDA for AXS-07 for the acute treatment of migraine in adults with or without aura, pursuant to the Company's special protocol assessment for the MOMENTUM clinical trial; the Company's ability to successfully defend its intellectual property or obtain the necessary licenses at a cost acceptable to the Company, if at all; the successful implementation of the Company's research and development programs and collaborations; the success of the Company's license agreements; the acceptance by the market of the Company's products and product candidates, if approved; the Company's anticipated capital requirements, including the amount of capital required for the continued commercialization of Sunosi and Auvelity and for the Company's commercial launch of its other product candidates, if approved, and the potential impact on the Company's anticipated cash runway; the Company's ability to convert sales to recognized revenue and maintain a favorable gross to net sales; unforeseen circumstances or other disruptions to normal business operations arising from or related to domestic political climate, geo-political conflicts or a global pandemic and other factors, including general economic conditions and regulatory developments, not within the Company's control. The factors discussed herein could cause actual results and developments to be materially different from those expressed in or implied by such statements. The forward-looking statements are made only as of the date of this press release and the Company undertakes no obligation to publicly update such forward-looking statements to reflect subsequent events or circumstance.
本新聞稿中討論的某些事項爲「前瞻性聲明」。公司在某些情況下可能使用諸如「預測」,「相信」,「潛力」,「持續」,「估計」,「預計」,「計劃」,「打算」,「可能」,「可能」,「將會」,「應該」或其他能傳達未來事件或結果不確定性的詞語來識別這些前瞻性聲明。特別是,公司在趨勢和潛在未來結果方面的陳述是此類前瞻性聲明的例子。前瞻性聲明包括風險和不確定性,包括但不限於公司Sunosi和Auvelity產品的商業成功持續性以及公司獲得與solriamfetol和/或AXS-05有關的額外指明的努力的成功;公司維持和擴展支付方覆蓋範圍的能力;公司正在進行的臨床試驗以及公司目前的產品候選者的預期臨床試驗的成功、時間和成本,包括關於試驗啓動時間、招募速度和完成時間的聲明(包括公司能夠充分資助公司已公開披露的臨床試驗,其中不會發生公司當前預計的營業收入或費用的重大變化)、無效性分析和獲得中間結果,這些不一定能反映公司正在進行的臨床試驗的最終結果和/或數據結果以及支持提交新藥申請(「NDA」)所需的研究數量或類型或結果的性質(用於公司目前的任何產品候選者);公司繼續推進其產品候選者的臨床試驗所需的資金;公司獲得和維持美國食品和藥物管理局(「FDA」)或其他監管機構批准公司的產品候選者或採取其他行動的時間,包括關於任何NDA提交的時間;FDA在對AXS-07的完全回應信中提出的問題是否會影響公司根據MOMENTUm臨床試驗的特殊方案評估爲成年人急性偏頭痛治療而提交的AXS-07的NDA的批准可行性;公司成功捍衛其知識產權或以公司可接受的成本獲得必要的許可的能力,如果有的話;公司的研究和開發項目和合作的成功實施;公司的許可協議的成功接受;市場對公司產品和產品候選者的接受程度,如果獲得批准的話;公司預期的資本需求,包括繼續銷售Sunosi和Auvelity以及公司其他產品候選者的商業化發展所需的資本金額,以及對公司預期現金運營時間的潛在影響;公司將銷售轉爲確認收入並保持有利的毛銷售淨額的能力;由於國內政治環境、地緣政治衝突或全球大流行等原因,未預料到的情況或其他對正常業務運營的干擾以及公司無法控制的其他因素,包括一般經濟狀況和監管發展。本文所討論的因素可能導致實際結果和發展與這些陳述中表達或暗示的結果存在重大差異。前瞻性聲明僅適用於發表本新聞稿之日,並且公司無義務公開更新此類前瞻性聲明以反映隨後發生的事件或情況。
Investors:
Mark Jacobson
Chief Operating Officer
(212) 332-3243
mjacobson@axsome.com
投資者:
馬克·雅各布森
首席運營官
(212) 332-3243
mjacobson@axsome.com
Media:
Darren Opland
Director, Corporate Communications
(929) 837-1065
dopland@axsome.com
媒體:
Darren Opland
董事,企業通信
(929)837-1065
dopland@axsome.com