Axsome Therapeutics将于 7月 21日在纽约市举行的脑健康研发前沿日活动上展示其创新的中枢神经系统 (CNS)管线-动脉网

Axsome Therapeutics to Showcase Its Innovative CNS Pipeline at Upcoming Frontiers in Brain Health R&D Day in New York City on July 21

Axsome Therapeutics 等信源发布 2025-07-07 19:03

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NEW YORK

纽约

，

July 07, 2025

2025年7月7日

(GLOBE NEWSWIRE) --

（环球新闻社）--

Axsome Therapeutics, Inc.

(NASDAQ: AXSM), a biopharmaceutical company leading a new era in the treatment of central nervous system (CNS) disorders, today announced that it will host its Frontiers in Brain Health R&D Day on July 21, 2025, starting at

(NASDAQ: AXSM)，一家引领中枢神经系统（CNS）疾病治疗新时代的生物制药公司，今天宣布将于2025年7月21日举办其“脑健康研发前沿日”活动，开始时间为

11:00 a.m. Eastern Time

东部时间上午11点

在

New York City

纽约市

. The event will highlight Axsome’s singular, innovative late-stage CNS pipeline.

该活动将突出展示Axsome独特、创新的晚期中枢神经系统（CNS）管线。

At the event, physician key opinion leaders will discuss the company’s current indications in neurology and psychiatry. Members of the Axsome management team will provide an overview of the clinical development programs. The presenters will be available to answer questions at the end of the presentations..

在活动中，医生关键意见领袖将讨论该公司在神经病学和精神病学领域的当前适应症。Axsome管理团队的成员将概述临床开发计划。报告人将在报告结束后回答问题。

This event is intended for institutional investors and sell-side analysts. To attend, please RSVP by emailing

该活动面向机构投资者和卖方分析师。如需参加，请通过电子邮件回复确认。

ir@axsome.com

, as space is limited.

，因为名额有限。

To register for the live webcast, please click

要注册实时网络直播，请点击

here

这里

. The live webcast and a replay of the event will also be publicly available on the “Webcasts & Presentations” page of the “Investors” section of the Company’s website at

现场直播和活动回放也将在公司网站“投资者”部分的“网络广播与演示”页面上公开提供。

www.axsome.com

。

About

关于

Axsome Therapeutics

is a biopharmaceutical company leading a new era in the treatment of central nervous system (CNS) conditions. We deliver scientific breakthroughs by identifying critical gaps in care and develop differentiated products with a focus on novel mechanisms of action that enable meaningful advancements in patient outcomes.

是一家引领中枢神经系统（CNS）疾病治疗新时代的生物制药公司。我们通过识别护理中的关键空白，开发具有新颖作用机制的差异化产品，从而实现科学突破，显著改善患者的治疗效果。

Our industry-leading neuroscience portfolio includes FDA-approved treatments for major depressive disorder, excessive daytime sleepiness associated with narcolepsy and obstructive sleep apnea, and migraine, and multiple late-stage development programs addressing a broad range of serious neurological and psychiatric conditions that impact over 150 million people in .

我们的行业领先的神经科学产品组合包括FDA批准的治疗重度抑郁症、与嗜睡症和阻塞性睡眠呼吸暂停相关的白天过度嗜睡以及偏头痛的药物，并且有多个后期开发项目，针对影响超过1.5亿人的各种严重的神经和精神疾病。

the United States

美国

. Together, we are on a mission to solve some of the brain’s biggest problems so patients and their loved ones can flourish. For more information, please visit us at

。我们一起致力于解决大脑的一些最大问题，以便患者及其亲人能够茁壮成长。欲了解更多信息，请访问我们的网站

www.axsome.com

and follow us on

关注我们

领英

and

和

。

Forward Looking Statements

前瞻性声明

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.

本新闻稿中讨论的某些事项属于“前瞻性陈述”。公司在某些情况下可能会使用“预测”、“相信”、“潜在”、“继续”、“估计”、“预期”、“计划”、“打算”、“可能”、“能够”、“也许”、“将”、“应该”等词语来传达未来事件或结果的不确定性，以此识别这些前瞻性陈述。

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 commercial success of the Company’s SUNOSI.

特别是，公司关于趋势和潜在未来结果的声明是此类前瞻性陈述的示例。前瞻性陈述包含风险和不确定性，包括但不限于公司SUNOSI的商业成功。

, AUVELITY

，AUVELITY

, and SYMBRAVO

，以及SYMBRAVO

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 .

产品以及公司为solriamfetol和/或AXS-05获得任何额外适应症的努力的成功；公司维持和扩大支付方覆盖的能力；公司正在进行的临床试验及预计开展的针对公司现有候选产品的临床试验的成功、时间安排和成本，包括关于试验启动时间、入组进度和完成情况的声明（包括公司充分资助其已披露临床试验的能力，此假设基于公司目前预计的收入或支出无重大变化），无效性分析以及中期结果的接收，这些结果不一定反映公司正在进行的临床试验的最终结果，和/或数据读出，以及支持公司现有候选产品中新药申请（“NDA”）所需的研究数量或类型或结果性质；公司为继续推进候选产品而资助额外临床试验的能力；公司获得并维持的时间和能力。

U.S. Food and Drug Administration

美国食品药品监督管理局

(“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; 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 Company’s ability to successfully resolve any intellectual property litigation, and even if such disputes are settled, whether the applicable federal agencies will approve of such settlements; 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 commercialization of SUNOSI, AUVELITY, and SYMBRAVO 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.

（“FDA”）或其他监管机构对公司产品候选物的批准或其他行动，包括任何新药申请（NDA）提交的时间；公司成功捍卫其知识产权或以公司可接受的成本获得必要许可的能力（如果能够获得）；公司成功解决任何知识产权诉讼的能力，即使这些争议得以解决，相关联邦机构是否会批准此类和解；公司研究与开发计划及合作的成功实施；公司许可协议的成功；市场对公司产品及其候选产品的接受度（如果获批）；公司的预期资本需求，包括用于商业化SUNOSI、AUVELITY和SYMBRAVO所需的资本，以及公司其他候选产品商业化发布所需的资金（如果获批），以及对预期现金跑道的潜在影响；公司将销售额转化为确认收入并保持有利的销售毛利净额的能力；由于国内政治气候、地缘政治冲突或全球疫情引发的不可预见情况或其他对正常业务运营的干扰，以及其他因素，包括一般经济状况和不在公司控制范围内的监管发展。

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 sta.

本文讨论的因素可能导致实际结果和发展与这些陈述所表达或暗示的有重大差异。前瞻性陈述仅在本新闻稿发布之日作出，公司不承担公开更新此类前瞻性陈述的义务。

Investors:

投资者：

Mark Jacobson

马克·雅各布森

Chief Operating Officer

首席运营官

(212) 332-3243

mjacobson@axsome.com

Media:

媒体：

Darren Opland