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Axsome Therapeutics to Report Second Quarter 2024 Financial Results on August 5

Axsome Therapeutics to Report Second Quarter 2024 Financial Results on August 5

axsome therapeutics将于2024年8月5日公布第二季度财报。
Axsome Therapeutics ·  07/11 00:00
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NEW YORK, July 11, 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 it will report its financial results for the second quarter of 2024 on Monday, August 5, 2024, before the opening of the U.S. financial markets. Axsome's management team will host a conference call at 8:00 a.m. Eastern Time on August 5, 2024, to discuss these results and provide a business update.

纽约,2024年7月11日(环球新闻社)——Axsome Therapeutics,Inc.(NASDAQ: AXSM)是一家生物制药公司,专注于开发和提供治疗中枢神经系统(CNS)疾病的新疗法。今天宣布将于2024年8月5日星期一,在美国金融市场开盘前公布其2024年第二季度财务业绩。Axsome的管理团队将于2024年8月5日上午8:00(美国东部时间)举行电话会议,讨论这些结果并提供业务更新。

To participate in the live conference call, please dial (877) 405-1239 (toll-free domestic). A live webcast of the conference call can be accessed on the "Webcasts & Presentations" page of the "Investors" section of the Company's website at . A recording of the conference call will be available on the Company's website for approximately 30 days following the live event.

请拨打电话(877)405-1239(国内免费),参加现场电话会议。可以通过公司网站上“Webcasts&Presentations”页面访问电话会议的现场网络广播。电话会议的记录将在现场活动后大约30天内在公司网站上提供访问。

About Axsome Therapeutics, Inc.

关于Axsome Therapeutics公司,Inc。

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.com. The Company may occasionally disseminate material, nonpublic information on the company website.

Axsome Therapeutics,Inc.是一家生物制药公司,开发和提供中枢神经系统(CNS)条件创新疗法,治疗选择有限的情况。通过开发具有新的作用机制的治疗选择,我们正在改变治疗中枢神经系统疾病的方法。在Axsome,我们致力于开发能够显著改善患者生命和为医生提供新的治疗选择的产品。有关更多信息,请访问公司网站axsome.com。该公司可能偶尔在公司网站上发布非公开信息。

Forward Looking Statements

前瞻性声明

Certain matters discussed in this press release are "forward-looking statements". We 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 our Sunosi and Auvelity products and the success of our efforts to obtain any additional indication(s) with respect to solriamfetol and/or AXS-05; the success, timing and cost of our ongoing clinical trials and anticipated clinical trials for our current product candidates, including statements regarding the timing of initiation, pace of enrollment and completion of the trials (including our ability to fully fund our disclosed clinical trials, which assumes no material changes to our currently projected revenues or expenses), futility analyses and receipt of interim results, which are not necessarily indicative of the final results of our 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 our current product candidates; our ability to fund additional clinical trials to continue the advancement of our product candidates; the timing of and our ability to obtain and maintain U.S. Food and Drug Administration ("FDA") or other regulatory authority approval of, or other action with respect to, our 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 our 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; unforeseen circumstances or other disruptions to normal business operations arising from or related to 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.

本新闻稿中讨论的某些事项是“前瞻性声明”。我们在某些情况下使用“预测”,“相信”,“潜力”,“继续”,“估计”,“预期”,“计划”,“打算”, “可能”,“可能”,“将”,“应该”或其他传达未来事件或结果的不确定性的单词来识别这些前瞻性声明。特别是,公司关于趋势和潜在未来结果的陈述是此类前瞻性声明的示例。前瞻性声明包括风险和不确定性,包括但不限于继续商业化Sunosi和Auvelity产品的成功以及我们取得任何关于solriamfetol和/或AXS-05的额外指示(s)的努力成功;我们当前product候选者的进行中的临床试验以及预期的临床试验的成功,包括有关试验启动的时间,招募步伐和完成情况的陈述(包括我们能否全额资助所披露的临床试验,这假设我们当前预计的收入或支出未发生实质性变化),无效分析和获得中期结果,不一定是正在进行的临床试验的最终结果,和/或数据读取,及支持提出新药申请(“NDA”)所需的研究数量或类型或结果的性质(目前的任何product候选者);我们能够为继续推进我们的product候选者而资助额外的临床试验的时间;我们获得并维护美国食品和药物管理局(“FDA”)或其他监管机构批准或采取行动的时间与能力涉及我们的product候选者,包括有关提交任何NDA的时间的声明;是否FDA在完整回复信中确定的问题可能会影响AXS-07 NDA的潜在批准性,用于有或无视幻象的成人偏头痛,依据我们对MOMENTUm临床试验的特殊协议评估;本公司成功捍卫其知识产权或以可接受成本获得必要的许可证,如果有的话;本公司的研究和开发计划和合作的成功实施;本公司授权协议的成功;市场对公司产品和product候选者(如果获得批准)的接受程度;我们所预计的资本需求,包括继续商业化Sunosi和Auvelity的资本要求以及本公司商业化其他product候选者的资本要求(如果获得批准),以及本公司预期现金离岸期潜在影响;由地缘政治冲突或全球大流行引起的或与之相关的其他未预料到的情况或其他干扰正常业务运营的因素,包括但不限于总体经济条件和监管发展,不在公司控制范围内。所讨论的因素可能会导致实际结果和发展与所述声明中明示或暗示的结果和发展有实质不同。前瞻性声明仅作为本新闻稿的发布日期,并且本公司无义务公开更新此类前瞻性声明以反映随后发生的事件或情况。

Axsome Contacts:

Axsome联络人:

Investors:
Mark Jacobson
Chief Operating Officer
Axsome Therapeutics, Inc.
One World Trade Center, 22nd Floor
New York, NY 10007
Tel: 212-332-3243
Email: mjacobson@axsome.com

投资者:
马克·雅各布森
首席运营官
Axsome Therapeutics公司
One World Trade Center,22楼
纽约市10007
电话:212-332-3243
电子邮件:mjacobson@axsome.com

Media:
Darren Opland
Director, Corporate Communications
Axsome Therapeutics, Inc.
One World Trade Center, 22nd Floor
New York, NY 10007
Tel: 929-837-1065
Email: dopland@axsome.com

媒体:
Darren Opland
董事,企业通信
Axsome Therapeutics公司
One World Trade Center,22楼
纽约市10007
电话:929-837-1065
电子邮件:dopland@axsome.com


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Source: Axsome Therapeutics, Inc.

来源:Axsome Therapeutics,Inc。

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