share_log

PaxMedica Files Nasdaq Delisting Appeal Notice and Prepares for Upcoming FDA Meeting on PAX-101

PaxMedica Files Nasdaq Delisting Appeal Notice and Prepares for Upcoming FDA Meeting on PAX-101

PaxMedica 提交纳斯达克退市上诉通知并为即将到来的 FDA PAX-101 会议做准备
PaxMedica ·  05/15 08:30

Share:

分享:

Created on:

创建于:

May 15, 2024 8:30 AM

2024 年 5 月 15 日上午 8:30

PaxMedica Files Nasdaq Delisting Appeal Notice and Prepares for Upcoming FDA Meeting on PAX-101

PaxMedica 提交纳斯达克退市上诉通知并为即将到来的 FDA PAX-101 会议做准备

PaxMedica today announced it has timely filed a formal notice of appeal with the Nasdaq Office of Appeals and Review to reverse the decision of a Nasdaq Hearings Panel to delist the Company from Nasdaq.

PaxMedica今天宣布,它已及时向纳斯达克上诉和复审办公室提交了正式的上诉通知书,要求推翻纳斯达克听证小组将该公司从纳斯达克退市的决定。

TARRYTOWN, NY / ACCESSWIRE / May 15, 2024 / PaxMedica,Inc. (the "Company" or "PaxMedica") (OTC:PXMD),a biopharmaceutical company dedicated to advancing treatments for neurological disorders, today announced it has timely filed a formal notice of appeal with the Nasdaq Office of Appeals and Review to reverse the decision of a Nasdaq Hearings Panel to delist the Company from Nasdaq. Following receipt of notification from Nasdaq on April 30th, PaxMedica determined to appeal the decision and intends to maintain that the Hearings Panel did not consider sufficiently or appropriately crucial aspects of PaxMedica's recent achievements and ongoing actions to regain compliance with all applicable requirements for continued listing.  PaxMedica has retained Jacob Frenkel, Dickinson Wright, PLLC as its lead counsel in the appeal, working with the consulting firm that interacted previously with the Hearings Panel.

纽约州塔里敦/ACCESSWIRE /2024 年 5 月 15 日/PaxMedica, Inc.(“公司” 或 “PaxMedica”)(场外交易:PXMD)是一家致力于推进神经系统疾病治疗的生物制药公司,今天宣布,它已及时向纳斯达克上诉和复审办公室提交了正式的上诉通知,要求推翻纳斯达克听证小组将该公司从纳斯达克除名的决定。在4月30日收到纳斯达克的通知后,PaxMedica决定对该决定提出上诉,并打算坚持认为,听证会小组没有充分或适当地考虑PaxMedica最近取得的成就和正在采取的行动的关键方面,以恢复对继续上市的所有适用要求的遵守。PaxMedica聘请雅各布·弗伦克尔、狄金森·赖特律师事务所作为上诉的首席律师,与之前与听证小组进行过互动的咨询公司合作。

Howard Weisman, CEO of PaxMedica, commented, "We are seeking a reevaluation of Nasdaq's recent action based on new developments that underscore our ongoing progress and commitment to addressing global health challenges. Notably, following our announcements on the completion of registration lots of PAX-101 in mid-April, the Company just submitted a briefing book for an important FDA Type C meeting scheduled for June 27th, during which we will present key updates on our plans for NDA submission later this year.  We believe this, as well as our financing plans which we made known to the Hearings Panel, support persuasively our arguments to appeal and restore trading on Nasdaq."

PaxMedica首席执行官霍华德·韦斯曼评论说:“我们正在寻求根据新的事态发展重新评估纳斯达克最近的行动,这些进展突显了我们对应对全球健康挑战的持续进展和承诺。值得注意的是,继我们于4月中旬宣布完成 PAX-101 的注册批次之后,该公司刚刚为定于6月27日举行的美国食品药品管理局C类重要会议提交了一份简报,届时我们将介绍今年晚些时候提交保密协议的计划的重要更新。我们认为,这以及我们向听证小组公布的融资计划有说服力地支持了我们对纳斯达克上诉和恢复交易的论点。”

Recent milestones for PaxMedica include:

PaxMedica 最近的里程碑包括:

  • April 11th: Completion of three pivotal registration/validation batches of PAX-101, an IV formulation of suramin, crucial for ongoing regulatory     submissions.

  • April 16th: Receipt of an urgent request from Malawi's Ministry of Health for emergency access to suramin to address a looming humanitarian crisis     due to the scarcity of treatment for TBr HAT, a fatal form of African     Sleeping Sickness.

  • April 23rd: Agreement to supply Malawi with PAX-101 from our stock, reinforcing our role in combating global health emergencies.

  • May 10th: PaxMedica submits FDA Briefing Book for June 27, 2024, Type C meeting.

  • 4 月 11 日:完成三批关键注册/验证批次 PAX-101(一种舒拉明的静脉注射配方),对持续的监管申报至关重要。

  • 4月16日:收到了马拉维卫生部的紧急请求,要求紧急提供苏拉明,以应对由于缺乏治疗tbR HAT(一种致命的非洲昏睡病)的治疗而迫在眉睫的人道主义危机。

  • 4月23日:协议从我们的库存中向马拉维供应PAX-101,以加强我们在应对全球突发卫生事件中的作用。

  • 5月10日:PaxMedica提交了2024年6月27日C类会议的美国食品药品管理局简报。

Weisman stated "these actions not only demonstrate our operational effectiveness, but also our vital role in the global healthcare landscape.  We are encouraged that the upcoming FDA meeting, and our continuous efforts to supply life-saving treatments, will result in favorable consideration by Nasdaq in our appeal." Nevertheless, PaxMedica acknowledges that it cannot predict the outcome of the appeal.  Weisman added that "we are committed to advancing expeditiously our efforts to maximize shareholder opportunities and value and pursue approval of our solutions for neurological disorders."

韦斯曼表示:“这些行动不仅表明了我们的运营效率,而且表明了我们在全球医疗保健领域的重要作用。令我们感到鼓舞的是,即将举行的美国食品药品管理局会议以及我们为提供挽救生命的治疗所做的持续努力将使纳斯达克在上诉中给予积极考虑。”尽管如此,PaxMedica承认它无法预测上诉的结果。韦斯曼补充说:“我们致力于迅速推进我们的努力,以最大限度地提高股东的机会和价值,并争取我们的神经系统疾病解决方案获得批准。”

PaxMedica remains resolute in its mission to develop and provide innovative treatments for neurological disorders, ensuring significant contributions to public health worldwide. For more information on PaxMedica's ongoing initiatives and developments, please visit www.paxmedica.com.

PaxMedica坚定不移地履行其使命,为神经系统疾病开发和提供创新的治疗方法,确保对全球公共卫生做出重大贡献。如需了解有关 PaxMedica 正在进行的举措和发展的更多信息,请访问 paxmedica.com。

About PaxMedica

关于 PaxMedica

PaxMedica, Inc. is a forward-looking clinical-stage biopharmaceutical firm specializing in cutting-edge anti-purinergic drug therapies (APT) aimed at addressing a range of challenging neurologic disorders. Our comprehensive portfolio encompasses a spectrum of conditions,including neurodevelopmental disorders such as Autism Spectrum Disorder (ASD),as well as other critical areas within the neurology field. Additionally, we intend to provide the rest of the world with an additional, reliable source of suramin, the accepted standard of care for Stage 1, Trypanosoma Brucei Rhodesiense.

PaxMedica, Inc. 是一家具有前瞻性的临床阶段生物制药公司,专门从事尖端的抗嘌呤能药物疗法(APT),旨在解决一系列具有挑战性的神经系统疾病。我们全面的产品组合涵盖一系列疾病,包括自闭症谱系障碍(ASD)等神经发育障碍,以及神经病学领域的其他关键领域。此外,我们打算向世界其他地区提供额外的、可靠的苏拉明来源,这是第一阶段,即布鲁塞伊·罗得西亚锥虫的公认护理标准。

We are dedicated to the continuous development and evaluation of our pioneering program, PAX-101, an intravenous suramin formulation that lies at the heart of our efforts, particularly focused on innovative ASD treatment solutions. Our ongoing research initiatives not only prioritize the needs of ASD patients, but also extend to exploring potential therapeutic applications for related conditions. To learn more about our transformative work, please visit www.paxmedica.com.

我们致力于持续开发和评估我们的开创性计划 PAX-101,这是一种静脉注射舒拉明配方,是我们工作的核心,特别侧重于创新的自闭症治疗解决方案。我们正在进行的研究计划不仅优先考虑自闭症患者的需求,而且还扩展到探索相关疾病的潜在治疗应用。要详细了解我们的变革性工作,请访问www.paxmedica.com。

Interested investors and shareholders are encouraged to signup for press releases and industry updates by registering for Email Alerts at https://www.paxmedica.com/email-alerts and by following PaxMedica on Twitter and LinkedIn.

鼓励感兴趣的投资者和股东通过在 https://www.paxmedica.com/email-alerts 注册电子邮件提醒和关注 PaxMedica 来订阅新闻稿和行业动态 推特 领英

Forward-Looking Statements

前瞻性陈述

This press release contains "forward-looking statements."Forward-looking statements reflect our current view about future events.Investors can identify these forward-looking statements by words or phrases such as "may," "will," "could," "expect," "anticipate," "aim," "estimate,""intend," "plan," "believe," "is/are likely to," "propose," "potential,""continue" or similar expressions. These forward-looking statements include our anticipated clinical program, the timing and success of our anticipated data announcements,pre-clinical and clinical trials and regulatory filings, and distribution and demand for our product candidates. These forward-looking statements involve known and unknown risks and uncertainties and are based on the Company's current expectations and projections about future events that the Company believes may affect its financial condition, results of operations, business strategy and financial needs. Such risks and uncertainties include, but are not limited to, risks associated with the Company's development work, including any delays or changes to the timing, cost and success of the Company's product development and clinical trials, risk of insufficient capital resources, cash funding and cash burn, regulatory approvals and risks associated with intellectual property and infringement claims. The Company undertakes no obligation to update or revise publicly any forward-looking statements to reflect subsequent occurring events or circumstances, or changes in its expectations, except as may be required by law. Although the Company believes that the expectations expressed in these forward-looking statements are reasonable, it cannot assure you that such expectations will turn out to be correct, and the Company cautions investors that actual results may differ materially from the anticipated results and encourages investors to review other factors that may affect its future results described in the Company's"Risk Factors" section and other sections in its most recent Annual Report on Form 10-K, and subsequent quarterly and other filings with the U.S. Securities and Exchange Commission.

本新闻稿包含 “前瞻性陈述”。前瞻性陈述反映了我们目前对未来事件的看法。投资者可以通过诸如 “可能”、“将”、“可能”、“期望”、“预测”、“目标”、“估计”、“打算”、“计划”、“相信”、“提议”、“潜在”、“继续” 或类似表述等词语或短语来识别这些前瞻性陈述。这些前瞻性陈述包括我们预期的临床计划、我们预期数据公告的时机和成功、临床前和临床试验及监管申报,以及候选产品的分布和需求。这些前瞻性陈述涉及已知和未知的风险和不确定性,基于公司当前对未来事件的预期和预测,公司认为这些预期和预测可能会影响其财务状况、经营业绩、业务战略和财务需求。此类风险和不确定性包括但不限于与公司开发工作相关的风险,包括公司产品开发和临床试验的时机、成本和成功的任何延迟或变化、资本资源不足、现金资金和现金消耗的风险、监管部门的批准以及与知识产权和侵权索赔相关的风险。除非法律要求,否则公司没有义务公开更新或修改任何前瞻性陈述以反映随后发生的事件或情况或预期的变化。尽管公司认为这些前瞻性陈述中表达的预期是合理的,但它无法向你保证这些预期是正确的。公司提醒投资者,实际业绩可能与预期业绩存在重大差异,并鼓励投资者审查可能影响公司最新10-K表年度报告中 “风险因素” 部分和其他章节以及随后向美国证券提交的季度和其他文件中描述的未来业绩的其他因素。和交易委员会。

Contacts

联系人

PaxMedica, Inc.

PaxMedica, Inc.

303 S Broadway,
Suite 125.
Tarrytown, NY 10591
www.paxmedica.com

百老汇街 303 号,
125 号套房
纽约州塔里敦 10591
paxmedica.com

Media Contact

媒体联系人

Investor Contact

投资者联系人

Scott McGowan
InvestorBrandNetwork (IBN)
Phone: 310.299.1717
ir@paxmedica.com
www.paxmedica.com/investors

斯科特·麦克高恩
投资者品牌网络 (IBN)
电话:310.299.1717
ir@paxmedica.com
www.paxmedica.com/投资者

声明:本内容仅用作提供资讯及教育之目的,不构成对任何特定投资或投资策略的推荐或认可。 更多信息
    抢沙发