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May 15, 2024 8:30 AM
PaxMedica Files Nasdaq Delisting Appeal Notice and Prepares for Upcoming FDA Meeting on PAX-101
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.
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.
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."
Recent milestones for PaxMedica include:
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.
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."
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.
About 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.
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.
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.
Forward-Looking Statements
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.
Contacts
PaxMedica, Inc.
303 S Broadway,
Suite 125.
Tarrytown, NY 10591
www.paxmedica.com
Media Contact
media@paxmedica.com
Investor Contact
Scott McGowan
InvestorBrandNetwork (IBN)
Phone: 310.299.1717
ir@paxmedica.com
www.paxmedica.com/investors
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2024 年 5 月 15 日上午 8:30
PaxMedica 提交納斯達克退市上訴通知併爲即將到來的 FDA PAX-101 會議做準備
PaxMedica今天宣佈,它已及時向納斯達克上訴和複審辦公室提交了正式的上訴通知書,要求推翻納斯達克聽證小組將該公司從納斯達克退市的決定。
紐約州塔裏敦/ACCESSWIRE /2024 年 5 月 15 日/PaxMedica, Inc.(“公司” 或 “PaxMedica”)(場外交易:PXMD)是一家致力於推進神經系統疾病治療的生物製藥公司,今天宣佈,它已及時向納斯達克上訴和複審辦公室提交了正式的上訴通知,要求推翻納斯達克聽證小組將該公司從納斯達克除名的決定。在4月30日收到納斯達克的通知後,PaxMedica決定對該決定提出上訴,並打算堅持認爲,聽證會小組沒有充分或適當地考慮PaxMedica最近取得的成就和正在採取的行動的關鍵方面,以恢復對繼續上市的所有適用要求的遵守。PaxMedica聘請雅各布·弗倫克爾、狄金森·賴特律師事務所作爲上訴的首席律師,與之前與聽證小組進行過互動的諮詢公司合作。
PaxMedica首席執行官霍華德·韋斯曼評論說:“我們正在尋求根據新的事態發展重新評估納斯達克最近的行動,這些進展突顯了我們對應對全球健康挑戰的持續進展和承諾。值得注意的是,繼我們於4月中旬宣佈完成 PAX-101 的註冊批次之後,該公司剛剛爲定於6月27日舉行的美國食品藥品管理局C類重要會議提交了一份簡報,屆時我們將介紹今年晚些時候提交保密協議的計劃的重要更新。我們認爲,這以及我們向聽證小組公佈的融資計劃有說服力地支持了我們對納斯達克上訴和恢復交易的論點。”
PaxMedica 最近的里程碑包括:
4 月 11 日:完成三批關鍵註冊/驗證批次 PAX-101(一種舒拉明的靜脈注射配方),對持續的監管申報至關重要。
4月16日:收到了馬拉維衛生部的緊急請求,要求緊急提供蘇拉明,以應對由於缺乏治療tbR HAT(一種致命的非洲昏睡病)的治療而迫在眉睫的人道主義危機。
4月23日:協議從我們的庫存中向馬拉維供應PAX-101,以加強我們在應對全球突發衛生事件中的作用。
5月10日:PaxMedica提交了2024年6月27日C類會議的美國食品藥品管理局簡報。
韋斯曼表示:“這些行動不僅表明了我們的運營效率,而且表明了我們在全球醫療保健領域的重要作用。令我們感到鼓舞的是,即將舉行的美國食品藥品管理局會議以及我們爲提供挽救生命的治療所做的持續努力將使納斯達克在上訴中給予積極考慮。”儘管如此,PaxMedica承認它無法預測上訴的結果。韋斯曼補充說:“我們致力於迅速推進我們的努力,以最大限度地提高股東的機會和價值,並爭取我們的神經系統疾病解決方案獲得批准。”
PaxMedica堅定不移地履行其使命,爲神經系統疾病開發和提供創新的治療方法,確保對全球公共衛生做出重大貢獻。如需了解有關 PaxMedica 正在進行的舉措和發展的更多信息,請訪問 paxmedica.com。
關於 PaxMedica
PaxMedica, Inc. 是一傢俱有前瞻性的臨床階段生物製藥公司,專門從事尖端的抗嘌呤能藥物療法(APT),旨在解決一系列具有挑戰性的神經系統疾病。我們全面的產品組合涵蓋一系列疾病,包括自閉症譜系障礙(ASD)等神經發育障礙,以及神經病學領域的其他關鍵領域。此外,我們打算向世界其他地區提供額外的、可靠的蘇拉明來源,這是第一階段,即布魯塞伊·羅得西亞錐蟲的公認護理標準。
我們致力於持續開發和評估我們的開創性計劃 PAX-101,這是一種靜脈注射舒拉明配方,是我們工作的核心,特別側重於創新的自閉症治療解決方案。我們正在進行的研究計劃不僅優先考慮自閉症患者的需求,而且還擴展到探索相關疾病的潛在治療應用。要詳細了解我們的變革性工作,請訪問www.paxmedica.com。
鼓勵感興趣的投資者和股東通過在 https://www.paxmedica.com/email-alerts 註冊電子郵件提醒和關注 PaxMedica 來訂閱新聞稿和行業動態 推特 和 領英。
前瞻性陳述
本新聞稿包含 “前瞻性陳述”。前瞻性陳述反映了我們目前對未來事件的看法。投資者可以通過諸如 “可能”、“將”、“可能”、“期望”、“預測”、“目標”、“估計”、“打算”、“計劃”、“相信”、“提議”、“潛在”、“繼續” 或類似表述等詞語或短語來識別這些前瞻性陳述。這些前瞻性陳述包括我們預期的臨床計劃、我們預期數據公告的時機和成功、臨床前和臨床試驗及監管申報,以及候選產品的分佈和需求。這些前瞻性陳述涉及已知和未知的風險和不確定性,基於公司當前對未來事件的預期和預測,公司認爲這些預期和預測可能會影響其財務狀況、經營業績、業務戰略和財務需求。此類風險和不確定性包括但不限於與公司開發工作相關的風險,包括公司產品開發和臨床試驗的時機、成本和成功的任何延遲或變化、資本資源不足、現金資金和現金消耗的風險、監管部門的批准以及與知識產權和侵權索賠相關的風險。除非法律要求,否則公司沒有義務公開更新或修改任何前瞻性陳述以反映隨後發生的事件或情況或預期的變化。儘管公司認爲這些前瞻性陳述中表達的預期是合理的,但它無法向你保證這些預期是正確的。公司提醒投資者,實際業績可能與預期業績存在重大差異,並鼓勵投資者審查可能影響公司最新10-K表年度報告中 “風險因素” 部分和其他章節以及隨後向美國證券提交的季度和其他文件中描述的未來業績的其他因素。和交易委員會。
聯繫人
PaxMedica, Inc.
百老匯街 303 號,
125 號套房
紐約州塔裏敦 10591
paxmedica.com
媒體聯繫人
media@paxmedica.com
投資者聯繫人
斯科特·麥克高恩
投資者品牌網絡 (IBN)
電話:310.299.1717
ir@paxmedica.com
www.paxmedica.com/投資者