share_log

Eupraxia Pharmaceuticals Begins Trading on Nasdaq Today

Eupraxia Pharmaceuticals Begins Trading on Nasdaq Today

Eupraxia Pharmicals今天開始在納斯達克交易
PR Newswire ·  04/05 19:00

VICTORIA, BC, April 5, 2024 /PRNewswire/ - Eupraxia Pharmaceuticals Inc. ("Eupraxia" or the "Company") (TSX: EPRX); (NASDAQ: EPRX), a clinical-stage biotechnology company leveraging its proprietary Diffusphere technology to optimize drug delivery for applications with significant unmet need, announced today that trading of the Company's common shares will begin today, April 5, 2024, on the Nasdaq Capital Market ("Nasdaq"), under the ticker symbol "EPRX".

不列顛哥倫比亞省維多利亞市,2024年4月5日 /PRNewswire/-Eupraxia Pharmicals Inc.(“Eupraxia” 或 “公司”)(多倫多證券交易所股票代碼:EPRX);(納斯達克股票代碼:EPRX)是一家臨床階段的生物技術公司,利用其專有的Diffusphere技術來優化有大量未滿足需求的應用的藥物交付。該公司今天宣佈,該公司普通股將於今天,即2024年4月5日開始交易納斯達克資本市場(“納斯達克”),股票代碼爲 “EPRX”。

The Company's shares also continue to trade on the Toronto Stock Exchange under the ticker symbol "EPRX".

該公司的股票還繼續在多倫多證券交易所上市,股票代碼爲 “EPRX”。

About Eupraxia Pharmaceuticals Inc.
關於 Eupraxia 製藥公司

Eupraxia is a clinical-stage biotechnology company focused on the development of locally delivered, extended-release products that have the potential to address therapeutic areas with high unmet medical need. The Company strives to provide improved patient benefit and has developed technology designed to deliver targeted, long-lasting activity with fewer side effects. Diffusphere, a proprietary, polymer-based micro-sphere technology, is designed to facilitate targeted drug delivery, with extended duration of effect, and offers multiple, highly tuneable PK profiles. This investigational technology can be engineered for use with multiple active pharmaceutical ingredients and delivery methods.

Eupraxia是一家處於臨床階段的生物技術公司,專注於開發本地交付的緩釋產品,這些產品有可能滿足大量未得到滿足的醫療需求的治療領域。該公司致力於改善患者的福利,並開發了旨在提供有針對性的長期活性且減少副作用的技術。Diffusphere是一種基於聚合物的專有微球技術,旨在促進靶向藥物遞送,延長效果持續時間,並提供多種高度可調的PK曲線。這項研究性技術可以設計用於多種活性藥物成分和交付方法。

Eupraxia recently completed a Phase 2b clinical trial (SPRINGBOARD) for its lead product candidate, EP-104IAR, for the treatment of pain due to osteoarthritis of the knee. The trial met its primary endpoint and three of the four secondary endpoints. Eupraxia has expanded the EP-104 platform into gastrointestinal disease with the Phase 1b/2a RESOLVE trial for treating eosinophilic esophagitis. Eupraxia is also developing a pipeline of later- and earlier-stage long-acting formulations. Potential pipeline indications include candidates for other inflammatory joint indications and oncology, each designed to improve on the activity and tolerability of currently approved drugs. For further details about Eupraxia, please visit the Company's website at: .

Eupraxia最近完成了其主要候選產品 EP-104IAR 的2b期臨床試驗(SPRINGBOARD),該產品用於治療膝蓋骨關節炎引起的疼痛。該試驗達到了其主要終點和四個次要終點中的三個。Eupraxia 通過治療嗜酸性食管炎的 1b/2a 期RESOLVE試驗,已將 EP-104 平台擴展到胃腸道疾病。Eupraxia還在開發後期和早期階段的長效配方產品線。潛在的臨床適應症包括其他炎症性關節適應症和腫瘤學的候選藥物,每種適應症都旨在改善當前批准藥物的活性和耐受性。有關Eupraxia的更多詳細信息,請訪問該公司的網站:。

Notice Regarding Forward-looking Statements and Information
關於前瞻性陳述和信息的通知

This news release includes forward-looking statements and forward–looking information within the meaning of applicable securities laws. Often, but not always, forward–looking information can be identified by the use of words such as "plans", "is expected", "expects", "scheduled", "intends", "contemplates", "anticipates", "believes", "proposes", "potential" or variations (including negative and grammatical variations) of such words and phrases, or state that certain actions, events or results "may", "could", "would", "might" or "will" be taken, occur or be achieved. Forward looking statements in this news release include statements regarding Eupraxia's listing on the Nasdaq and the potential of Eupraxia's product candidates. Such statements and information are based on the current expectations of Eupraxia's management, and are based on assumptions, including but not limited to: future research and development plans for the Company proceeding substantially as currently envisioned; industry growth trends, including with respect to projected and actual industry sales; the Company's ability to obtain positive results from the Company's research and development activities, including clinical trials; and the Company's ability to protect patents and proprietary rights. Although Eupraxia's management believes that the assumptions underlying these statements and information are reasonable, they may prove to be incorrect. The forward–looking events and circumstances discussed in this news release may not occur by certain dates or at all and could differ materially as a result of known and unknown risk factors and uncertainties affecting Eupraxia, including, but not limited to: risks and uncertainties related to the Company's limited operating history; the Company's novel technology with uncertain market acceptance; if the Company breaches any of the agreements under which it licenses rights to its product candidates or technology from third parties, the Company could lose license rights that are important to its business; the Company's current license agreement may not provide an adequate remedy for its breach by the licensor; the Company's technology may not be successful for its intended use; the Company's future technology will require regulatory approval, which is costly and the Company may not be able to obtain it; the Company may fail to obtain regulatory approvals or only obtain approvals for limited uses or indications; the Company's clinical trials may fail to demonstrate adequately the safety and efficacy of our product candidates at any stage of clinical development; the Company may be required to suspend or discontinue clinical trials due to side effects or other safety risks; the Company completely relies on third parties to provide supplies and inputs required for its products and services; the Company relies on external contract research organizations to provide clinical and non-clinical research services; the Company may not be able to successfully execute its business strategy; the Company will require additional financing, which may not be available; any therapeutics the Company develops will be subject to extensive, lengthy and uncertain regulatory requirements, which could adversely affect the Company's ability to obtain regulatory approval in a timely manner, or at all; the impact of health pandemics or epidemics on the Company's operations; the Company's restatement of its consolidated financial statements, which may lead to additional risks and uncertainties, including loss of investor confidence and negative impacts on the Company's common share price; and other risks and uncertainties described in more detail in Eupraxia's public filings on SEDAR+ (sedarplus.ca) and EDGAR (sec.gov). Although Eupraxia has attempted to identify important factors that could cause actual actions, events or results to differ materially from those described in forward–looking statements and information, there may be other factors that cause actions, events or results to differ from those anticipated, estimated or intended. No forward–looking statement or information can be guaranteed. Except as required by applicable securities laws, forward–looking statements and information speak only as of the date on which they are made and Eupraxia undertakes no obligation to publicly update or revise any forward–looking statement or information, whether as a result of new information, future events or otherwise.

本新聞稿包括適用證券法所指的前瞻性陳述和前瞻性信息。通常,但並非總是如此,前瞻性信息可以通過使用諸如 “計劃”、“預期”、“預期”、“計劃”、“打算”、“考慮”、“預期”、“相信”、“提議”、“潛在” 或變體(包括負面和語法變體)等詞語來識別,或聲明某些行動、事件或結果 “可能”,“可以”、“將”、“可能” 或 “將” 被採取、發生或實現。本新聞稿中的前瞻性聲明包括有關Eupraxia在納斯達克上市的聲明以及Eupraxia候選產品的潛力。此類陳述和信息基於Eupraxia管理層當前的預期,並基於假設,包括但不限於:公司未來的研發計劃基本按目前的設想進行;行業增長趨勢,包括預計和實際的行業銷售;公司從包括臨床試驗在內的公司研發活動中獲得積極成果的能力;以及公司保護專利和專有權利的能力。儘管Eupraxia的管理層認爲這些陳述和信息所依據的假設是合理的,但它們可能被證明是不正確的。本新聞稿中討論的前瞻性事件和情況可能不會在特定日期之前發生,也可能根本不會發生,並且由於影響Eupraxia的已知和未知的風險因素和不確定性,可能存在重大差異,包括但不限於:與公司有限運營歷史相關的風險和不確定性;市場接受度不確定的公司新技術;如果公司違反了向第三方許可其候選產品或技術權利的任何協議,公司可能會失去執照對其業務至關重要的權利;公司目前的許可協議可能無法爲許可方的違約行爲提供充分的補救措施;公司的技術可能無法成功實現其預期用途;公司的未來技術將需要監管部門的批准,這很昂貴,公司可能無法獲得批准;公司可能無法獲得監管部門的批准或僅獲得有限用途或適應症的批准;公司的臨床試驗可能無法證明充分保證我們產品的安全性和有效性處於臨床開發任何階段的候選人;由於副作用或其他安全風險,公司可能被要求暫停或終止臨床試驗;公司完全依賴第三方提供其產品和服務所需的供應和投入;公司依賴外部合同研究機構提供臨床和非臨床研究服務;公司可能無法成功執行其業務戰略;公司將需要額外的融資,但可能無法獲得;任何療法公司發展將受到廣泛、漫長和不確定的監管要求的約束,這可能會對公司及時或根本獲得監管部門批准的能力產生不利影響;健康流行病或流行病對公司運營的影響;公司重報合併財務報表,這可能會導致額外的風險和不確定性,包括投資者信心喪失和對公司普通股價格的負面影響;以及更多內容中描述的其他風險和不確定性 Eupraxia 的詳細信息關於SEDAR+(sedarplus.ca)和EDGAR(sec.gov)的公開文件。儘管Eupraxia試圖確定可能導致實際行動、事件或結果與前瞻性陳述和信息中描述的重大差異的重要因素,但可能還有其他因素導致行動、事件或結果與預期、估計或預期的不同。無法保證任何前瞻性的陳述或信息。除非適用的證券法要求,否則前瞻性陳述和信息僅代表其發佈之日,Eupraxia沒有義務公開更新或修改任何前瞻性聲明或信息,無論是由於新信息、未來事件還是其他原因。

SOURCE Eupraxia Pharmaceuticals Inc.

來源 Eupraxia Pharmicals Inc.

譯文內容由第三人軟體翻譯。


以上內容僅用作資訊或教育之目的,不構成與富途相關的任何投資建議。富途竭力但無法保證上述全部內容的真實性、準確性和原創性。
    搶先評論