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Eupraxia Pharmaceuticals Announces Closing of Overnight Marketed Offering for Gross Proceeds of C$33.9 Million

Eupraxia Pharmaceuticals Announces Closing of Overnight Marketed Offering for Gross Proceeds of C$33.9 Million

Eupraxia Pharmicals宣佈完成隔夜上市發行,總收益爲3,390萬加元
GlobeNewswire ·  03/15 08:26

NOT FOR DISSEMINATION IN THE UNITED STATES OR THROUGH U.S. NEWSWIRE SERVICES

不得在美國或通過美國新聞線服務傳播

VICTORIA, British Columbia, March 15, 2024 (GLOBE NEWSWIRE) -- Eupraxia Pharmaceuticals Inc. ("Eupraxia" or the "Company") (TSX: EPRX), a clinical-stage biotechnology company, today announced that it has closed its previously announced overnight marketed public offering (the "Offering") of common shares of the Company (the "Shares"). Pursuant to the Offering, Eupraxia issued 8,260,435 Shares at a price of C$4.10 per Share for gross proceeds of C$33,867,784, which includes the issuance of 943,435 Shares upon exercise of the over-allotment option.

2024年3月15日,卑詩省維多利亞社—Eupraxia Pharmaceuticals Inc. ("Eupraxia" or the "Company") (TSX: EPRX),一家臨床生物技術公司,今天宣佈已完成公司的公開發行("Offering")並賣出了共8,260,435股普通股("Shares"),每股出售價爲4.10加元,總募集資金爲33,867,784加元。該募集資金包括943,435股超額認購權的股份。

Eupraxia expects to use the net proceeds of the Offering, together with its existing cash and cash equivalents, primarily to fund research and development activities, general and administrative expenses, a milestone payment, working capital needs and other general corporate purposes.

Eupraxia預計將與現有的現金及現金等價物一起,主要用於資助研究開發,一般和行政支出,里程碑付款,經營資本需求和其他一般公司用途。

The Common Shares were offered pursuant to a final prospectus supplement dated March 12, 2024 to the Company's short form base shelf prospectus dated February 5, 2024. The Common Shares were offered in each of the provinces of Canada, except Québec.

普通股是根據公司2024年2月5日的短期基準股份發售備忘錄和2024年3月12日的最終發售備忘錄內容進行發售的。該股票在加拿大各省(不包括魁北克)中發售。

Raymond James Ltd. acted as sole underwriter and bookrunner for the Offering.

Raymond James Ltd.代表公司擔任本次公開發售的唯一承銷商和包銷商。

No securities regulatory authority has either approved or disapproved the contents of this press release. This press release shall not constitute an offer to sell or the solicitation of an offer to buy nor shall there be any sale of the common shares in the United States or in any province, state or jurisdiction in which such offer, solicitation or sale would be unlawful prior to the registration or qualification under the securities laws of any such province, state or jurisdiction. The securities have not been registered under the United States Securities Act of 1933, as amended, and may not be offered or sold in the United States absent registration or an applicable exemption from the registration requirements thereunder. The Company does not intend to register any part of the Offering in the United States, and any public offering of securities to be made in the United States will only be made by means of a prospectus that may be obtained from the issuer and that will contain detailed information about the Company and management, as well as financial statements.

沒有證券監管機構批准或駁回本新聞稿的內容。該新聞稿不構成任何出售或要約購買的要約,也不應在任何國家、地區或司法管轄區中出售。該證券未根據《美國證券法》修正案進行註冊,除非在任何此類省份、州份或司法管轄區中根據證券法的註冊或資格,否則不得提供或出售上述證券。公司不打算在美國註冊任何發售股票的部分,任何在美國發售的證券都只能通過發佈將詳細信息可從發行人處獲得的發售說明書進行。該說明書將包含有關公司、管理層以及財務報表的詳細信息。

About Eupraxia Pharmaceuticals Inc.

有關前瞻性聲明和信息的注意事項

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.

Eupraxia是一家臨床生物技術公司,專注於開發具有高未滿足醫療需求的治療領域潛力的局部遞送延遲釋放產品。公司致力於提供更好的患者受益,並開發了旨在提供有針對性,持久活性和副作用較少的技術。

Notice Regarding Forward-Looking Statements and Information

有關前瞻性聲明和信息的注意事項

This press 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", "estimates", "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 press release include statements regarding the use of the proceeds of the Offering and the business of the Company.

本新聞稿包含有關前瞻性陳述和前瞻性信息,根據適用證券法的規定進行。通常情況下,但並非總是如此,前瞻性信息可以通過使用諸如"計劃","期望","預計","安排","打算","考慮","預測","相信","建議","估計","潛在"或這些字詞和短語(包括否定的和語法上的變化)的變體,或者說明某些行動、事件或結果"可能","可能","將","可能"或"將要"被採取、發生或實現。本新聞稿中的前瞻性聲明包括有關Eupraxia的業務情況和本發售所募集資金的用途的聲明。

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 press 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). 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.

此類陳述和信息基於Eupraxia管理層的當前預期,並基於假設,包括但不限於:公司未來的研究和開發計劃將基本按照當前的設想進行;行業增長趨勢,包括關於預計和實際行業銷售的情況;公司能否從其研究開發活動,包括臨床試驗中獲得積極結果;公司能否保護專利和專有權利。儘管Eupraxia的管理層認爲這些聲明和信息的基礎是合理的,但它們可能被證明是不正確的。這個新聞稿中討論的前景和情況可能不會在某些日期或根本不會發生,並且可能因已知和未知的風險因素和不確定性影響Eupraxia,包括但不限於:與公司有限的經營歷史有關的風險和不確定性;公司新技術的市場認可性不確定;如果公司違反任何授權第三方許可其產品候選品或技術的協議,公司可能會失去對其業務具有重要意義的授權權利;公司的現有許可協議可能無法爲其被授權方的違約提供足夠的賠償;公司的技術可能無法成功用於其預期用途;公司未來的技術將需要獲得監管審批,這是昂貴的,公司可能無法獲得它;公司可能無法成功獲得監管批准或僅獲批准用於有限的用途或適應症;公司的臨床試驗可能無法充分證明其產品候選品在任何臨床開發階段的安全性和有效性;公司可能需要暫停或終止臨床試驗,因爲存在副作用或其他安全風險;公司完全依靠第三方提供其產品和服務所需的用品和輸入;公司依賴外部合同研究組織提供臨床和非臨床研究服務;公司可能無法成功執行其商業策略;公司將需要額外融資,這可能無法獲得;公司開發的任何治療方法都將受到廣泛的、漫長的和不確定的監管要求的影響,這可能會對公司及時獲得監管批准,或者根本不會獲得批准,產生不利影響;健康大流行或流行病對公司的運營的影響;公司的合併財務報表的重新陳述,可能導致其他風險和不確定性,包括投資者信心的喪失和對公司普通股價格的負面影響;以及在更多細節上更多地描述在Eupraxia對加拿大各省證券管理機構提出的申請,其公共檔案可在SEDAR+ (sedarplus.ca)上獲得的其他風險和不確定性。雖然Eupraxia已盡力確定可能導致實際行動、事件或結果與前瞻性陳述和信息所述行動、事件或結果有所不同的重要因素,但可能存在其他導致行動、事件或結果與預期、估計或意圖不符的因素。沒有任何前瞻性陳述或信息能夠保證實現。除非受到適用證券法的規定要求,否則前瞻性陳述和信息僅於發表日期起專屬於Eupraxia,Eupraxia沒有義務公開更新或修訂任何前瞻性陳述或信息,無論是有新信息、未來事件或其他原因引起的。

For investor and media inquiries, please contact:

投資者和媒體諮詢,請聯繫:

Danielle Egan, Eupraxia Pharmaceuticals Inc.
778.401.3302
degan@eupraxiapharma.com

Danielle Egan,Eupraxia Pharmaceuticals Inc。
778.401.3302
degan@eupraxiapharma.com

or

或者

Adam Peeler, on behalf of:
Eupraxia Pharmaceuticals Inc.
416.427.1235
adam.peeler@loderockadvisors.com

代表Eupraxia Pharmaceuticals Inc。的Adam Peeler
Eupraxia Pharmaceuticals Inc。
416.427.1235
adam.peeler@loderockadvisors.com

Source: Eupraxia Pharmaceuticals Inc.

來源:Eupraxia Pharmaceuticals Inc。


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