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VICTORIA, BC,Feb. 11, 2021/CNW/ – Eupraxia Pharmaceuticals Inc. (“Eupraxia” or the “Company”), a Phase 2 clinical-stage biotechnology company with an innovative drug delivery technology platform, today announced that it has filed a preliminary prospectus in connection with a proposed initial public offering (the “Offering“) of common shares of the Company (the “Common Shares“) for gross proceeds of up to$50,000,000. The Offering will be conducted on a best efforts basis by a syndicate of agents (the “Agents“) led by Raymond James Ltd., as lead agent and sole bookrunner, together with BMO Nesbitt Burns Inc. and Canaccord Genuity Corp.
The preliminary prospectus has been filed with the securities commissions in each of the provinces of Canada, except Québec, and contains important information relating to the Company, the Offering and the Common Shares. The preliminary prospectus remains subject to completion or amendment. There will not be any sale or any acceptance of an offer to buy the Common Shares until a receipt for the final prospectus has been issued by the relevant securities commissions in Canada.
A copy of the preliminary prospectus may be obtained under the Company’s profile at www.sedar.com.
No securities regulatory authority has either approved or disapproved of the contents of this press release. The Common Shares have not been and will not be registered under the United States Securities Act of 1933, as amended (the “U.S. Securities Act“) or any state securities laws. Accordingly, the Common Shares may not be offered or sold, directly or indirectly, in theUnited States, except pursuant to an exemption from the registration requirements of the U.S. Securities Act and applicable state securities laws. This press release does not constitute an offer to sell or a solicitation of an offer to buy any securities of the Company in any jurisdiction in which such offer, solicitation or sale would be unlawful.
Eupraxia is a clinical-stage biotechnology company focused on the development of locally delivered, extended-release alternatives to currently approved drugs. Each of Eupraxia’s product candidates has the potential to address therapeutic areas with high unmet medical need, and strives to provide improved patient benefit by delivering targeted, long-lasting activity with fewer side effects.
Eupraxia’s lead product candidate, EP-104IAR, is currently in Phase 2 development for the treatment of pain due to osteoarthritis of the knee.
In addition to EP-104IAR, Eupraxia is developing a pipeline of earlier-stage long-acting formulations. Potential pipeline candidates include a range of drugs for indications such as post-surgical pain (EP-105), and post-surgical site infections (EP-201), each designed to improve on the activity and tolerability of approved drugs. Eupraxia is also developing a formulation of EP-104IAR for use in canine and equine osteoarthritis.
Notice Regarding Forward-looking Statements and Information:
This news release includes forward-looking statements and forward–looking information within the meaning of Canadian 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” 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 Offering, including the successful completion of the Offering and the company obtaining a receipt for a final prospectus, the Company’s plans, focus and objectives 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 and subject to risks and uncertainties. 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 the risk factors set forth in the Company’s preliminary prospectus under the heading “Risk Factors”. 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.
SOURCE Eupraxia Pharmaceuticals Inc.
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