Stock Markets February 19, 2026

Eupraxia Pharmaceuticals Shares Decline After $55 Million Equity Offering Is Priced

Clinical-stage biotech sells common stock and pre-funded warrants to raise capital for EP-104GI development and broader pipeline work

By Ajmal Hussain EPRX
Eupraxia Pharmaceuticals Shares Decline After $55 Million Equity Offering Is Priced
EPRX

Eupraxia Pharmaceuticals Inc. (NASDAQ:EPRX) saw its shares fall about 8% on Thursday following the announcement of a priced public offering expected to raise roughly $55 million in gross proceeds. The clinical-stage company is issuing common shares and pre-funded warrants, and has granted underwriters an option to purchase additional shares. Proceeds will be directed primarily to development of EP-104GI for Eosinophilic Esophagitis and related gastrointestinal programs, with remaining funds earmarked for pipeline R&D, business development, and general corporate needs.

Key Points

  • Eupraxia priced a public offering totaling 6,428,574 common shares at $7.00 per share and pre-funded warrants for 1,428,571 common shares at $6.99999 each, expected to raise about $55 million in gross proceeds.
  • Underwriters can purchase an additional 1,178,571 common shares within 30 days on the same terms; closing is expected on February 20, 2026, subject to customary conditions.
  • Proceeds are primarily allocated to advancing EP-104GI for Eosinophilic Esophagitis and related gastrointestinal indications, plus R&D, business development, and general corporate purposes, impacting the biotech and healthcare sectors as well as market financing activity.

Eupraxia Pharmaceuticals Inc. (NASDAQ:EPRX) experienced an approximate 8% drop in its share price on Thursday after the company disclosed the pricing terms for a previously announced public offering.

The company is offering 6,428,574 common shares at $7.00 per share and is also selling pre-funded warrants exercisable for up to 1,428,571 common shares at $6.99999 per warrant. The transaction is anticipated to produce around $55 million in gross proceeds prior to underwriting commissions and other offering expenses.

Underwriters have been granted a 30-day option to buy up to an additional 1,178,571 common shares on the same terms as the base offering. The deal is scheduled to close on February 20, 2026, subject to customary closing conditions.

Cantor and LifeSci Capital are acting as joint book-running managers, while Bloom Burton and Craig-Hallum are serving as co-managers for the offering.

Use of proceeds

  • The company intends to use the majority of the proceeds to advance EP-104GI for the treatment of Eosinophilic Esophagitis, including completing ongoing preclinical studies and Phase 2 clinical trials, preparing for Phase 3 trials, and funding manufacturing activities.
  • Proceeds will also support the expansion of clinical studies for EP-104GI into other gastrointestinal indications such as esophageal strictures and fibrostenotic Crohn's disease.
  • A portion of the funds is planned for research and development of additional pipeline candidates, business development initiatives, and general corporate purposes, which the company identifies to include employee salaries, working capital, and facility leases.

Eupraxia bases its therapeutic approach on its Diffusphere™ technology, designed to enable localized, controlled drug delivery for conditions with important unmet medical needs.


The market reaction - an immediate decline in the company's stock price - followed the financing announcement. The offering structure combines direct common share issuance with pre-funded warrants, and includes an overallotment option for the underwriters.

Risks

  • Market risk associated with the dilutive effect of the new shares and pre-funded warrants, which influenced the immediate decline in the company’s stock price - a concern for equity investors and capital markets participants.
  • Financing-related closing risk, since the offering is subject to customary closing conditions and has not yet closed, affecting transaction certainty for stakeholders.
  • Clinical and development risk implicit in allocating proceeds to EP-104GI and additional pipeline R&D, where advancement through clinical stages and manufacturing activities may influence future corporate value and resource needs, affecting the biotech and pharmaceutical sectors.

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