Northwire Canada EditionFriday, October 16, 2026
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GOLD 4184.00 +0.3% SILVER 57.27 +0.2% COPPER 6.57 +0.2% OIL 98.64 +0.7% PALLADIUM 1116.25 −1.1% MON 0.385 −6.1% OMI 0.250 +0.0% BUFF 0.800 +2.6% FEO 0.650 +0.0% LIB 0.700 −2.8% NPR 0.620 +0.0% QZM 0.380 +0.0% BVA 0.770 +1.3% ONAU 0.530 +1.9% FMR 0.225 +0.0% GSVR 0.350 +2.9% PHNM 0.345 +1.5% SLG 5.54 −3.0% CASA 0.060 +0.0% DRY 0.220 +2.3% SOMA 0.570 +1.8% GOLD 4184.00 +0.3% SILVER 57.27 +0.2% COPPER 6.57 +0.2% OIL 98.64 +0.7% PALLADIUM 1116.25 −1.1% MON 0.385 −6.1% OMI 0.250 +0.0% BUFF 0.800 +2.6% FEO 0.650 +0.0% LIB 0.700 −2.8% NPR 0.620 +0.0% QZM 0.380 +0.0% BVA 0.770 +1.3% ONAU 0.530 +1.9% FMR 0.225 +0.0% GSVR 0.350 +2.9% PHNM 0.345 +1.5% SLG 5.54 −3.0% CASA 0.060 +0.0% DRY 0.220 +2.3% SOMA 0.570 +1.8%
Financings

Eupraxia Pharmaceuticals Announces Proposed Public Offering

EPRX · Price

Executive Summary

  • Eupraxia Pharmaceuticals filed a preliminary prospectus supplement to its short‑form base shelf prospectus in connection with a proposed public offering of common shares (or pre‑funded warrants).
  • The company has granted underwriters a 30‑day option to purchase up to an additional 15% of the offered securities.
  • Net proceeds are intended primarily for advancing EP‑104GI (Eosinophilic Esophagitis) through preclinical work, Phase 2 and Phase 3 clinical development, manufacturing scale‑up, and broader gastrointestinal indications, as well as other R&D, business development, IP expansion, and general corporate purposes.

Key Details

  • Supplement Filing: Preliminary prospectus supplement filed with the SEC (Form‑10) and SEDAR; Base Prospectus dated February 5 2024.
  • Offering Structure: Common shares (or pre‑funded warrants to purchase common shares). Underwriters may exercise a 30‑day option for up to an additional 15% of the offered securities.
  • Book‑Running Managers: Cantor and LifeSci Capital (joint book‑running managers); Bloom Burton acting as co‑manager.
  • Pricing & Size: To be determined at pricing; final terms will be set in the market context. No specific price or gross proceeds disclosed.
  • Use of Proceeds – Primary:
  • Completion of ongoing preclinical studies for EP‑104GI.
  • Execution of Phase 2 clinical trials and preparation for Phase 3, including regulatory submissions.
  • Manufacturing activities to support eventual product launch.
  • Use of Proceeds – Secondary:
  • Expansion of EP‑104GI into additional gastrointestinal indications (esophageal strictures, fibrostenotic Crohn’s disease).
  • Research & development of other pipeline candidates.
  • Business development initiatives and general corporate purposes (salaries, working capital, leases, administrative expenses, capex).
  • Expansion of intellectual property portfolio and strengthening of corporate infrastructure.

Notable Quotes

No executive quotes were included in the release.

Read the original news release →

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