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Eupraxia Pharmaceuticals Inc. (T:EPRX)

Business Focus: Biotechnology & Medical Research (NEC)

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Insider Chart - Past 6 Months

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Insider Filings

Latest 10 SEDI filings for EPRX within the last 6 months
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Company News

May 05, 2022 17:00 ET
Eupraxia Pharmaceuticals Reports First Quarter 2022 Financial Results
VICTORIA, BC, May 5, 2022 /CNW/ - Eupraxia Pharmaceuticals Inc. ("Eupraxia" or the "Company") (TSX: EPRX), a Phase 2 clinical-stage biotechnology company with an innovative drug delivery technology platform, today announced its unaudited financial results (prepared in accordance with International Financial Reporting Standards or "IFRS") and operational highlights for the first quarter ended March 31, 2022. All amounts are expressed in Canadian dollars unless otherwise indicated.
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Apr 20, 2022 09:39 ET
IIROC Trade Resumption - EPRX.WT.A
TORONTO, April 20, 2022 /CNW/ - Trading resumes in:
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Valuation Ratios

Price to Sales - TTM
Price to Book - most recent quarter
Price to Cash Flow per share - TTM
Price to Free Cash Flow per share - TTM
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Short Report

DateNumber of Shares ShortedNet Change
Apr 30, 20226,775-145,585
Apr 15, 2022152,360147,150
Mar 31, 20225,210-3,039
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Business Summary

Sector:  Healthcare Industry:  Biotechnology & Medical Research

Eupraxia Pharmaceuticals Inc. is a Canada-based clinical-stage biotechnology company. The Company is focused on the development of locally delivered, extended-release alternatives to existing pharmaceuticals. Its lead product candidate, EP-104IAR, is designed to meet the unmet medical need and market demand for long-lasting pain relief for knee osteoarthritis (OA). EP-104IAR contains a solid core of the active ingredient Fluticasone Propionate (FP) with an outer layer of the biocompatible polymer, PVA. In addition to EP-104IAR, the Company is also developing a pipeline of earlier-stage long-acting formulations. It develops pipeline candidates for a range of indications, such as post-surgical pain (EP-105), and post-surgical site infections (EP-201). The Company has completed a phase I, double-blind, placebo-controlled clinical study at three sites in Canada.

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