
Eupraxia Pharmaceuticals (NASDAQ: EPRX) is drawing fresh investor attention as Craig-Hallum raises its price target to $14 following a series of noteworthy pipeline updates and recent clinical trial momentum for its lead asset, EP-104GI, targeting eosinophilic esophagitis (EoE) and broader gastrointestinal indications.
Craig-Hallum Report Highlights
Craig-Hallum’s October 2, 2025, note reiterates a Buy rating for Eupraxia and boosts its price target from $12 to $14, citing EP-104GI’s eventful year ahead, strong clinical data in EoE, and plans to expand the asset to new GI indications in 2026. The report underscores Eupraxia’s robust cash position (~$100M) post-September 2025 offering and clinical runway now stretching into 2028, allowing the company to leverage its proprietary Diffusphere drug delivery technology. Key financial modeling includes projected royalty streams from EP-104IAR in knee osteoarthritis and EP-104GI in Crohn’s disease, estimating total revenues from EP-104 to possibly reach $1 billion by 2035 and $1.7 billion by 2038.
Latest Clinical Momentum
Operational updates in September 2025 confirm first patient dosing in the placebo-controlled Phase 2b portion of the RESOLVE trial for EP-104GI, with topline data expected in H2 2026. The positive nine-month data from cohorts in the Phase 1b/2a dose-escalation segment supports EP-104GI’s promise for durable, deep tissue responses—three patients showed sustained or improved outcomes after nine months, with no serious adverse events. Eupraxia now plans to expand Phase 2b to 120 patients, with critical data readouts in late 2025 and early 2026, reinforcing its leadership in EoE innovation.
Competitive Landscape
EP-104GI’s extended-release, localized delivery mechanism sets it apart from oral or injectable biologics, potentially offering up to 12 months of treatment from a single injection—addressing major pain points like cost, compliance, and repeated administration. This innovation comes as the EoE market, currently dominated by Takeda’s Eohilia and Sanofi’s (SNY) Dupixent, is expected to reach $2.8 billion by 2030. Eupraxia also faces competitive pressure from emerging therapies such as Bristol Myers Squibb’s (BMY) Cendakimab and AstraZeneca’s (AZN) Tezepelumab. Nevertheless, EP-104GI’s unique profile and expanding label opportunities position it as a disruptive contender.
Analyst Consensus and Investor Sentiment
Eupraxia’s stock has seen marked volatility, surging 20% post-market after groundbreaking RESOLVE data in late September 2025. Independent analyst forecasts reflect consensus “Strong Buy” ratings, with price targets as high as $14 (Craig-Hallum), $12 (Chimera Research Group), and $11.50 from broader market consensus, projecting substantial upside from current levels. Analysts cite upcoming clinical catalysts, strong cash reserves, and significant addressable markets as fueling Eupraxia’s investment thesis. Eupraxia’s stock at $5.92 is currently up +124.24% over the last year period.
Looking Forward
With pipeline expansion planned into new GI indications including Crohn’s disease and benign esophageal strictures, Eupraxia is expected to initiate new trials in 2026—potentially unlocking additional revenue streams and opportunities for partnerships. Key risks remain, including clinical, regulatory, and commercial uncertainty, but ongoing investor interest and Wall Street analyst support suggest growing optimism for Eupraxia’s future.
The Sum…
Eupraxia Pharmaceuticals (NASDAQ: EPRX) stands at a strategic crossroads, armed with robust clinical momentum and capital resources, poised to challenge entrenched therapies and redefine long-term care standards in the EoE treatment market and beyond.
The Sources…
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