Northwire Canada EditionMonday, July 13, 2026
Northwire
GLDN 0.055 +0.0% BRON 0.040 +0.0% BTO 5.43 −0.7% ESK 0.365 −2.7% AUMN 0.275 +0.0% GGX 0.040 +0.0% S 0.155 +29.2% NNX 0.035 +0.0% ABX 51.90 −0.6% TTS 2.40 −4.0% FCI 0.400 −9.1% GR 0.075 +0.0% AII 23.38 +12.4% TUNG 1.72 +1.8% LGO 1.01 −2.9% EMM 0.080 +0.0% GLDN 0.055 +0.0% BRON 0.040 +0.0% BTO 5.43 −0.7% ESK 0.365 −2.7% AUMN 0.275 +0.0% GGX 0.040 +0.0% S 0.155 +29.2% NNX 0.035 +0.0% ABX 51.90 −0.6% TTS 2.40 −4.0% FCI 0.400 −9.1% GR 0.075 +0.0% AII 23.38 +12.4% TUNG 1.72 +1.8% LGO 1.01 −2.9% EMM 0.080 +0.0%
Earnings Routine +

NervGen Pharma Reports Full Year 2025 Financial Results and Provides Business Updates

Clinical Validation Confirmed, Capital Runway Tightens Ahead of Phase 3 Pivot

Executive Summary
  • The March 31, 2026 release provides full-year 2025 financial results alongside a comprehensive business and clinical update.
  • Financials show $22.1M in cash and investments, up from $17.3M at year-end 2024, following a $10.05M private placement in November 2025. The reported net loss was $44.1M, heavily weighted by $24.8M in non-cash expenses.
  • Clinical data confirms the Phase 1b/2a CONNECT SCI trial met its primary endpoint, highlighting an 825% improvement in hand function versus placebo and statistically significant reductions in maladaptive reticulospinal activity.
  • Regulatory and development timelines are reiterated: FDA End-of-Phase 2 meeting completed, regulatory update expected early Q2 2026, and Phase 3 initiation targeted for mid-2026.
  • Management changes include the retirement of the CFO, the hiring of a Chief Regulatory Affairs Officer and an SVP of Patient Advocacy, and the termination of a negligible ATM program alongside a voluntary TSXV delisting.
Material Impact
  • The release is a scheduled confirmation of previously disclosed clinical and regulatory milestones. The 825% functional improvement and primary endpoint success were already communicated in November 2025, meaning the market has largely priced in this positive signal.
  • The financial disclosure is standard for a pre-revenue clinical-stage biotech. While the headline net loss is large, the actual cash burn is moderate relative to the raised capital. The $22.1M cash balance provides a clear runway to initiate Phase 3 but will not fund trial completion.
  • Leadership transitions and the TSXV delisting are administrative and operational adjustments that streamline costs but do not alter the fundamental investment thesis.
  • Overall, the news reinforces the existing trajectory without introducing new, unexpected catalysts or altering near-term valuation drivers.
NGEN · Price
Company Overview
  • NervGen Pharma is a clinical-stage biopharmaceutical company focused on developing neuroregenerative therapies for neurotraumatic and neurologic conditions.
  • Flagship asset: NVG-291, a neuroreparative peptide designed to restore neural connectivity and function following spinal cord injury (SCI). The program holds FDA Fast Track and EMA Orphan Drug designations.
  • The CONNECT SCI Phase 1b/2a trial targets chronic tetraplegia, demonstrating statistically significant improvements in upper-limb function, bladder control, and spasticity reduction, with durability observed up to 364 days post-treatment.
Read the original news release →

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