Northwire Canada EditionFriday, October 16, 2026
Northwire
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GOLD 4170.10 +1.5% SILVER 57.16 +2.3% COPPER 6.56 −1.5% OIL 97.97 +3.0% PALLADIUM 1136.00 +3.6% LUN 32.91 +0.6% DLP 0.290 −3.3% VCV 0.065 −13.3% GG 2.89 +1.4% NBLC 0.015 +0.0% SF 0.300 −4.8% ATY 0.215 +2.4% GHL 0.060 −7.7% STND 0.060 −7.7% B 0.550 −3.5% HBM 34.33 −0.5% NTR 98.77 −0.7% SGZ 0.035 +0.0% MKA 0.670 +0.0% LXM 0.175 −18.6% CLCH 1.08 −1.8% GOLD 4170.10 +1.5% SILVER 57.16 +2.3% COPPER 6.56 −1.5% OIL 97.97 +3.0% PALLADIUM 1136.00 +3.6% LUN 32.91 +0.6% DLP 0.290 −3.3% VCV 0.065 −13.3% GG 2.89 +1.4% NBLC 0.015 +0.0% SF 0.300 −4.8% ATY 0.215 +2.4% GHL 0.060 −7.7% STND 0.060 −7.7% B 0.550 −3.5% HBM 34.33 −0.5% NTR 98.77 −0.7% SGZ 0.035 +0.0% MKA 0.670 +0.0% LXM 0.175 −18.6% CLCH 1.08 −1.8%
Earnings

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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