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May 17, 20260 citationsOpen Access

Anti-Nogo-A NG101 treatment induces changes in spinal cord micro- and macrostructure following spinal cord injury

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LFLynn FarnerPSPaulina S ScheurenKSKiomars Sharifi

Key Points

  • This research aims to evaluate the structural changes induced by NG101 treatment in patients with spinal cord injury using MRI biomarkers.
  • Phase 2b NISCI trial involving 106 participants with acute cervical SCI.
  • Assessed lesion volume, tissue bridges, cross-sectional cord area, and myelin-sensitive metrics over six months.
  • Compared NG101 treatment group to placebo.
  • NG101-treated participants showed faster lesion volume reduction compared to placebo (exact metrics not specified).
  • Slower decline in cross-sectional cord area and MTsat in corticospinal tracts and dorsal columns was observed.
  • Multimodal analysis enhanced detection of clinical effects significantly.

Abstract

NG101 is a recombinant antibody that neutralizes the nerve growth inhibitor Nogo-A, promoting neural repair and improving upper extremity motor function in spinal cord injury (SCI). This study evaluated spinal cord MRI biomarkers to detect treatment-related structural changes and enhance patient stratification using data from 106 participants with acute cervical SCI in the phase 2b NISCI trial. We assessed lesion volume, tissue bridges, and remote changes in cross-sectional cord area (CSA), and tract-specific myelin-sensitive magnetization transfer saturation (MTsat) over six months. Compared to placebo, NG101-treated participants exhibited faster lesion volume reduction and a slower decline of CSA and MTsat in the corticospinal tracts and dorsal columns. Crucially, multimodal stratification incorporating MRI and electrophysiological measures substantially enhanced the detection of clinical treatment effects. These findings suggest NG101 slows trauma-induced progressive macro- and microstructural degeneration or promotes fiber sprouting. Combining MRI with electrophysiology enables sensitive detection of treatment effects and efficient trial designs. ClinicalTrials.gov identifier: NCT03935321.

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Cite This Study

Farner et al. (2026) studied this question.

synapsesocial.com/papers/6a095b1b7880e6d24efe0eafhttps://doi.org/10.5167/uzh-434121
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