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Allothera

Treating neuropathic pain at the source

Allothera is developing first-in-class small-molecule STOML3 antagonists for neuropathic pain, with the goal of shifting treatment from broad symptomatic pain control to mechanism-based modulation of pain perception at the peripheral origin. The project is built on a decade of high-quality research and aims to translate validated biology into a differentiated therapeutic and diagnostic platform.

Problem​

Neuropathic pain affects a large patient population and remains poorly treated: current options such as pregabalin, gabapentinoids, antidepressants, lidocaine/​capsaicin, and opioids often deliver limited relief, while causing sedation, dizziness, burning, addiction risk, or other side effects. The core issue is that today’s standard of care mostly dampens pain transmission rather than addressing the underlying peripheral sensitization that drives touch-evoked pain.

Solution​

Allothera’s solution is to inhibit STOML3, a peripheral mechanotransduction regulator that amplifies mechanosensitive channel activity and drives pathological mechanical hypersensitivity. The lead program has already shown strong preclinical and translational validation: STOML3 antagonists reverse mechanically evoked currents in sensory models, reduce pain behavior in animal models, and have evidence of activity in human iPSC-derived sensory neurons, supporting both therapeutic and biomarker-guided patient stratification potential.

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News and Background

Founding Team

Funded by

Helmholtz enterprise

Website

Allothera.com