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GRIN Therapeutics, Inc.

New York, New York, United Statesgrintherapeutics.com ↗

Ownership: Private
Development stage: Phase 3

Overview

Radiprodil showed positive results in Phase 1b Honeycomb trial, with patients experiencing a median 86% reduction in countable motor seizure frequency. The drug appeared generally well-tolerated, with 71% of patients having greater than 50% reduction in seizures. The company received FDA Breakthrough Therapy designation in February 2025 and Orphan Drug designation in March 2025 for radiprodil.

Therapeutic areas: Rare DiseasesNeurology
Modalities: Small molecules (specifically radiprodil, a negative allosteric modulator)
Industry: Biotech

Drug pipeline

1 asset

radiprodil

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