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Radiprodil

GRIN-related Neurodevelopmental Disorder (GRIN-NDD) with gain-of-function variants

Phase 3Active

Key Facts

Indication
GRIN-related Neurodevelopmental Disorder (GRIN-NDD) with gain-of-function variants
Phase
Phase 3
Status
Active
Company

About GRIN Therapeutics

GRIN Therapeutics, founded in 2020 and based in Cambridge, USA, is a private, pre-revenue biotech focused on developing small molecule therapeutics for severe pediatric neurodevelopmental disorders. The company's lead asset is radiprodil, an investigational therapy targeting dysregulated NMDA receptor activity, which is currently in a global Phase 3 trial for GRIN-NDD and being explored for other conditions like tuberous sclerosis complex. GRIN Therapeutics represents a precision medicine approach to a high-need, rare disease space with significant scientific and clinical validation potential.

View full company profile

About GRIN Therapeutics

GRIN Therapeutics, founded in 2020 and based in Cambridge, USA, is a private, pre-revenue biotech focused on developing small molecule therapeutics for severe pediatric neurodevelopmental disorders. The company's lead asset is radiprodil, an investigational therapy targeting dysregulated NMDA receptor activity, which is currently in a global Phase 3 trial for GRIN-NDD and being explored for other conditions like tuberous sclerosis complex. GRIN Therapeutics represents a precision medicine approach to a high-need, rare disease space with significant scientific and clinical validation potential.

View full company profile

About GRIN Therapeutics

GRIN Therapeutics, founded in 2020 and based in Cambridge, USA, is a private, pre-revenue biotech focused on developing small molecule therapeutics for severe pediatric neurodevelopmental disorders. The company's lead asset is radiprodil, an investigational therapy targeting dysregulated NMDA receptor activity, which is currently in a global Phase 3 trial for GRIN-NDD and being explored for other conditions like tuberous sclerosis complex. GRIN Therapeutics represents a precision medicine approach to a high-need, rare disease space with significant scientific and clinical validation potential.

View full company profile