GRIN Therapeutics Inc., a leader in development of therapies to treat GRIN-related disorders, today announced that the first patient has been dosed in the Honeycomb Study, the Company’s Phase 1B clinical trial of radiprodil, an investigational NR2B-negative allosteric modulator in development for the treatment of GRIN-related disorders. Radiprodil targets the hyperactive receptors associated with the development and progression of GRIN-related disorders by potently and selectively modulating the Nmethyl-D-aspartate (NMDA) receptor subtype 2B (NR2B).

“GRIN-related disorders represent a significant area of unmet need in healthcare and the initiation of the Honeycomb Study is a historic milestone for GRIN Therapeutics and for patients around the world who are in desperate need of new treatments,” said Michael A. Panzara, M.D., MPH, chief medical officer of Neurvati Neurosciences, the parent company of GRIN Therapeutics. “We continue to be inspired by the children and families affected by GRIN-related disorders and by the leaders from the treatment community who have supported this important research and are very grateful for their partnership.”

GRIN-related disorders are genetically defined, rare pediatric developmental and epileptic encephalopathies (DEEs) caused by mutations in the gene coding on the NMDA glutamate receptor. People living with GRIN-related disorders present with a spectrum of symptoms including epilepsy, behavioral disorders, autism, intellectual disability, and movement disorders. Currently, there are no disease-specific treatment options for GRIN-related disorders. Radiprodil is a small molecule that selectively targets NR2B-NMDA receptors that are overactive in GRIN-related disorders and that represent important potential targets in effective therapeutic intervention.

“When we identified the genes that cause GRIN-related disorders in 2014, we never imagined the collaboration that would be undertaken to get into the clinic so quickly,” stated Johannes Lemke, M.D., Head of Leipzig University Hospitals' Institute of Human Genetics. “Working together with GRIN Therapeutics to evaluate radiprodil in patients with GRIN-related disorders represents an important advancement and I look forward to the study results with anticipation and optimism.”

The open label Honeycomb phase 1B study will evaluate the safety, tolerability, pharmacokinetics, and effects on seizures, behavioral symptoms, sleep, and motor functions of multiple individually titrated doses of radiprodil in children with GRIN-related disorders. The trial will include up to 24 participants between the ages of six months and 12 years with confirmed gain-of-function (GoF) variants causing GRIN-related disorders, including variants on GRIN2B, GRIN2A, GRIN2D, and GRIN1. The trial will include one cohort of patients who have experienced drug resistant seizures with a frequency of at least once weekly and a second cohort including patients with behavioral and other symptoms who have experienced fewer or no seizures. The study will consist of a screening period, a titration period, and a maintenance period on the highest tolerated dose. Upon completion of treatment, participants will have the option to enter a long-term extension study.

 

Source:businesswire.com

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