Clinical Trials Logo

GM2 Gangliosidoses clinical trials

View clinical trials related to GM2 Gangliosidoses.

Filter by:
  • Completed  
  • Page 1

NCT ID: NCT00672022 Completed - Sandhoff Disease Clinical Trials

Pharmacokinetics, Safety and Tolerability of Zavesca (Miglustat) in Patients With Infantile Onset Gangliosidosis: Single and Steady State Oral Doses

Start date: July 2004
Phase: Phase 3
Study type: Interventional

We want to see if Zavesca (or miglustat) is safe and can be tolerated by patients with acute infantile onset GM2 gangliosidosis - classical Tay-Sachs and infantile onset Sandhoff disease. We know that miglustat inhibits the formation of GM2 ganglioside, the compound that is stored in the brains of children with Tay-Sachs and Sandhoff disease. Since it inhibits the synthesis of ganglioside, miglustat may be able to reduce or delay the onset of clinical symptoms.