Acceptability Study of a New Paediatric Form of Vigabatrin in Infants and Children With Infantile Spasms or Pharmacoresistant Partial Epilepsy

• Status: Completed
• Trial end date: 2016-12-01

Summary

The sponsor is developing a new paediatric formulation of vigabatrin to better adjust the dose to body weight and to limit waste of unused drug. The currently marketed vigabatrin (Sabril™) form only exists as 500 mg film coated tablets (for adults and children above 6 years) and 500 mg granules for oral solution sachets (for infants and children below 6 years). Sabril™ is not adapted for administration to infants when a fraction of the sachet is needed. Manual splitting of the sachet or lengthy and error-prone dilutions are often required.

This study is a descriptive, non-randomized, open label multi-centric acceptability study in infants and children affected with infantile spasms. The primary objective is to describe the adherence to the new formulation. Secondary objectives include:

• evaluation of the palatability and user-friendliness of the new treatment,

• evaluation of the pharmacokinetic parameters of the new formulation,

• PK parameters,

• evaluation of the tolerance,

• measurement of taurine plasma levels. This study will recruit up to 40 patients with infantile spasms and pharmacoresistant partial epilepsy aged 1 month to 6 years in 23 clinical sites in France.

• Phase: N/A

Details

• Lead Sponsor: Orphelia Pharma; Targeon SAS
• Collaborators: Hospices Civils de Lyon; Institut National de la Santé Et de la Recherche Médicale, France; National Research Agency, France
• Treatments: Vigabatrin