Your browser doesn't support javascript.
loading
Clinical Trials in Mitochondrial Disease: An Update on EPI-743 and RP103
Enns, Gregory M.; NeuroDevelopmental Science CenterCohen, Bruce H..
Afiliação
  • Enns, Gregory M.; Stanford University. Department of Pediatrics. Division of Medical Genetics. Stanford. US
  • NeuroDevelopmental Science CenterCohen, Bruce H.; Akron Children's Hospital. Department of Pediatrics. NeuroDevelopmental Science CenterCohen, Bruce H.. Akron.
J. inborn errors metab. screen ; 5: e170011, 2017. tab
Article em En | LILACS-Express | LILACS | ID: biblio-1090926
Biblioteca responsável: BR1.1
ABSTRACT
Abstract Mitochondrial dysfunction results in the production of an abnormally high amount of reactive oxygen and nitrogen species, which results in redox imbalance and glutathione deficiency. Therapeutics such as EPI-743 (?-tocotrienol quinone) and RP103 (cysteamine bitartrate) have the theoretical potential to improve redox imbalance by increasing intracellular glutathione and are currently under investigation in multiple clinical trials. This review provides an update on the use of these compounds in clinical trials related to primary and secondary mitochondrial disorders. These clinical trials have not only provided hope to affected patients and their families and caregivers, but also will serve as important stepping stones for further studies as our understanding of mitochondrial disease pathogenesis continues to improve.
Palavras-chave

Texto completo: 1 Índice: LILACS Idioma: En Revista: J. inborn errors metab. screen Assunto da revista: Medicina Cl¡nica / Patologia Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Índice: LILACS Idioma: En Revista: J. inborn errors metab. screen Assunto da revista: Medicina Cl¡nica / Patologia Ano de publicação: 2017 Tipo de documento: Article