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Effects of triheptanoin (UX007) in patients with long-chain fatty acid oxidation disorders: Results from an open-label, long-term extension study.
Vockley, Jerry; Burton, Barbara; Berry, Gerard; Longo, Nicola; Phillips, John; Sanchez-Valle, Amarilis; Chapman, Kimberly; Tanpaiboon, Pranoot; Grunewald, Stephanie; Murphy, Elaine; Lu, Xiaoxiao; Cataldo, Jason.
Afiliação
  • Vockley J; University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
  • Burton B; Ann & Robert H. Lurie Children's Hospital, Chicago, Illinois, USA.
  • Berry G; Boston Children's Hospital, Boston, Massachusetts, USA.
  • Longo N; University of Utah, Salt Lake City, Utah, USA.
  • Phillips J; Vanderbilt University Medical Center, Nashville, Tennessee, USA.
  • Sanchez-Valle A; USF Health, Morsani College of Medicine, Tampa, Florida, USA.
  • Chapman K; Children's National Health System, Washington, District of Columbia, USA.
  • Tanpaiboon P; Children's National Health System, Washington, District of Columbia, USA.
  • Grunewald S; Great Ormond Street Hospital and Institute of Child Health, NIHR Biomedical Research Center (BRC), UCL, London, UK.
  • Murphy E; National Hospital for Neurology and Neurosurgery, London, UK.
  • Lu X; Ultragenyx Pharmaceutical Inc., Novato, California, USA.
  • Cataldo J; Ultragenyx Pharmaceutical Inc., Novato, California, USA.
J Inherit Metab Dis ; 44(1): 253-263, 2021 01.
Article em En | MEDLINE | ID: mdl-32885845
ABSTRACT
Long-chain fatty acid oxidation disorders (LC-FAOD) are autosomal recessive conditions that impair conversion of long-chain fatty acids into energy, leading to significant clinical symptoms. Triheptanoin is a highly purified, 7-carbon chain triglyceride approved in the United States as a source of calories and fatty acids for treatment of pediatric and adult patients with molecularly confirmed LC-FAOD. CL202 is an open-label, long-term extension study evaluating triheptanoin (Dojolvi) safety and efficacy in patients with LC-FAOD. Patients rolled over from the CL201 triheptanoin clinical trial (rollover); were triheptanoin-naïve (naïve); or had participated in investigator-sponsored trials/expanded access programs (IST/other). Results focus on rollover and naïve groups, as pretreatment data allow comparison. Primary outcomes were annual rate and duration of major clinical events (MCEs; rhabdomyolysis, hypoglycemia, and cardiomyopathy events). Seventy-five patients were enrolled (24 rollover, 20 naïve, 31 IST/other). Mean study duration was 23.0 months for rollover, 15.7 months for naïve, and 34.7 months for IST/other. In the rollover group, mean annualized MCE rate decreased from 1.76 events/year pre-triheptanoin to 0.96 events/year with triheptanoin (P = .0319). Median MCE duration was reduced by 66%. In the naïve group, median annualized MCE rate decreased from 2.33 events/year pre-triheptanoin to 0.71 events/year with triheptanoin (P = .1072). Median MCE duration was reduced by 80%. The most common related adverse events (AEs) were diarrhea, abdominal pain/discomfort, and vomiting, most mild to moderate. Three patients had serious AEs (diverticulitis, ileus, rhabdomyolysis) possibly related to drug; all resolved. Two patients had AEs leading to death; neither drug related. Triheptanoin reduced rate and duration of MCEs. Safety was consistent with previous observations.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Oxirredução / Triglicerídeos / Ácidos Graxos / Erros Inatos do Metabolismo Lipídico Tipo de estudo: Clinical_trials Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged País como assunto: America do norte / Europa Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Oxirredução / Triglicerídeos / Ácidos Graxos / Erros Inatos do Metabolismo Lipídico Tipo de estudo: Clinical_trials Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged País como assunto: America do norte / Europa Idioma: En Ano de publicação: 2021 Tipo de documento: Article