324. メチルグルタコン酸尿症 Methylglutaconic aciduria Clinical trials / Disease details


臨床試験数 : 4 薬物数 : 4 - (DrugBank : 3) / 標的遺伝子数 : 1 - 標的パスウェイ数 : 10

  
1 trial found
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1EUCTR2015-001382-10-GB
(EUCTR)
21/01/201924/08/2015A study comparing the drug 'bezafibrate' against a placebo in the treatment of Barth SyndromeTreatment of Barth Syndrome by CARDIOlipin MANipulation (CARDIOMAN): A randomised placebo controlled pilot trial conducted by the nationally commissioned Barth Syndrome Service - CARDIOMAN Barth Syndrome is a rare, life threatening, genetic disease which affects young males. It is caused by abnormal fats (lipids) in the powerhouses of cells (mitochondria) and those who suffer with it often develop heart failure, heart rhythm abnormalities, bacterial infections, poor growth or feeding, weak muscles, developmental delay, severe exercise intolerance, lethargy and fatigue.
MedDRA version: 20.0;Level: SOC;Classification code 10010331;Term: Congenital, familial and genetic disorders;System Organ Class: 10010331 - Congenital, familial and genetic disorders ;Therapeutic area: Diseases [C] - Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Trade Name: Bezafibrate
Product Name: Bezafibrate
INN or Proposed INN: Bezafibrate (INN 3968)
University Hospitals Bristol NHS Foundation TrustNULLAuthorised-recruitment may be ongoing or finished Female: no
Male: yes
15 Human pharmacology (Phase 1): no Therapeutic exploratory (Phase 2): yes Therapeutic confirmatory - (Phase 3): no Therapeutic use (Phase 4): noUnited Kingdom