Congenital hyperammonemia, type I

Search Trials
A Study to Evaluate the Efficacy and Safety of Maralixibat in Subjects With Progressive Familial Intrahepatic Cholestasis (MARCH-PFIC)
Status:
Recruiting
Last Changed:
Aug 7, 2019
First Changed:
Apr 5, 2019
Disease(s):
Progressive Familial Intrahepatic Cholestasis (PFIC)
Intervention(s):
MaralixibatPlacebo
A Placebo-controlled Study of Maralixibat (SHP625) in Pediatric Subjects With Progressive Familial Intrahepatic Cholestasis (PFIC)
Status:
Withdrawn
Last Changed:
Mar 18, 2019
First Changed:
Nov 27, 2017
Disease(s):
Progressive Familial Intrahepatic Cholestasis (PFIC)
Intervention(s):
MaralixibatPlacebo
Second-line Therapy of Unresectable Cholangiocarcinoma by RADIOEMBOLIZATION
Status:
Terminated
Last Changed:
Aug 7, 2013
First Changed:
Jun 28, 2011
Disease(s):
Cholestasis, Progressive Familial Intrahepatic 3
Intervention(s):
Yttrium microsphere injection
Human Heterologous Liver Cells for Infusion in Children With Urea Cycle Disorders
Status:
Completed
Last Changed:
Feb 8, 2016
First Changed:
Jul 18, 2008
Disease(s):
Urea Cycle Disorders
Intervention(s):
Human Heterologous Liver Cells
Manipulating the Gut Microbiome Study
Status:
Terminated
Last Changed:
Apr 5, 2019
First Changed:
Jun 9, 2017
Disease(s):
Urea Cycle Disorder
Intervention(s):
Acetohydroxamic Acid Oral Tablet [Lithostat]

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