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Biliary atresia

MONDO:0008867

A rare, biliary tract disease characterized by progressive obliterative cholangiopathy of the intra- and extrahepatic bile ducts, occurring in the embryonic/ perinatal period, leading to severe and persistent neonatal jaundice and acholic stool.

Also known as: atresia of bile ducts, biliary atresia, congenital, congenital biliary atresia, isolated atresia of bile ducts, non-syndromic biliary atresia, isolated biliary atresia

31 clinical trials for this condition and its sub-types, 24 tagged with Biliary atresia itself.

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Where it sits in the disease tree

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Part of

↑ Non-neoplastic bile duct disorder (172) ↑ Cholestasis (91)

Sub-types of Biliary atresia

Biliary atresia intrahepatic non syndromic form 0 trials
Biliary atresia intrahepatic syndromic form 0 trials
Extrahepatic biliary atresia 0 trials

Including sub-types (31) Tagged with Biliary atresia (24)

Trials to join now! 18 Not yet recruiting 1 Not yet finished but already full! 5 Completed 6 Terminated 1

Liver drug trial for kids with biliary atresia ends early

Disease control Stopped early

This study tested the drug obeticholic acid in children with biliary atresia who had already undergone Kasai surgery. The goal was to see if the drug could improve outcomes like avoiding liver transplant or death. The trial was terminated early and enrolled only 28 participants, …

Phase 2/3 • Sponsor: Intercept Pharmaceuticals • Aim: Disease control

Last updated Jul 09, 2026 00:00 UTC

Biliary atresia

Where it sits in the disease tree

Liver drug trial for kids with biliary atresia ends early