Autosomal dominant polycystic liver disease

MONDO:0000447

An autosomal dominant inherited condition characterized by many cysts of various sizes scattered throughout the liver.

Also known as: AD polycystic liver disease, ADPLD, PCLD, isolated congenital polycystic liver disease, isolated polycystic liver disease, polycystic liver disease, congenital cystic liver disease, congenital hepatic cyst

3 clinical trials for this condition and its sub-types, 3 tagged with Autosomal dominant polycystic liver disease itself.

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Where it sits in the disease tree

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Part of

↑ Liver disorder (3621) ↑ Autosomal dominant disease (699)

Sub-types of Autosomal dominant polycystic liver disease

SEC61B-related polycystic liver disease 0 trials
Polycystic liver disease 1 0 trials
Polycystic liver disease 2 0 trials
Polycystic liver disease 3 with or without kidney cysts 0 trials
Polycystic liver disease 4 with or without kidney cysts 0 trials

Including sub-types (3) Tagged with Autosomal dominant polycystic liver disease (3)

Trials to join now! 2 Not yet finished but already full! 1

New shot could shrink enlarged livers and ease pain

Disease control Ongoing

This study tests a drug called CAM2029 (octreotide) given as a weekly or every-other-week shot to people with symptomatic polycystic liver disease. The goal is to see if it can shrink the liver and reduce symptoms like belly pain, bloating, and nausea. About 71 adults with an enl…

Phase 2/3 • Sponsor: Camurus AB • Aim: Disease control

Last updated Jun 27, 2026 13:02 UTC

Autosomal dominant polycystic liver disease

Where it sits in the disease tree

New shot could shrink enlarged livers and ease pain