drugset / Trial / NCT01315795

Lanreotide Autogel in the Treatment of Symptomatic Polycystic Liver Disease

NCT01315795

Phase 2/3 Completed 59 enrolled Universitaire Ziekenhuizen KU Leuven Ipsen · collab
NaSingle-groupOpen-labelTreatment

Summary

An open-label, Phase II clinical study to evaluate the efficacy and safety of lanreotide autogel 90mg every 4 weeks in the treatment of symptomatic polycystic liver disease, including a dose escalation at month 6 to lanreotide autogel 120mg for non responders.

Timeline

Start
2011-03
Primary completion
2014-07
Completion
2014-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Lanreotide Other / unclassified 90 mg Subcutaneous
Subject Lanreotide Other / unclassified 120 mg Subcutaneous

Indications