Overview

Lanreotide as Treatment of Polycystic Livers

Status:
Completed
Trial end date:
1969-12-31
Target enrollment:
0
Participant gender:
All
Summary
To assess the efficacy of lanreotide in controling total liver volume in patients with polycystic livers this study will be performed. A minimum of 38 patients will be recruited and randomized (1:1) to receive either verum or placebo. Lanreotide is already used in other disease states and found to be safe and non-toxic.
Phase:
Phase 2/Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Radboud University
Collaborator:
Ipsen
Treatments:
Angiopeptin
Lanreotide
Somatostatin
Criteria
Inclusion Criteria:

- 18 yrs-of age

- Multiple cysts > 20

- Cooperating patient

- Is willing and able to comply with the study drug regimen and all other study
requirements

- Willingness to give written informed consent

Exclusion Criteria:

- Use of oral anticonceptives or estrogen suppletion

- Females who are pregnant or breast-feeding

- History or other evidence of chronic pulmonary disease associated with functional
limitation

- History of severe cardiac disease

- History or other evidence of severe illness or any other conditions which would make
the patient, in the opinion of the investigator, unsuitable for the study

- Symptomatic gallstones

- Renal failure requiring hemodialysis