Clinical Trials · NCT00216372

Efficacy and Safety of Lanreotide Microparticles as Palliative Treatment in Peritoneal Carcinomatosis

CompletedPhase 3Lanreotide (Approved)
Phase
Phase 3
Recruitment status
Completed
Sponsor
Ipsen
Enrollment
80
Start date
Sep 2003
Locations
53 sites, 3 countries
Primary endpoint
Percentage of responder patients (patient with 1 or less vomiting episode per day during at least 3 consecutive days or in whom nasogastric tube (NGT) has been removed during at least three consecutive days without vomiting recurrence)
View Lanreotide compound reference