Clinical Trials · NCT02396953

Study to Determine the Maximum Tolerated Dose, Safety and Tolerability of a Single Dose of Lanreotide Prolonged Release Formulation (PRF) in Subjects With Acromegaly

Phase
Phase 1/Phase 2
Recruitment status
Completed
Sponsor
Ipsen
Enrollment
28
Start date
Mar 2015
Locations
36 sites, 12 countries
Primary endpoint
Determination of the Maximum Tolerated Dose (MTD) by Number of Subjects With DLTs.
View Lanreotide compound reference