29
Participants
Start Date
February 1, 2011
Primary Completion Date
October 6, 2021
Study Completion Date
March 2, 2023
Pasireotide Long Acting Release (LAR)
Pasireotide will be administered as an intramuscular injection at the beginning of every cycle which is defined as 28 days (+/- 3 days). Study treatment should begin within 14 days following enrollment into the study and continue until disease progression, unacceptable toxicity, or withdrawal of consent.
H. Lee Moffitt Cancer Center and Research Institute, Tampa
Stanford Cancer Institute, Stanford
Collaborators (1)
Novartis Pharmaceuticals
INDUSTRY
RECORDATI GROUP
INDUSTRY
H. Lee Moffitt Cancer Center and Research Institute
OTHER