123
Participants
Start Date
March 31, 2015
Primary Completion Date
January 8, 2018
Study Completion Date
September 27, 2018
Pasireotide LAR
Pasireotide 40 mg and 60 mg. Pasireotide 20 mg which was allowed for dose decrease in case of adverse event.
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Lead Sponsor
Novartis Pharmaceuticals
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