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Clinical Trial Summary

This study designed to determine the Maximum Tolerated Dose (MTD) for patients with advanced Neuroendocrine Tumors (NETs) and to characterize the safety, tolerability, Pharmacokinetics and preliminary efficacy of pasireotide LAR administered i.m. once every 28 days.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01364415
Study type Interventional
Source Novartis
Contact
Status Completed
Phase Phase 1
Start date August 2011
Completion date April 2016

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