drugset / Trial / NCT01364415

Dose Escalation Study of Pasireotide (SOM230) in Patients With Advanced Neuroendocrine Tumors (NETs)

NCT01364415

Phase 1 Completed 29 enrolled Novartis Pharmaceuticals
NaSingle-groupOpen-labelTreatment

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.

Timeline

Start
2011-08
Primary completion
2016-04
Completion
2016-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Pasireotide Other / unclassified 80 mg Intramuscular
Subject Pasireotide Other / unclassified 120 mg Intramuscular