drugset / Trial / NCT00446082

Study of Pasireotide Long Acting Release (LAR) Injection in Patients With Acromegaly and Patients With Carcinoid Disease

NCT00446082

Phase 1 Completed 85 enrolled Novartis Pharmaceuticals
NaSingle-groupOpen-labelTreatment

Summary

This study will assess the pharmacokinetic profile and the safety/tolerability profile of single and monthly doses of pasireotide LAR intramuscular (i.m.) injection in patients with acromegaly and patients with carcinoid disease

Timeline

Start
2006-06
Primary completion
2013-11
Completion
2013-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Pasireotide Other / unclassified 20 mg Intramuscular
Subject Pasireotide Other / unclassified 40 mg Intramuscular
Subject Pasireotide Other / unclassified 60 mg Intramuscular