drugset / Trial / NCT01582061

An Open-label, Multi-center, Expanded Access Study of Pasireotide s.c. in Patients With Cushing's Disease.

NCT01582061

Phase 3 Completed 104 enrolled Novartis Pharmaceuticals
Non-randomizedSingle-groupOpen-labelTreatment

Summary

This study provided access to pasireotide sc in patients with Cushing's disease.and provided additional information for safety and efficacy of pasireotide s.c.

Timeline

Start
2011-08-16
Primary completion
2017-01-26
Completion
2017-01-26

Drugs

EvaluationDrugModalityDoseRoute
Subject Pasireotide Other / unclassified 600 ug Subcutaneous
Subject Pasireotide Other / unclassified 900 ug Subcutaneous

Indications