drugset / Trial / NCT01374906

Efficacy and Safety of Pasireotide Administered Monthly in Patients With Cushing's Disease

NCT01374906 ↗

Phase 3 Completed 150 enrolled Novartis Pharmaceuticals
RandomizedParallel-groupTriple-blindTreatment

Summary

This is a randomized, double-blind, multicenter, phase III study to evaluate the safety and efficacy of 2 dosing regiments of Pasireotide long acting release (LAR) in patients with Cushing's disease.

Timeline

Start
2011-11-04
Primary completion
2016-12-21
Completion
2016-12-21

Outcome

Met primary endpoint

paper The primary efficacy endpoint was met by 31 (41·9% [95% CI 30·5-53·9]) of 74 patients in the 10 mg group and 31 (40·8% [29·7-52·7]) of 76 in the 30 mg group. PMID 29032078 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Pasireotide Other / unclassified 10 mg Intramuscular
Subject Pasireotide Other / unclassified 30 mg Intramuscular