drugset / Trial / NCT02668172

Pasireotide LAR and Pegvisomant Study in Acromegaly

NCT02668172

Phase 4 Unknown 60 enrolled Erasmus Medical Center Novartis · collab
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The objective of this study is to assess the efficacy of Pasireotide Long Acting Release (LAR) alone and in combination with weekly Pegvisomant (PEGV) in acromegaIy patients previously controlled with combination treatment of long-acting Somatostatin analogs (LA-SSAs) and PEGV.

Timeline

Start
2015-08
Primary completion
2017-03
Completion
2017-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Pasireotide Other / unclassified 60 mg
Subject Pegvisomant Protein / enzyme biologic

Indications