drugset / Trial / NCT02668172
Pasireotide LAR and Pegvisomant Study in Acromegaly
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Pasireotide | Other / unclassified | 60 mg | — |
| Subject | Pegvisomant | Protein / enzyme biologic | — | — |