drugset / Trial / NCT01582061
An Open-label, Multi-center, Expanded Access Study of Pasireotide s.c. in Patients With Cushing's Disease.
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Pasireotide | Other / unclassified | 600 ug | Subcutaneous |
| Subject | Pasireotide | Other / unclassified | 900 ug | Subcutaneous |