drugset / Trial / NCT02780882
SOM230 Ectopic ACTH-producing Tumors
NaSingle-groupOpen-labelTreatment
Summary
The purpose of this prospective open-label phase II study, is to evaluate the efficacy of pasireotide twice daily subcutaneous injections for normalizing 24 hour urine free cortisol in patients with ectopic ACTH-producing tumors as measured by the proportion of patients achieving normal UFC at the end of the study period.
Timeline
- Start
- 2015-12
- Primary completion
- 2018-12
- Completion
- 2019-06
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Pasireotide | Other / unclassified | 900 ug | Subcutaneous |