Long Term Safety and Efficacy of Pasireotide s.c. in Patients With Cushing's Disease
Status:
Recruiting
Trial end date:
2024-05-01
Target enrollment:
Participant gender:
Summary
This is a non-interventional, multinational, multi-center post-marketing study, to further
document the safety and efficacy of pasireotide s.c. administered in routine clinical
practice in patients with Cushing's disease. Patients with Cushing's disease and treated with
pasireotide s.c. alone and in combination with other therapies will be monitored. For this
study, each enrolled patient will be followed up for 3 years after enrollment. Patients who
permanently discontinue pasireotide s.c. prior to completing the 3-year observation period
will be followed up for 3 months after the last dose of pasireotide s.c.