An Observational Study of Octreotide Subcutaneous Depot in Patients With Acromegaly
Conditions: Acromegaly
Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Enrollment: 200
Sponsor: Camurus AB
Location: Universitaetsklinikum Aachen Aachen
Summary
The purpose of this study is to collect long-term (up to two years) safety and effectiveness of octreotide subcutaneous depot in patients with acromegaly in the real-world setting.
Eligibility Criteria
Inclusion Criteria:
* Have started or will be starting treatment with octreotide SC depot for acromegaly
Exclusion Criteria:
* Have started or will be starting treatment with octreotide SC depot for other conditions not related to acromegaly
* Currently taking part in an interventional clinical trial or is still within a 30-day washout period from the end of taking part in an interventional clinical trial.
Interested in this study? View the official listing for contact and enrollment details.