A Real-world Study of Octreotide Microspheres in Chinese Patients With Neuroendocrine Tumors
Condition(s) studied
Investigational drug(s) / intervention(s)
Octreotide microspheres: 20mg/30mg Q4W
Study summary
The aim of this multicenter, open-label, observational study is to evaluate the safety and efficacy of octreotide microspheres in the treatment of advanced neuroendocrine tumors in real clinical practice, especially to evaluate the treatment of octreotide microspheres in various subgroups of neuroendocrine tumor patients.
Eligibility
Primary outcome measure(s)
- Treatment Emergent Adverse Events — up to 46 months
Treatment emergent adverse events were recorded according to Common Terminology Criteria for Adverse Events (version 5.0) of the National Cancer Institute that participants received at least one dose of protocol treatment.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Qilu hospital of Shandong University | Jinan | Shandong |
More Qilu Hospital of Shandong University trials in China
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06300216 on ClinicalTrials.gov ↗ ← All trials in China