Ireland
--:--IST
Starting soon Observational

A Real-world Study of Octreotide Microspheres in Chinese Patients With Neuroendocrine Tumors

NCT06300216 · tracked via the Priya Life Science China tracker
Phase
Observational
Started
2024-03-26
Last updated
2024-03-08

Condition(s) studied

Neuroendocrine Tumors

Investigational drug(s) / intervention(s)

Octreotide microspheres

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

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. Sign an informed consent form and voluntarily participate in this study; 2. Patients with unresectable or metastatic neuroendocrine tumors confirmed by histopathology. Patients with recurrence and progression after surgery or local treatment can also be included in the study; 3. Age ≥ 18 years old; 4. Treatment with octreotide microspheres. Exclusion Criteria: 1. Confirmed pregnant or lactating women; 2. Participating in any research with intervention measures outside of routine clinical practice; 3. Other situations unsuitable for inclusion in the study determined by the researcher.

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)

FacilityCityRegionStatus
Qilu hospital of Shandong University Jinan Shandong
Official registry record

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