CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 71 enrolled
Drug / intervention
Lanreotide autogeldrug
Likely dose
Lanreotide autogel 120 mcgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04696042
NCT04696042N/ACompleted

Prospective Observational Study to Assess the Effectiveness and Safety of Lanreotide Autogel® in Patients With Locally Advanced or Metastatic Gastroenteropancreatic Neuroendocrine Tumors (GEP-NETs) in Asia Region

Asan Medical Center·observational·Posted Jan 6, 2021·Updated Jan 28, 2025

In Brief

An observational study evaluating Lanreotide autogel for Neuroendocrine Tumors. Completed, enrolled 71 participants across 1 site.

Detailed Summary

Lanreotide Autogel® has been established as a standard of care for patients with locally advanced or metastatic GEP-NETs based on the success of CLARINET trial. However, only few patients with Asian ethnicity were included in the trial. According to the nationwide comprehensive study of patients with GEP-NET in Korea, hindgut primary NETs(Rectal) occured more frequently than western countries. However, small intestine or lung primary NET is relatively rare compared with western countries.1) Considering the clinical characteristics of GEP-NETs are distinct between the patients in Asian and Western countries, further evaluation on the efficacy and safety of Lanreotide Autogel® in Asian patients with GEP-NETs is needed.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesSouth Korea

Timeline

N/ACompletedFinished
202120222023202420252026
First PostedJan 6, 2021
Enrollment StartJan 1, 2021
Primary CompletionJan 30, 2024
Study CompletionJan 27, 2025
TodayJul 2, 2026
Enrollment to primary: 3.1 yearsPosted 5.5 years ago

Interventions

Lanreotide autogeldrug

Lanreotide autogel 90-120 mcg, every 4 weeks