LUTATHERA Injection General Use Result Survey

NCT05844332 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 347

Last updated 2025-12-22

No results posted yet for this study

Summary

This study was a multicenter observational study with a central registration system and all-case surveillance system without a control group.

Conditions

  • Somatostatin Receptor-positive Neuroendocrine Tumor

Interventions

OTHER

LUTATHERA

There was no treatment allocation. Patients administered LUTATHERA by prescription could be enrolled.

Sponsors & Collaborators

Principal Investigators

  • Novartis Pharmaceuticals · Novartis Pharmaceuticals

Eligibility

Min Age
18 Years
Max Age
99 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-12-17
Primary Completion
2024-06-27
Completion
2024-06-27

Countries

  • Japan

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05844332 on ClinicalTrials.gov