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Clinical Trial Summary

This is a multicentre long-term non-interventional study of adult subjects diagnosed with unresectable or metastatic, progressive, well differentiated (G1 and G2), somatostatin receptor positive GEP-NETs who have been prescribed Lutathera® in standard clinical practice.


Clinical Trial Description

Data on patients will be collected from the date when patient consent was obtained, during treatment with Lutathera® and for a follow-up period until end of study (EOS), defined as the time when the last enrolled patient has completed 36 months of assessments (unless early termination) after enrolment. Data will be collected in accordance with routine clinical visits. The study duration will be 48 months in total: 12 months recruitment and 36 of follow-up from the last patient in. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04727723
Study type Observational
Source Advanced Accelerator Applications
Contact
Status Active, not recruiting
Phase
Start date March 9, 2021
Completion date April 1, 2025

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