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Clinical Trial Summary

The objective of the PRELUDE study is to describe the use of lanreotide Autogel® (LAN ATG) combined with Peptide Receptor Radionuclide Therapy (PRRT) in the treatment of progressive neuroendocrine tumours located in the lung or in the digestive system as there is currently limited data on these treatments used together for these types of neuroendocrine tumours.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02788578
Study type Observational
Source Ipsen
Contact
Status Terminated
Phase
Start date June 2016
Completion date July 2017

See also
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Completed NCT00326469 - Efficacy and Safety of Lanreotide Autogel in Tumour Stabilization of Patients With Progressive Neuroendocrine Tumours Phase 2
Completed NCT01840449 - Somatuline Predictive Factors in Acromegaly and NET
Completed NCT02698410 - Efficacy and Safety of Lanreotide Autogel (ATG) in Combination With Temozolomide in Subjects With Thoracic Neuroendocrine Tumors. Phase 2
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Completed NCT01673906 - 68-Ga-labeled Octreotide Analogues PET in Duodenal-pancreatic Neuroendocrine Tumours Phase 2
Active, not recruiting NCT04579679 - Open-Label Surufatinib in European Patients With NET Phase 2