Last updated on March 2019

Efficacy and Safety Study in Pancreatic or Midgut Neuroendocrine Tumours Having Progressed Radiologically While Previously Treated With Lanreotide Autogel 120 mg


Brief description of study

This study aims to explore the efficacy and safety of lanreotide Autogel 120 mg administered every 14 days in subjects with grade 1 or 2, metastatic or locally advanced, unresectable pancreatic or intestinal neuroendocrine tumours (NETs) once they have progressed on the standard dose of lanreotide Autogel 120 mg every 28 days.

Clinical Study Identifier: NCT02651987

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Universit tsklinikum Erlangen

Erlangen, Germany
8.68miles
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Recruitment Status: Open


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