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Clinical Trial Summary

To assess the efficacy of Lanreotide Autogel 120 mg for the relief of vomiting due to inoperable malignant intestinal obstruction in patients without nasogastric tube (NGT) and to assess the efficacy of lanreotide Autogel 120 mg on removal of nasogastric tube without the recurrence of vomiting in patients with an inoperable malignant intestinal obstruction with a nasogastric tube.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02275338
Study type Interventional
Source Ipsen
Contact
Status Completed
Phase Phase 2
Start date November 19, 2014
Completion date November 9, 2017

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