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Clinical Trial Summary

The primary objective of the study is to evaluate the impact on quality of life of Lanreotide Autogel 120 mg in combination with standard care, in comparison to the standard care alone, in subjects affected by inoperable malignant bowel obstruction.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02365584
Study type Interventional
Source Ipsen
Contact
Status Terminated
Phase Phase 2
Start date January 2015
Completion date January 16, 2018

See also
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