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Clinical Trial Summary

The primary aim of this study is to assess which method of lanreotide Autogel administration patients with neuroendocrine tumours prefer - self/partner administrations or healthcare provided administrations. The study will also assess if self/partner administration can be performed without loss of efficacy and with a preserved safety profile. The impact of self/partner administration on resource utilisation and costs will be studied. In addition, we will also assess the healthcare provider's experience of the two administration practices.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT00681187
Study type Interventional
Source Ipsen
Contact
Status Completed
Phase Phase 4
Start date June 2008
Completion date August 2010