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Clinical Trial Summary

The purpose of the protocol is to assess the efficacy and safety of BIM 23A760 on patient's overall satisfaction in terms of symptom relief (diarrhoea and/or flushes) in patients with carcinoid syndrome after 24 weeks of treatment.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01018953
Study type Interventional
Source Ipsen
Contact
Status Terminated
Phase Phase 2
Start date February 2010
Completion date January 2011

See also
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