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Clinical Trial Summary

The purpose of this study is to evaluate the safety and tolerability of telotristat etiprate (LX1606) versus a placebo control in participants with symptomatic carcinoid syndrome not managed by stable-dose long-acting octreotide therapy. Following determination of the maximally tolerated or effective dose, cohort expansion will occur to confirm effect on symptoms and safety profile.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT00853047
Study type Interventional
Source Lexicon Pharmaceuticals
Contact
Status Completed
Phase Phase 2
Start date March 2009
Completion date June 2014

See also
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