drugset / Trial / NCT01677910

TELESTAR (Telotristat Etiprate for Somatostatin Analogue Not Adequately Controlled Carcinoid Syndrome)

NCT01677910

Phase 3 Completed 135 enrolled Lexicon Pharmaceuticals
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objective of the study is to confirm that at least 1 or more doses of telotristat etiprate compared to placebo is effective in reducing the number of daily bowel movements (BMs) from baseline averaged over the 12-week double-blind portion (Treatment Period) of the trial in patients not adequately controlled by current SSA therapy.

Timeline

Start
2013-01-08
Primary completion
2016-03-21
Completion
2016-03-21

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Telotristat etiprate Unknown 250 mg Oral
Subject Telotristat etiprate Unknown 500 mg Oral

Indications