drugset / Trial / NCT02026063

Telotristat Etiprate - Expanded Treatment for Patients With Carcinoid Syndrome Symptoms

NCT02026063

Phase 3 Completed 124 enrolled Lexicon Pharmaceuticals
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The primary objective of this study is to evaluate the long-term safety and tolerability of orally administered telotristat etiprate.

Timeline

Start
2014-01-14
Primary completion
2018-09-12
Completion
2018-09-12

Drugs

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

Indications