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NCT00853047 · ClinicalTrials.gov registry record · Phase 2

Study of Telotristat Etiprate (LX1606) in Participants With Symptomatic Carcinoid Syndrome Not Managed by Stable-Dose Octreotide Therapy

A Phase 2 study, sponsored by Lexicon Pharmaceuticals.

Completed
Registry status
Phase 2
Development phase
23
Enrollment target

NCT00853047 is a Phase 2 study that has completed, run by Lexicon Pharmaceuticals. The registered enrollment target is 23 participants.

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The verdict

NCT00853047, a Phase 2 study, has completed, sponsored by Lexicon Pharmaceuticals.

COMPLETED
Registry status
Phase 2
Development phase
23 participants
Enrollment target

Study 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.

Interventions

  • DRUG Placebo
  • DRUG Telotristat etiprate
  • DRUG Octreotide LAR Depot

Trial Details

FieldValue
Enrollment Target 23 participants
Start Date 2009-03
Est. Completion 2014-06
Phase Phase 2

Sponsor

Lexicon Pharmaceuticals

56 total trials

What the Registry Record Tells You About NCT00853047

The ClinicalTrials.gov registry entry for NCT00853047 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 23 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Lexicon Pharmaceuticals, which has 56 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 3 interventions - of which Placebo is the first listed.

NCT00853047 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00853047 about?

NCT00853047 is a clinical study titled "Study of Telotristat Etiprate (LX1606) in Participants With Symptomatic Carcinoid Syndrome Not Managed by Stable-Dose Octreotide Therapy". 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 effectiv...

What is the current status of trial NCT00853047?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 23 participants. The study started on 2009-03. Estimated completion is 2014-06.

What interventions are being tested in trial NCT00853047?

The interventions under investigation include: Placebo (DRUG), Telotristat etiprate (DRUG), Octreotide LAR Depot (DRUG).

Who is sponsoring clinical trial NCT00853047?

This trial is sponsored by Lexicon Pharmaceuticals, which has 56 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.