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Completed Phase 2 Interventional

Study to Assess the Efficacy of Larazotide Acetate for the Treatment of Celiac Disease

ClinicalTrials.gov ID: NCT00492960

Public ClinicalTrials.gov record NCT00492960. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 29, 2026, 4:06 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase IIb, Randomized, Double-Blind, Placebo Controlled, Dose Ranging, Multicenter Study to Determine the Safety, Tolerance, and Efficacy of Larazotide Acetate (AT-1001) in Celiac Disease Subjects During a Gluten Challenge

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study was conducted to evaluate the efficacy of multiple doses of larazotide acetate in preventing intestinal permeability changes induced by a 6- week gluten challenge in subjects with celiac disease.

Study identification

NCT ID
NCT00492960
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
9 Meters Biopharma, Inc.
Industry
Enrollment
171 participants

Conditions and interventions

Conditions

Interventions

Drug · Dietary Supplement

Eligibility (public fields only)

Age range
18 Years to 72 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 2007 (Actual)
Primary completion
Oct 2008 (Actual)
Completion
Mar 2009 (Actual)
Last update posted
Sep 20, 2017

2007 – 2009

United States locations

U.S. sites
17
U.S. states
15
U.S. cities
17
Facility City State ZIP Site status
Study Site Scottsdale Arizona 85259 —
Study Site Colorado Springs Colorado 80907 —
Study Site Chicago Illinois 60637 —
Study Site Lexington Kentucky 40536 —
Study Site Hagerstown Maryland 21740 —
Study Site Boston Massachusetts 02215 —
Study Site Troy Michigan 48084 —
Study Site Rochester Minnesota 55905 —
Study Site New York New York 10032 —
Study Site Asheville North Carolina 28801 —
Study Site Cleveland Ohio 44195 —
Study Site Philadelphia Pennsylvania 19107 —
Study Site Pittsburgh Pennsylvania 15243 —
Study Site Houston Texas 77030 —
Study Site Plano Texas 75093 —
Study Site Richmond Virginia 23298 —
Study Site Seattle Washington 98101 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 6 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00492960, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 20, 2017 · Synced Oct 29, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00492960 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →