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Completed Phase 2 Interventional

Study of the Efficacy of Larazotide Acetate to Treat Celiac Disease

ClinicalTrials.gov ID: NCT00889473

Public ClinicalTrials.gov record NCT00889473. 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 Jul 22, 2026, 6:38 PM 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

Study identification

NCT ID
NCT00889473
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
9 Meters Biopharma, Inc.
Industry
Enrollment
42 participants

Conditions and interventions

Conditions

Interventions

  • Larazotide acetate Drug
  • Placebo Drug
  • Gluten 900 mg Dietary Supplement

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
Mar 31, 2009
Primary completion
Oct 31, 2009
Completion
Mar 31, 2010
Last update posted
Sep 19, 2017

2009 – 2010

United States locations

U.S. sites
14
U.S. states
10
U.S. cities
14
Facility City State ZIP Site status
Study Site Orange California
Study Site Topeka Kansas
Study Site Lexington Kentucky
Study Site Hagerstown Maryland
Study Site Silver Spring Maryland
Study Site Chesterfield Michigan
Study Site Troy Michigan
Study Site Rochester Minnesota
Study Site New York New York
Study Site Oklahoma City Oklahoma
Study Site Paoli Pennsylvania
Study Site Philadelphia Pennsylvania
Study Site Pittsburgh Pennsylvania
Study Site Franklin Tennessee

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 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00889473, 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 19, 2017 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00889473 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →