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Completed Phase 2 Interventional

Safety and Efficacy of Once-daily Oral Administrations of TZP-102 for Gastroparesis in Patients With Diabetes Mellitus

ClinicalTrials.gov ID: NCT00889486

Public ClinicalTrials.gov record NCT00889486. 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 30, 2026, 6:56 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 Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Phase 2 Evaluation of the Safety and Efficacy of Once-Daily Administrations of TZP 102 for the Treatment of Symptomatic Gastroparesis in Patients With Diabetes Mellitus

Brief summary

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

The purpose of this study is to evaluate the effect of TZP-102 on gastric emptying rate, gastroparesis symptoms and health-related quality of life in diabetic patients with gastroparesis.

Study identification

NCT ID
NCT00889486
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Tranzyme, Inc.
Industry
Enrollment
92 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 80 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
Apr 2009 (Type not available)
Primary completion
Apr 2010 (Actual)
Completion
Apr 2010 (Actual)
Last update posted
Dec 11, 2012

2009 – 2010

United States locations

U.S. sites
11
U.S. states
9
U.S. cities
11
Facility City State ZIP Site status
Long Beach VA Medical Center Long Beach California 90822 —
Impact Clinical Trials Los Angeles California 90036 —
California Pacific Medical Center Research Institute San Francisco California 94115 —
University of South Florida/Tampa General Hospital Tampa Florida 33606 —
Saint John's Research Institute Anderson Indiana 46012 —
University of Kansas Medical Center Kansas City Kansas 66160 —
Univ. of Louisville Medical-Dental Complex Louisville Kentucky 40202 —
Beth Israel Deaconess Medical Center Boston Massachusetts 02215 —
Dartmouth Hitchcock Medical Center Lebanon New Hampshire 03756 —
Wake Research Associates Raleigh North Carolina 27612 —
Texas Tech Univ. Health Sciences Center Dept. of Medicine El Paso Texas 79905 —

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 12 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00889486, 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 Dec 11, 2012 · Synced Oct 30, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00889486 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →