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Completed Phase 2 Interventional

A Safety and Efficacy Study of T0903131 (INT131) Besylate to Treat Type 2 Diabetes Mellitus

ClinicalTrials.gov ID: NCT00952445

Public ClinicalTrials.gov record NCT00952445. 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 24, 2026, 4:52 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 Randomized, Double-Blind, Placebo-Controlled, 4-week Study to Evaluate the Safety and Efficacy of T0903131 Besylate in Subjects With Type 2 Diabetes Mellitus

Brief summary

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

The purpose of the study is to determine if repeated daily doses of T0903131 (INT131) Besylate over 4 weeks can lower fasting blood glucose in patients with Type 2 Diabetes Mellitus.

Study identification

NCT ID
NCT00952445
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
InteKrin Therapeutics, Inc.
Industry
Enrollment
70 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
30 Years to 75 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
Dec 2003 (Type not available)
Primary completion
Not listed
Completion
Jun 2004 (Actual)
Last update posted
Oct 19, 2022

2003 – 2004

United States locations

U.S. sites
21
U.S. states
13
U.S. cities
17
Facility City State ZIP Site status
Whittier Diabetes Institute La Jolla California — —
Charles R. Drew University Los Angeles California — —
National Research Institute Los Angeles California — —
Lovelace Research Institute Santa Ana California — —
University of Miami Miami Florida — —
GFI Research Center Evansville Indiana — —
Joslin Diabetes Center Boston Massachusetts — —
Radiant Research Edina Minnesota — —
Radiant Research St Louis Missouri — —
St Louis Center for Clinical Research St Louis Missouri — —
Kaleida Health Diabetes Center Buffalo New York — —
Rochester Clinical Research Rochester New York — —
Duke University Medical Center Durham North Carolina — —
Radiant Research Portland Oregon — —
Radiant Research Anderson South Carolina — —
Baylor University Endocrine Center Dallas Texas — —
Dallas Diabetes and Endocrine Research Center Dallas Texas — —
Endocrine Associates of Dallas Dallas Texas — —
Diabetes and Grandular Disease Clinic and Reseach Center San Antonio Texas — —
Endocrine Research Specialists Ogden Utah — —
Salem VA Medical Center Salem Virginia — —

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00952445, 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 Oct 19, 2022 · Synced Oct 24, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00952445 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →