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Terminated Phase 2 Interventional

Long-term Extension Study to Evaluate the Safety of Dutogliptin/PHX1149T in Subjects With Type 2 Diabetes Mellitus

ClinicalTrials.gov ID: NCT01101945

Public ClinicalTrials.gov record NCT01101945. 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 20, 2026, 2:11 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

An Open Label, Multi-Center, Long-Term Follow-up Study to Evaluate the Safety of PHX1149T in Subjects With Type 2 Diabetes Mellitus - Extension to Protocol PHX1149-PROT202

Brief summary

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

The purpose of this study is to demonstrate that dutogliptin/PHX1149T is safe and tolerable.

Study identification

NCT ID
NCT01101945
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Phenomix
Industry
Enrollment
339 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 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
Jul 2007 (Type not available)
Primary completion
Jan 2010 (Estimated)
Completion
Mar 2010 (Estimated)
Last update posted
Aug 11, 2010

2007 – 2010

United States locations

U.S. sites
27
U.S. states
16
U.S. cities
27
Facility City State ZIP Site status
Not listed Fullerton California — —
Not listed Long Beach California — —
Not listed Orange California — —
Not listed San Diego California — —
Not listed Kissimmee Florida — —
Not listed Melbourne Florida — —
Not listed New Port Richey Florida — —
Not listed Gurnee Illinois — —
Not listed Wichita Kansas — —
Not listed Kansas City Missouri — —
Not listed Henderson Nevada — —
Not listed Las Vegas Nevada — —
Not listed Berlin New Jersey — —
Not listed Margate City New Jersey — —
Not listed Trenton New Jersey — —
Not listed Charlotte North Carolina — —
Not listed Winston-Salem North Carolina — —
Not listed Cincinnati Ohio — —
Not listed Oklahoma City Oklahoma — —
Not listed Medford Oregon — —
Not listed Warminster Pennsylvania — —
Not listed Columbia South Carolina — —
Not listed Greer South Carolina — —
Not listed Dallas Texas — —
Not listed San Antonio Texas — —
Not listed Salt Lake City Utah — —
Not listed Norfolk Virginia — —

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 28 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01101945, 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 Aug 11, 2010 · Synced Oct 20, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01101945 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →