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Completed Phase 2 Interventional

A Study to Evaluate Safety and Efficacy of TTP054 for 12 Weeks in Subjects With Type 2 Diabetes

ClinicalTrials.gov ID: NCT01665352

Public ClinicalTrials.gov record NCT01665352. 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 Nov 9, 2026, 2:14 PM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Phase 2, Randomized, Double-Blind, Placebo-Controlled, Dose-Ranging, Parallel Group Study to Evaluate the Safety and Efficacy of TTP054 for 12 Weeks in Subjects With Type 2 Diabetes Mellitus Inadequately Controlled on Metformin

Brief summary

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

The purpose of this study is to compare the safety and effect of TTP054 versus placebo on glucose control in patients with type 2 diabetes.

Study identification

NCT ID
NCT01665352
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
vTv Therapeutics
Industry
Enrollment
186 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 70 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 2012 (Type not available)
Primary completion
May 2013 (Actual)
Completion
May 2013 (Actual)
Last update posted
Feb 10, 2017

2012 – 2013

United States locations

U.S. sites
19
U.S. states
14
U.S. cities
18
Facility City State ZIP Site status
Site 18 Chula Vista California 91911 —
Site 1 Los Angeles California 90057 —
Site 13 Denver Colorado 80220 —
Site 4 Coral Gables Florida 33134 —
Site 5 Port Orange Florida 32127 —
Site 3 Honolulu Hawaii 96814 —
Site 17 Indianapolis Indiana 46254 —
Site 7 Louisville Kentucky 40213 —
Site 8 Auburn Maine 04210 —
Site 9 Las Vegas Nevada 89101 —
Site 26 Trenton New Jersey 08611 —
Site 12 Rochester New York 14609 —
Site 14 Cincinnati Ohio 45219 —
Site 6 Mt. Pleasant South Carolina 29464 —
Site 16 Dallas Texas 75230 —
Site 10 Houston Texas 77072 —
Site 2 Houston Texas 77074 —
Site 11 Katy Texas 77450 —
Site 15 Richmond Virginia 23294 —

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 NCT01665352, 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 Feb 10, 2017 · Synced Nov 9, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01665352 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →