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Completed Phase 1Phase 2 Interventional

Safety Study of Mesenchymal Precursor Cells in Type 2 Diabetes

ClinicalTrials.gov ID: NCT01576328

Public ClinicalTrials.gov record NCT01576328. 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 Sep 22, 2026, 5:49 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, Placebo-Controlled Dose-Escalation Study to Assess the Safety and Tolerability of a Single Intravenous Infusion of Allogeneic Mesenchymal Precursor Cells (MPCs) in Patients With Type 2 Diabetes Sub-optimally Controlled on Metformin

Brief summary

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

This study is being conducted to assess the overall safety and tolerability of a single intravenous infusion of three doses of Mesenchymal Precursor Cells versus Placebo in subjects with Type 2 Diabetes inadequately controlled on Metformin.

Study identification

NCT ID
NCT01576328
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Mesoblast, Ltd.
Industry
Enrollment
61 participants

Conditions and interventions

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
Mar 31, 2012
Primary completion
Sep 30, 2013
Completion
Sep 30, 2015
Last update posted
Jun 1, 2020

2012 – 2015

United States locations

U.S. sites
18
U.S. states
11
U.S. cities
18
Facility City State ZIP Site status
SC Clinical Research Garden Grove California 92844
Diabetes Research Institute Miami Florida 33136
Compass Research Orlando Florida 32806
Pennington Biomedical Research Center Baton Rouge Louisiana 70808
Tulane University Medical Center New Orleans Louisiana 70112
Big Sky Clinical Research Butte Montana 59701
Desert Endocrinology Clinical Research Center-Henderson Henderson Nevada 89052
Alliance Against Diabetes/AAD Clinical Research Las Vegas Nevada 89101
Active Practices and Research Newington New Hampshire 03801
The Carl and Edyth Lindner Center for Research and Education at The Christ Hospital Cincinnati Ohio 45219
Providence Health Partners - Center for Clinical Reseach Dayton Ohio 45439
Dallas Diabetes and Endocrine Center Dallas Texas 75230
West Houston Clinical Research Services Houston Texas 77055
Paragon Research Center San Antonio Texas 78205
Wasatch Clinical Research Salt Lake City Utah 84107
National Clinical Research - Norfolk, Inc Norfolk Virginia 23502
National Clinical Research - Richmond, Inc. Richmond Virginia 23294
Capital Clinical Research Center Olympia Washington 98502

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 NCT01576328, 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 Jun 1, 2020 · Synced Sep 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01576328 live on ClinicalTrials.gov.

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