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Completed Phase 2 Interventional Results available

Study of AC-201 in Patients With Type 2 Diabetes Mellitus

ClinicalTrials.gov ID: NCT01276106

Public ClinicalTrials.gov record NCT01276106. 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 1, 2026, 3:46 PM EST

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, Dose-Ranging Phase II Study of AC-201 in Patients With Type 2 Diabetes Mellitus

Brief summary

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

This is a 24-week randomized placebo-controlled study to investigate the effect of an oral IL-1beta inhibitor AC-201 in patients with type 2 diabetes mellitus already treated on different background diabetes therapies.

Study identification

NCT ID
NCT01276106
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
TWi Biotechnology, Inc.
Industry
Enrollment
259 participants

Conditions and interventions

Eligibility (public fields only)

Age range
20 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
Jan 2011 (Type not available)
Primary completion
Feb 2012 (Actual)
Completion
Mar 2012 (Actual)
Last update posted
May 22, 2018

2011 – 2012

United States locations

U.S. sites
13
U.S. states
9
U.S. cities
13
Facility City State ZIP Site status
Catalina Research Institute, LLC Chino California — —
National Research Institute Los Angeles California — —
Clinical Research of South Florida Coral Gables Florida — —
Jacksonville Impotence Treatment Center Jacksonville Florida — —
Chicago Clinical Research Institute, Inc. Chicago Illinois — —
Clinical Investigation Specialists, Inc. Gurnee Illinois — —
Midwest Institute for Clinical Research, Inc. Indianapolis Indiana — —
L-MARC Research Center Louisville Kentucky — —
New Orleans Center for Clinical Research New Orleans Louisiana — —
Sterling Research Group, Ltd Cincinnati Ohio — —
PriMed Clinical Research Kettering Ohio — —
National Clinical Research-Richmond, Inc. Richmond Virginia — —
Rainier Clinical Research Center, Inc. Renton Washington — —

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 8 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01276106, 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 May 22, 2018 · Synced Nov 1, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01276106 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →