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Terminated Phase 2Phase 3 Interventional Results available

Dose Finding, Safety and Efficacy of Monthly Subcutaneous Canakinumab Administration in Metformin Monotherapy Treated Type 2 Diabetic Patients

ClinicalTrials.gov ID: NCT00900146

Public ClinicalTrials.gov record NCT00900146. 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 19, 2026, 1:34 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

Dose Finding, Safety and Efficacy of Monthly Subcutaneous Canakinumab Administration for the Treatment of Hyperglycemia in Metformin Monotherapy Treated Type 2 Diabetic Patients: a Randomized, Double-Blind, Placebo-Controlled, Multi-Center Study

Brief summary

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

This was a four month dose ranging study followed by a 24 to 48 month extension at the selected dose to characterize the safety and efficacy of the injectable IL-1B (interleukin 1, beta) antagonist canakinumab in the treatment of patients with Type 2 diabetes mellitus (T2DM) already treated on maximum dose metformin.

Study identification

NCT ID
NCT00900146
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2, Phase 3
Lead sponsor
Novartis
Industry
Enrollment
556 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 74 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
Apr 2009 (Type not available)
Primary completion
Nov 2010 (Actual)
Completion
Nov 2010 (Actual)
Last update posted
Feb 20, 2012

2009 – 2010

United States locations

U.S. sites
18
U.S. states
11
U.S. cities
18
Facility City State ZIP Site status
Anasazi Internal Medicine Phoenix Arizona — —
Whittier Institute of Diabetes La Jolla California — —
Novartis Investigative Site Los Gatos California — —
Novartis Investigative Site Santa Monica California 90404 —
Orange County Research Center Tustin California — —
Novartis Investigative Site Atlanta Georgia — —
Deaconess Clinic Evansville Indiana — —
Novartis Investigative Site Jackson Mississippi — —
Novartis Investigative Site Picayune Mississippi — —
Novartis Investigative Site Trenton New Jersey — —
Diabetes Research Center Columbus Ohio — —
Tri-State Medical Group Beaver Pennsylvania — —
Preferred Primary Care Physicians Pittsburgh Pennsylvania — —
Novartis Investigative Site Columbia South Carolina — —
R/D Clinical Research Lake Jackson Texas — —
Novartis Investigative Site Pasadena Texas — —
Novartis Investigative Site San Antonio Texas — —
Medical Research Initiatives Inc Virginia Beach 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 88 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00900146, 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 20, 2012 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00900146 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →