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Completed Phase 3 Interventional Results available

An Efficacy, Safety, and Tolerability Study of Canagliflozin in Patients With Type 2 Diabetes Mellitus Who Have Moderate Renal Impairment

ClinicalTrials.gov ID: NCT01064414

Public ClinicalTrials.gov record NCT01064414. 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, 3:14 PM 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, Double-Blind, Placebo-Controlled, 3-Arm, Parallel-Group, 26-Week, Multicenter Study With a 26-Week Extension, to Evaluate the Efficacy, Safety and Tolerability of Canagliflozin in the Treatment of Subjects With Type 2 Diabetes Mellitus Who Have Moderate Renal Impairment

Brief summary

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

The purpose of this study is to evaluate the efficacy and safety of 2 different doses of canagliflozin compared with placebo in patients with type 2 diabetes mellitus who have reduced kidney function.

Study identification

NCT ID
NCT01064414
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
272 participants

Conditions and interventions

Eligibility (public fields only)

Age range
25 Years and older
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
Jun 2010 (Type not available)
Primary completion
Dec 2011 (Actual)
Completion
Aug 2012 (Actual)
Last update posted
Aug 14, 2013

2010 – 2012

United States locations

U.S. sites
26
U.S. states
17
U.S. cities
26
Facility City State ZIP Site status
Not listed Concord California — —
Not listed Fountain Valley California — —
Not listed San Diego California — —
Not listed Denver Colorado — —
Not listed Pembroke Pines Florida — —
Not listed Tampa Florida — —
Not listed West Palm Beach Florida — —
Not listed Augusta Georgia — —
Not listed Nampa Idaho — —
Not listed Baton Rouge Louisiana — —
Not listed Jackson Mississippi — —
Not listed Picayune Mississippi — —
Not listed Chesterfield Missouri — —
Not listed Las Vegas Nevada — —
Not listed Albuquerque New Mexico — —
Not listed Durham North Carolina — —
Not listed Canal Fulton Ohio — —
Not listed Cincinnati Ohio — —
Not listed Columbus Ohio — —
Not listed Zanesville Ohio — —
Not listed Oklahoma City Oklahoma — —
Not listed Meridian Pennsylvania — —
Not listed Pittsburgh Pennsylvania — —
Not listed North Charleston South Carolina — —
Not listed Salt Lake City Utah — —
Not listed Fairfax 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 80 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01064414, 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 14, 2013 · 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 NCT01064414 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →