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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 Jun 26, 2026, 2:51 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, 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

Study identification

NCT ID
NCT01064414
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Janssen Research & Development, LLC
Industry
Enrollment
272 participants

Conditions and interventions

Interventions

  • Canagliflozin Drug
  • Placebo Drug

Drug

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
May 31, 2010
Primary completion
Nov 30, 2011
Completion
Jul 31, 2012
Last update posted
Aug 13, 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 13, 2013 · Synced Jun 26, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01064414 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →