This trial has been completed.

Condition diabetes mellitus, type 2
Treatments canagliflozin, 100 mg, canagliflozin, 300 mg, placebo
Phase phase 1
Sponsor Janssen Research & Development, LLC
Start date September 2014
End date January 2017
Trial size 59 participants
Trial identifier NCT02009488, 28431754DIA1054, CR103062


The purpose of this study is to assess changes from baseline in insulin sensitivity, hepatic fat content and beta cell function after approximately 24-25 weeks of treatment with canagliflozin compared to placebo in participants with type 2 diabetes mellitus (T2DM) with inadequate glycemic (blood sugar) control on metformin monotherapy or on combination therapy with metformin and a dipeptidyl peptidase-4 (DPP-4) inhibitor.

United States No locations recruiting
Other countries No locations recruiting

Study Design

Allocation randomized
Intervention model parallel assignment
Primary purpose treatment
Masking participant, care provider
Each patient will receive canagliflozin 100 mg once daily during the first 4 weeks of the 25 weeks double-blind period, then the dose may be increased to 300 mg once daily, till the end of the period.
canagliflozin, 100 mg
One 100 mg capsule taken orally (by mouth) once daily
canagliflozin, 300 mg
One 300 mg capsule taken orally (by mouth) once daily
(Placebo Comparator)
One placebo capsule taken orally (by mouth) once daily for approximately 28 days during the Pre-Treatment Run-In and the Baseline Periods, then during double-blind study for 178 days (approximately 24-25 weeks).
One placebo capsule (inactive medication) once daily.

Primary Outcomes

Change from baseline in hepatic insulin sensitivity
time frame: Baseline, 25 weeks
Change from baseline in peripheral tissue insulin sensitivity
time frame: Baseline, 25 weeks
Change from baseline in liver fat content, determined using magnetic resonance spectroscopy (MRS)
time frame: Baseline, 25 weeks
Change from baseline in insulin secretion rate (ISR) during mixed-meal tolerance test (MMTT)
time frame: Baseline, 25 weeks
Change from baseline in beta-cell glucose sensitivity, determined as a slope of ISR vs. plasma glucose concentration during MMTT
time frame: Baseline, 25 weeks

Secondary Outcomes

Changes from baseline in substrate oxidation and energy production rates during MMTT and euglycemic clamp
time frame: Baseline, 25 weeks
Changes from baseline in insulin clearance during MMTT and euglycemic clamp
time frame: Baseline, 25 weeks
Change from baseline in suppression of free fatty acids (FFAs) during euglycemic clamp
time frame: Baseline, 25 weeks
Changes from baseline in basal and postprandial plasma glucagon, FFAs and β-hydroxybutyrate during MMTT
time frame: Baseline, 25 weeks
Change from baseline in renal threshold for glucose (RTG), estimated using an MMTT-based method
time frame: Baseline, 25 weeks

Eligibility Criteria

All participants from 25 years up to 70 years old.

Inclusion Criteria: - Must have a diagnosis of T2DM for at least 3 months and be on either metformin monotherapy at a stable dose of >=1,000 mg per day or on combination therapy of metformin >=1,000 mg per day and a DPP-4 inhibitor at stable daily doses for at least 12 weeks prior to screening with an HbA1c of >=7.0% and <= 9.5% at Screening - Fasting plasma glucose >=120 mg/dL and <=240 mg/dL at the Week -4 visit - Fasting fingerstick glucose >=120 mg/dL and <=240 mg/dL performed at clinical research center on Day -14 - Must be medically stable on the basis of clinical laboratory tests performed at screening Exclusion Criteria: - Has a history of diabetic ketoacidosis, type 1 diabetes mellitus (T1DM), pancreas or β-cell transplantation, or diabetes secondary to pancreatitis or pancreatectomy - Has claustrophobia or anxiety, related to previous negative experiences with magnetic resonance imaging procedures which cannot be managed with an anxiolytic drug - Has a history of brittle or labile glycemic control, with widely varying glucose measurements - Has proliferative diabetic retinopathy (based on an eye examination within one year prior to Screening), currently receiving or requiring treatment - Has a history of 1 or more severe hypoglycemic episodes within 6 months before screening - Has history of hereditary glucose-galactose malabsorption or primary renal glucosuria.

Additional Information

Official title A Double-Blind, Placebo-Controlled, Randomized, Parallel Groups, Multicenter Study to Investigate the Effects of Canagliflozin on Insulin Sensitivity, Hepatic Fat Content and Beta Cell Function in Subjects With Type 2 Diabetes Mellitus
Description This is a double-blind (neither physician nor participants knows the treatment that the participant receives), randomized (the study medication is assigned by chance), placebo-controlled (an inactive substance is compared with a medication to test whether the medication has a real effect in a clinical study), parallel-groups study which will be conducted at 2 clinical research centers (CRC) in the US. Approximately 56 participants, ages 25-70 years, with T2DM inadequately controlled on either metformin monotherapy or combination therapy with metformin and a DPP-4 inhibitor, will be enrolled. The study has 3 phases: pre-treatment, double-blind treatment, and post-treatment. Pre-Treatment Phase will consist of a screening visit (Week -5), 14 days Single- Blind Placebo Run-in period, followed by 14 days of Single-Blind Placebo Baseline Period, during which participants will be randomized (1:1) to one of 2 treatment groups, either canagliflozin or placebo. Double-Blind Treatment Phase begins on Day 1, and ends at approximately Week 25, during which participants will be assessed at least biweekly at outpatient visits or by telephone contact. Canagliflozin treatment will be initiated at 100 mg/day, with up-titration to 300 mg/day, consistent with the approved INVOKANA® US Prescribing Information 2013. During post-treatment phase, a follow-up visit will occur within approximately 28 days after the last dose of study drug. At baseline and after 24 weeks of treatment with canagliflozin, hepatic and peripheral insulin sensitivity will be assessed using tracer labeled euglycemic clamp technique; hepatic fat content will be determined using 1H nuclear magnetic resonance spectroscopy (MRS); beta cell function (insulin secretion rate and beta cell glucose sensitivity) will be assessed during mixed meal tolerance test (MMTT); substrate oxidation and energy production rates will be measured using indirect calorimetry during euglycemic clamp and MMTT. During the study, participants will remain on their stable dose regimens of metformin or combination metformin DPP-4 inhibitor therapy, unless the investigator considers dose modification to be medically necessary. The total study duration for each participant participating in this study will be up to approximately 34 weeks.
Trial information was received from ClinicalTrials.gov and was last updated in March 2017.
Information provided to ClinicalTrials.gov by Janssen Research & Development, LLC.