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Completed

NCT Number: NCT01273558

A Study of Two Methods for Determining the Renal Threshold for Glucose in Patients With Type 2 Diabetes Mellitus

The purpose of this study is to compare the results from two methods used to determine the renal threshold for glucose excretion (defined as the lowest plasma glucose concentration at which appreciable amounts of glucose appear in the urine) in untreated patients with type 2 diabetes mellitus and in patients with type 2 diabetes mellitus who are treated with 100 mg once-daily canigliflozin for 8 days.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Neuss, Germany

About this study

This is an open-label (patients will know if they are receiving treatment and the identity of the treatment) study that will compare renal threshold of glucose (RTG) values obtained by 2 different methods: an established method (ie, the stepwise hyperglycemic clamp method) and a new method (the mixed meal tolerance test [MMTT] method). The RTG is defined as the lowest plasma glucose concentration at which appreciable amounts of glucose appear in the urine. Each method for determining the RTG value will be performed in untreated patients with type 2 diabetes mellitus (T2DM) and in patients with T2DM who are treated with canagliflozin 100 mg once daily for 8 days. Canagliflozin (a Sodium-Glucose Cotransporter 2 inhibitor) is currently under development to lower blood sugar levels in patients with T2DM. Patients will not take study drug (canagliflozin 100 mg overencapsulated tablets) in Part 1 of the study. In Part 2 of the study, patients will take study drug once daily on Study Days 1 through 8.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients with T2DM who are not receiving treatment with any anti-hyperglycemic agents (AHAs) for at least 12 weeks, or who are receiving treatment with a stable dose and regimen of metformin monotherapy for at least 12 weeks and have a hemoglobin A1c (HbA1c) in the range of >=7% to <=10%

Exclusion criteria

  • History of Type 1, "brittle" diabetes or secondary forms of diabetes
  • History of 1 or more severe hypoglycemic episodes
  • History of diabetic complications considered to be clinically significant by the Investigator
  • History of or current illness considered to be clinically significant by the investigator

Treatment and study plan

Canagliflozin

Drug

One 100 mg capsule taken orally (by mouth) on Days Days 1-8

Primary outcomes

  1. RTG values using the MMTT and the stepwise hyperglycemic clamp methods

    Time frame: On Days 1 and 2 (Part 1)

  2. RTG values using the MMTT and the stepwise hyperglycemic clamp methods

    Time frame: On Days 7 and 8 (Part 2)

Secondary outcomes

  1. Plasma glucose (PG) concentration during the MMT and the hyperglycemic clamp procedure

    Time frame: On Days 1 and 2 (Part 1)

  2. Plasma glucose (PG) concentration during the MMT and the hyperglycemic clamp procedure

    Time frame: On Days 7 and 8 (Part 2)

  3. Rate of Urinary glucose excretion (UGE) during the MMTT and the hyperglycemic clamp procedure

    Time frame: On Days 1 and 2 (Part 1)

  4. Rate of Urinary glucose excretion (UGE) during the MMTT and the hyperglycemic clamp procedure

    Time frame: On Days 7 and 8 (Part 2)

Sponsors and collaborators

Lead sponsor

Johnson & Johnson Pharmaceutical Research & Development, L.L.C.

Industry

Registry information

Official study title

An Open-Label Study to Compare Two Methods for Determining the Renal Threshold for Glucose in Subjects With Type 2 Diabetes Mellitus

Important dates

Study start
2011
Study completion
2011
First posted
Jan 10, 2011
Registry last updated
Apr 22, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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