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Completed

NCT Number: NCT02545842

Assessment Study of Three Different Fasting Plasma Glucose Targets in Chinese Patients With Type 2 Diabetes Mellitus (BEYOND III/FPG GOAL)

Primary Objective:

To identify a best fasting plasma glucose (FPG) target for Chinese type 2 diabetes patients using insulin glargine which can provide the highest control rate of glycated hemoglobin (HbA1c) < 7%.

Secondary Objectives:

The control rate of HbA1c ≤6.5% achievement. The control rate of HbA1c <7.0% in patients achieving their FPG target. The percentage of HbA1c <7% without hypoglycemia. The percentage of patients achieving the FPG target without hypoglycemia. The percentage of patients achieving the FPG target and post prandial glucose (PPG) target (2-hour post breakfast <10 mmol/L).

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Investigational Site Number 156053, Anshan, China

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About this study

The study duration for each patient will be 27 weeks.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • 18 to 65 years old.
  • Type 2 diabetes patients insufficient controlled by 1-3 oral anti-hyperglycemic drugs (OADs) with stable dose at least 3 months:
  • If on 1 OAD, provided with the following doses (including but not limited to):
  • α-glucosidase inhibitor: 100mg, three times a day (tid);
  • metformin: 1.5-2.0 g/day;
  • sulphonylureas: sub-maximum (half dose above) to maximum tolerated dose;
  • thiazolidinediones: eg. pioglitazone, 30-40 mg/day.
  • Besides the medications listed above, if on 1 OAD, others should be maximum tolerated dose allowed in package insert.
  • If on 2-3 OADs, any range of dose is acceptable.
  • HbA1c >7%, and ≤10.5%.
  • FPG >7 mmol/L.
  • Body mass index (BMI) ≥20 kg/m^2, and ≤40 kg/m^2.
  • Diabetes duration ≥1 year.
  • Physician decides to and the patient is willing to start basal insulin (BI) treatment.
  • Willing to join the study and sign the informed consent.

Exclusion criteria

  • Type 1 diabetes patients.
  • Patients with acute diabetic complications (including unexplained severe hypoglycemia in the last 6 months).
  • Previous treatment with insulin for more than 1 month cumulatively in last 1 year, or treatment with insulin in the last 3 months before the screening.
  • Known hypoglycemia unawareness or recurrent hypoglycemia.
  • Hypersensitivity to study drug or its excipients.
  • Any clinically significant acute major organ or systemic disease, or any other situation judged by the Investigator, that is difficult for the 24 weeks follow-up.
  • Pregnancy or breastfeeding women.
  • Have any mental disorders, lack self-control or not able to express accurately.
  • Involved in another clinical trial simultaneously or within a 1 month before start of trial.

The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

Treatment and study plan

insulin glargine

Drug

Pharmaceutical form: solution

Route of administration: subcutaneous

Other names: HOE901

Primary outcomes

  1. Percentage of patients with HbA1c <7% achievement

    Time frame: 24 weeks

Secondary outcomes

  1. Percentage of patients achieving HbA1c <=6.5%

    Time frame: 24 weeks

  2. Percentage of patients achieving FPG target with HbA1c <7%

    Time frame: 24 weeks

  3. Percentage of patients achieving HbA1c <7% without hypoglycemia

    Time frame: 24 weeks

  4. Percentage of patients achieving the FPG target without hypoglycemia

    Time frame: 24 weeks

  5. Percentage of patients achieving FPG target

    Time frame: 24 weeks

  6. Percentage of patients achieving PPG target (2-hour post-breakfast <10 mmol/L)

    Time frame: 24 weeks

  7. Change from baseline in HbA1c

    Time frame: Baseline to 24 weeks

  8. Change in FPG

    Time frame: 8 weeks to 24 weeks

  9. Change in PPG

    Time frame: Baseline to 24 weeks

  10. Change in insulin doses in each arm

    Time frame: 1 week to 24 weeks

  11. Change in body weight in each treatment arm

    Time frame: Baseline to 24 weeks

  12. Percentage of patients experienced hypoglycemic events

    Time frame: 24 weeks

Sponsors and collaborators

Lead sponsor

Sanofi

Industry

Registry information

Official study title

Titration Target for Chinese Type 2 Diabetes Mellitus Patients Using Insulin Glargine to Achieve Glycaemic Goals: An Assessment of Three Different Fasting Plasma Glucose Targets - BEYOND III/FPG GOAL Study

Important dates

Study start
2015
Primary completion
2018
Study completion
2018
First posted
Sep 10, 2015
Registry last updated
Apr 25, 2022

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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