Location-F: Comparison of Dapagliflozin, Lobeglitazone, and Its Combination in Efficacy and Safety

Sponsor
Seoul National University Bundang Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT05915949
Collaborator
(none)
99
1
3
24
4.1

Study Details

Study Description

Brief Summary

Diabetes is the most frequently occurring chronic disease along with obesity, hypertension, and hyperlipidemia. The number of patients with diabetes is increasing worldwide. Despite rapid progress in management of diabetes, the problem is that glycemic target goal is still low showing 30-40%. Thus, diabetes has become a serious social, economic, and public health problem beyond individual health problems due to its increasing prevalence.

Condition or Disease Intervention/Treatment Phase
  • Drug: Dapagliflozin 10mg Tab
  • Drug: Lobeglitazone 0.5 mg
  • Drug: Dapagliflozin + Lobeglitazone
Phase 4

Detailed Description

Previously, metformin, sulfonylurea, and insulin injections were used to treat diabetes, but since then, various new drugs such as thiazolidinedione (TZD), sodium-glucose cotransporter-2 (SGLT-2) inhibitor, dipeptidyl peptidase-4 (DPP-4) inhibitor, and glucagon like peptide-1 (GLP-1) receptor agonist have been released. Among them, metformin and TZD are known to improve insulin resistance, SGLT-2 inhibitor has a mechanism to excrete glucose into urine, and other drugs have a mechanism to promote insulin secretion.

After a report in 2007 that rosiglitazone could increase cardiovascular disease, use of TZD has been limited. However, more people are having insulin resistance, and this is more evident in developing countries. In this circumstance, TZD can be a main stay for diabetic patients with insulin resistance. TZDs improve insulin sensitivity by activating peroxisome proliferator-activated receptor γ (PPARγ). They have shown excellent glycemic durability. On the other hand, SGLT-2 inhibitors are attracting attention as a mechanism that directly excretes excess glucose in diabetic patients through urine. Many cardiovascular outcome trials have proven its efficacy in cardiovascular and renal outcomes. Current guidelines proposed a new paradigm in the management of T2DM, with a preferential place for SGLT-2 inhibitors, after metformin, in patients with atherosclerotic cardiovascular disease, heart failure and progressive kidney disease.

As such, combination therapy of TZD and SGLT-2 inhibitors, two drugs that have mechanisms for improving insulin resistance and urinary glucose excretion, would have compensatory effects, which would be effective for diabetes treatment. In addition, since studies that investigated effect of TZD and SGLT-2 inhibitor combination on changes in body fat mass and metabolic phenotype are lacking, we investigated the effect of reducing visceral fat (abdominal visceral fat mass/abdominal subcutaneous fat mass) in combination therapy with dapagliflozin, an SGLT-2 inhibitor, and lobeglitazone, a TZD.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
99 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
Evaluation of the Efficacy of Combination of Dapagliflozin and Lobeglitazone on Glucose Concentrations and Body Fat in Patients With Type 2 Diabetes
Actual Study Start Date :
Jan 1, 2022
Anticipated Primary Completion Date :
Oct 30, 2023
Anticipated Study Completion Date :
Dec 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Dapagliflozin

Dapagliflozin 10 mg once daily will be given to participants.

Drug: Dapagliflozin 10mg Tab
Forxiga 10mg Tab once daily will be given to participants for 24 weeks.
Other Names:
  • Forxiga 10mg
  • Active Comparator: Lobeglitazone

    Lobeglitazone 0.5 mg once daily will be given to participants.

    Drug: Lobeglitazone 0.5 mg
    Duvie 0.5mg Tab once daily will be given to participants for 24 weeks.
    Other Names:
  • Duvie 0.5 mg
  • Active Comparator: Dapagliflozin and Lobeglitazone combined

    Dapagliflozin 10 mg and lobeglitazone 0.5 mg once daily together will be given to participants.

    Drug: Dapagliflozin + Lobeglitazone
    Duvie 0.5mg Tab once daily will be given to participants for 24 weeks.
    Other Names:
  • Forxiga 10mg + Duvie 0.5mg
  • Outcome Measures

    Primary Outcome Measures

    1. HbA1c [6 months]

      Glycemic control

    Secondary Outcome Measures

    1. Fasting plasma glucose [6 months]

      Glucose metabolism

    2. Postprandial glucose [6 months]

      Glucose metabolism

    3. Whole body muscle [6 months]

      Body composition

    4. Whole body fat [6 months]

      Body composition

    5. Abdominal subcutaneous fat [6 months]

      Body composition

    6. Abdominal visceral fat [6 months]

      Body composition

    7. NTproBNP [6 months]

      Cardiac marker

    8. Troponin T [6 months]

      Cardiac marker

    9. Lipids [6 months]

      Lipid profiles (TG, HDL, and LDL)

    10. Lipoprotein (a) [6 months]

      Lipid metabolism

    11. Urinary microalbumin-Creatinine ratio [6 months]

      Lipid metabolism

    12. Hepatic fibrosis marker [6 months]

      Liver markers

    Other Outcome Measures

    1. Adverse events [6 months]

      Side effects.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    20 Years to 75 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • type 2 diabetic patients between the ages of 20 and 80 who are taking oral diabetes medications (metformin and/or DPP-4 inhibitors) for more than 8 weeks without dose adjustment

    • body mass index (BMI) ≥ 20 kg/m2

    • eGFR ≥ 50 mL/min/1.73 m2

    • HbA1c: 7-10%.

    Exclusion Criteria:
    • patients with type 1 diabetes; HbA1c <7% or HbA1c >10%

    • fasting blood glucose (FPG) >15 mmol/L (270 mg/dL) at the first visit (screening) and pre-randomization screening

    • women of childbearing potential (if not using proper contraception)

    • history of gastric surgery (including gastric banding within 3 years)

    • history of diabetic ketoacidosis or non-ketogenic hyperosmotic coma

    • average of 3 blood pressure measurements is systolic blood pressure (SBP) >180 mmHg or diastolic blood pressure (DBP) >100 mmHg

    • heart failure NYHA class III or IV

    • AST or ALT greater than 3 times the upper limit of normal

    • systemic corticosteroids have been used for 10 consecutive days within 90 days (topical, eye drop, topical or inhalation agents)

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Seoul National University Bundang Hospital Seongnam Gyeonggi Korea, Republic of 463-707

    Sponsors and Collaborators

    • Seoul National University Bundang Hospital

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Soo Lim, Professor, Seoul National University Bundang Hospital
    ClinicalTrials.gov Identifier:
    NCT05915949
    Other Study ID Numbers:
    • B-1910-568-001
    First Posted:
    Jun 23, 2023
    Last Update Posted:
    Jun 23, 2023
    Last Verified:
    Jun 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Soo Lim, Professor, Seoul National University Bundang Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jun 23, 2023