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NCT03499704CompletedPhase 4

A Study to Evaluate the Effect of add-on Pioglitazone or Dapagliflozin in Participants With Type 2 Diabetes Mellitus Inadequately Controlled by DPP-4 Inhibitor and Metformin Therapy

A Multicenter, Randomized, Open-label, Two-arm, Phase 4 Study to Evaluate the Effect of Add-on Pioglitazone or Dapagliflozin in Subjects With Type 2 Diabetes Mellitus Inadequately Controlled by Dipeptidyl Peptidase-4 Inhibitor and Metformin Therapy

Source: ClinicalTrials.gov · Last updated 18 Mar 2026

Brief summary (registry, in English)

The purpose of this study is to assess the pioglitazone plus alogliptin plus metformin is non-inferior to dapagliflozin plus alogliptin plus metformin on glycosylated haemoglobin (HbA1c) change from baseline at Week 26.

Status (registry)
Completed
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
133 (actual)
First submitted
9 Apr 2018
Start date
11 Feb 2020
Primary completion date
2 Jan 2024
Lead sponsor
Celltrion Pharm, Inc.
NCT number
NCT03499704

What you commit to

  • Study type: Interventional · Phase 4
  • Participants enrolled: 133
  • From 11 Feb 2020 to the primary completion date, 2 Jan 2024
  • 15 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • The use of any medications ie, oral or systemically injected glucocorticoids (including intra-articular injection), weight-loss drugs, insulin or other anti-diabetic drugs except DPP-4 inhibitor and metformin, within 3 months prior to randomization. Strong Cytochrome P450 2C8 (CYP2C8) inhibitors (eg, gemfibrozil, montelukast, quercetin, phenelzine) and CYP2C8 inducers (eg, rifampin) that in the opinion of the Investigator or Sponsor require treatment contraindicated during the study. The diuretics, angiotensin receptor blockers (ARBs), angiotensin-converting enzyme (ACE) -inhibitors and nonsteroidal anti-inflammatory drugs (NSAIDs) are to be used per product label with close monitoring under Investigator's supervision.
  • Has a history of alcohol abuse within 2 years prior to randomization.

Other illness

  • The subject has type 1 diabetes, diabetic ketoacidosis, diabetic coma or diabetic precoma.
  • The subject has an active bladder cancer or a history of bladder cancer.

Lab values

  • Has genetic problems such as galactose intolerance, Lapp lactose dehydrogenase deficiency or glucose-galactose uptake disorder, etc.

Who the study is looking for

  • The subject is a regular outpatient with an has a historical diagnosis of type 2 diabetes.
  • The subject has metabolic syndrome as jointly defined by the International Diabetes Federation (IDF); National Heart, Lung, and Blood Institute (NHLBI) / American Heart Association (AHA); and International Association for the Study of Obesity (IASO). If any 3 of the following 5 risk factors are present, metabolic syndrome can be considered:
    • High waist circumference: male ≥ 90 cm, female ≥ 85 cm.
    • High TGs (drug treatment for high TGs is an alternate indicator): ≥ 150 mg/dL (1.7 mmol/L).
    • Low HDL-C (drug treatment for low HDL-C is an alternate indicator): \< 40 mg/dL(1.0 mmol/L) in males, \< 50 mg/dL (1.3 mmol/L) in females.
    • High blood pressure (antihypertensive drug treatment in a subject with a history of hypertension is an alternate indicator): Systolic ≥ 130 mmHg and/or diastolic ≥ 85 mmHg.
    • High fasting glucose (drug treatment of high glucose is an alternate indicator): ≥ 100 mg/dL.
  • The subject has been receiving a stable dose of DPP-4 inhibitor + metformin therapy with diet and exercise for ≥ 3 months prior to Randomization.
  • The subject has a HbA1c value between 7.0 and 11% inclusively within 28 days of Randomization via central laboratory test or after run-in period for 4 weeks via central laboratory test.

Age in the registry: 19 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (15)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
The Catholic University of Korea, Bucheon, St. Marys Hospital
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Bucheon-siSouth KoreaUnknown status
Inje University Haeundae Paik Hospital
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BusanSouth KoreaUnknown status
Pusan National University Hospital
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BusanSouth KoreaUnknown status
Yeungnam University Hospital
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DaeguSouth KoreaUnknown status
Daejeon Eulji Medical center, Eulji University
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DaejeonSouth KoreaUnknown status
Chosun University Hospital
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GwangjuSouth KoreaUnknown status
Seoul National University Bundang Hospital
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Seongnam-siSouth KoreaUnknown status
Yonsei University Health System, Severance Hospital
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SeoulSouth KoreaUnknown status
Kangbuk Samsung Hospital
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SeoulSouth KoreaUnknown status
Korea University Anam Hospital
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SeoulSouth KoreaUnknown status
Samsung Medical Center
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SeoulSouth KoreaUnknown status
Kyung Hee University Hospital at Gangdong
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SeoulSouth KoreaUnknown status
The Catholic University of Korea St Vincents Hospital
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SuwonSouth KoreaUnknown status
Ajou University Hospital
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SuwonSouth KoreaUnknown status
Ulsan University Hospital
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UlsanSouth KoreaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.