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N/A Completed N=3,281

Alogliptin/Pioglitazone (Liovel) Combination Tablets Survey on Long-term Use in Patients With Type 2 Diabetes Mellitus

Source: ClinicalTrials.gov NCT01990300 ↗
Enrolled (actual)
3,281
Serious AEs
0.1%
Results posted
Jan 2019
Primary outcomePrimary: Number of Participants Who Experience at Least One Adverse Events — 206 Participants

Summary

The purpose of this survey is to examine the safety and efficacy of long-term use of alogliptin/pioglitazone(Liovel) combination tablets in patients with type 2 diabetes mellitus determined as warranting combination therapy with alogliptin benzoate and pioglitazone hydrochloride

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants Who Experience at Least One Adverse Events
206 —
PRIMARY
Changes From Baseline in Glycosylated Hemoglobin (HbA1c)
-0.26; -0.58; -0.66; -0.66; -0.65 —
SECONDARY
Changes From Baseline in Fasting Blood Glucose (FBG)
-14.7; -18.7; -18.4; -19.6; -19.8 —

Eligibility Criteria

Inclusion Criteria

  • Patients with type 2 diabetes mellitus

Exclusion Criteria

  • Patients meeting any of the following criteria will be excluded:
  • Patients with current cardiac failure or a past history of cardiac failure
  • Patients with severe ketosis, diabetic coma or precoma, or type 1 diabetes mellitus
  • Patients with serious hepatic dysfunction
  • Patients with serious renal dysfunction
  • Patients with severe infection, pre- or post-operative patients, or patients with serious traumatic injury
  • Patients with a history of hypersensitivity to any ingredients of Alogliptin/Pioglitazone
  • Pregnant or possibly pregnant women
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01990300). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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