Combination therapy for Type 2 diabetes: Repaglinide plus rosiglitazone

Philip Raskin, J. McGill, M. F. Saad, J. M. Cappleman, W. Kaye, N. Khutoryansky, P. M. Hale

Research output: Contribution to journalArticlepeer-review

24 Scopus citations

Abstract

Aims: This 24-week, randomized, multicentre, open-label, parallel-group clinical trial compared efficacy and safety of repaglinide monotherapy, rosiglitazone monotherapy, and combination therapy (repaglinide plus rosiglitazone) in Type 2 diabetes after unsatisfactory response to sulphonylurea or metformin monotherapy. Methods: Enrolled patients (n = 252) were adults having Type 2 diabetes for at least 1 year, with HbA1c values > 7.0% after previous monotherapy (sulphonylurea or metformin, ≥ 50% maximal dose). Prior therapy was withdrawn for 2 weeks, followed by randomization to repaglinide, rosiglitazone, or repaglinide/rosiglitazone. Study treatments were initiated with a 12-week dose optimization period (doses optimized according to labelling), followed by a 12-week maintenance period. Efficacy endpoints were changes in HbA1c values (primary) or fasting plasma glucose values (secondary). Results: Baseline HbA1c values were comparable (9.3% for repaglinide, 9.0% for rosiglitazone, 9.1% for combination). Mean changes in HbA1c values at the end of treatment were greater for repaglinide/rosiglitazone therapy (-1.43%) than for repaglinide (-0.17%) or rosiglitazone (-0.56%) monotherapy. Reductions of fasting plasma glucose values were also greater for combination therapy (-5.2 mmol/l, -94 mg/dl) than for repaglinide monotherapy (-3.0 mmol/l, -54 mg/dl) or rosiglitazone monotherapy (-3.7 mmol/l, -67 mg/dl). Minor hypoglycaemic events occurred in 9% of combination therapy patients, vs. 6% for repaglinide and 2% for rosiglitazone. Individual weight gains for combination therapy were correlated to HbA1c response. Conclusions: The combination therapy regimen was well tolerated. In patients previously showing unsatisfactory response to oral monotherapy, glycaemic reductions were greater for the repaglinide/rosiglitazone combination regimen than for use of either repaglinide or rosiglitazone alone.

Original languageEnglish (US)
Pages (from-to)329-335
Number of pages7
JournalDiabetic Medicine
Volume21
Issue number4
DOIs
StatePublished - Apr 2004

Keywords

  • Insulin secretagogue
  • Lipids
  • Oral antidiabetic drug
  • Thiazolidinedione

ASJC Scopus subject areas

  • Internal Medicine
  • Endocrinology, Diabetes and Metabolism
  • Endocrinology

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