A dose-response study of glimepiride in patients with NIDDM who have previously received sulfonylurea agents

Ronald B. Goldberg, Sherman M. Holvey, Jill Schneider

Research output: Contribution to journalArticle

88 Scopus citations

Abstract

OBJECTIVE - To assess the efficacy, safety, and dose-response relationship of glimepiride in patients with NIDDM. RESEARCH DESIGN AND METHODS - After a 21-day placebo washout period, 304 patients were randomized to receive either placebo or glimepiride, 1, 4, or 8 mg once daily. Fasting plasma glucose (FPG), 2-h postprandial glucose (PPG), and HbA(1c) were measured at predetermined intervals during the washout period and the 14-week study. Adverse events were tabulated. RESULTS - At each patient visit, reduction from baseline FPG was greater in each glimepride group than in the placebo group (P < 0.001). Changes from baseline to endpoint after 1, 4, and 8 mg glimepride exceeded those after placebo (P < 0.001) by 2.4, 3.9, and 4.1 mmol/l, respectively, for FPG; by 1.2, 1.8, and 1.9 percentage points, respectively, for HbA(1c) and by 3.5, 5.1, and 5.2 mmol/l, respectively, for 2-h PPG. Greater reductions in these parameters were observed with 8 and 4 mg than with 1 mg (P < 0.05), indicating a dose- response relationship. When patients with baseline HbA(1c) levels ≤8% were assessed, more patients who received 8 mg glimepiride had HbA(1c) values <8% at endpoint compared with patients receiving 4 mg. Glimepiride had a favorable safety profile. CONCLUSIONS - Glimepiride in 1-, 4-, or 8-mg once- daily doses was effective and well tolerated. Although the 4- and 8-mg doses were significantly more potent than the 1-mg dose, all three doses yielded clinical improvement. Because the 8-mg dose controlled HbA(1c) values in a greater number of patients with high baseline HbA(1c) levels than did the 4- mg dose, this higher dose might be beneficial for patients who are difficult to treat.

Original languageEnglish (US)
Pages (from-to)849-856
Number of pages8
JournalDiabetes care
Volume19
Issue number8
DOIs
StatePublished - Aug 1996

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ASJC Scopus subject areas

  • Internal Medicine
  • Endocrinology, Diabetes and Metabolism
  • Advanced and Specialized Nursing

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