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Diabetes Care, Vol 19, Issue 8 849-856, Copyright © 1996 by American Diabetes Association
A dose-response study of glimepiride in patients with NIDDM who have previously received sulfonylurea agents. The Glimepiride Protocol #201 Study Group
RB Goldberg, SM Holvey and J Schneider
Diabetes Research Institute, University of Miami School of Medicine, Florida 33136, USA.
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 HbA1c 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 glimepiride group than in the placebo
group (P < 0.001). Changes from baseline to endpoint after 1, 4, and 8
mg glimepiride 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 HbA1c; 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 HbA1c levels > or = 8% were assessed, more
patients who received 8 mg glimepiride had HbA1c values < 8% at endpoint
compared with patients receiving 4 mg. Glimepiride had a favorable safety
profile. CONCLUSIONS: Glimepiride in 1-, 4-, or 8-mg doses was effective
and well tolerated. Although the 4- and 8-mg once-daily doses were
significantly more potent than the 1-mg dose, all three doses yielded
clinical improvement. Because the 8-mg dose controlled HbA1c values in a
greater number of patients with high baseline HbA1c levels than did the
4-mg dose, this higher dose might be beneficial for patients who are
difficult to treat.

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Copyright © 1996 by the American Diabetes Association.
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