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The Lack of Bronchodilator Effect and the Short-term Safety of Cumulative Single Doses of an Inhaled Potassium Channel Opener (Bimakalim) in Adult Patients with Mild to Moderate Bronchial Asthma

✍ Scribed by P. Faurschou; K.L. Mikkelsen; I. Steffensen; B. Franke


Publisher
Elsevier
Year
1994
Tongue
English
Weight
230 KB
Volume
7
Category
Article
ISSN
0952-0600

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✦ Synopsis


SUMMARY: The aim of this study was to assess the bronchodilator effect and short-term safety of cumulative single doses of inhaled bimakalim (E Merck, Darmstadt), a potassium channel opener, compared to placebo in 12 adult patients with chronic, mild to moderate, non-allergic bronchial asthma. The study was a randomized, placebocontrolled, cross-over study and the only efficacy variable measured was the forced expiratory volume in one second (\left(\mathrm{FEV}{1}\right.) ). The patients had an (\mathrm{FEV}{-1}>50 %) of predicted normal value and a reversibility of more than (15 %) at entrance to the study. Inhaled bimakalim and placebo were delivered by a Pariboy nebulizer. The doses tested in a cumulative manner were (10,25,40) and (100 \mu \mathrm{g}) (total cumulative dose (175 \mu \mathrm{g}) ), each individual dose given at (60-\mathrm{min}) intervals. Plasma bimakalim concentrations were measured at time 0 and (60 \mathrm{~min}) after each dose. No bronchodilator effect was shown, with inhaled bimakalim at the doses tested. Reasons for the lack of efficacy of inhaled bimakalim in this study may be due to low doses of administrated drug or to a true lack of bronchodilatation effect in the study patients. Inhaled bimakalim was well tolerated. No headache or cardiovascular events were seen with the cumulative dose of (175 \mu \mathrm{g}) bimakalim.