candesartan cilexetil effective in moderate-to-severe hypertension

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Inpharma 1261 - 28 Oct 2000 Candesartan cilexetil is effective in moderate-to- severe hypertension when administered alone and in combination with amlodipine ± hydrochlorothiazide, report researchers from the UK and Israel Candesartan Investigator Group. In this study, 216 patients with moderate-to-severe essential hypertension received open-label candesartan cilexetil (maximum dosage 16 mg/day) with, if necessary, the addition of amlodipine 5 mg/day and hydrochlorothiazide 25 mg/day in a stepwise fashion in order to achieve BP control. * ; Among 162 evaluable patients, overall mean seated BP was reduced from 174/108mm Hg at baseline to 141/88mm Hg. 131 patients were then randomised to continue candesartan cilexetil (n = 64) or to have candesartan cilexetil replaced with placebo, for another 4 weeks. During this phase, BP increased by a significant extent in placebo recipients while no such change was seen in candesartan cilexetil recipients. * The study was supported by Takeda Euro R&D. † The dose-titration phase lasted 12 weeks. MacGregor GA, et al. Efficacy of candesartan cilexetil alone or in combination with amlodipine and hydrochlorothiazide in moderate-to-severe hypertension. Hypertension 36: 454-460, Sep 2000 800846871 1 Inpharma 28 Oct 2000 No. 1261 1173-8324/10/1261-0001/$14.95 Adis © 2010 Springer International Publishing AG. All rights reserved

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Inpharma 1261 - 28 Oct 2000

■ Candesartan cilexetil is effective in moderate-to-severe hypertension when administered alone and incombination with amlodipine ± hydrochlorothiazide,report researchers from the UK and Israel CandesartanInvestigator Group. In this study, 216 patients withmoderate-to-severe essential hypertension receivedopen-label candesartan cilexetil (maximum dosage 16mg/day) with, if necessary, the addition of amlodipine5 mg/day and hydrochlorothiazide 25 mg/day in astepwise fashion in order to achieve BP control.*;†

Among 162 evaluable patients, overall mean seated BPwas reduced from 174/108mm Hg at baseline to141/88mm Hg. 131 patients were then randomised tocontinue candesartan cilexetil (n = 64) or to havecandesartan cilexetil replaced with placebo, foranother 4 weeks. During this phase, BP increased by asignificant extent in placebo recipients while no suchchange was seen in candesartan cilexetil recipients.* The study was supported by Takeda Euro R&D.† The dose-titration phase lasted 12 weeks.

MacGregor GA, et al. Efficacy of candesartan cilexetil alone or in combinationwith amlodipine and hydrochlorothiazide in moderate-to-severe hypertension.Hypertension 36: 454-460, Sep 2000 800846871

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Inpharma 28 Oct 2000 No. 12611173-8324/10/1261-0001/$14.95 Adis © 2010 Springer International Publishing AG. All rights reserved