Literature DB >> 9829158

Candesartan cilexetil. A review of its use in essential hypertension.

K J McClellan1, K L Goa.   

Abstract

UNLABELLED: Candesartan cilexetil is completely converted to the nonpeptide angiotensin II receptor blocker candesartan during absorption from the gastrointestinal tract. Candesartan selectively blocks and dissociates slowly from the angiotensin II subtype 1 (AT1) receptor which mediates most of the known activities of angiotensin II. When administered once daily, oral candesartan cilexetil 8 to 32 mg dose-dependently and effectively reduces blood pressure in patients with mild to moderate essential hypertension. In comparative studies, candesartan cilexetil 8 mg/day was as effective as usual therapeutic dosages of enalapril, losartan potassium, hydrochlorothiazide and amlodipine. One study showed candesartan cilexetil 16 mg/day to be more effective than losartan potassium 50 mg/day. Furthermore, the combination of candesartan cilexetil with either hydrochlorothiazide or amlodipine resulted in additive antihypertensive effects. Preliminary evidence suggests that the blood pressure-lowering effects of candesartan cilexetil are associated with the prevention or improvement of end-organ damage in patients with hypertension. However, this requires further confirmation in clinical studies. Candesartan cilexetil improves insulin sensitivity in patients with hypertension and does not affect glucose homeostasis or the serum lipid profile in those with coexisting type 2 (non-insulin-dependent) diabetes mellitus. Candesartan cilexetil is well tolerated in patients with hypertension. Pooled data indicate that the tolerability profile of the drug is not significantly different from that of placebo, with headache being the most commonly reported event. Adverse events are not dose related and are mostly mild to moderate in severity. Candesartan cilexetil is better tolerated than enalapril, primarily because of a reduced incidence of cough, and was not associated with the hypokalaemia or hyperuricaemia seen with hydrochlorothiazide in a study in patients aged > or = 75 years. The drug has an adverse events profile similar to that of losartan potassium in patients with mild to moderate hypertension.
CONCLUSIONS: once daily candesartan cilexetil is effective and well tolerated when used once daily (as monotherapy or in combination with other antihypertensive agents) in patients with mild, moderate or severe hypertension. Initially, however, the drug is likely to be used as an alternative to other agents in patients not responding to or intolerant of their current drug therapy.

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Year:  1998        PMID: 9829158     DOI: 10.2165/00003495-199856050-00013

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  60 in total

1.  Protective effects of candesartan cilexetil (TCV-116) against stroke, kidney dysfunction and cardiac hypertrophy in stroke-prone spontaneously hypertensive rats.

Authors:  Y Inada; T Wada; M Ojima; T Sanada; Y Shibouta; R Kanagawa; Y Ishimura; Y Fujisawa; K Nishikawa
Journal:  Clin Exp Hypertens       Date:  1997-10       Impact factor: 1.749

2.  Bioavailability of candesartan is unaffected by food in healthy volunteers administered candesartan cilexetil.

Authors:  J G Riddell
Journal:  J Hum Hypertens       Date:  1997-09       Impact factor: 3.012

3.  Twenty-four hour blood pressure profile of different doses of candesartan cilexetil in patients with mild to moderate hypertension.

Authors:  H J Heuer; G Schöndorfer; A M Högemann
Journal:  J Hum Hypertens       Date:  1997-09       Impact factor: 3.012

4.  Candesartan cilexetil, a new generation angiotensin II antagonist, provides dose dependent antihypertensive effect.

Authors:  D Elmfeldt; M George; R Hübner; B Olofsson
Journal:  J Hum Hypertens       Date:  1997-09       Impact factor: 3.012

5.  Angiotensin II type I receptor antagonist inhibits the gene expression of transforming growth factor-beta 1 and extracellular matrix in cardiac and vascular tissues of hypertensive rats.

Authors:  S Kim; K Ohta; A Hamaguchi; T Omura; T Yukimura; K Miura; Y Inada; Y Ishimura; F Chatani; H Iwao
Journal:  J Pharmacol Exp Ther       Date:  1995-04       Impact factor: 4.030

Review 6.  Angiotensin II receptor subtypes: selective antagonists and functional correlates.

Authors:  P B Timmermans; R D Smith
Journal:  Eur Heart J       Date:  1994-12       Impact factor: 29.983

7.  1993 guidelines for the management of mild hypertension. Memorandum from a World Health Organization/International Society of Hypertension meeting. Guidelines Subcommittee of the WHO/ISH Mild Hypertension Liaison Committee.

Authors: 
Journal:  Hypertension       Date:  1993-09       Impact factor: 10.190

8.  An angiotensin II receptor antagonist reduces myocardial damage in an animal model of myocarditis.

Authors:  A Tanaka; A Matsumori; W Wang; S Sasayama
Journal:  Circulation       Date:  1994-10       Impact factor: 29.690

Review 9.  Blockade of the renin-angiotensin system.

Authors:  M G Nicholls; C J Charles; I G Crozier; E A Espiner; H Ikram; M J Rademaker; A M Richards; T G Yandle
Journal:  J Hypertens Suppl       Date:  1994-12

Review 10.  Modulation of the renin-angiotensin-aldosterone system and cough.

Authors:  Y Lacourcière; J Lefebvre
Journal:  Can J Cardiol       Date:  1995-08       Impact factor: 5.223

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  18 in total

1.  Enhanced solubility and intestinal absorption of candesartan cilexetil solid dispersions using everted rat intestinal sacs.

Authors:  S Gurunath; Baswaraj K Nanjwade; P A Patila
Journal:  Saudi Pharm J       Date:  2013-04-08       Impact factor: 4.330

Review 2.  Clinical pharmacokinetics of candesartan.

Authors:  Christoph H Gleiter; Klaus E Mörike
Journal:  Clin Pharmacokinet       Date:  2002       Impact factor: 6.447

Review 3.  Noncholestatic acute hepatocellular injury following candesartan administration.

Authors:  Jan Antonio Lammel-Lindemann; Eduardo Flores-Villalba; Alexandro Jose Martagón; Eduardo DeObeso-Gonzalez; Francisco Puente-Gallegos
Journal:  Br J Clin Pharmacol       Date:  2017-10-22       Impact factor: 4.335

4.  Quantification of Candesartan in Mouse Plasma by MALDI-TOFMS and in Tissue Sections by MALDI-Imaging Using the Stable-Isotope Dilution Technique.

Authors:  Toyofumi Nakanishi; Shinji Takai; Denan Jin; Takayuki Takubo
Journal:  Mass Spectrom (Tokyo)       Date:  2013-06-01

Review 5.  Comparative safety and tolerability of angiotensin II receptor antagonists.

Authors:  L Mazzolai; M Burnier
Journal:  Drug Saf       Date:  1999-07       Impact factor: 5.606

Review 6.  Candesartan cilexetil: a review of its use in the management of chronic heart failure.

Authors:  Caroline Fenton; Lesley J Scott
Journal:  Drugs       Date:  2005       Impact factor: 9.546

7.  Spectrum of use for the angiotensin-receptor blocking drugs.

Authors:  M E Fabiani; C I Johnston
Journal:  Curr Hypertens Rep       Date:  1999-10       Impact factor: 5.369

8.  Randomised controlled trial of dual blockade of renin-angiotensin system in patients with hypertension, microalbuminuria, and non-insulin dependent diabetes: the candesartan and lisinopril microalbuminuria (CALM) study.

Authors:  C E Mogensen; S Neldam; I Tikkanen; S Oren; R Viskoper; R W Watts; M E Cooper
Journal:  BMJ       Date:  2000-12-09

Review 9.  Candesartan cilexetil: an update of its use in essential hypertension.

Authors:  Stephanie E Easthope; Blair Jarvis
Journal:  Drugs       Date:  2002       Impact factor: 9.546

Review 10.  Drug interactions with angiotensin receptor blockers: a comparison with other antihypertensives.

Authors:  Thomas Unger; Elena Kaschina
Journal:  Drug Saf       Date:  2003       Impact factor: 5.606

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