Bioequivalence of losartan/amlodipine fixed dose combination tablets (losanet AM) compared with concomitant administration of Single components of losartan and amlodipine tablets in healthy human volunteers

A fixed dose combination of losartan, an angiotensin receptor blocker and amlodipine, a calcium channel blocker, can potentially provide complementary mechanism of action to improve blood pressure control and clinical outcomes. The current study was conducted to compare the pharmacokinetics of a new...

Full description

Saved in:
Bibliographic Details
Main Author: Bustami, Rana (author)
Other Authors: Khasawneh, Sewar (author), Absi, Wafaa (author), Feddah, Hamzeh (author), Mroueh, Mohamad (author), Daccache, Elie (author), Sarraf, Jean-Charles (author), Kyriacos, Soula (author)
Format: article
Published: 2015
Online Access:http://hdl.handle.net/10725/6797
http://dx.doi.org/10.4172/jbb.1000243
http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php
https://www.walshmedicalmedia.com/abstract/bioequivalence-of-losartanamlodipine-fixed-dose-combination-tabletslosanet-am-compared-with-concomitant-administration-o-34627.html
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1864513480960245760
author Bustami, Rana
author2 Khasawneh, Sewar
Absi, Wafaa
Feddah, Hamzeh
Mroueh, Mohamad
Daccache, Elie
Sarraf, Jean-Charles
Kyriacos, Soula
author2_role author
author
author
author
author
author
author
author_facet Bustami, Rana
Khasawneh, Sewar
Absi, Wafaa
Feddah, Hamzeh
Mroueh, Mohamad
Daccache, Elie
Sarraf, Jean-Charles
Kyriacos, Soula
author_role author
dc.creator.none.fl_str_mv Bustami, Rana
Khasawneh, Sewar
Absi, Wafaa
Feddah, Hamzeh
Mroueh, Mohamad
Daccache, Elie
Sarraf, Jean-Charles
Kyriacos, Soula
dc.date.none.fl_str_mv 2015
2017-12-15T10:17:37Z
2017-12-15T10:17:37Z
2017-12-15
dc.identifier.none.fl_str_mv 0975-0851
http://hdl.handle.net/10725/6797
http://dx.doi.org/10.4172/jbb.1000243
Bustami, R., Khasawneh, S., Absi, W., Feddah, H., & Mroueh, M. (2015). Bioequivalence of Losartan/Amlodipine Fixed Dose Combination Tablets (Losanet AM) Compared with Concomitant Administration of Single Components of Losartan and Amlodipine Tablets in Healthy Human Volunteers. Journal of Bioequivalence & Bioavailability, 7(5), 216-224.
http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php
https://www.walshmedicalmedia.com/abstract/bioequivalence-of-losartanamlodipine-fixed-dose-combination-tabletslosanet-am-compared-with-concomitant-administration-o-34627.html
dc.language.none.fl_str_mv en
dc.relation.none.fl_str_mv Bioequivalence & Bioavailability
dc.rights.*.fl_str_mv info:eu-repo/semantics/openAccess
dc.title.none.fl_str_mv Bioequivalence of losartan/amlodipine fixed dose combination tablets (losanet AM) compared with concomitant administration of Single components of losartan and amlodipine tablets in healthy human volunteers
dc.type.none.fl_str_mv Article
info:eu-repo/semantics/publishedVersion
info:eu-repo/semantics/article
description A fixed dose combination of losartan, an angiotensin receptor blocker and amlodipine, a calcium channel blocker, can potentially provide complementary mechanism of action to improve blood pressure control and clinical outcomes. The current study was conducted to compare the pharmacokinetics of a new combination product of losartan potassium and amlodipine besylate with separate co-administration of losartan potassium and amlodipine besylate tablets in 40 healthy human volunteers after a single oral dose in a randomized three-period crossover study. The study protocol was prepared in accordance to the requirements set in the EMA guidance for conducting bioequivalence studies. Reference (Cozaar 100 mg, Merck Sharp & Dohme Ltd, UK and Norvasc 10 mg, Pfizer, Canada) and test (Losanet AM, Pharmaline, Lebanon) drugs were administered to fasted volunteers and blood samples were collected up to 168 hours and assayed for losartan, carboxylic acid losartan metabolite and amlodipine using a validated LC-MS/MS method. The pharmacokinetic parameters AUC0-t, AUC0- ∞,Cmax, Tmax, T1/2, MRTinf, residual area (%) and elimination rate constant were determined from plasma concentration-time profile by non-compartmental analysis method using WinNonlin V5.3. The analysis of variance did not show any significant difference between the two formulations and 90% confidence intervals fell within the acceptable range for bioequivalence (80-125%). The resulting data demonstrated that when administered as fixed dose combination or individual tablets, the pharmacokinetics of losartan and amlodipine were bioequivalent and were well-tolerated.
eu_rights_str_mv openAccess
format article
id LAURepo_df818140423daabb65f2d68784941955
identifier_str_mv 0975-0851
Bustami, R., Khasawneh, S., Absi, W., Feddah, H., & Mroueh, M. (2015). Bioequivalence of Losartan/Amlodipine Fixed Dose Combination Tablets (Losanet AM) Compared with Concomitant Administration of Single Components of Losartan and Amlodipine Tablets in Healthy Human Volunteers. Journal of Bioequivalence & Bioavailability, 7(5), 216-224.
language_invalid_str_mv en
network_acronym_str LAURepo
network_name_str Lebanese American University repository
oai_identifier_str oai:laur.lau.edu.lb:10725/6797
publishDate 2015
repository.mail.fl_str_mv
repository.name.fl_str_mv
repository_id_str
spelling Bioequivalence of losartan/amlodipine fixed dose combination tablets (losanet AM) compared with concomitant administration of Single components of losartan and amlodipine tablets in healthy human volunteersBustami, RanaKhasawneh, SewarAbsi, WafaaFeddah, HamzehMroueh, MohamadDaccache, ElieSarraf, Jean-CharlesKyriacos, SoulaA fixed dose combination of losartan, an angiotensin receptor blocker and amlodipine, a calcium channel blocker, can potentially provide complementary mechanism of action to improve blood pressure control and clinical outcomes. The current study was conducted to compare the pharmacokinetics of a new combination product of losartan potassium and amlodipine besylate with separate co-administration of losartan potassium and amlodipine besylate tablets in 40 healthy human volunteers after a single oral dose in a randomized three-period crossover study. The study protocol was prepared in accordance to the requirements set in the EMA guidance for conducting bioequivalence studies. Reference (Cozaar 100 mg, Merck Sharp & Dohme Ltd, UK and Norvasc 10 mg, Pfizer, Canada) and test (Losanet AM, Pharmaline, Lebanon) drugs were administered to fasted volunteers and blood samples were collected up to 168 hours and assayed for losartan, carboxylic acid losartan metabolite and amlodipine using a validated LC-MS/MS method. The pharmacokinetic parameters AUC0-t, AUC0- ∞,Cmax, Tmax, T1/2, MRTinf, residual area (%) and elimination rate constant were determined from plasma concentration-time profile by non-compartmental analysis method using WinNonlin V5.3. The analysis of variance did not show any significant difference between the two formulations and 90% confidence intervals fell within the acceptable range for bioequivalence (80-125%). The resulting data demonstrated that when administered as fixed dose combination or individual tablets, the pharmacokinetics of losartan and amlodipine were bioequivalent and were well-tolerated.PublishedN/A2017-12-15T10:17:37Z2017-12-15T10:17:37Z20152017-12-15Articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article0975-0851http://hdl.handle.net/10725/6797http://dx.doi.org/10.4172/jbb.1000243Bustami, R., Khasawneh, S., Absi, W., Feddah, H., & Mroueh, M. (2015). Bioequivalence of Losartan/Amlodipine Fixed Dose Combination Tablets (Losanet AM) Compared with Concomitant Administration of Single Components of Losartan and Amlodipine Tablets in Healthy Human Volunteers. Journal of Bioequivalence & Bioavailability, 7(5), 216-224.http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.phphttps://www.walshmedicalmedia.com/abstract/bioequivalence-of-losartanamlodipine-fixed-dose-combination-tabletslosanet-am-compared-with-concomitant-administration-o-34627.htmlenBioequivalence & Bioavailabilityinfo:eu-repo/semantics/openAccessoai:laur.lau.edu.lb:10725/67972024-01-31T13:55:31Z
spellingShingle Bioequivalence of losartan/amlodipine fixed dose combination tablets (losanet AM) compared with concomitant administration of Single components of losartan and amlodipine tablets in healthy human volunteers
Bustami, Rana
status_str publishedVersion
title Bioequivalence of losartan/amlodipine fixed dose combination tablets (losanet AM) compared with concomitant administration of Single components of losartan and amlodipine tablets in healthy human volunteers
title_full Bioequivalence of losartan/amlodipine fixed dose combination tablets (losanet AM) compared with concomitant administration of Single components of losartan and amlodipine tablets in healthy human volunteers
title_fullStr Bioequivalence of losartan/amlodipine fixed dose combination tablets (losanet AM) compared with concomitant administration of Single components of losartan and amlodipine tablets in healthy human volunteers
title_full_unstemmed Bioequivalence of losartan/amlodipine fixed dose combination tablets (losanet AM) compared with concomitant administration of Single components of losartan and amlodipine tablets in healthy human volunteers
title_short Bioequivalence of losartan/amlodipine fixed dose combination tablets (losanet AM) compared with concomitant administration of Single components of losartan and amlodipine tablets in healthy human volunteers
title_sort Bioequivalence of losartan/amlodipine fixed dose combination tablets (losanet AM) compared with concomitant administration of Single components of losartan and amlodipine tablets in healthy human volunteers
url http://hdl.handle.net/10725/6797
http://dx.doi.org/10.4172/jbb.1000243
http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php
https://www.walshmedicalmedia.com/abstract/bioequivalence-of-losartanamlodipine-fixed-dose-combination-tabletslosanet-am-compared-with-concomitant-administration-o-34627.html