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Pharmacokinetics and anti-emetic efficacy of BRL43694, a new selective 5HT-3 antagonist.

Twenty patients receiving a variety of emetogenic cytotoxics (including cisplatin in 5) were given a single i.v. infusion of 40 micrograms kg-1 of BRL43694 (as the hydrochloride salt) in successive groups of 3-4 patients between 0-6 hours after chemotherapy. Eleven patients were completely protected...

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Autores principales: Cassidy, J., Raina, V., Lewis, C., Adams, L., Soukop, M., Rapeport, W. G., Zussman, B. D., Rankin, E. M., Kaye, S. B.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1988
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2246838/
https://www.ncbi.nlm.nih.gov/pubmed/2851312
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author Cassidy, J.
Raina, V.
Lewis, C.
Adams, L.
Soukop, M.
Rapeport, W. G.
Zussman, B. D.
Rankin, E. M.
Kaye, S. B.
author_facet Cassidy, J.
Raina, V.
Lewis, C.
Adams, L.
Soukop, M.
Rapeport, W. G.
Zussman, B. D.
Rankin, E. M.
Kaye, S. B.
author_sort Cassidy, J.
collection PubMed
description Twenty patients receiving a variety of emetogenic cytotoxics (including cisplatin in 5) were given a single i.v. infusion of 40 micrograms kg-1 of BRL43694 (as the hydrochloride salt) in successive groups of 3-4 patients between 0-6 hours after chemotherapy. Eleven patients were completely protected from vomiting; 9 had mild to moderate nausea and vomiting, but none severe enough to require alternative anti-emetic 'rescue'. In 4 of the patients in whom BRL43694 was delayed until 4-6 h after chemotherapy, vomiting had already begun; in each case immediate termination of vomiting occurred when BRL43694 was infused. No adverse effects attributable to the anti-emetic were observed. Mean pharmacokinetic parameters in 14 patients in whom plasma assay data are available were: Maximum observed concentration = 30.7 ng ml-1; terminal phase half-life = 8.96 h; total body clearance = 0.376 (1 h-1) kg-1; apparent volume of distribution = 2.85 l kg-1. This study shows BRL43694 to be an effective and well tolerated anti-emetic. Further studies aimed at defining an optimal dose and schedule for use against the most emetogenic cytotoxics are in progress.
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spelling pubmed-22468382009-09-10 Pharmacokinetics and anti-emetic efficacy of BRL43694, a new selective 5HT-3 antagonist. Cassidy, J. Raina, V. Lewis, C. Adams, L. Soukop, M. Rapeport, W. G. Zussman, B. D. Rankin, E. M. Kaye, S. B. Br J Cancer Research Article Twenty patients receiving a variety of emetogenic cytotoxics (including cisplatin in 5) were given a single i.v. infusion of 40 micrograms kg-1 of BRL43694 (as the hydrochloride salt) in successive groups of 3-4 patients between 0-6 hours after chemotherapy. Eleven patients were completely protected from vomiting; 9 had mild to moderate nausea and vomiting, but none severe enough to require alternative anti-emetic 'rescue'. In 4 of the patients in whom BRL43694 was delayed until 4-6 h after chemotherapy, vomiting had already begun; in each case immediate termination of vomiting occurred when BRL43694 was infused. No adverse effects attributable to the anti-emetic were observed. Mean pharmacokinetic parameters in 14 patients in whom plasma assay data are available were: Maximum observed concentration = 30.7 ng ml-1; terminal phase half-life = 8.96 h; total body clearance = 0.376 (1 h-1) kg-1; apparent volume of distribution = 2.85 l kg-1. This study shows BRL43694 to be an effective and well tolerated anti-emetic. Further studies aimed at defining an optimal dose and schedule for use against the most emetogenic cytotoxics are in progress. Nature Publishing Group 1988-11 /pmc/articles/PMC2246838/ /pubmed/2851312 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Research Article
Cassidy, J.
Raina, V.
Lewis, C.
Adams, L.
Soukop, M.
Rapeport, W. G.
Zussman, B. D.
Rankin, E. M.
Kaye, S. B.
Pharmacokinetics and anti-emetic efficacy of BRL43694, a new selective 5HT-3 antagonist.
title Pharmacokinetics and anti-emetic efficacy of BRL43694, a new selective 5HT-3 antagonist.
title_full Pharmacokinetics and anti-emetic efficacy of BRL43694, a new selective 5HT-3 antagonist.
title_fullStr Pharmacokinetics and anti-emetic efficacy of BRL43694, a new selective 5HT-3 antagonist.
title_full_unstemmed Pharmacokinetics and anti-emetic efficacy of BRL43694, a new selective 5HT-3 antagonist.
title_short Pharmacokinetics and anti-emetic efficacy of BRL43694, a new selective 5HT-3 antagonist.
title_sort pharmacokinetics and anti-emetic efficacy of brl43694, a new selective 5ht-3 antagonist.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2246838/
https://www.ncbi.nlm.nih.gov/pubmed/2851312
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