Literature DB >> 2851312

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

J Cassidy1, V Raina, C Lewis, L Adams, M Soukop, W G Rapeport, B D Zussman, E M Rankin, S B Kaye.   

Abstract

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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Year:  1988        PMID: 2851312      PMCID: PMC2246838          DOI: 10.1038/bjc.1988.278

Source DB:  PubMed          Journal:  Br J Cancer        ISSN: 0007-0920            Impact factor:   7.640


  7 in total

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Authors:  B Costall; A M Domeney; R J Naylor; F D Tattersall
Journal:  Neuropharmacology       Date:  1986-08       Impact factor: 5.250

2.  First results with ICS 205-930 (5-HT3 receptor antagonist) in prevention of chemotherapy-induced emesis.

Authors:  U Leibundgut; I Lancranjan
Journal:  Lancet       Date:  1987-05-23       Impact factor: 79.321

3.  Identification of serotonin M-receptor subtypes and their specific blockade by a new class of drugs.

Authors:  B P Richardson; G Engel; P Donatsch; P A Stadler
Journal:  Nature       Date:  1985 Jul 11-17       Impact factor: 49.962

4.  Blockade of neuronal tryptamine receptors by metoclopramide.

Authors:  J R Fozard; A T Mobarok ALI
Journal:  Eur J Pharmacol       Date:  1978-05-01       Impact factor: 4.432

5.  Inhibition of cisplatin-induced vomiting by selective 5-hydroxytryptamine M-receptor antagonism.

Authors:  W D Miner; G J Sanger
Journal:  Br J Pharmacol       Date:  1986-07       Impact factor: 8.739

6.  Prevention of emesis in patients receiving cytotoxic drugs by GR38032F, a selective 5-HT3 receptor antagonist.

Authors:  D Cunningham; J Hawthorn; A Pople; J C Gazet; H T Ford; T Challoner; R C Coombes
Journal:  Lancet       Date:  1987-06-27       Impact factor: 79.321

7.  Immediate termination of intractable vomiting induced by cisplatin combination chemotherapy using an intensive five-drug antiemetic regimen.

Authors:  P M Plezia; D S Alberts; J Kessler; M S Aapro; V Graham; E A Surwit
Journal:  Cancer Treat Rep       Date:  1984-12
  7 in total
  15 in total

1.  Human responses to inhaled capsaicin are not inhibited by granisetron.

Authors:  N B Choudry; J R McEwan; E A Lavender; A J Williams; R W Fuller
Journal:  Br J Clin Pharmacol       Date:  1991-03       Impact factor: 4.335

Review 2.  5-HT3 receptor antagonists. An overview of their present status and future potential in cancer therapy-induced emesis.

Authors:  M S Aapro
Journal:  Drugs       Date:  1991-10       Impact factor: 9.546

3.  Ondansetron--a new safe and effective antiemetic in patients receiving high-dose melphalan.

Authors:  C V Viner; P J Selby; G B Zulian; M E Gore; M E Butcher; C M Wootton; T J McElwain
Journal:  Cancer Chemother Pharmacol       Date:  1990       Impact factor: 3.333

4.  Pharmacokinetics and tolerability of ascending intravenous doses of granisetron, a novel 5-HT3 antagonist, in healthy human subjects.

Authors:  A Allen; C C Asgill; D M Pierce; J Upward; B D Zussman
Journal:  Eur J Clin Pharmacol       Date:  1994       Impact factor: 2.953

Review 5.  5-HT3 receptor antagonists for the prevention of chemotherapy-induced nausea and vomiting. A comparison of their pharmacology and clinical efficacy.

Authors:  R E Gregory; D S Ettinger
Journal:  Drugs       Date:  1998-02       Impact factor: 9.546

6.  A dose-finding study of granisetron, a novel antiemetic, in patients receiving high-dose cisplatin. Granisetron Study Group.

Authors:  M Soukop
Journal:  Support Care Cancer       Date:  1994-05       Impact factor: 3.603

7.  Serotonin and vasoactive intestinal peptide antagonists attenuate rotavirus diarrhoea.

Authors:  S Kordasti; H Sjövall; O Lundgren; L Svensson
Journal:  Gut       Date:  2004-07       Impact factor: 23.059

Review 8.  Signals for nausea and emesis: Implications for models of upper gastrointestinal diseases.

Authors:  Paul L R Andrews; Charles C Horn
Journal:  Auton Neurosci       Date:  2006-03-23       Impact factor: 3.145

9.  Randomized, double-blind, crossover study of palonosetron compared with granisetron for the prevention of chemotherapy-induced nausea and vomiting in a Chinese population.

Authors:  Weihua Tian; Zhiqiang Wang; Juntian Zhou; Shucai Zhang; Jinghui Wang; Qiang Chen; Cheng Huang; Liangxi Pan; Lili Zhang; Jianjin Huang; Hong Shen; Tongyu Lin
Journal:  Med Oncol       Date:  2010-01-05       Impact factor: 3.064

Review 10.  Granisetron. An update of its therapeutic use in nausea and vomiting induced by antineoplastic therapy.

Authors:  Y E Yarker; D McTavish
Journal:  Drugs       Date:  1994-11       Impact factor: 9.546

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