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A double-blind comparison of the efficacy of two dose regimens of oral granisetron in preventing acute emesis in patients receiving moderately emetogenic chemotherapy

โœ Scribed by David S. Ettinger; Peter D. Eisenberg; David Fitts; Carl Friedman; Karen Wilson-Lynch; Karen Yocom


Publisher
John Wiley and Sons
Year
1996
Tongue
English
Weight
848 KB
Volume
78
Category
Article
ISSN
0008-543X

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โœฆ Synopsis


The purpose of this study was to define an optimal administration schedule of granisetron for patients receiving moderately ernetogenic chemotherapy by comparing the antiemetic efficacy and safety of 2 mg of the drug administered orally.

METHODS.

In this double-blind, randomized, parallel study, 2-dose regimens of oral granisetron were evaluated in 697 adult cancer patients. Patients were stratified by gender and randomized to receive 2 mg oral granisetron, either as a divided dose given 1 hour prior to chemotherapy and 12 hours after the start of chemotherapy, or as a single dose 1 hour prior to chemotherapy at Cycle 1. The primary efficacy endpoints assessed were the percentage of patients with complete response (no


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