European Journal of Clinical Pharmacology

, Volume 27, Issue 6, pp 721–725 | Cite as

Alizapride, a new substituted benzamide, as an antiemetic during cancer chemotherapy

  • R. A. Joss
  • R. L. Galeazzi
  • A. K. Bischoff
  • K. W. Brunner
Originals

Summary

In early clinical trials alizapride showed a better antiemetic activity with fewer side effects than metoclopramide. Alizapride has now been evaluated in an open dose — ranging study in 24 patients receiving strongly emetic chemotherapy. Alizapride 4–8 mg/kg was given as a 15 min infusion 0.5 h before and 1.5, 3.5, 5.5 and 8.5 h after the chemotherapy. At the dose levels of 6 and 8 mg/kg × 5, respectively 6 out-of 9 and 4 of 4 patients experienced side effects (hypotension, dizziness, profuse sweating, general malaise and diarrhoea). At 4 mg/kg × 54 of 15 patients experienced side effects due to alizapride (dyspnoea 1, diarrhoea 2, extrapyramidal syndrome 1 patient). Overall, 9 of 24 patients were partially or completely protected from nausea and vomiting. Based on this experience alizapride has antiemetic activity and few side effects in the dose of 4 mg/kg × 5.

Key words

alizapride cancer chemotherapy substituted benzamide nausea vomiting side-effects antiemetic therapy 

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Copyright information

© Springer-Verlag 1985

Authors and Affiliations

  • R. A. Joss
    • 1
  • R. L. Galeazzi
    • 2
  • A. K. Bischoff
    • 2
  • K. W. Brunner
    • 1
  1. 1.Institute for Medical OncologyUniversity of BernBernSwitzerland
  2. 2.Department of Internal MedicineUniversity of BernBernSwitzerland

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