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Phase I trial with pharmacokinetics of CB10-277 given by 24 hours continuous infusion.

The dose limiting toxicities of the short infusion trial of the dacarbazine analog, CB10-277, were nausea and vomiting which appeared to be related to the peak plasma level of the parent drug. In addition, based on mouse studies, these dose limiting toxicities occurred at a less than optimal level o...

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Hlavní autoři: Foster, B. J., Newell, D. R., Gumbrell, L. A., Jenns, K. E., Calvert, A. H.
Médium: Artigo
Jazyk:Inglês
Vydáno: Nature Publishing Group 1993
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1968159/
https://ncbi.nlm.nih.gov/pubmed/8431368
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