Literature DB >> 8040140

Pharmacologically based phase I trials in cancer chemotherapy.

D R Newell1.   

Abstract

Recent developments in Phase I trial methodology are reviewed. Preclinical pharmacological studies can be used in Phase I trials to improve patient selection, starting dose identification, and dose escalation. Establishing pharmacokinetic-pharmacodynamic relationships is also an important new aspect of Phase I trial methodology; these relationships can be exploited in subsequent efficacy studies. Finally, the inclusion of molecular pharmacodynamic studies in Phase I trials is increasing with a view to identifying the mechanism of action of a new agent in patients.

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Year:  1994        PMID: 8040140

Source DB:  PubMed          Journal:  Hematol Oncol Clin North Am        ISSN: 0889-8588            Impact factor:   3.722


  1 in total

1.  Adaptive Estimation of Personalized Maximum Tolerated Dose in Cancer Phase I Clinical Trials Based on All Toxicities and Individual Genomic Profile.

Authors:  Zhengjia Chen; Zheng Li; Run Zhuang; Ying Yuan; Michael Kutner; Taofeek Owonikoko; Walter J Curran; Jeanne Kowalski
Journal:  PLoS One       Date:  2017-01-26       Impact factor: 3.240

  1 in total

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