Induction of Phase I and Phase II Drug-Metabolizing Enzyme mRNA, Protein, and Activity by BHA, Ethoxyquin, and Oltipraz

1995 ◽  
Vol 135 (1) ◽  
pp. 45-57 ◽  
Author(s):  
T.M. Buetler ◽  
E.P. Gallagher ◽  
C.H. Wang ◽  
D.L. Stahl ◽  
J.D. Hayes ◽  
...  
2008 ◽  
Vol 36 (3) ◽  
pp. 420-427 ◽  
Author(s):  
Toshihiko Makino ◽  
Kayoko Ishikawa ◽  
Isao Igarashi ◽  
Takashi Yamoto ◽  
Sunao Manabe ◽  
...  

2012 ◽  
Vol 30 (15_suppl) ◽  
pp. 2611-2611
Author(s):  
Kehua Wu ◽  
Larry House ◽  
Jacqueline Ramirez ◽  
Mark J. Ratain

2611 Background: There are many phase I clinical combination trials including drug-drug interaction (DDI) studies, but very few of them report positive results. We hypothesized that the utility of DDI studies is low in the absence of a mechanistic hypothesis. Methods: We retrospectively reviewed 119 phase I (2 drug) combination studies published in 2007-2011. Results: Only 23 (19%) studies had a positive rationale, either inhibition/induction of a drug metabolizing enzyme or transporter, co-substrates for the same enzyme or transporter, potential for end-organ toxicity, or protein- binding. Only 9 (8%) studies demonstrated a statistically significant effect DDI, based on AUC of parent drug or active metabolite. There was a strong association between lack of rationale and a lack of interaction, as only 2% of studies without a rationale demonstrated a DDI, compared to 30% of studies with a rationale (Fisher’s exact test, p=0.0004) (Table). Conclusions: DDI studies should not be routinely performed as part of phase I clinical trials. [Table: see text]


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