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All enrolled people who received at the least one dose of zosuquidar or placebo all through induction were monitored to the incidence of adverse events (439 individuals, 219 on zosuquidar and 210 on placebo). The most typical adverse gatherings were being associated with the duration of extended and substantial myelosuppression as is predicted with induction chemotherapy. As summarized in Desk five, a lot more than ninety% of people seasoned clinically important fever and neutropenia or infection with neutropenia and thrombocytopenia.

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The HRs were being expressed as zosuquidar/placebo. A ratio < one would point out an enhanced consequence with zosuquidar.

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Just about every situation was repeated in four wells, and consequence expressed because the mean of your four wells. The viability is expressed given that the ratio of your OD of the cells in presence of every drug at distinctive focus with or with no modulator as well as the OD of Manage cells in media with no drug. The IC50 (the 50 % maximal inhibitory focus) was firm by Software Piceatannol 4'-O-?-D-glucopyranoside program (Biosoft, Cambridge, UK) adhering to the viability success. All experiments were being performed in triplicate.

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Forest plot illustration of subgroup analysis of OS. A ratio a lot less than one signifies a profit to zosuquidar.

In conclusion, the addition of zosuquidar, a powerful and selective modulator of P-gp–mediated drug efflux in vitro, to straightforward induction chemotherapy didn't improve the final result of more mature patients with recently diagnosed AML.

Paclitaxel pharmacokinetic parameters from the basic and covariate (categorical and continous) population pharmacokinetic types

Unadjusted and modified hazard ratios for procedure impact: influence of baseline characteristics on comparison of OS amongst patients handled with zosuquidar or placebo

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