Examples of using Ctrough in English and their translations into Polish
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Medicine
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Computer
Ctrough values are not presented in the table because they are not available from all studies.
The fluctuations between Cmax and Ctrough were higher for the every 4 weeks dosage regimen.
the once-daily dosing is associated with a reduction in the Cmin/Ctrough values of approximately 50.
For subjects weighing 90 kg, Ctrough values were the same for the intravenous
As weight increases from 65 to 200 kg, Cmax is expected to decrease 24% and Ctrough is expected to increase by 5.
Geometric mean Ctrough and geometric mean AUCτ from the BP22333
steady-state trastuzumab Ctrough value at the end of treatment Cycle 7,
bid dosing schedule†† Ctrough values.
Similarly, for subjects in the high BSA tritile, Ctrough values were the same for the intravenous
Cmax24,ss+ 99% and Ctrough+ 18%)
All but one of the patients achieved Ctrough values of saquinavir above the therapeutic threshold(100 ng/ml) in the fasted state.
The objective of the Part 1 was to select a MabThera subcutaneous formulation dose that resulted in comparable MabThera serum Ctrough levels compared with MabThera intravenous formulation.
low BSA tritiles, average Ctrough values following intravenous dosing were approximately 12% and 26% lower compared to the subcutaneous regimen.
bid dosing schedule†† Ctrough values.
A To report analysis of primary endpoint(Ctrough non-inferiority) for Part 2 and available safety
Cmax was 6.14 2.48g/ml, and Ctrough was.
The objective of the Part 2 was to establish the non-inferiority in observed Ctrough levels between the confirmed MabThera subcutaneous dose
In Study 1005, the adjusted geometric mean Ctrough, ss of crizotinib in mild(N=191)
and trough(Ctrough) concentrations were not impacted markedly with changes in BMI or lung function.
In Study 1001, the adjusted geometric mean of plasma Ctrough, ss in mild(N=35) and moderate(N=8)
or lower(Ctrough- 24%)
As a conservative approach, based on enhanced amprenavir Ctrough levels, the twice daily dosing regimen of fosamprenavir with ritonavir was recommended for optimal therapeutic management of this population see section 4.2.
INR measurement can be used at the Ctrough of rivaroxaban(24 hours after the previous intake of rivaroxaban)
The pharmacokinetic results for the co primary endpoint, Ctrough at pre dose Cycle 8(Ctrough), showed non-inferiority of the Herceptin subcutaneous compared to the Herceptin intravenous dose adjusted by body weight.
The objective of the first stage was to establish the rituximab subcutaneous dose that resulted in comparable MabThera subcutaneous formulation serum Ctrough levels compared with MabThera intravenous formulation, when given as part of induction treatment every 3 weeks see section 5.2.
while fixed subcutaneous dosing leads to larger differences in exposure(Ctrough and AUCτ) between subjects with low and high body sizes compared to body-weight-adjusted intravenous dosing, it allows to maintain Ctrough and AUCτ values for all body-size groups at the levels not lower than levels attained by intravenous dosing,