Примери за използване на Primary analysis на Английски и техните преводи на Български
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Ecclesiastic
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Ecclesiastic
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Primary analysis.
Best overall response- Primary analysis.
Primary analysis.
Secondary endpoints Progression-free survival- Primary analysis 6.
Primary analysis(ITT).
Хората също превеждат
Overall survival- primary analysis Hazard ratio(95% CI).
Primary analysis(3-point MACE) CV Death.
Kaplan-Meier Curve of Primary Analysis of PFS in Study MMY3007.
Primary Analysis(26 February 2016 Cutoff).
Patients with Outcome Events in TRITON Primary Analysis.
Pooled primary analysis set.
The analysis of OS was performed approximately 13 months after the primary analysis of PFS.
Primary analysis Minimum follow-up: 10.6 months.
N: Number of patients included in the primary analysis of complete response.
The primary analysis is based on all events accrued.
N: Number of adult patients included in the primary analysis of complete response.
Primary analysis All(blinded independent central review).
Table 9 Survival data from the primary analysis and post-hoc analyses. .
Primary analysis at clinical cut-off 31 January 2006.
Summary of efficacy in the primary analysis population(all comers)*(OAK).
The primary analysis will be conducted in our diplomatic office.
Table 5 EXIST-2- Angiomyolipoma response rates by time-averaged Cmin category, at primary analysis.
At the time of the primary analysis there were 1,633 patients randomised.
The primary objective was to evaluate the effect of brentuximab vedotin on cardiac ventricular re-polarization and the predefined primary analysis was the change in QTc from baseline to multiple time points in Cycle 1.
One primary analysis and one updated analysis were performed.
Summary of efficacy from IMpower130 in the primary analysis(ITT-WT population) Efficacy endpoints.
The primary analysis was combination group vs. pooled monotherapy groups.
The efficacy results at the time of the primary analysis of OS including all randomized patients are summarized in Figure 2 and Table 10.
Primary analysis was performed with a data cut-off date of 14 November 2011.
The trial met its primary endpoint at the primary analysis, demonstrating a statistically significant improvement in PFS by investigator.