Examples of using Primary analysis in English and their translations into Norwegian
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Ecclesiastic
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Ecclesiastic
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Primary Analysis ORR Intent-.
Blinded independent review protocol-defined primary analysis.
The primary analysis was combination group vs. pooled monotherapy groups.
Table 3: Patients with Outcome Events in TRITON Primary Analysis.
At the time of the primary analysis, the median follow-up time for both arms was 30 months[range, 0 to 50].
Values in parentheses correspond to 25 months median observation time primary analysis.
Table 9 Survival data from the primary analysis and post-hoc analyses. .
Table 5 EXIST-2- Angiomyolipoma response rates by time-averaged Cmin category, at primary analysis.
Table 6: Efficacy outcomes at week 24(primary analysis) and week 48 in MYRROR study Full Analysis Set with LOCFA.
These patients were classified as week-2 responders andwere included in the primary analysis see Table 5.
Primary analysis was performed with a data cut-off date of 12 December 2012 and is considered the final analysis. .
In CD Study III, at Week 4,58%(499/854) of patients were in clinical response and were assessed in the primary analysis.
The primary analysis was done when all patients had a follow-up of greater than 5 years median follow-up time of 77 months.
Results in patients with wild-type RAS mCRC andmutant RAS mCRC from the primary analysis are presented in the table below.
At the time of primary analysis data for 19 of 20 tumour and symptomatic responders were censored due to on-going response.
Table 8: Efficacy results for GIOTRIF vs erlotinib in LUX-Lung 8, based on primary analysis of OS, including all randomized patients.
Efficacy results from the primary analysis and a post-hoc analysis with 6-months additional follow up are summarised in Table 8.
Observation after 48 months median observation time(compared with results of primary analysis based on 25 months median observation time).
Primary analysis, which assigns a person of any doctor to whom he addresses with complaints- a general analysis of capillary blood.
She has been involved in the planning, carried out the data collection,conducted a primary analysis, participated in the manuscript preparation and has approved the submitted manuscript.
At the time of primary analysis, the median follow-up for overall survival in the full analysis set was 18.3 months.
Progression-free survival(PFS) was assessed by a blinded independent radiology review committee, and the primary analysis was conducted among the first 375 subjects randomized.
In the prospectively defined primary analysis statistical significance was not reached at the primary efficacy endpoint at week 24.
Table 4 Maintenance phase: overview of efficacy results MabThera vs. observation after 48 months median observation time compared with results of primary analysis based on 25 months median observation time.
This was demonstrated in both the primary analysis at one year and in the confirmatory analysis at two years endpoint Table 2.
The primary analysis of progression free survival(PFS) was performed in 645 patients with measurable disease and assessed by independent radiology review.
The PFS results in the post hoc analysis are consistent with the primary analysis and its significance is unchanged and the safety profile is consistent with the primary analysis.
In the primary analysis for DFS in the ITT population, XELOX was shown to be significantly superior to 5-FU/LV HR=0.80, 95% CI=[0.69; 0.93]; p=0.0045.
Observation after 73 months median observation time(compared with results of primary analysis based on 25 months median observation time, and updated analysis based on 48 months median observation time).
The primary analysis of this study was performed on the population of all patients randomly assigned to a treatment arm who received study drug randomised and treated.