Examples of using Primary efficacy endpoint in English and their translations into Polish
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Medicine
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Ecclesiastic
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Official/political
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Computer
The primary efficacy endpoint, Complete Response(CR:
significantly more patients treated with adefovir dipivoxil achieved the primary efficacy endpoint and obtained significant reductions in serum HBV DNA(23%)
no significant difference was observed in the primary efficacy endpoint, i.e. the proportion of patients who required a RBC transfusion after Day 28 62% of epoetin alfa patients versus 69% of standard therapy patients.
In both studies, the primary efficacy endpoint was the proportion of patients who maintained vision,
The primary efficacy endpoint in all four studies was the proportion of patients in each treatment group who achieved the PASI 75(i.e.,
With respect to the primary efficacy endpoint, the proportion(%) of patients achieving HIV RNA< 50 copies/ml at Week 48 was 241/280(86.1%)
In this subgroup ADENURIC achieved the primary efficacy endpoint in 41%(80 mg QD), 48%(120 mg QD),
In both of these studies tenofovir disoproxil fumarate was significantly superior to adefovir dipivoxil for the primary efficacy endpoint of complete response defined as HBV DNA levels<
In this subgroup ADENURIC achieved the primary efficacy endpoint(sUA< 6.0 mg/dL at the last 3 visits)
The incidence of the primary efficacy endpoint defined as first recurrence of AF
The primary efficacy endpoint, time to first biopsy-proven acute rejection(BPAR) episode or treatment failure defined as graft loss, death or presumptive rejection within the first 6 months post transplantation,
was terminated early when it was determined that the primary efficacy endpoint could not be met ARTEMIS-IPF study.
Primary efficacy endpoints.
The primary efficacy endpoints were.
The primary efficacy endpoint was overall survival.
The primary efficacy endpoint was progression free survival PFS.
The primary efficacy endpoint in both studies was time to progression TTP.
The primary efficacy endpoint was the ASAS20 response rate at Week 12.
The primary efficacy endpoint was ORR, based on Response Evaluation Criteria in Solid Tumours RECIST.
The primary efficacy endpoint was the change from baseline at week 16 in 6-minute walk distance.