Примери за използване на Efficacy endpoint на Английски и техните преводи на Български
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Secondary efficacy endpoints.
Efficacy endpoint or haematological parameter a.
Primary efficacy endpoint.
Efficacy endpoints(Part A)(per RECIST v1.1, IERC).
Key secondary efficacy endpoints.
Хората също превеждат
The number of oocytes retrieved was a key secondary efficacy endpoint.
Primary efficacy endpoint OS.
Secondary efficacy endpoints included OS and ORR.
Twelve-month persistent infection was evaluated as additional efficacy endpoint.
Summary of Other Key Efficacy Endpoints(AEGIS 1/2).
The efficacy endpoints were based on 29 patients with 13 weeks of follow-up.
A summary of the key efficacy endpoints is presented below.
Table 10: IRC assessed efficacy results for study MMY2002 Efficacy endpoint.
Summary of Efficacy Endpoints at Day 35(Intent to Treat Population).
Time to First Occurrence of Primary Efficacy Endpoint(CV death, MI or stroke).
Secondary efficacy endpoints included Progression Free Survival and Overall Survival.
Effect of ivacaftor on other efficacy endpoints in studies 1 and 2.
Secondary efficacy endpoints included progression-free survival and objective response rate.
The results for the other key efficacy endpoints are shown in Table 2.
Primary efficacy endpoint was fixed flexion contracture in the treated joint pair subgroup.
The interim analysis results indicated that it failed to achieve statistical significance in any evaluated efficacy endpoint.
The main secondary efficacy endpoint was progression-free survival(PFS).
Table 11: Efficacy results following the final survival update to VISTA study Efficacy endpoint.
As secondary efficacy endpoint overall survival(Table 6) was assessed.
These studies were of poor methodological quality: uncontrolled,open designed and without any well-defined primary efficacy endpoint.
The key efficacy endpoint was the sponsor-defined clinical outcome at test-of-cure(TOC), which was defined by a blinded medical director.
For larger molecules(e.g. monoclonal antibodies), even when robust quality and in vitro comparability data are provided,a comparative study in patients using a conventional clinical efficacy endpoint is usually required.
Primary efficacy endpoint(International Myeloma Working Group criteria) CI=confidence interval; NE=not estimable; MR=minimal response.
In combined dataanalysis of VIEW1 and VIEW2, Eylea demonstrated clinically meaningful changes from baseline in pre-specified secondary efficacy endpoint National Eye Institute Visual Function Questionnaire(NEI VFQ-25) without clinically meaningful differences to ranibizumab.