Примери за използване на Efficacy endpoints на Английски и техните преводи на Български
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All rates of efficacy endpoints improved or were maintained through 2 years of treatment.
Proportion of patients meeting efficacy endpoints at week 8(OCTAVE induction study 1
Efficacy endpoints included sub maximal exercise capacity,
The primary objective of this study was safety, while efficacy endpoints were exploratory.
placebo-controlled study evaluating efficacy endpoints at Week 6 and Week 52.
The clinical significance of this finding is unknown since there were no consistent relationships between IgG antibody level and clinical efficacy endpoints.
Additional analyses suggest that the surgical procedure type did not influence the trends in efficacy endpoints and the efficacy of IONSYS was similar across the range of body mass indices studied< 25 to> 40 kg/m2.
Table 6 summarises the subsequent interim analysis of efficacy endpoints including an estimate of the 6-month rates by Kaplan-Meier for DOR
These patients also experienced comparable clinical improvement, in terms of the efficacy endpoints and haematological parameters detailed above,
Data collected in the post-marketing phase will also be examined to determine if a suitable Naglazyme maintenance dose can be recommended relative to the efficacy endpoints used in the clinical studies.
Proportion of adolescent patients with≥4-point improvement on the pruritus NRS in AD-1526 studya(FAS)b a In the primary analyses of the efficacy endpoints, subjects who received rescue treatment or with missing data were considered non-responders.
Primary efficacy endpoints were haemoglobin stabilization(patients who maintained a haemoglobin concentration above the haemoglobin set-point
In all studies, the efficacy endpoints were“Count of episodes of laughing
the Marketing Authorisation Holder bridged the efficacy of Emulgel to Spraygel based on a cross-study comparison of the efficacy endpoints, which are however confounded by differences in study methods and populations.
Study BO22227 was designed to demonstrate non-inferiority of treatment with Herceptin subcutaneous formulation versus Herceptin intravenous formulation based on co-primary PK and efficacy endpoints(trastuzumab Ctrough at pre-dose Cycle 8, and pCR rate at definitive surgery, respectively).
The pivotal trial BO22227 was designed to demonstrate non-inferiority of treatment with Herceptin subcutaneous formulation versus treatment with Herceptin intravenous formulation based on coprimary PK and efficacy endpoints(trastuzumab Ctrough at pre-dose Cycle 8,
The main secondary efficacy endpoint was progression-free survival(PFS).
Efficacy endpoint or haematological parameter a.
Time to First Occurrence of Primary Efficacy Endpoint(CV death,
As secondary efficacy endpoint overall survival(Table 6) was assessed.