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antal evaluerbare patienter
number of evaluable patients

f antal evaluerbare patienter.
f number of patients evaluable.

a antal af evaluerbare patienter.
a number of patients evaluable.

virologisk respons hos evaluerbare patientera
virologic response in evaluable subjectsa

36 patienter var evaluerbare for effekt.
36 patients were evaluable for efficacy.

behandlingsuger n = antal evaluerbare patienter
weeks of treatment n = number of patients evaluable

40 patienter var fuldt evaluerbare for respons.
forty patients were fully evaluable for response.

figur 1 : evaluerbare virkninger af en politik
figure 1 policy effects to be evaluated

disse virkninger eller evaluerbare kriterier fremgår af figur 1.
figure 1 shows these effects and evaluation criteria.

studie med aktiv komparator (n=2569) evaluerbare patienter
active comparator trials (n=2569) evaluable patients

populationen af alle evaluerbare patienter (itt) (n=41)
all evaluable patients (itt) population (n=41)

effektresultaterne efter 24 timer vises i tabel 2 for den evaluerbare patientpopulation.
efficacy results at the end of 24 hours, are presented in table 2 below for the evaluable patient population.

atten var evaluerbare for effekt og sikkerhed og yderligere fem patienter var kun evaluerbare for toksicitet.
eighteen were evaluable for efficacy and safety and a further five patients were evaluable for toxicity only.

den samlede molekylære responsrate var 48% (49 ud af 102 evaluerbare patienter).
the complete molecular response rate was 48% (49 out of 102 evaluable patients).

kun patienter, der bådehavde baseline samt ≥ 1 evaluerbare vurderinger efter baseline blev inkluderet idenneanalyse.
only subjects that had both baseline and ≥ 1 evaluable post-baseline assessments were included in this analysis.

en tæt latenstid til frembrud (≤ 2 uger) efter behandlingsstart med umec/vi blev rapporteret i 7/12 evaluerbare sager.
a close latency to onset (≤ 2 weeks) following start of treatment with umec/vi was reported in 7/12 evaluable cases.

ved den kumulative gennemgang af bronkokonstriktion identificeredes 45 evaluerbare tilfælde efter administration af regadenoson, hvor der ikke var symptomer på overfølsomhedsreaktioner.
the cumulative review of bronchoconstriction identified 45 evaluable cases following regadenoson administration that did not have features of a hypersensitivity reaction.

i de tre studier, havde respektivt 16, 19 og 28 patienter evaluerbare baseline isolater og blev derfor i studiet i mindst 24 måneder.
of the three study groups, 16, 19 and 28 patients respectively had evaluable baseline isolates and subsequently remained in the study for at least 24 weeks.