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patients who met virologic but not serologic or biochemical response criteria continued blinded treatment.
pazjenti li ssodisfaw il-kriterji għar-rispons viroloġiku iżda mhux il- kriterji għar-rispons seroloġiku jew bijokimiku komplew bit-trattament blinded.
all adverse events of acute ipf exacerbation reported by the investigator were adjudicated by a blinded adjudication committee.
l-avvenimenti avversi kollha ta' taħrix akut tal-ipv irrappurtati mill-investigatur kienu aġġudikati minn kumitat tal-aġġudikazzjoni "blinded".
the pfs primary endpoint, orr and dcr were based on centralized, independent blinded review of the imaging data.
il-mira ewlenija (pfs), orr u dcr kienu ibbażati fuq reviżjoni indipendenti magħmula bl-għama, ċentralizzata tad-dejta bl-immaġni.
a total of 52 cases of invasive disease caused by vaccine serotypes had accumulated in a blinded follow- up period through april 20, 1999.
total ta’ 52 każ ta’ mard invażiv ikkawżat minn serotipi tat-tilqima, akkumula f’perjodu blinded follow-up sal-20 t’april, 1999.
1reactions reported more frequently in the active arm of the placebo-controlled study than the placebo arm; frequency determined from 39 patients of the blinded phase 3 study.
1reazzjonijiet rrappurtati aktar ta’ spiss fil-grupp attiv tal-istudju kkontrollat bil-plaċebo milli fil-grupp tal-plaċebo; frekwenza determinata minn 39 pazjent tal-istudju blinded ta’ fażi 3.