Examples of using Multicentre in English and their translations into Hungarian
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Medicine
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Ecclesiastic
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Financial
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Official/political
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Computer
wherein the recruitment for international, multicentre examination is of a“competitive type”,
In a Phase I/II 48 week multicentre, open-label study(P1093/ING112578),
Study AVF3694g was a Phase III, multicentre, randomised, placebo-controlled trial designed to evaluate the efficacy and safety of Avastin
DESCARTES was an international, multicentre, double-blind, randomised,
In an open-label, active-controlled, multicentre clinical study,
The GOG-0218 study was a phase III multicentre, randomised, double-blind,
The results for clinically relevant responders pooled from two flexible dose studies out of the three pivotal 26-week multicentre studies in patients with mild-to-moderately severe Alzheimer's Dementia, are provided in Table 4 below.
double- blind, multicentre, multinational study of primarily non-neutropenic patients with candidaemia and a limited number
A Phase IV randomised, multicentre, double-blind study was conducted to compare the efficacy of NeuroBloc(10,000 U) to Botulinum Toxin Type A(150 U)
To submit the preliminary results from Study 20110266(a phase 2, multicentre, randomised, open-label trial assessing the efficacy
double-masked, multicentre, 24-month studies(BPD OCR 003 AMD, or Verteporfin in Photodynamic Therapy-AMD[VIP-AMD],
A further randomised, multicentre, double-blind study was conducted to compare the efficacy of NeuroBloc(10,000 U) to Botulinum Toxin Type A(150 U)
Data from two multicentre phase II clinical trials support the use of capecitabine monotherapy for treatment of patients after failure of taxanes
Efficacy of enzalutamide was established in two randomized placebo-controlled multicentre phase 3 clinical studies[CRPC2(AFFIRM),
double-blind, multicentre study).
The difference between treatment groups in the average weekly frequency of≥3 SCBMs per week was not statistically significant over Weeks 1-12 which is inconsistent with the 5 other multicentre, randomised, double-blind, 12-week placebo controlled
placebo-controlled, multicentre phase 3 clinical trial.
An open-label, uncontrolled, multicentre Phase II study was conducted to determine the efficacy of Tasigna in patients with imatinib resistant or intolerant CML with
controlled, multicentre, multidose, adaptive phase II/III study aimed to compare four regimens of propranolol(1
The data described below reflect exposure to Tasigna in 458 patients in an open-label multicentre Phase II study in patients with imatinib-resistant