Примери за използване на There were no clinically relevant на Английски и техните преводи на Български
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There were no clinically relevant differences in Cmax compared to healthy volunteers.
Based on pharmacokinetic data from studies in Japanese andChinese patients with prostate cancer, there were no clinically relevant differences in exposure among the populations.
There were no clinically relevant differences in the clearance of tigecycline between men and women.
In vitro, interaction studies to determine the potential inhibitory effects on transporters concluded that there were no clinically relevant effects, except for OAT3.
There were no clinically relevant pharmacokinetic interactions between Abraxane and carboplatin.
Potential for interference with opioid-mediated analgesia There were no clinically relevant differences between naloxegol 12.5 mg, 25 mg, and placebo in average pain intensity, daily opioid dose or in opioid withdrawal scores over the 12-week study.
There were no clinically relevant differences in systemic exposures between White, Black or Asian races.
Dapagliflozin: There were no clinically relevant differences in systemic exposures between White, Black or Asian races.
There were no clinically relevant differences in pharmacokinetic properties between young children, children, adolescents and adults.
Based on population pharmacokinetic analysis, there were no clinically relevant differences in apalutamide pharmacokinetics between White(Caucasian or Hispanic or Latino; N=761), Black(of African heritage or African American; N=71), Asian(non-Japanese; N=58) and Japanese(N=58).
There were no clinically relevant changes in deferasirox pharmacokinetics when EXJADE granules were administered with food.
There were no clinically relevant pharmacokinetic interactions between human serum albumin-paclitaxel nanoparticlesand carboplatin.
There were no clinically relevant differences in empagliflozin pharmacokinetics between healthy volunteers and patients with type 2 diabetes.
There were no clinically relevant changes in pain scores from baseline in either the methylnaltrexone bromide or placebo-treated patients.
There were no clinically relevant changes from baseline in pain scores in either the methylnaltrexone bromide or placebo-treated patients.
There were no clinically relevant mean increases of C-reactive protein from baseline following long-term treatment with teduglutide for up to 30 months.
There were no clinically relevant differences in the safety population of the elderly subjects who received oseltamivir or placebo compared with the adult population aged up to 65 years.
There are no clinically relevant differences due to age in the pharmacokinetics of cinacalcet.
There are no clinically relevant differences between genders in pharmacokinetic properties of Levemir.
Elderly There are no clinically relevant differences due to age in the pharmacokinetics of cinacalcet.
There are no clinically relevant differences in pharmacokinetics between Caucasian and Asian subjects.
There is no clinically relevant pharmacokinetic drug-drug interaction between nalmefene and alcohol.
There was no clinically relevant difference in pharmacokinetic properties.
There was no clinically relevant effect on the overall exposure of either ethinyloestradiol or levonorgestrel.
There is no clinically relevant interaction with food.
There are no clinically relevant differences in serum insulin or glucose levels after abdominal, deltoid or thigh administration of Semglee.
There are no clinically relevant differences in the rate of absorption when lixisenatide is administered subcutaneously in the abdomen, thigh, or arm.
There are no clinically relevant differences in the rate of absorption when lixisenatide as monotherapy is administered subcutaneously in the abdomen, deltoid, or thigh.
Population pharmacokinetic analyses in patients with advanced NSCLC andhealthy volunteers indicate that there are no clinically relevant effects of age, gender, race, body weight, and phenotypes for CYP3A5 and CYP2C19.
There are no clinically relevant differences in serum insulin or glucose levels after abdominal, deltoid or thigh administration of insulin glargine.