Examples of using Active-controlled in English and their translations into Croatian
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placebo and active-controlled clinical studies with Exelon transdermal patches for a duration of 24-48 weeks and from post-marketing data.
placebom i aktivno kontroliranim kliničkim ispitivanjima s Exelon transdermalnim flasterom u trajanju od 24-48 tjedana te iz podataka nakon stavljanja lijeka u promet.parallel-group, active-controlled with Zinbryta 150 mg every 4 weeks(n=919)
randomizirano, aktivnim lijekom kontrolirano ispitivanje usporednih skupina sa Zinbrytom od 150 mg svaka 4 tjedna(n 919)The efficacy and safety of Numient in patients with advanced stage Parkinson's disease have been evaluated in 2 double-blind, active-controlled studies: parallel study ADVANCE-PD(study IPX066-B09-02; 22 weeks) and cross-over study ASCEND-PD study IPX066-B-09-06 Part 1; 11 weeks.
Djelotvornot i sigurnost Numienta u bolesnika The first pivotal(phase III) clinical study XM22-03 was an active-controlled study in 202 patients with stage II-IV breast cancer receiving up to 4 cycles of chemotherapy consisting of doxorubicin and docetaxel.
Prvo glavno(faze III) kliničko ispitivanje XM22-03 serological responses after 48 weeks of treatment in active-controlled clinical trials of 1,633 adults with chronic hepatitis B infection,
seroloških odgovora nakon 48 tjedana liječenja u aktivno kontroliranim kliničkim ispitivanjima 1633 odrasla bolesnika s infekcijom kroničnim hepatitisom B,was evaluated in a multicenter, randomized, double-blind, active-controlled, 8-week, parallel-arm study.
dvostruko slijepom ispitivanju s aktivnom kontrolom, u trajanju od 8 tjedana, with Ilaris in the active-controlled clinical studies versus the comparator(7.7%)
s Ilarisom u aktivno kontroliranim kliničkim ispitivanjimastratified, active-controlled study of 833 men and women aged 18-85 years mean age for men.
dvostruko-slijepom, stratificiranom ispitivanju s aktivnom kontrolom u.in metastatic carcinoma of the colon or rectum were studied in three randomised, active-controlled clinical trials in combination with fluoropyrimidine-based first-line chemotherapy.
rektuma ispitane su u tri randomizirana, aktivno kontrolirana klinička ispitivanja u kombinaciji s kemoterapijom prve linije baziranom na fluoropirimidinu.The safety population of Gilenya is derived from two Phase III placebo-controlled clinical studies and one Phase III active-controlled clinical study in patients with relapsing remitting multiple sclerosis.
Populacija za za ocjenu sigurnosti primjene lijeka Gilenya izvedena je iz dva placebom This was a phase III randomised, active-controlled, open-label trial investigating Avastin 10 mg/kg in combination with leucovorin with 5-fluorouracil bolus
Riječ je o randomiziranom, aktivno kontroliranom, otvorenom kliničkom ispitivanju faze III u kojemu se ispitivao Avastin u dozi od 10 mg/kg svaka 2 tjedna u kombinaciji s leukovorinomIn a double-blind, randomized, active-controlled clinical study of 516 patients with invasive fungal disease caused by Aspergillus species or other filamentous fungi, elevated liver transaminases(alanine aminotransferase
U dvostruko-slijepom, randomiziranom, aktivnim lijekom kontroliranom kliničkom ispitivanju s 516 bolesnika s invazivnom gljivičnom bolesti uzrokovanom vrstama Aspergillus ili drugim filamentoznim gljivicama,one long-term double-blind, active-controlled, non-inferiority study.
dugotrajnom dvostruko slijepom, aktivno kontroliranom ispitivanju neinferiornosti.double-blind, active-controlled clinical study used the recommended dose of 400 mg twice daily in combination with a fixed dose of emtricitabine 200 mg(+) tenofovir 245 mg in 281 patients, in comparison to 282 patients taking efavirenz(EFV)
dvostruko slijepom, aktivnim lijekom kontroliranom kliničkom ispitivanju u bolesnika koji prethodno nisu bili liječeni 281 bolesnik primao je preporučenu dozu od 400 mg in a 4-way crossover, double-blind, placebo- and active-controlled(moxifloxacin 400 mg)
dvoslijepom ispitivanju s double-blind, active-controlled, parallel group study,
dvostruko-slijepoj, aktivno kontroliranoj studiji na paralelnim skupinama,double-blind, active-controlled studies in patients with frequent gouty arthritis(≥ 3 attacks in the previous 12 months) unable to use NSAIDs
dvostruko slijepa, aktivno kontrolirana ispitivanja kod bolesnika s učestalim uričnim artritisom(≥3 napada u prethodnih 12 mjeseci) koji nisu mogli koristiti NSAIL-overeceived silodosin 8 mg once daily in two Phase III placebo-controlled clinical studies conducted in the United States and in one placebo- and active-controlled clinical study conducted in Europe.
mg jedanput na dan, u dva placebom kontrolirana klinička ispitivanja faze III koja su se provela u Sjedinjenim Američkim Državama i jednom kliničkom ispitivanju s placebom i aktivnom kontrolom provedenima u Europi.evaluated in a randomised, placebo- and active-controlled(moxifloxacin 400 mg),
randomiziranom ispitivanju s placebom i aktivnom kontrolom(moksifloksacin od 400 mg),In FLAMINGO(ING114915), an open-label, randomised and active-controlled study, 484 HIV-1 infected antiretroviral naïve adults received one dose of either dolutegravir 50 mg once daily(n=242)
U otvorenom, randomiziranom i aktivno kontroliranom ispitivanju FLAMINGO(ING114915), 484 odrasle osobe s HIV-1 infekcijom koje prethodno nisu bile liječene antiretrovirusnim lijekovima primile su jednu
