Examples of using Secondary endpoint in English and their translations into Hungarian
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Medicine
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After 4 weeks, the secondary endpoint of hydration was statistically greater in the Top-To-Toe® Bath group, but not to a clinically significant extent.
Statistically significant improvements were observed for the primary endpoint of PFS and secondary endpoint of overall response rate(ORR).
In study MenACWY-TT-039, serum bactericidal activity was also measured using human serum as the source of complement(hSBA) as a secondary endpoint(Table 2).
scores, a secondary endpoint in the study.
Adjusted mean change from baseline in trough FEV1 was also evaluated as a secondary endpoint.
Total Score≥ 30% and CGI-C Score≤ 2) as a secondary endpoint.
Efficacy was also evaluated by calculation of treatment response(defined as decrease in PANSS Total Score≥ 30%) as a secondary endpoint.
In study MenACWY-TT-104, serum bactericidal activity was also measured using hSBA as a secondary endpoint.
In the pivotal clinical trials the rate of recurrence in the 30 days following treatment was assessed as a secondary endpoint.
The key secondary endpoint defined as the proportion of patients achieving complete haematological remission at week 28 was also met(23.0% in the Jakavi arm versus 5.3% in the BAT arm).
The main secondary endpoint“change in best VA” was measured as the difference between best VA in either the left or right eye at
The major secondary endpoint was the proportion of patients who achieved a sPGA score of clear(0)
A key secondary endpoint was the continuous abstinence(CA) rate for week 13 through week 52.
The secondary endpoint of PFS showed no difference between Tarceva and placebo in maintenance treatment(HR=0.94,
The secondary endpoint, PFS, demonstrated a 29% risk reduction of progression
A key secondary endpoint was the incidence of proven/ probable IFIs during the on-treatment period(first dose to last dose of study medicinal product+ 7 days).
A key secondary endpoint was the incidence of proven/ probable IFIs at 100 days post-randomization.
After the 40 week non-treatment phase, a key secondary endpoint for both studies was the Continuous Abstinence Rate(CA) at week 52.
Another secondary endpoint, all cause mortality, occurred at a rate of 5.1%
The main secondary endpoint was MCyR by total daily dose level in the imatinib-resistant patients.