Exact(2)
This study was a randomized, open label comparison that was designed to determine efficacy and safety of miltefosine as the first oral drug for the treatment of zoonotic cutaneous leishmaniasis caused by Leishmania major in comparison with meglumine antimoniate.
The study was designed as a 12-week open label comparison of the plant-based mixture and a fixed dose combination ICS/LABA therapy compared to the ICS/LABA alone in patients with stable COPD.
Similar(58)
We use two metrics for scene-level labeling comparison, i.e., total accuracy and average accuracy.
For object-level labeling comparison, the baseline methods include E-SVM and HV+GC, similar to that of [15].
For scene-level labeling comparison, the baseline is referred to that of Shotton et al. [4], which is the typical method in scene-level manner.
This was a randomized, open-label comparison of 3 regimens of AS monotherapy given as a single oral dose of 2, 4 or 6 mg/kg/day (AS2, AS4 and AS6) for 7 days (total doses 14, 28 and 42 mg/kg) in otherwise healthy adult patients with acute falciparum malaria.
Moreover, the study incorporated an open-label comparison with tiotropium 18 mcg once daily for 7 days.
We previously reported the first stage, a randomized open-label comparison of exenatide QW to exenatide BID in patients with type 2 diabetes over 30 weeks (17).
DURATION-1 and -5 were randomized control trials with open-label comparison of safety and efficacy profile of weekly versus 10 µg twice-daily exenatide use.
The study was a randomized, exploratory, active-controlled, open-label comparison of etravirine (n = 59) and a protease inhibitor chosen by the investigator (n = 57).
This 2-stage protocol consisted of a randomized, open-label comparison of exenatide QW and exenatide BID for 30 weeks, followed by an open-ended assessment period in which all patients received exenatide QW.
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