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The primary endpoint of this study is overall survival (OS).
The primary endpoint of this study was the baseline-adjusted, placebo-corrected QT interval corrected using the Fridericia method (ΔΔQTcF).
The primary endpoint of this study was adverse outcome.
The primary endpoint of this study is 90-day all-cause mortality.
The primary endpoint of this study was comparison of the change in COPD symptoms assessed by the CCQ questionnaire between the intervention and control group at 26 weeks.
The primary endpoint of this study was overall survival (OS).
Last, serum PSA was the primary endpoint of this study.
The primary endpoint of this study was response rates (RR).
The primary endpoint of this study was safety.
In-hospital mortality was the primary endpoint of this study.
The primary endpoint of this study is the hospital stays.
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