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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.
For the primary endpoint of this trial, parasitological cure at Day 28 (PP population), CDA was highly efficacious (94%).
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 trial was survival rate.
The primary endpoint of this study was safety.
In-hospital mortality was the primary endpoint of this study.
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