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Treatment‐emergent adverse events (TEAEs) were recorded and assessed for severity. Serious TEAEs were recorded. Routine physical and clinical laboratory evaluations included measurement of vital signs and weight and administration of electrocardiograms.
Copyright and License information: ©2020 The Authors. published by John Wiley & Sons Ltd on behalf of European Sleep Research Society
This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
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