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10.1111/jcmm.16052 102 LiQ.XingC.YuanY

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Patients who held their protein targets and training will have rebuilt at least partial lean mass, improving RMR relative to its post-medication nadir

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This is an expensive, time-consuming, and utterly demoralizing scenario that our team has seen derail promising research projects

Food and Drug Administration (FDA) and the European Medicines Agency (EMA) usually require specific endpoints to be met in clinical trials for a drug to be considered for approval