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However, test re-test %CV of our GSH acquisition was 15%, which is within range of previous research (83, 84)
They are not suitable for self-administration or individuals without proper clinical training
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The primary end point for this trial was at 14 weeks, by which point 51% of the patients receiving golimumab 50 mg and 45% of those receiving golimumab 100 mg had achieved an ACR20 response compared with 9% in the placebo arm (Figure 7-15)
10.2174/2210315510999201210143035 288 TsaiL.-C.LinY.-W.HsiehC.-L
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