Pooled analysis of routine safety parameters observed in healthy participants at baseline and following placebo administration in early phase clinical studies
Abstract Phase I trials inform on the initial safety profile of a new molecule and impact whether further development is pursued or not. Understanding the effect of non‐pharmacological factors on the variability of routine safety parameters could improve decision making in these early clinical trial...
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Wiley,
2024-01-01T00:00:00Z.
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A1234.567 |
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| Kopie 1 | Beschikbaar |