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. 2005 Feb 3;6(1):1.
doi: 10.1186/1468-6708-6-1.

Methodological considerations in the design of trials for safety assessment of new drugs and chemical entities

Affiliations

Methodological considerations in the design of trials for safety assessment of new drugs and chemical entities

Cornel Pater. Curr Control Trials Cardiovasc Med. .
No abstract available

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Figures

Figure 1A
Figure 1A
"Humps" on the terminal part of the T-wave reflecting early ADPs. Figure 1b EAD degenerating in tachycardia.
Figure 2A
Figure 2A
12-lead ECG sampling pattern in the run-in period (baseline). Minimum number of recordings are highlighted at 8, 14 and 20 hours. Figure 2B Plasma concentration-time profiles (PK/PD analysis).
Figure 3A
Figure 3A
Plasma concentration-time profile of parent drug. Figure 3B Plasma concentration-time profile of metabolite.
Figure 4
Figure 4
Normal ECG highlighting the common parameters measured when assessing the QT/QTc interval.
Figure 5
Figure 5
Visual Anlogues Scale to assist in reconciliating the inter-observer assessment of TU morphology.

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