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US and European regulatory initiatives to improve R&D performance.
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Biomarkers and surrogate end points for fit-for-purpose development and regulatory evaluation of new drugs.
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Efficacy and tolerability of the dipeptidyl peptidase-4 inhibitor sitagliptin as monotherapy over 12 weeks in patients with type 2 diabetes.
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Recent evidence of sustained benefit with exenatide in Type 2 diabetes.
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Quantitative clinical pharmacology: Making paradigm shifts a reality.
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