Author: Rayner, Craig R.; Smith, Patrick F.; Andes, David; Andrews, Kayla; Derendorf, Hartmut; Friberg, Lena E.; Hanna, Debra; Lepak, Alex; Mills, Edward; Polasek, Thomas M.; Roberts, Jason A.; Schuck, Virna; Shelton, Mark J.; Wesche, David; Rowlandâ€Yeo, Karen
Title: Modelâ€Informed Drug Development for Antiâ€Infectives: State of the Art and Future Cord-id: rfyzbwsf Document date: 2021_3_9
ID: rfyzbwsf
Snippet: Modelâ€informed drug development (MIDD) has a long and rich history in infectious diseases. This review describes foundational principles of translational antiâ€infective pharmacology, including choice of appropriate measures of exposure and pharmacodynamic (PD) measures, patient subpopulations, and drugâ€drug interactions. Examples are presented for stateâ€ofâ€theâ€art, empiric, mechanistic, interdisciplinary, and realâ€world evidence MIDD applications in the development of antibacterial
Document: Modelâ€informed drug development (MIDD) has a long and rich history in infectious diseases. This review describes foundational principles of translational antiâ€infective pharmacology, including choice of appropriate measures of exposure and pharmacodynamic (PD) measures, patient subpopulations, and drugâ€drug interactions. Examples are presented for stateâ€ofâ€theâ€art, empiric, mechanistic, interdisciplinary, and realâ€world evidence MIDD applications in the development of antibacterials (review of minimum inhibitory concentrationâ€based models, mechanismâ€based pharmacokinetic/PD (PK/PD) models, PK/PD models of resistance, and immune response), antifungals, antivirals, drugs for the treatment of global health infectious diseases, and medical countermeasures. The degree of adoption of MIDD practices across the infectious diseases field is also summarized. The future application of MIDD in infectious diseases will progress along two planes; “depth†and “breadth†of MIDD methods. “MIDD depth†refers to deeper incorporation of the specific pathogen biology and intrinsic and acquiredâ€resistance mechanisms; host factors, such as immunologic response and infection site, to enable deeper interrogation of pharmacological impact on pathogen clearance; clinical outcome and emergence of resistance from a pathogen; and patient and population perspective. In particular, improved early assessment of the emergence of resistance potential will become a greater focus in MIDD, as this is poorly mitigated by current development approaches. “MIDD breadth†refers to greater adoption of modelâ€centered approaches to antiâ€infective development. Specifically, this means how various MIDD approaches and translational tools can be integrated or connected in a systematic way that supports decision making by key stakeholders (sponsors, regulators, and payers) across the entire development pathway.
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