Dose-proportionality Study Design
Dose-Proportionality Study Design is a research methodology that systematically varies drug dosage levels in a predetermined fashion to assess whether changes in exposure are directly proportional to changes in administered dose, thereby enabling pharmacokinetic evaluation of dose-proportionality across a defined therapeutic range.
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2017–2026
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Patricia Barditch‐Crovo, Steven G. Deeks, Ann Collier et al. · Antimicrobial Agents and Chemotherapy · 2001 · 333 citations · Full text
Christie M. Ballantyne, Nicola Abate, Žhong Yuan et al. · American Heart Journal · 2005 · 240 citations
The pharmacokinetics of meropenem in volunteers
Richard Bax, W Bastain, A. Featherstone et al. · Journal of Antimicrobial Chemotherapy · 1989 · 160 citations
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W.E. Upjohn Institute for Employment Research, United States
2 publications · 134 citations
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AstraZeneca (United Kingdom)
Cambridge, United Kingdom
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10 publications
1.4K citations
Pfizer (United States)
New York, United States
2 h-index
15 publications
977 citations
Certara (United States)
St Louis, United States
2 h-index
2 publications
89 citations
GlaxoSmithKline (United States)
Philadelphia, United States
2 h-index
5 publications
90 citations
Gilead Sciences (United States)
Foster City, United States
2 h-index
7 publications
2K citations
United States Military Academy
West Point, United States
2 h-index
6 publications
795 citations
Celerion (United States)
Lincoln, United States
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4 publications
223 citations
Shanghai Clinical Research Center
Shanghai, China
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11 publications
825 citations
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3 publications · 150 citations
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3 publications · 131 citations
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Repository · 2 publications · 42 citations
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DIA · 2 publications · 278 citations
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