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.

39

Publications

2.8K

Citations

287

Authors

115

Institutions

Publications per year

2017–2026

8

Authors

287

  1. MG
    Michael G. Hutchison

    University of Toronto, Canada

    2 publications · 426 citations

    2

    h-index

  2. SR
    Steven R. Cox

    W.E. Upjohn Institute for Employment Research, United States

    2 publications · 134 citations

    2

    h-index

  3. JF
    Joseph F. Boucher

    Pfizer (United States), United States

    2 publications · 134 citations

    2

    h-index

  4. SP
    S. P. LESMAN

    Pfizer (United States), United States

    2 publications · 134 citations

    2

    h-index

  5. AM
    A Marco

    PharmacoGenetics (China), China

    1 publications · 31 citations

    1

    h-index

1–5 of 287

Venues

  1. 3

    h-index

  2. The Journal of Clinical Pharmacology

    3 publications · 131 citations

    3

    h-index

  3. PubMed

    Repository · 2 publications · 42 citations

    2

    h-index

  4. Drug Information Journal

    DIA · 2 publications · 278 citations

    2

    h-index

  5. Clinical Therapeutics

    2 publications · 73 citations

    2

    h-index

1–5