Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

A note on multiple testing procedures in dose finding

P Bauer1

  • 1Department of Medical Statistics, University of Vienna, Austria.

Biometrics
|October 23, 1997
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Torque regulation is affected by joint angle during isometric contraction in young male adults.

Scientific reports·2026
Same author

Evidence for the Collective Nature of Radial Flow in Pb+Pb Collisions with the ATLAS Detector.

Physical review letters·2026
Same author

Evidence for the Dimuon Decay of the Higgs Boson in pp Collisions with the ATLAS Detector.

Physical review letters·2025
Same author

Evidence for Longitudinally Polarized W Bosons in the Electroweak Production of Same-Sign W Boson Pairs in Association with Two Jets in pp Collisions at sqrt[s]=13  TeV with the ATLAS Detector.

Physical review letters·2025
Same author

Observation of tt[over ¯] Production in Pb+Pb Collisions at sqrt[s_{NN}]=5.02  TeV with the ATLAS Detector.

Physical review letters·2025
Same author

Search for Dark Matter Produced in Association with a Dark Higgs Boson in the bb[over ¯] Final State Using pp Collisions at sqrt[s]=13  TeV with the ATLAS Detector.

Physical review letters·2025
Same journal

Fast penalized generalized estimating equations for large longitudinal functional datasets.

Biometrics·2026
Same journal

Causally-interpretable random-effects meta-analysis.

Biometrics·2026
Same journal

Statistical inference for mean function of partially observed functional time series.

Biometrics·2026
Same journal

Subgroup identification via Interaction Tree and Mixed Model for Repeated Measures with application to Alzheimer's disease.

Biometrics·2026
Same journal

Finite mixtures of linear quantile regressions with concomitant variables: a solution to endogeneity in longitudinal data modeling.

Biometrics·2026
Same journal

Discussion on "INTACT: a method for integration of longitudinal physical activity data from multiple sources" by Jingru Zhang, Erjia Cui, Hongzhe Li, and Haochang Shou.

Biometrics·2026
See all related articles

New dose-finding methods require order assumptions for error control. Safer procedures use classical many-one comparisons, avoiding restrictions on dose-response means.

Area of Science:

  • Biostatistics
  • Pharmacometrics
  • Statistical methods

Background:

  • Multiple testing procedures are crucial for dose-finding studies.
  • Recently proposed methods by Tamhane, Hochberg, and Dunnett (1996) offer advanced statistical approaches.
  • These methods aim to control the familywise error rate (FWER) in dose-response assessments.

Purpose of the Study:

  • To evaluate the assumptions underlying recently proposed multiple test procedures for dose finding.
  • To identify conditions under which strong control of the familywise error rate is guaranteed.
  • To propose alternative, broadly applicable procedures for dose-finding analysis.

Main Methods:

  • The study analyzes the theoretical properties of multiple test procedures for dose finding.

Related Experiment Videos

  • It examines the impact of assuming order relations among treatment group means.
  • It contrasts these with procedures based on classical many-one comparisons to a zero-dose control.
  • Main Results:

    • Strong control of the familywise error rate in the cited procedures is contingent upon assuming monotonic dose-response relationships.
    • Without such order assumptions, these specific procedures may not reliably control the overall error rate.
    • Procedures utilizing many-one comparisons with the zero dose offer robust error control without requiring pre-specified order relations.

    Conclusions:

    • The reliability of certain dose-finding multiple test procedures depends on assumptions about dose-response monotonicity.
    • Researchers should exercise caution when applying these methods without order restrictions.
    • Classical many-one comparisons provide a safer, assumption-free alternative for dose-finding when order cannot be guaranteed.