Literature DB >> 10576409

Establishing equivalence by showing that a specified percentage of the effect of the active control over placebo is maintained.

E B Holmgren1.   

Abstract

We propose a procedure for establishing equivalence that determines whether a specified percentage of the treatment effect of a known active agent over placebo is maintained. This procedure accounts for the error in the estimates from the historical studies of the known active agent and placebo as well as the error in the estimates from the equivalence study of the new test treatment versus the active control. After the procedure is presented, it is compared analytically to a procedure in which the equivalence boundary is estimated from historical data and then used with a one-sided test. We address sample size requirements for the proposed equivalence procedure. We also illustrate the use of the proposed procedure with an example from the clinical area of thrombolytic therapy in acute myocardial infarction.

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Year:  1999        PMID: 10576409     DOI: 10.1081/bip-100101201

Source DB:  PubMed          Journal:  J Biopharm Stat        ISSN: 1054-3406            Impact factor:   1.051


  2 in total

1.  Defining the noninferiority margin and analysing noninferiority: An overview.

Authors:  Turki A Althunian; Anthonius de Boer; Rolf H H Groenwold; Olaf H Klungel
Journal:  Br J Clin Pharmacol       Date:  2017-04-06       Impact factor: 4.335

2.  A note on the determination of non-inferiority margins with application in oncology clinical trials.

Authors:  Binbing Yu; Harry Yang; Antony Sabin
Journal:  Contemp Clin Trials Commun       Date:  2019-09-23
  2 in total

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