Skip to main content
Top
Published in: BMC Medical Research Methodology 1/2013

Open Access 01-12-2013 | Research article

Phase IV non-inferiority trials and additional claims of benefit

Authors: Rosemarie DLC Bernabe, Grace Wangge, Mirjam J Knol, Olaf H Klungel, Johannes JM van Delden, Anthonius de Boer, Arno W Hoes, Jan AM Raaijmakers, Ghislaine JMW van Thiel

Published in: BMC Medical Research Methodology | Issue 1/2013

Login to get access

Abstract

Background

Non-inferiority (NI) trials in drug research are used to demonstrate that a new treatment is not less effective than an active comparator. Since phase IV trials typically aim at informing a clinical decision, the value of a phase IV non-inferiority trial hinges also on its clinical relevance. In such trials, clinical relevance would refer to the added benefit claims of a specific drug, apart from efficacy, relative to its comparator drug in the trial.

Methods

In this study, we reviewed 41 phase IV trials and extracted information on whether the authors mentioned any additional benefit beyond the NI (efficacy) claim of the drug and whether the additional benefit was proven in the trial. We checked whether the additional claim was based on descriptions only or on formal statistical analyses.

Results

Our results showed that 22 out of the 41 NI trials mentioned additional benefit of the test drug and most of these claims were related to the safety profile. Of all the post-authorization NI trials that claimed additional benefit, 10 out of 22 NI trials used formal statistical analyses to show additional benefit, and only one included a sample size calculation for the additional benefit prior to the trial.

Conclusion

We conclude that there is room for improvement in terms of designing phase IV NI trials with added benefit claims and in proving these additional claims.
Appendix
Available only for authorised users
Literature
4.
go back to reference Eichler HG, Bloechl-Daum B, Abadie E, Barnett D, Konig F, Pearson S: Relative efficacy of drugs: an emerging issue between regulatory agencies and third-party payers. Nat Rev Drug Discov. 2010, 9 (4): 277-291. 10.1038/nrd3079.CrossRefPubMed Eichler HG, Bloechl-Daum B, Abadie E, Barnett D, Konig F, Pearson S: Relative efficacy of drugs: an emerging issue between regulatory agencies and third-party payers. Nat Rev Drug Discov. 2010, 9 (4): 277-291. 10.1038/nrd3079.CrossRefPubMed
5.
go back to reference van der Graaf R, van Delden JJ: Equipoise should be amended, not abandoned. Clin Trials. 2011, 8 (4): 408-416. 10.1177/1740774511409600.CrossRefPubMed van der Graaf R, van Delden JJ: Equipoise should be amended, not abandoned. Clin Trials. 2011, 8 (4): 408-416. 10.1177/1740774511409600.CrossRefPubMed
6.
go back to reference Wangge G, Klungel OH, Roes KC, de Boer A, Hoes AW, Knol MJ: Interpretation and inference in noninferiority randomized controlled trials in drug research. Clin Pharmacol Ther. 2010, 88 (3): 420-423. 10.1038/clpt.2010.134.CrossRefPubMed Wangge G, Klungel OH, Roes KC, de Boer A, Hoes AW, Knol MJ: Interpretation and inference in noninferiority randomized controlled trials in drug research. Clin Pharmacol Ther. 2010, 88 (3): 420-423. 10.1038/clpt.2010.134.CrossRefPubMed
7.
go back to reference Marano N, Plikaytis BD, Martin SW, Rose C, Semenova VA, Martin SK: Effects of a reduced dose schedule and intramuscular administration of anthrax vaccine adsorbed on immunogenicity and safety at 7 months: a randomized trial. JAMA. 2008, 300 (13): 1532-1543. 10.1001/jama.300.13.1532.CrossRefPubMed Marano N, Plikaytis BD, Martin SW, Rose C, Semenova VA, Martin SK: Effects of a reduced dose schedule and intramuscular administration of anthrax vaccine adsorbed on immunogenicity and safety at 7 months: a randomized trial. JAMA. 2008, 300 (13): 1532-1543. 10.1001/jama.300.13.1532.CrossRefPubMed
12.
go back to reference Eichler HG, Pignatti F, Flamion B, Leufkens H, Breckenridge A: Balancing early market access to new drugs with the need for benefit/risk data: a mounting dilemma. Nat Rev Drug Discov. 2008, 7 (10): 818-826. 10.1038/nrd2664.CrossRefPubMed Eichler HG, Pignatti F, Flamion B, Leufkens H, Breckenridge A: Balancing early market access to new drugs with the need for benefit/risk data: a mounting dilemma. Nat Rev Drug Discov. 2008, 7 (10): 818-826. 10.1038/nrd2664.CrossRefPubMed
14.
go back to reference Wangge G, Klungel OH, Roes KC, de Boer A, Hoes AW, Knol MJ: Should non-inferiority drug trails be banned altogether?:. Drug Discov Today. 2013, 18 (11-12): 601-604. 10.1016/j.drudis.2013.01.003.CrossRefPubMed Wangge G, Klungel OH, Roes KC, de Boer A, Hoes AW, Knol MJ: Should non-inferiority drug trails be banned altogether?:. Drug Discov Today. 2013, 18 (11-12): 601-604. 10.1016/j.drudis.2013.01.003.CrossRefPubMed
Metadata
Title
Phase IV non-inferiority trials and additional claims of benefit
Authors
Rosemarie DLC Bernabe
Grace Wangge
Mirjam J Knol
Olaf H Klungel
Johannes JM van Delden
Anthonius de Boer
Arno W Hoes
Jan AM Raaijmakers
Ghislaine JMW van Thiel
Publication date
01-12-2013
Publisher
BioMed Central
Published in
BMC Medical Research Methodology / Issue 1/2013
Electronic ISSN: 1471-2288
DOI
https://doi.org/10.1186/1471-2288-13-70

Other articles of this Issue 1/2013

BMC Medical Research Methodology 1/2013 Go to the issue