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- Design
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1. An introduction to randomization for clinical trials 1
- Prof. William Rosenberger
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2. An introduction to randomization for clinical trials 2
- Prof. William Rosenberger
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3. Randomisation, blinding and drug supply in interactive voice response trials
- Mr. Damian McEntegart
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4. Randomization in clinical trials: time for fresh consideration?
- Dr. Alex Sverdlov
- Analysis
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5. Design and conduct of non-inferiority trials
- Prof. Valerie Durkalski-Mauldin
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6. Nonparametric covariate adjustment
- Prof. Michael Akritas
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7. The impact of randomization on the evidence of a clinical trial
- Prof. Nicole Heussen
- Theory
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8. Historical and ethical issues in trial design
- Dr. J. Rosser Matthews
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9. Likelihood ratios and the strength of statistical evidence
- Prof. Jeffrey Blume
- Randomization, Masking and Allocation Concealment
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11. Detection of and adjustment for selection bias in randomized controlled clinical trials
- Prof. Lieven Nils Kennes
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12. Innovative and effective subject randomization methods
- Prof. Wenle Zhao
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13. Selection bias in studies with unequal allocation
- Dr. Olga M. Kuznetsova
- Archived Lectures *These may not cover the latest advances in the field
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14. Design and conduct of equivalence trials
- Prof. Valerie Durkalski-Mauldin
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15. Dose-finding trials in oncology
- Prof. Anastasia Ivanova
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16. Allocation concealment, prediction and selection bias
- Prof. David Torgerson
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17. Pseudo cluster randomization
- Dr. George Borm
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18. Introduction to flexible, adaptive trial design
- Dr. Cyrus Mehta
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19. Randomization in clinical trials
- Prof. William Rosenberger
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20. Novel methods for randomizing
- Dr. William Grant
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21. Permutation tests
- Dr. YanYan Zhou
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23. Multiple analyses in clinical trials
- Prof. Lemuel Moye
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24. Handling of missing data in clinical trials
- Dr. Linda Yau
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26. N-of-1 randomized clinical trials
- Prof. Patrick Onghena
Printable Handouts
Navigable Slide Index
- Introduction
- Objectives
- Outline of presentation
- Jargon
- Active control trials
- Motivation for non-inferiority (NI) trials
- ICH E9 guidelines (1998)
- FDA draft guidance (2010)
- Key points from 2016 FDA guidance
- Motivation behind non-inferiority (1)
- Motivation behind non-inferiority (2)
- Examples of non-inferiority trials
- ‘Good’ design components
- Trial design issues
- Trial design – step 1
- Formulating the correct question
- Superiority or non-inferiority
- Trial design – step 2
- Choice of active control [ICH E9]
- Post-ERCP example
- Trial design – step 3
- Choice of NI margin (δ) (ICH 1999)
- Dilemma with NI margin
- Aim & choice of non-inferiority studies
- Combination of statistical & clinical judgment
- Choice of NI margin for PEP trial
- Clinical judgment
- Define the difference
- Trial design – step 4
- Assay sensitivity (primary potential problem)
- Biocreep
- Assay sensitivity (factors that reduce sensitivity)
- Assay sensitivity (placebo)
- Sample size
- Analysis approach
- Non-inferiority scenarios
- Hypothesis testing (1)
- Hypothesis testing (2)
- Analysis population (per-protocol’ set of subjects)
- Analysis population (‘ITT’ set of subjects)
- Analysis population (conclusions and summary)
- Key points (1)
- Key points (2)
- Caution signs
- Superiority ↔ non-inferiority
- Interpretation
- Summary
- Related guidances
- Thank you
Topics Covered
- When is ‘non-inferiority’ the correct question for your trial
- Selection of an acceptable margin of non-inferiority
- Selection of the control arm (placebo/active/both)
- How to interpret the study results
Links
Series:
Categories:
Talk Citation
Durkalski-Mauldin, V. (2018, May 31). Design and conduct of non-inferiority trials [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved December 26, 2024, from https://doi.org/10.69645/YJNK5774.Export Citation (RIS)
Publication History
Financial Disclosures
- Prof. Valerie Durkalski-Mauldin has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.
A selection of talks on Methods
Transcript
Please wait while the transcript is being prepared...
0:00
Greetings everyone. My name is Valerie Durkalski-Mauldin,
I'm a professor of Biostatistics in
the Department of Public Health Sciences at the Medical University of South Carolina.
Today I'll be speaking with you about the design and conduct of non-inferiority trials.
0:16
The objectives of today's talk are to review
when non-inferiority is the correct question for your trial,
how to choose the margin of non-inferiority,
what is the importance of maintaining
trial validity when conducting a non-inferiority trial,
and how do you interpret the results.
0:32
The outline of my presentation will first begin
with the actual definition of a non-inferiority trial,
we'll talk about key trial design issues such as
the choice of the active control and the choice of the margin,
we'll review analysis approaches as well as key points to consider.
0:48
So, when we talk about non-inferiority trials,
there's other terminology or jargon that comes into play.
Some might say, an active control trial or
an equivalence trial or a bio-equivalence trial,
and these are all legitimate terms
but they really are talking about different types of studies.
Today, we're going to be focusing on when we're concerned about a one-sided questions.
So, it'll be the non-inferiority trial setting.
1:14
But let's first review what an active control trial is.
It's a trial in which an experimental intervention is
compared with an accepted standard intervention which we call the active control.
These trials have the objective to show efficacy of the test treatment by showing one,
it is superior to the active control,
or your question might be it is as good as the active control,
or it is not inferior to the active control.
All of these are active controlled trials because of
the comparator arm, meaning the active control.
However, you might have different questions and depending on your question,
we'll tell you which design you're actually choosing for your study.