

REVIEW ARTICLE 

Year : 2020  Volume
: 11
 Issue : 6  Page : 890894 


Understanding superiority, noninferiority, and equivalence for clinical trials
Kamal Kishore^{1}, Rahul Mahajan^{2}
^{1} Department of Biostatistics, Postgraduate Institute of Medical Education and Research, Chandigarh, India ^{2} Department of Dermatology, Venereology, and Leprology, Postgraduate Institute of Medical Education and Research, Chandigarh, India
Date of Submission  06Mar2020 
Date of Decision  09May2020 
Date of Acceptance  20Jul2020 
Date of Web Publication  19Sep2020 
Correspondence Address: Rahul Mahajan Associate Professor, Department of Dermatology, Venereology, and Leprology, Postgraduate Institute of Medical Education and Research, Chandigarh  160 012 India
Source of Support: None, Conflict of Interest: None  Check 
DOI: 10.4103/idoj.IDOJ_130_20
Abstract   
Randomized control trialsare the gold standard for testing the efficacy of new interventions. Historically, superiority trials were methods of choice as reference (standard) interventions were not established for many disease conditions. However currently, reference interventions are available for most of adverse conditions. Despite this, many investigators are using superiority trials in comparison to more suitable noninferiority and equivalence trials. The application of noninferiority and equivalence trials is on the rise, but by and large, these trials are poorly understood, illconceived, inappropriately analyzed, and reported and misinterpreted.
Keywords: Clinical trials, equivalence, methodology, noninferiority, superiority
How to cite this article: Kishore K, Mahajan R. Understanding superiority, noninferiority, and equivalence for clinical trials. Indian Dermatol Online J 2020;11:8904 
How to cite this URL: Kishore K, Mahajan R. Understanding superiority, noninferiority, and equivalence for clinical trials. Indian Dermatol Online J [serial online] 2020 [cited 2021 Jan 19];11:8904. Available from: https://www.idoj.in/text.asp?2020/11/6/890/295420 
Introduction   
The efficacy of a drug in randomized control trials (RCTs) is established using null hypothesis significance testing (NHST) approach.^{[1],[2]} An insightful clinical trial meticulously documents the specific objectives, hypotheses, data analysis, and reporting plans. Traditionally, the investigators were investigating the superiority of the intervention group with a control group in the absence of reference interventions. Therefore, the classical approach was to frame twosided (there is a significant difference in the outcome variable between two groups) alternative hypothesis. The Consolidated standard of Reporting (CONSORT) for RCTs recommend twosided P value and confidence interval approach to declare the statistical significance.^{[3]} After rejecting the null hypothesis, investigators used to compare the average score of the outcome variable between the intervention group (experimental group) and the control group to declare superiority. Recently, many authors are comparing novel interventions (NI) as compared to reference interventions (RI). The competing intervention may not significantly differ in terms of their efficacy. Although, there maybe various other reasons such as safety, low cost, ease of administration, and lesser side effects of a novel intervention.^{[4],[5]} Therefore, the traditional approach of superiority trial do not work in these types of situations. The noninferiority and equivalence trials are better methods of investigations for comparing NI against standard treatment. The primary objectives of noninferiority and equivalence trials are to demonstrate that NI is better or not worse than active control (standard intervention or reference intervention) beyond clinically significant margins.^{[5],[6]} By contrast, noninferiority trials investigate NI (e.g., new drug or treatment claimed to be better than existing standard drug by the company in terms of ease of administration, etc.) is not worse than active control in terms of either or both safety and efficacy beyond a specified margin of clinical significance. However, NI may be better than active control. Equivalence trial investigates novel intervention (e.g., generic drugs claimed by the govt. to have similar efficacy and safety but lower cost as compared to company supplied drug) is not better and worse than active control beyond the prespecified margin of clinical significance. Thus, null and alternative hypothesis and typeI and typeII error will change as per the objectives of the trial. There will also be certain modifications in sample size and statistical analysis plan. The classical approaches of the null hypothesis, sample size, statistical analysis using the P value are not justifiable for noninferiority and equivalence trials. Therefore, the framing of appropriate hypotheses is foundations for the application of appropriate superiority, noninferiority, and equivalence trials. Further, it facilitates sample size, statistical analysis, reporting, and conclusions. Initially, we attempt to disentangle the various intricacies of noninferiority and equivalence trial along with familiar superiority trial. Finally, we proposed a brief table of important characteristics to plan and analyses these types of trials.
Clinically meaningful difference (Δ)
The concept of statistical significance and clinical importance is at the heart of clinical research. The clinically relevant difference should always take precedence over statistical significance. A change in score of few points (e.g., 7065) in the severity of alopecia assessment tool (SALT; range 0100) among alopecia patients may be statistically significant but may not be clinically relevant.^{[7]} Typically, a clinically meaningful difference is determined clinically and statistically after consulting literature, personal experience and discussion with colleagues. It is denoted with symbol Δ and is usually challenging to select. A very small Δ may lead to rejection of a promising drug, whereas large Δ may lead to a selection of potentially inferior drug. Generally, superiority trials justify Δ after analysis as compared to equivalence and noninferiority trials. Whereas, a prerequisite knowledge about Δ is vital to frame hypotheses for equivalence and noninferiority trials.^{[8]} The conclusion about equivalence and noninferiority also depends on Δ. It is compelling to specify Δ after data inspection, but it may give rise to bias.^{[9]} Therefore, it is essential to fix Δ with suitable reasons in advance while finalizing research protocol. A conservative rule is to set a clinically significant difference (Δ) of 50% from the value of lower confidence interval in a superiority trial.^{[6]} The FDA recommended the Δ value of 20, 15, 10, and 5% for the antiinfective drugs with the efficacy of 5080, 8090, 9095, and >95%, respectively, measured as the binary outcome.^{[10]}
Hypothesis and error
An initial step in almost all the studies is to formulate the hypothesis. A superiority trial investigates whether NIis better than active control (AC) or placebo by a specified margin (Δ). The null and alternative hypothesis for superiority trials are H_{0}:μ_{NI} μ_{AC}≤Δ and H_{1}:μ_{NT} μ_{AC}>Δ, respectively. However, in practice, a superiority trial is a twostep NHST process. Therefore, as per NHST, null and alternative hypothesis are formulated as H_{0}:μ_{NT} μ_{AC}= 0 and H_{1}:μ_{NT} μ_{AC}≠ 0. After rejecting the null hypothesis,^{ th}e adequacy of Δ is determined while reporting results. The authors can read an excellent article written by Farrugia et al. on formulating the research question, hypotheses and objectives.^{[11]} The equivalence trial investigates whether NI is equally good as compared to AC. The active control is the standard intervention for noninferiority and equivalence trials as compared to placebo or nonstandard intervention for superiority trial. The equally good margin ranges from Δ to +Δ and known as tolerance range for equivalence studies. The noninferiority trials examine whether NI is not noninferior to AC. The NI will be noninferior to AC (standard intervention) if the noninferiority margin is to right of Δ. The typeI error is critical for conclusions. TypeI error is falsely rejecting a null hypothesis (i.e., falsely declaring statistical significance). The interpretation is inherently confusing to investigators in general for equivalence and noninferiority trials. The objectives of null and alternative hypotheses for superiority (rejection of null) and equivalence trials (rejection of difference) are opposite to each other. Whereas alternative hypothesis for noninferiority trial is onetailed as compared to twotailed for superiority trials. Researchers can refer [Table 1] for a lucid explanation of hypotheses and errors for the different type of trials.  Table 1: The hypotheses and errors for different type of clinical trials
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Sample size
The optimum sample size is one of the crucial requirements to conduct systematic and objective research. It is unethical and unscientific to conduct underpowered studies. Typically, there are four fundamental requirements, such as variance, confidence interval (CI), power, and effect size to calculate the sample size. However, it is essential to prespecify with an appropriate explanation for noninferiority and equivalence trials. [Table 2] gives the formula for calculating sample size for continuous and binary outcome variables in different types of clinical trials. The researcher interested in detailed discussion regarding sample size for many other types of designs can consult “Sample Size Calculations in Clinical Research” by Chow et al.^{[10]} The total sample size (n) is sum (n_{1}+n_{2}) of sample sizes in each arm. The value of k = 0.5, 1 and 2 represent 1:2, 1:1, and 2:1 participants in treatment and control group, respectively. Typically, the value of is taken as zero for superiority trials as the null hypothesis is usually framed as a hypothesis of no difference. In general, sample size to conduct noninferiority and equivalence studies are higher as compared to superiority trials.^{[9]} Let us assume the effectiveness of achieving an intended endpoint (say PASI75) with a placebo and a drug under investigation is 25% and 60%, respectively. Normally, = 0 for superiority trials. The and values at 95% CI and 80% power are 1.96 and 0.84, respectively. The values of P_{1}= 0.25 and P_{2}= 0.60 and d = 0.25–0.60 = 0.35. Assuming, investigator need equal number of cases to controls (K = 1). The application of sample size formula for superiority trial from [Table 2] give a sample of approximately 29 individuals to be recruited in each group. Similarly, assume the effectiveness of achieving PASI75 for noninferiority trial with a standard drug and novel interventions are 55% and 60%, respectively. The and values at 95% CI and 80% power are 1.64 and 0.84, respectively. The values of P_{1}= 0.55 and P_{2}= 0.60 and d = 0.55–0.60 = 0.05. A noninferiority margin of 10% (= 0.10) is considered meaningful for the outcome. Assuming, investigator need equal number of cases to controls (K = 1). The application of sample size formula for noninferiority trial from [Table 2] give a sample of approximately 134 individuals to be recruited in each group. Similarly, assuming researcher is interested in equivalence trial for the measures given for noninferiority trials. All the values except values at 95% CI and 80% power are 1.96 and 1.28 will remain the same. The application of sample size formula for equivalence trial from [Table 2] give a sample of approximately 2047 individuals to be recruited in each group.  Table 2: Sample size formulae for different type of trials for continuous and binary outcome variable
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Statistical analysis
The CONSORT guidelines recommend using the P value and CI approach for declaring the superiority of one intervention over others.^{[3]} However, many studies still report results using the P value approach. The superiority using CI can be declared if the CIdoes not include 0 (1 for odds and risk ratio). When it comes to making inference about noninferiority and equivalence trials, CI approach is recommended in comparison to the P value approach. The intention to treat (ITT) and perprotocol analysis have advantages and disadvantages. ITT is the preferred analytic approach for reporting results from superiority trials in comparison to both ITT and perprotocol analysis for equivalence and noninferiority trials.^{[6],[12]} Usually, both lead to the same conclusion. However, in case of disagreement, a judicious and careful approach after consulting literature needs to be adopted. The clinically significant difference (Δ) plays an essential role in declaring noninferiority and equivalence. The CI to declare equivalence lies between –Δ and +Δ. For the noninferiority trial, novel intervention needs to be similar or better than reference intervention. Therefore, the CI to declare noninferiority lies on the right side of –Δ. [Figure 1] and [Figure 2] display the confidence interval approach to declare significance for positive (higher the better) and negative (lower the better) outcome variable, respectively, for various trials.  Figure 1: Interpretation of results from confidence intervals with different type of trials for positive outcome
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 Figure 2: Interpretation of results from confidence intervals with different type of trials for negative outcome
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Contextualizing   
Scenario
Understanding the choice of trial design based on the evolution of firstline systemic therapies in severe psoriasis from methotrexate to biologics and biosimilars.
The relevance of understanding the trial design for superiority, inferiority, or equivalence can be understood in context to the gradual emergence of biologic response modifiers in the management of severe psoriasis. At the turn of the century, there were limited data on the clinical efficacy and adverse effect profile as targeted therapies were emerging for treating severe psoriasis. The early randomized controlled trials were placebocontrolled.^{[13]} It leads to establishing of methotrexate as a standard drug. Subsequently, a threearm noninferiority trial popularly known as CHAMPION trial compared adalimumab (NI) with the gold standard drug methotrexate,^{[14]} and a placebo. Despite being designed as a noninferiority trial, the CHAMPION trial declared the superiority of adalimumab as compared to methotrexate. The Committee for Proprietary Medicinal Products (CPMP) have discussed conditions under which results of noninferiority trial can be reported as a superiority trial.^{[9]}
As mentioned above, placebocontrolled superiority trials were the first steps for new drugs to show its potential benefits. The recommendations are for noninferiority designs to compare the new drug (adalimumab in this case) relative to an established one (methotrexate here). The CHAMPION trial was designed as a doubleblind, doubledummy placebocontrolled study with an adequate sample size of 90% power to detect noninferiority of adalimumab relative to methotrexate (based on the primary outcome of achieving PASI75 assuming effectiveness of adalimumab to be 62% and of methotrexate to be 60%, and placebo 4%).^{[14]} Despite few limitations or criticisms of the trial, CHAMPION trial proved to be a vital trial in turning the tide toward the more widespread use of biologics in comparison to the traditional systemic agents in managing moderate to severe psoriasis. Recently, many biosimilars came into the market after the expiry of patent for adalimumab (Humira) in both the United States and Europe. Hercogova et al. compared the efficacy, safety, and immunogenicity of the biosimilar MSB11022 (a new agent here) with reference adalimumab (now an established agent).^{[15]} Before the clinical trial, the biosimilar was shown to have structural, functional, and pharmacokinetic equivalence to adalimumab. The researchers can consult [Table 3] as a ready reference to decide about the selection of one trial over another.  Table 3: Summary of important characteristics of difference between different type of trials
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Conclusion   
By default, superiority trials are preferred by researchers. However, the usage and reporting of noninferiority and equivalence trials are increasing. These trials are more complex and challenging to understand and interpret as compared to superiority trials. The researchers need to better equip themselves with the intricacies and subtle differences between various trials to keep themselves abreast with the latest developments. Careful attention will help researchers to make an informed decision about the claimed safety and efficacy of interventions.
Financial support and sponsorship
Nil.
Conflicts of interest
There are no conflicts of interest.
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[Figure 1], [Figure 2], [Figure 1], [Figure 2]
[Table 1], [Table 2], [Table 3], [Table 1], [Table 2], [Table 3]
