Adaptive design

Short description: Concept in medicine referring to design of clinical trials

In an adaptive design of a clinical trial, the parameters and conduct of the trial for a candidate drug or vaccine may be changed based on an interim analysis.[1][2][3] Adaptive design typically involves advanced statistics to interpret a clinical trial endpoint.[2] This is in contrast to traditional single-arm (i.e. non-randomized) clinical trials or randomized clinical trials (RCTs) that are static in their protocol and do not modify any parameters until the trial is completed. The adaptation process takes place at certain points in the trial, prescribed in the trial protocol. Importantly, this trial protocol is set before the trial begins with the adaptation schedule and processes specified. Adaptions may include modifications to: dosage, sample size, drug undergoing trial, patient selection criteria and/or "cocktail" mix.[4] The PANDA (A Practical Adaptive & Novel Designs and Analysis toolkit) provides not only a summary of different adaptive designs, but also comprehensive information on adaptive design planning, conduct, analysis and reporting.[5]

Schematic block diagram of an adaptive design for a clinical trial[2]

## Contents

* 1 Purpose
* 2 History
* 3 Characteristics
* 4 Types
* 4.1 Overview
* 4.2 Dose finding design
* 4.3 Group sequential design
* 5 Usage
* 5.1 In 2020 COVID-19 related trials
* 5.2 Breast cancer
* 5.2.1 I-SPY 1
* 5.2.2 I-SPY 2
* 5.3 Alzheimer's
* 6 Bayesian designs
* 7 Statistical analysis
* 8 Added complexity
* 9 Risks
* 10 Resources (external links)
* 11 See also
* 12 References
* 13 Sources
* 14 External links

## Purpose

The aim of an adaptive trial is to more quickly identify drugs or devices that have a therapeutic effect, and to zero in on patient populations for whom the drug is appropriate.[6] When conducted efficiently, adaptive trials have the potential to find new treatments while minimizing the number of patients exposed to the risks of clinical trials. Specifically, adaptive trials can efficiently discover new treatments by reducing the number of patients enrolled in treatment groups that show minimal efficacy or higher adverse-event rates. Adaptive trials can adjust almost any part of its design, based on pre-set rules and statistical design, such as sample size, adding new groups, dropping less effective groups and changing the probability of being randomized to a particular group, for example.

## History

In 2004, a Strategic Path Initiative was introduced by the United States Food and Drug Administration (FDA) to modify the way drugs travel from lab to market. This initiative aimed at dealing with the high attrition levels observed in the clinical phase. It also attempted to offer flexibility to investigators to find the optimal clinical benefit without affecting the study's validity. Adaptive clinical trials initially came under this regime.[7]

The FDA issued draft guidance on adaptive trial design in 2010.[6] In 2012, the President's Council of Advisors on Science and Technology (PCAST) recommended that FDA "run pilot projects to explore adaptive approval mechanisms to generate evidence across the lifecycle of a drug from the pre-market through the post-market phase." While not specifically related to clinical trials, the council also recommended that FDA "make full use of accelerated approval for all drugs meeting the statutory standard of addressing an unmet need for a serious or life-threatening disease, and demonstrating an impact on a clinical endpoint other than survival or irreversible morbidity, or on a surrogate endpoint, likely to predict clinical benefit."[8]

By 2019, the FDA updated their 2010 recommendations and issued "Adaptive Design Clinical Trials for Drugs and Biologics Guidance".[9]

## Characteristics

Traditionally, clinical trials are conducted in three steps:[2]

1. The trial is designed.
2. The trial is conducted as prescribed by the design.
3. Once the data are ready, they are analysed according to a pre-specified analysis plan.

## Types

### Overview

Any trial design that can change its design, during active enrollment, could be considered an adaptive clinical trial. There are a number of different types, and real life trials may combine elements from these different trial types:[2][10][11][12][13][14] In some cases, trials have become an ongoing process that regularly adds and drops therapies and patient groups as more information is gained.[7]

Trial Design Type  | Adaptable Element  | Description

|
|

Dose-finding  | Treatment dose  | Dose may be changed to find minimally toxic, and maximally effective dosing.
Adaptive hypothesis  | Trial endpoints  | According to pre-set protocols, these trials can adapt to investigate new hypothesis, and add new endpoints accordingly. An example would be switch from a superiority to a non-inferiority design.
Group sequential  | Sample size, by a set interval at a time.  | Sample sizes can be changed. These trials usually change the sample size by adding or removing set-blocks of patients such as adding 20 patients at a time, and then re-evaluating. This type of design is explained in detail on PANDA.[5]
Response adaptive randomisation  | Randomization ratios  | The chance of being randomized into one particular group, can change. Treatment groups are not added or dropped, but the chance of being randomized, for example, into the treatment group could increase after interim analysis. This type of design is explained in detail on PANDA.[5]
Adaptive treatment-switching  | Treatment  | These trials, based on pre-set rules, can change individual patients from one group to another.
Biomarker adaptive  | Multiple, on the basis of biomarker discoveries  | These trials incorporated biomarkers into their decision making process. Examples including focusing on a sub-population that may be more biological receptive to a treatment, or choosing new treatments for a trial as more becomes known about the biology of the disease.
Population enrichment  | Population enrolled  | The population that the trial enrolls from may change based on, for example, improved epidemiological understanding of a disease. This type of design is explained in detail on PANDA.[5]
Platform Trial | Multiple, on the basis that all different treatment groups share the same, single control group  | Platform trials are defined by having a constant control group, against which variable treatment groups are compared.
Multi-arm multi-stage  | The current treatment arms  | These trials adapt to stop recruitment to treatment arms that show less efficacy and therefore they do not allocate new participants to the least effective-seeming treatment arms. This type of design is explained in detail on PANDA.[5]
Sample size re-estimation  | Sample size  | Sample sizes of either the whole trial or individual groups may change as more becomes known about effect sizes. This type of design is explained in detail on PANDA.[5]
Seamless Phase I/II  | Entry into phase II trials  | These trials collect data on safety and dosing simultaneously.
Seamless Phase II/III  | Entry into phase III trials  | These trials collect data on dosing and efficacy simultaneously.

### Dose finding design

Phase I of clinical research focuses on selecting a particular dose of a drug to carry forward into future trials. Historically, such trials have had a "rules-based" (or "algorithm-based") design, such as the 3+3 design.[15] However, these "A+B" rules-based designs are not appropriate for phase I studies and are inferior to adaptive, model-based designs.[16] An example of a superior design is the continual reassessment method (CRM).[17][18][19]

### Group sequential design

Group sequential design is the application of sequential analysis to clinical trials. At each interim analysis, investigators will use the current data to decide whether the trial should either stop or should continue to recruit more participants. The trial might stop either because the evidence that the treatment is working is strong ("stopping for benefit") or weak ("stopping for futility"). Whether a trial may stop for futility only, benefit only, or either, is stated in advance. A design has "binding stopping rules" when the trial must stop when a particular threshold of (either strong or weak) evidence is crossed at a particular interim analysis. Otherwise it has "non-binding stopping rules", in which case other information can be taken into account, for example safety data. The number of interim analyses is specified in advance, and can be anything from a single interim analysis (a "two-stage" design") to an interim analysis after every participant ("continuous monitoring").

For trials with a binary (response/no response) outcome and a single treatment arm, a popular and simple group sequential design with two stages is the Simon design. In this design, there is a single interim analysis partway through the trial, at which point the trial either stops for futility or continues to the second stage.[20] Mander and Thomson also proposed a design with a single interim analysis, at which point the trial could stop for either futility or benefit.[21]

For single-arm, single-stage binary outcome trials, a trial's success or failure is determined by the number of responses observed by the end of the trial. This means that it may be possible to know the conclusion of the trial (success or failure) with certainty before all the data are available. Planning to stop a trial once the conclusion is known with certainty is called non-stochastic curtailment. This reduces the sample size on average. Planning to stop a trial when the probability of success, based on the results so far, is either above or below a certain threshold is called stochastic curtailment. This reduces the average sample size even more than non-stochastic curtailment. Stochastic and non-stochastic curtailment can also be used in two-arm binary outcome trials, where a trial's success or failure is determined by the number of responses observed on each arm by the end of the trial.

An example of a Simon design, a two-stage design for a binary outcome trial. Two possible occurrences for a two-stage trial: stopping at stage one (top) and stopping at stage two (bottom) An example of a three-stage group sequential design, shown in terms of the test statistic.

## Usage

See also: Phases of clinical research

The adaptive design method developed mainly in the early 21st century.[2] In November 2019, the US Food and Drug Administration provided guidelines for using adaptive designs in clinical trials.[3]

### In 2020 COVID-19 related trials

In April 2020, the World Health Organization published an "R&D Blueprint (for the) novel Coronavirus" (Blueprint). The Blueprint documented a "large, international, multi-site, individually randomized controlled clinical trial" to allow "the concurrent evaluation of the benefits and risks of each promising candidate vaccine within 3–6 months of it being made available for the trial." The Blueprint listed a Global Target Product Profile (TPP) for COVID‑19, identifying favorable attributes of safe and effective vaccines under two broad categories: "vaccines for the long-term protection of people at higher risk of COVID‑19, such as healthcare workers", and other vaccines to provide rapid-response immunity for new outbreaks.[22]

The international TPP team was formed to 1) assess the development of the most promising candidate vaccines; 2) map candidate vaccines and their clinical trial worldwide, publishing a frequently-updated "landscape" of vaccines in development;[23] 3) rapidly evaluate and screen for the most promising candidate vaccines simultaneously before they are tested in humans; and 4) design and coordinate a multiple-site, international randomized controlled trial - the "Solidarity trial" for vaccines[22][24] - to enable simultaneous evaluation of the benefits and risks of different vaccine candidates under clinical trials in countries where there are high rates of COVID‑19 disease, ensuring fast interpretation and sharing of results around the world.[22] The WHO vaccine coalition will prioritize which vaccines should go into Phase II and III clinical trials, and determine harmonized Phase III protocols for all vaccines achieving the pivotal trial stage.[22]

The global "Solidarity" and European "Discovery" trials of hospitalized people with severe COVID‑19 infection apply adaptive design to rapidly alter trial parameters as results from the four experimental therapeutic strategies emerge.[25][26][27][28] The US National Institute of Allergy and Infectious Diseases (NIAID) initiated an adaptive design, international Phase III trial (called "ACTT") to involve up to 800 hospitalized COVID‑19 people at 100 sites in multiple countries.[29]

### Breast cancer

An adaptive trial design enabled two experimental breast cancer drugs to deliver promising results after just six months of testing, far shorter than usual. Researchers assessed the results while the trial was in process and found that cancer had been eradicated in more than half of one group of patients. The trial, known as I-Spy 2, tested 12 experimental drugs.[6]

#### I-SPY 1

For its predecessor I-SPY 1, 10 cancer centers and the National Cancer Institute (NCI SPORE program and the NCI Cooperative groups) collaborated to identify response indicators that would best predict survival for women with high-risk breast cancer. During 2002–2006, the study monitored 237 patients undergoing neoadjuvant therapy before surgery. Iterative MRI and tissue samples monitored the biology of patients to chemotherapy given in a neoadjuvant setting, or presurgical setting. Evaluating chemotherapy's direct impact on tumor tissue took much less time than monitoring outcomes in thousands of patients over long time periods. The approach helped to standardize the imaging and tumor sampling processes, and led to miniaturized assays. Key findings included that tumor response was a good predictor of patient survival, and that tumor shrinkage during treatment was a good predictor of long-term outcome. Importantly, the vast majority of tumors identified as high risk by molecular signature. However, heterogeneity within this group of women and measuring response within tumor subtypes was more informative than viewing the group as a whole. Within genetic signatures, level of response to treatment appears to be a reasonable predictor of outcome. Additionally, its shared database has furthered the understanding of drug response and generated new targets and agents for subsequent testing.[30]

#### I-SPY 2

I-SPY 2 is an adaptive clinical trial of multiple Phase 2 treatment regimens combined with standard chemotherapy. I-SPY 2 linked 19 academic cancer centers, two community centers, the FDA, the NCI, pharmaceutical and biotech companies, patient advocates and philanthropic partners. The trial is sponsored by the Biomarker Consortium of the Foundation for the NIH (FNIH), and is co-managed by the FNIH and QuantumLeap Healthcare Collaborative. I-SPY 2 was designed to explore the hypothesis that different combinations of cancer therapies have varying degrees of success for different patients. Conventional clinical trials that evaluate post-surgical tumor response require a separate trial with long intervals and large populations to test each combination. Instead, I-SPY 2 is organized as a continuous process. It efficiently evaluates multiple therapy regimes by relying on the predictors developed in I-SPY 1 that help quickly determine whether patients with a particular genetic signature will respond to a given treatment regime. The trial is adaptive in that the investigators learn as they go, and do not continue treatments that appear to be ineffective. All patients are categorized based on tissue and imaging markers collected early and iteratively (a patient's markers may change over time) throughout the trial, so that early insights can guide treatments for later patients. Treatments that show positive effects for a patient group can be ushered to confirmatory clinical trials, while those that do not can be rapidly sidelined. Importantly, confirmatory trials can serve as a pathway for FDA Accelerated Approval. I-SPY 2 can simultaneously evaluate candidates developed by multiple companies, escalating or eliminating drugs based on immediate results. Using a single standard arm for comparison for all candidates in the trial saves significant costs over individual Phase 3 trials. All data are shared across the industry.[30] As of January 2016[update] I-SPY 2 is comparing 11 new treatments against 'standard therapy', and is estimated to complete in Sept 2017.[31] By mid 2016 several treatments had been selected for later stage trials.[32]

### Alzheimer's

Researchers plan to use an adaptive trial design to help speed development of Alzheimer's disease treatments, with a budget of 53 million euros. The first trial under the initiative was expected to begin in 2015 and to involve about a dozen companies.[6]

| Parts of this medicine (those related to section) need to be updated. Please update this medicine to reflect recent events or newly available information. (July 2016)

|

## Bayesian designs

The adjustable nature of adaptive trials inherently suggests the use of Bayesian statistical analysis. Bayesian statistics inherently address updating information such as that seen in adaptive trials that change from updated information derived from interim analysis. The problem of adaptive clinical trial design is more or less exactly the bandit problem as studied in the field of reinforcement learning.

According to FDA guidelines, an adaptive Bayesian clinical trial can involve:[33]

* Interim looks to stop or to adjust patient accrual
* Interim looks to assess stopping the trial early either for success, futility or harm
* Reversing the hypothesis of non-inferiority to superiority or vice versa
* Dropping arms or doses or adjusting doses
* Modification of the randomization rate to increase the probability that a patient is allocated to the most appropriate treatment (or arm in the multi-armed bandit model)

The Bayesian framework Continuous Individualized Risk Index which is based on dynamic measurements from cancer patients can be effectively used for adaptive trial designs. Platform trials rely heavily on Bayesian designs.

## Statistical analysis

The problem of adaptive clinical trial design is more or less exactly the bandit problem as studied in the field of reinforcement learning.

## Added complexity

The logistics of managing traditional, non-adaptive design clinical trials may be complex. In adaptive design clinical trials, adapting the design as results arrive adds to the complexity of design, monitoring, drug supply, data capture and randomization.[7] Furthermore, it should be stated in the trial's protocol exactly what kind of adaptation will be permitted.[2] Publishing the trial protocol in advance increases the validity of the final results, as it makes clear that any adaptation that took place during the trial was planned, rather than ad hoc. According to PCAST "One approach is to focus studies on specific subsets of patients most likely to benefit, identified based on validated biomarkers. In some cases, using appropriate biomarkers can make it possible to dramatically decrease the sample size required to achieve statistical significance—for example, from 1500 to 50 patients."[34]

Adaptive designs have added statistical complexity compared to traditional clinical trial designs. For example, any multiple testing, either from looking at multiple treatment arms or from looking at a single treatment arm multiple times, must be accounted for. Another example is statistical bias, which can be more likely when using adaptive designs, and again must be accounted for.

While an adaptive design may be an improvement over a non-adaptive design in some respects (for example, expected sample size), it is not always the case that an adaptive design is a better choice overall: in some cases, the added complexity of the adaptive design may not justify its benefits. An example of this is when the trial is based on a measurement that takes a long time to observe, as this would mean having an interim analysis when many participants have started treatment but cannot yet contribute to the interim results.[35]

## Risks

Shorter trials may not reveal longer term risks, such as a cancer's return.[6]

## Resources (external links)

* "What are adaptive clinical trials?" (in en) (video). Medical Research Council Biostatistics Unit. November 17, 2022. https://www.youtube.com/watch?v=cCZnOFZ5Tww.
* Burnett, Thomas; Mozgunov, Pavel; Pallmann, Philip; Villar, Sofia S.; Wheeler, Graham M.; Jaki, Thomas (2020). "Adding flexibility to clinical trial designs: An example-based guide to the practical use of adaptive designs". BMC Medicine 18 (1): 352. doi:10.1186/s12916-020-01808-2. PMID 33208155.
* Jennison, Christopher; Turnbull, Bruce (1999). Group Sequential Methods with Applications to Clinical Trials. Taylor & Francis. ISBN 0849303168.
* Wason, James M. S.; Brocklehurst, Peter; Yap, Christina (2019). "When to keep it simple – adaptive designs are not always useful". BMC Medicine 17 (1): 152. doi:10.1186/s12916-019-1391-9. PMID 31370839.
* Wheeler, Graham M.; Mander, Adrian P.; Bedding, Alun; Brock, Kristian; Cornelius, Victoria; Grieve, Andrew P.; Jaki, Thomas; Love, Sharon B. et al. (2019). "How to design a dose-finding study using the continual reassessment method". BMC Medical Research Methodology 19 (1): 18. doi:10.1186/s12874-018-0638-z. PMID 30658575.
* Grayling, Michael John; Wheeler, Graham Mark (2020). "A review of available software for adaptive clinical trial design". Clinical Trials 17 (3): 323–331. doi:10.1177/1740774520906398. PMID 32063024. PMC 7736777. https://doi.org/10.1177/1740774520906398.

## See also

* Adverse Event Reporting System
* Clinical and Translational Science Awards
* Clinical study design
* Clinical trial protocol
* COVID-19 drug development
* COVID-19 drug repurposing research
* COVID-19 vaccine
* Food and Drug Administration Amendments Act of 2007
* Markov chain Monte Carlo
* Multiple Myeloma Research Consortium
* National Center for Advancing Translational Sciences
* WinBUGS

## References

1. ↑ "What are adaptive clinical trials?" (in en) (video). Medical Research Council Biostatistics Unit. November 17, 2022. https://www.youtube.com/watch?v=cCZnOFZ5Tww.
2. ↑ 2.0 2.1 2.2 2.3 2.4 2.5 2.6 "Adaptive designs in clinical trials: why use them, and how to run and report them". BMC Medicine 16 (1): 29. February 2018. doi:10.1186/s12916-018-1017-7. PMID 29490655.
3. ↑ 3.0 3.1 "Adaptive designs for clinical trials of drugs and biologics: Guidance for industry". U.S. Food and Drug Administration (FDA). 1 November 2019. https://www.fda.gov/media/78495/download.
4. ↑ Brennan 2013.
5. ↑ 5.0 5.1 5.2 5.3 5.4 5.5 "PANDA website". https://panda.shef.ac.uk/.
6. ↑ 6.0 6.1 6.2 6.3 6.4 Wang, Shirley S. (2013-12-30). "Health: Scientists Look to Improve Cost and Time of Drug Trials - WSJ.com". Online.wsj.com. https://www.wsj.com/news/articles/SB10001424052702304361604579290572010514840?KEYWORDS=adaptive+clinical+trial.
7. ↑ 7.0 7.1 7.2 "Adaptive Clinical Trials for Overcoming Research Challenges". News-medical.net. 16 September 2013. http://www.news-medical.net/whitepaper/20130916/Adaptive-Clinical-Trials-for-Overcoming-Research-Challenges.aspx.
8. ↑ President's Council of Advisors on Science and Technology 2012, p. xiii.
9. ↑ Research, Center for Drug Evaluation and (2020-04-21). "Adaptive Design Clinical Trials for Drugs and Biologics Guidance for Industry" (in en). https://www.fda.gov/regulatory-information/search-fda-guidance-documents/adaptive-design-clinical-trials-drugs-and-biologics-guidance-industry.
10. ↑ Bothwell, Laura E; Avorn, Jerry; Khan, Nazleen F; Kesselheim, Aaron S (2018-02-10). "Adaptive design clinical trials: a review of the literature and ClinicalTrials.gov". BMJ Open 8 (2): e018320. doi:10.1136/bmjopen-2017-018320. ISSN 2044-6055. PMID 29440155.
11. ↑ Pallmann, Philip; Bedding, Alun W.; Choodari-Oskooei, Babak; Dimairo, Munyaradzi; Flight, Laura; Hampson, Lisa V.; Holmes, Jane; Mander, Adrian P. et al. (December 2018). "Adaptive designs in clinical trials: why use them, and how to run and report them" (in en). BMC Medicine 16 (1): 29. doi:10.1186/s12916-018-1017-7. ISSN 1741-7015. PMID 29490655.
12. ↑ Bowalekar, Suresh (2011). "Adaptive designs in clinical trials". Perspectives in Clinical Research 2 (1): 23–27. doi:10.4103/2229-3485.76286. ISSN 2229-3485. PMID 21584178.
13. ↑ "Phase II trials in drug development and adaptive trial design". JACC. Basic to Translational Science 4 (3): 428–437. June 2019. doi:10.1016/j.jacbts.2019.02.005. PMID 31312766.
14. ↑ "Practical characteristics of adaptive design in Phase 2 and 3 clinical trials". Journal of Clinical Pharmacy and Therapeutics 43 (2): 170–180. April 2018. doi:10.1111/jcpt.12617. PMID 28850685.
15. ↑ Storer, Barry E. (1989). "Design and Analysis of Phase I Clinical Trials". Biometrics 45 (3): 925–937. doi:10.2307/2531693. PMID 2790129. https://doi.org/10.2307/2531693.
16. ↑ Adaptive Designs Working Group of the MRC Network of Hubs for Trials Methodology Research. "A quick guide why not to use A+B designs". https://www.methodologyhubs.mrc.ac.uk/files/6814/6253/2385/A_quick_guide_why_not_to_use_AB_designs.pdf.
17. ↑ Wheeler, Graham M.; Mander, Adrian P.; Bedding, Alun; Brock, Kristian; Cornelius, Victoria; Grieve, Andrew P.; Jaki, Thomas; Love, Sharon B. et al. (2019). "How to design a dose-finding study using the continual reassessment method". BMC Medical Research Methodology 19 (1): 18. doi:10.1186/s12874-018-0638-z. PMID 30658575.
18. ↑ Jaki, Thomas; Clive, Sally; Weir, Christopher J. (2013). "Principles of dose finding studies in cancer: A comparison of trial designs". Cancer Chemotherapy and Pharmacology 71 (5): 1107–1114. doi:10.1007/s00280-012-2059-8. PMID 23299793. PMC 3636432. https://doi.org/10.1007/s00280-012-2059-8.
19. ↑ Iasonos, Alexia; Wilton, Andrew S.; Riedel, Elyn R.; Seshan, Venkatraman E.; Spriggs, David R. (2008). "A comprehensive comparison of the continual reassessment method to the standard 3 + 3 dose escalation scheme in Phase I dose-finding studies". Clinical Trials 5 (5): 465–477. doi:10.1177/1740774508096474. PMID 18827039. PMC 2637378. https://doi.org/10.1177/1740774508096474.
20. ↑ Simon, Richard (1989). "Optimal two-stage designs for phase II clinical trials". Controlled Clinical Trials 10 (1): 1–10. doi:10.1016/0197-2456(89)90015-9. PMID 2702835. https://doi.org/10.1016/0197-2456(89)90015-9.
21. ↑ Mander, A.P.; Thompson, S.G. (2010). "Two-stage designs optimal under the alternative hypothesis for phase II cancer clinical trials". Contemporary Clinical Trials 31 (6): 572–578. doi:10.1016/j.cct.2010.07.008. PMID 20678585. PMC 3049867. https://doi.org/10.1016/j.cct.2010.07.008.
22. ↑ 22.0 22.1 22.2 22.3 "Update on WHO Solidarity Trial – Accelerating a safe and effective COVID-19 vaccine". World Health Organization. 27 April 2020. https://www.who.int/emergencies/diseases/novel-coronavirus-2019/global-research-on-novel-coronavirus-2019-ncov/solidarity-trial-accelerating-a-safe-and-effective-covid-19-vaccine. "It is vital that we evaluate as many vaccines as possible as we cannot predict how many will turn out to be viable. To increase the chances of success (given the high level of attrition during vaccine development), we must test all candidate vaccines until they fail. [The] WHO is working to ensure that all of them have the chance of being tested at the initial stage of development. The results for the efficacy of each vaccine are expected within three to six months and this evidence, combined with data on safety, will inform decisions about whether it can be used on a wider scale."
23. ↑ "Draft landscape of COVID 19 candidate vaccines". World Health Organization. 3 September 2020. https://www.who.int/who-documents-detail/draft-landscape-of-covid-19-candidate-vaccines.
24. ↑ "An international randomised trial of candidate vaccines against COVID-19: Outline of Solidarity vaccine trial". World Health Organization. 9 April 2020. https://www.who.int/blueprint/priority-diseases/key-action/Outline_CoreProtocol_vaccine_trial_09042020.pdf.
25. ↑ COVID-19 Clinical Research Coalition (April 2020). "Global coalition to accelerate COVID-19 clinical research in resource-limited settings". Lancet 395 (10233): 1322–1325. doi:10.1016/s0140-6736(20)30798-4. PMID 32247324.
26. ↑ "Therapeutic options for the 2019 novel coronavirus (2019-nCoV)". Nature Reviews. Drug Discovery 19 (3): 149–150. March 2020. doi:10.1038/d41573-020-00016-0. PMID 32127666.
27. ↑ "COVID-19, an emerging coronavirus infection: advances and prospects in designing and developing vaccines, immunotherapeutics, and therapeutics". Human Vaccines & Immunotherapeutics 16 (6): 1232–1238. March 2020. doi:10.1080/21645515.2020.1735227. PMID 32186952.
28. ↑ "Launch of a European clinical trial against COVID-19". INSERM. 22 March 2020. https://presse.inserm.fr/en/launch-of-a-european-clinical-trial-against-covid-19/38737/. "The great strength of this trial is its "adaptive" nature. This means that ineffective experimental treatments can very quickly be dropped and replaced by other molecules that emerge from research efforts. We will therefore be able to make changes in real time, in line with the most recent scientific data, in order to find the best treatment for our patients"
29. ↑ Clinical trial number NCT04280705 for "Adaptive COVID-19 Treatment Trial (ACTT)" at ClinicalTrials.gov
30. ↑ 30.0 30.1 President's Council of Advisors on Science and Technology 2012, p. 21-22.
31. ↑ I-SPY 2 TRIAL: Neoadjuvant and Personalized Adaptive Novel Agents to Treat Breast Cancer
32. ↑ Novel Agents are Targeting Drivers of TNBC - Several drug candidates in I-SPY2 have 'graduated' to later-phase studies. June 2016
33. ↑ Spiegelhalter 2010, p. 3.
34. ↑ President's Council of Advisors on Science and Technology 2012, p. 21.
35. ↑ Wason, James M. S.; Brocklehurst, Peter; Yap, Christina (2019). "When to keep it simple – adaptive designs are not always useful". BMC Medicine 17 (1): 152. doi:10.1186/s12916-019-1391-9. PMID 31370839.

## Sources

* Kurtz, Esfahani, Scherer (July 2019). "Dynamic Risk Profiling Using Serial Tumor Biomarkers for Personalized Outcome Prediction". Cell 178 (3): 699–713.e19. doi:10.1016/j.cell.2019.06.011. PMID 31280963.
* President's Council of Advisors on Science and Technology (September 2012). "Report To The President on Propelling Innovation in Drug Discovery, Development and Evaluation". Executive Office of the President. https://obamawhitehouse.archives.gov/sites/default/files/microsites/ostp/pcast-fda-final.pdf.
* Brennan, Zachary (2013-06-05). "CROs Slowly Shifting to Adaptive Clinical Trial Designs". Outsourcing-pharma.com. http://www.outsourcing-pharma.com/Clinical-Development/CROs-Slowly-Shifting-to-Adaptive-Clinical-Trial-Designs.
* Spiegelhalter, David (April 2010). "Bayesian methods in clinical trials: Has there been any progress?". http://www.mrc-bsu.cam.ac.uk/CHTMR/DJS_forweb.pdf.
* Carlin, Bradley P. (March 25, 2009). "Bayesian Adaptive Methods for Clinical Trial Design and Analysis". http://www.mbswonline.com/upload/presentation_Brad4-27-2009-15-29-36.pdf.

## External links

* Gottlieb K. (2016) The FDA adaptive trial design guidance in a nutshell - A review in Q&A format for decision makers. PeerJ Preprints 4:e1825v1 [1]
* Coffey, C. S.; Kairalla, J. A. (2008). "Adaptive clinical trials: Progress and challenges". Drugs in R&D 9 (4): 229–242. doi:10.2165/00126839-200809040-00003. PMID 18588354.
* Center for Drug Evaluation and Research (CDER); Center for Biologics Evaluation and Research (CBER) (February 2010). "Adaptive Design Clinical Trials for Drugs and Biologics". Food and Drug Administration. https://www.fda.gov/downloads/Drugs/.../Guidances/ucm201790.pdf.
* Yi, Cheng; Yu, Shen. "Bayesian Adaptive Designs for Clinical Trials". M. D. Anderson. http://www.mdanderson.org/education-and-research/departments-programs-and-labs/departments-and-divisions/division-of-quantitative-sciences/research/biostats-utmdabtr-012-04.pdf.
* Berry, Scott M.; Carlin, Bradley P.; Lee, J. Jack; Muller, Peter (20 July 2010). Bayesian Adaptive Methods for Clinical Trials. CRC Press. ISBN 978-1-4398-2551-8. https://books.google.com/books?id=_Wz0RlH6NssC. Berry on BAMCT on YouTube
* Press, W. H. (2009). "Bandit solutions provide unified ethical models for randomized clinical trials and comparative effectiveness research". Proceedings of the National Academy of Sciences 106 (52): 22387–92. doi:10.1073/pnas.0912378106. PMID 20018711.

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Controlled study
(EBM I to II-1)|

* Randomized controlled trial
* Scientific experiment
* Blind experiment
* Open-label trial

Observational study
(EBM II-2 to II-3)|

* Cross-sectional study vs. Longitudinal study, Ecological study
* Cohort study
* Retrospective
* Prospective
* Case–control study (Nested case–control study)
* Case series
* Case study
* Case report

Measures|

| Occurrence|

Incidence, Cumulative incidence, Prevalence, Point prevalence, Period prevalence

|

Association|

Risk difference, Number needed to treat, Number needed to harm, Risk ratio, Relative risk reduction, Odds ratio, Hazard ratio

Population impact|

Attributable fraction among the exposed, Attributable fraction for the population, Preventable fraction among the unexposed, Preventable fraction for the population

Other|

Clinical endpoint, Virulence, Infectivity, Mortality rate, Morbidity, Case fatality rate, Specificity and sensitivity, Likelihood-ratios, Pre- and post-test probability

Trial/test types|

* In vitro
* In vivo
* Animal testing
* Animal testing on non-human primates
* First-in-man study
* Multicenter trial
* Seeding trial
* Vaccine trial

Analysis of clinical trials|

* Risk–benefit ratio
* Systematic review
* Replication
* Meta-analysis
* Intention-to-treat analysis

Interpretation of results|

* Selection bias
* Survivorship bias
* Correlation does not imply causation
* Null result

* Category
* Glossary
* List of topics

* v
* t
* e

Product testing

Testing organizations|

* Standards organization
* Consumer organization
* Trade organization
* Food safety organization

Methodologies|

* Conformance testing
* Chemical test
* Destructive testing
* Discrimination testing
* Nondestructive testing
* Physical test
* Sensory analysis
* Survey research
* Test method
* Usability testing

Product fields|

* Cannabis testing
* Coffee cupping
* Crash test
* Clinical trial
* Package testing
* Software testing
* Whisky tasting
* Wine tasting

* v
* t
* e

Statistics

* Outline
* Index

Descriptive statistics

| Continuous data|

| Center|

* Mean
* arithmetic
* geometric
* harmonic
* Median
* Mode

|

Dispersion|

* Variance
* Standard deviation
* Coefficient of variation
* Percentile
* Range
* Interquartile range

Shape|

* Central limit theorem
* Moments
* Skewness
* Kurtosis
* L-moments

Count data|

* Index of dispersion

Summary tables|

* Grouped data
* Frequency distribution
* Contingency table

Dependence|

* Pearson product-moment correlation
* Rank correlation
* Spearman's rho
* Kendall's tau
* Partial correlation
* Scatter plot

Graphics|

* Bar chart
* Biplot
* Box plot
* Control chart
* Correlogram
* Fan chart
* Forest plot
* Histogram
* Pie chart
* Q–Q plot
* Run chart
* Scatter plot
* Stem-and-leaf display
* Radar chart
* Violin plot

Data collection

| Study design|

* Population
* Statistic
* Effect size
* Statistical power
* Optimal design
* Sample size determination
* Replication
* Missing data

|

Survey methodology|

* Sampling
* stratified
* cluster
* Standard error
* Opinion poll
* Questionnaire

Controlled experiments|

* Scientific control
* Randomized experiment
* Randomized controlled trial
* Random assignment
* Blocking
* Interaction
* Factorial experiment

Adaptive Designs|

* Adaptive clinical trial
* Up-and-Down Designs
* Stochastic approximation

Observational Studies|

* Cross-sectional study
* Cohort study
* Natural experiment
* Quasi-experiment

Statistical inference

| Statistical theory|

* Population
* Statistic
* Probability distribution
* Sampling distribution
* Order statistic
* Empirical distribution
* Density estimation
* Statistical model
* Model specification
* Lp space
* Parameter
* location
* scale
* shape
* Parametric family
* Likelihood (monotone)
* Location–scale family
* Exponential family
* Completeness
* Sufficiency
* Statistical functional
* Bootstrap
* U
* V
* Optimal decision
* loss function
* Efficiency
* Statistical distance
* divergence
* Asymptotics
* Robustness

|

Frequentist inference|

| Point estimation|

* Estimating equations
* Maximum likelihood
* Method of moments
* M-estimator
* Minimum distance
* Unbiased estimators
* Mean-unbiased minimum-variance
* Rao–Blackwellization
* Lehmann–Scheffé theorem
* Median unbiased
* Plug-in

|

Interval estimation|

* Confidence interval
* Pivot
* Likelihood interval
* Prediction interval
* Tolerance interval
* Resampling
* Bootstrap
* Jackknife

Testing hypotheses|

* 1- & 2-tails
* Power
* Uniformly most powerful test
* Permutation test
* Randomization test
* Multiple comparisons

Parametric tests|

* Likelihood-ratio
* Score/Lagrange multiplier
* Wald

Specific tests|

* Z-test (normal)
* Student's t-test
* F-test

Goodness of fit|

* Chi-squared
* G-test
* Kolmogorov–Smirnov
* Anderson–Darling
* Lilliefors
* Jarque–Bera
* Normality (Shapiro–Wilk)
* Likelihood-ratio test
* Model selection
* Cross validation
* AIC
* BIC

Rank statistics|

* Sign
* Sample median
* Signed rank (Wilcoxon)
* Hodges–Lehmann estimator
* Rank sum (Mann–Whitney)
* Nonparametric anova
* 1-way (Kruskal–Wallis)
* 2-way (Friedman)
* Ordered alternative (Jonckheere–Terpstra)

Bayesian inference|

* Bayesian probability
* prior
* posterior
* Credible interval
* Bayes factor
* Bayesian estimator
* Maximum posterior estimator

* Correlation
* Regression analysis

| Correlation|

* Pearson product-moment
* Partial correlation
* Confounding variable
* Coefficient of determination

|

Regression analysis|

* Errors and residuals
* Regression validation
* Mixed effects models
* Simultaneous equations models
* Multivariate adaptive regression splines (MARS)

Linear regression|

* Simple linear regression
* Ordinary least squares
* General linear model
* Bayesian regression

Non-standard predictors|

* Nonlinear regression
* Nonparametric
* Semiparametric
* Isotonic
* Robust
* Heteroscedasticity
* Homoscedasticity

Generalized linear model|

* Exponential families
* Logistic (Bernoulli) / Binomial / Poisson regressions

Partition of variance|

* Analysis of variance (ANOVA, anova)
* Analysis of covariance
* Multivariate ANOVA
* Degrees of freedom

Categorical / Multivariate / Time-series / Survival analysis

| Categorical|

* Cohen's kappa
* Contingency table
* Graphical model
* Log-linear model
* McNemar's test

|

Multivariate|

* Regression
* Manova
* Principal components
* Canonical correlation
* Discriminant analysis
* Cluster analysis
* Classification
* Structural equation model
* Factor analysis
* Multivariate distributions
* Elliptical distributions
* Normal

Time-series|

| General|

* Decomposition
* Trend
* Stationarity
* Seasonal adjustment
* Exponential smoothing
* Cointegration
* Structural break
* Granger causality

|

Specific tests|

* Dickey–Fuller
* Johansen
* Q-statistic (Ljung–Box)
* Durbin–Watson
* Breusch–Godfrey

Time domain|

* Autocorrelation (ACF)
* partial (PACF)
* Cross-correlation (XCF)
* ARMA model
* ARIMA model (Box–Jenkins)
* Autoregressive conditional heteroskedasticity (ARCH)
* Vector autoregression (VAR)

Frequency domain|

* Spectral density estimation
* Fourier analysis
* Wavelet
* Whittle likelihood

Survival|

| Survival function|

* Kaplan–Meier estimator (product limit)
* Proportional hazards models
* Accelerated failure time (AFT) model
* First hitting time

|

Hazard function|

* Nelson–Aalen estimator

Test|

* Log-rank test

Applications

| Biostatistics|

* Bioinformatics
* Clinical trials / studies
* Epidemiology
* Medical statistics

|

Engineering statistics|

* Chemometrics
* Methods engineering
* Probabilistic design
* Process / quality control
* Reliability
* System identification

Social statistics|

* Actuarial science
* Census
* Crime statistics
* Demography
* Econometrics
* Jurimetrics
* National accounts
* Official statistics
* Population statistics
* Psychometrics

Spatial statistics|

* Cartography
* Environmental statistics
* Geographic information system
* Geostatistics
* Kriging

* Category
* '
* Commons
* WikiProject

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