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Theoretical vs. Experimental Probability: How do they differ?

Theoretical vs. Experimental Probability

Probability is the study of chances and is an important topic in mathematics. There are two types of probability: theoretical and experimental.

So, how to define theoretical and experimental probability? Theoretical probability is calculated using mathematical formulas, while experimental probability is based on results from experiments or surveys. In order words, theoretical probability represents how likely an event is to happen. On the other hand, experimental probability illustrates how frequently an event occurs in an experiment.

Read on to find out the differences between theoretical and experimental probability. If you wonder How to Understand Statistics Easily , I wrote a whole article where I share 9 helpful tips to help you Ace statistics.

Table of Contents

What Is Theoretical Probability?

Theoretical probability is calculated using mathematical formulas. In other words, a theoretical probability is a probability that is determined based on reasoning. It does not require any experiments to be conducted. Theoretical probability can be used to calculate the likelihood of an event occurring before it happens.

Keep in mind that theoretical probability doesn’t involve any experiments or surveys; instead, it relies on known information to calculate the chances of something happening.

For example, if you wanted to calculate the probability of flipping a coin and getting tails, you would use the formula for theoretical probability. You know that there are two possible outcomes—heads or tails—and that each outcome is equally likely, so you would calculate the probability as follows: 1/2, or 50%.

How Do You Calculate Theoretical Probability?

  • First, start by counting the number of possible outcomes of the event.
  • Second, count the number of desirable (favorable) outcomes of the event.
  • Third, divide the number of desirable (favorable) outcomes by the number of possible outcomes.
  • Finally, express this probability as a decimal or percentage.

The theoretical probability formula is defined as follows: Theoretical Probability = Number of favorable (desirable) outcomes divided by the Number of possible outcomes.

How Is Theoretical Probability Used in Real Life?

Probability plays a vital role in the day to day life. Here is how theoretical probability is used in real life: 

  • Sports and gaming strategies
  • Analyzing political strategies.
  • Buying or selling insurance
  • Determining blood groups 
  • Online shopping
  • Weather forecast
  • Online games

What Is Experimental Probability?

Experimental probability, on the other hand, is based on results from experiments or surveys. It is the ratio of the number of successful trials divided by the total number of trials conducted. Experimental probability can be used to calculate the likelihood of an event occurring after it happens.

For example, if you flipped a coin 20 times and got heads eight times, the experimental probability of obtaining heads would be 8/20, which is the same as 2/5, 0.4, or 40%.

How Do You Calculate Experimental Probability?

The formula for the experimental probability is as follows:  Probability of an Event P(E) = Number of times an event happens divided by the Total Number of trials .

If you are interested in learning how to calculate experimental probability, I encourage you to watch the video below.

How Is Experimental Probability Used in Real Life?

Knowing experimental probability in real life provides powerful insights into probability’s nature. Here are a few examples of how experimental probability is used in real life:

  • Rolling dice
  • Selecting playing cards from a deck
  • Drawing marbles from a hat
  • Tossing coins

The main difference between theoretical and experimental probability is that theoretical probability expresses how likely an event is to occur, while experimental probability characterizes how frequently an event occurs in an experiment.

In general, the theoretical probability is more reliable than experimental because it doesn’t rely on a limited sample size; however, experimental probability can still give you a good idea of the chances of something happening.

The reason is that the theoretical probability of an event will invariably be the same, whereas the experimental probability is typically affected by chance; therefore, it can be different for different experiments.

Also, generally, the more trials you carry out, the more times you flip a coin, and the closer the experimental probability is likely to be to its theoretical probability.

Also, note that theoretical probability is calculated using mathematical formulas, while experimental probability is found by conducting experiments.

What to read next:

  • Types of Statistics in Mathematics And Their Applications .
  • Is Statistics Harder Than Algebra? (Let’s find out!)
  • Should You Take Statistics or Calculus in High School?
  • Is Statistics Hard in High School? (Yes, here’s why!)

Wrapping Up

Theoretical and experimental probabilities are two ways of calculating the likelihood of an event occurring. Theoretical probability uses mathematical formulas, while experimental probability uses data from experiments. Both types of probability are useful in different situations.

I believe that both theoretical and experimental probabilities are important in mathematics. Theoretical probability uses mathematical formulas to calculate chances, while experimental probability relies on results from experiments or surveys.

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Integration of theory and experiment in the modelling of heterogeneous electrocatalysis

  • Sharon Hammes-Schiffer   ORCID: orcid.org/0000-0002-3782-6995 1 &
  • Giulia Galli   ORCID: orcid.org/0000-0002-8001-5290 2 , 3  

Nature Energy volume  6 ,  pages 700–705 ( 2021 ) Cite this article

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  • Computational chemistry
  • Electrocatalysis
  • Hydrogen energy
  • Solar fuels

Heterogeneous electrocatalysis is critical to many energy conversion processes. Theoretical and computational approaches are essential to interpret experimental data and provide the mechanistic understanding necessary to design more effective catalysts. However, automated general procedures to build predictive theoretical and computational frameworks are not readily available; specific choices must be made in terms of the atomistic structural model and the level of theory, as well as the experimental data used to inform and validate these choices. Here we outline some best practices for modelling heterogeneous systems and present examples in the context of catalysis at metal electrodes and oxides. The level of theory should be chosen for the specific system and properties of interest, and experimental validation is essential from the beginning to the end of the study. Continuous feedback and ultimate integration between experiment and theory enhances the power of calculations to elucidate mechanisms, identify effective descriptors and clarify design principles.

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Acknowledgements

This material is based on work supported by the National Science Foundation grant no. CHE-1764399 (G.G.) and the Air Force Office of Scientific Research under awards FA9550-18-1-0420 and FA9550-18-1-0134 (S.H.-S.).

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Pritzker School of Molecular Engineering and Department of Chemistry, University of Chicago, Chicago, IL, USA

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Hammes-Schiffer, S., Galli, G. Integration of theory and experiment in the modelling of heterogeneous electrocatalysis. Nat Energy 6 , 700–705 (2021). https://doi.org/10.1038/s41560-021-00827-4

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Mastering Theoretical and Experimental Probability Comparisons Dive into the world of probability with our comprehensive guide. Learn to calculate, compare, and apply theoretical and experimental probability in real-world scenarios. Enhance your statistical skills today!

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  • Experimental probability VS. Theoretical probability

Die Outcome

Experimental results

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II

2

IIII

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I

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III

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IIIII

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I

Coin Outcome

Experimental Results

H, H

IIII

H, T

IIIII

T, H

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What is the experimental probability of both coins landing on heads?

  • Calculate the theoretical probability of both coins landing on heads.
  • Compare the theoretical probability and experimental probability.
  • What can Jessie do to decrease the difference between the theoretical probability and experimental probability?

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What is experimental probability?

In math, when we deal with probability , we may be asked for the experimental probability of an experiment. What this means is that they're looking for the probability of something happening based off the results of an actual experiment. This is the experimental probability definition.

So for example, if you're asked for the probability of getting heads after flipping a coin 10 times, the experimental probability will be the number of times you got heads after flipping a coin 10 times. Let's say that you got 6 heads out of your 10 throws. Then your experimental probability is 6/10, or 60%.

For theoretical probability, it doesn't require you to actually do the experiment and then look at the results. Instead, the theoretical probability is what you expect to happen in an experiment (the expected probability). This is the theoretical probability definition.

In the case of the coin flips, since there's 2 sides to a coin and there's an equal chance that either side will land when you flip it, the theoretical probability should be 1 2 \frac{1}{2} 2 1 ​ or 50%.

Why is there a difference in theoretical and experimental probability? The relationship between the two is that you'll find if you do the experiment enough times, the experimental probability will get closer and closer to the theoretical probability's answer. You can try this out yourself with a coin. You likely won't get exactly 50% for both heads and tails from your first 10 throws, but as you throw a coin 50 times or even 100 times, you'll see the experimental probability's answer getting closer to 50%.

We'll now see how experimental and theoretical probability works with these questions.

Question 1a: Two coins are flipped 20 times to determine the experimental probability of landing on heads versus tails. The results are in the chart below:

We are looking for the experimental probability of both coins landing on heads. Looking at the table in the question, we know that there were 4 out of 20 trials in which both coins landed on heads. So the experimental probability is 4 20 \frac{4}{20} 20 4 ​ , which equals to 1 5 \frac{1}{5} 5 1 ​ (20%) after simplifying the fraction

Question 1b: Calculate the theoretical probability of both coins landing on heads.

Now, we are looking for the theoretical probability. First, there are 4 possible outcomes (H,H), (H, T), (T,H), (T, T). 1 out of the 4 possible outcomes has both coins land on heads. So, the theoretical probability is 1 4 \frac{1}{4} 4 1 ​ or 25%

Question 1c: Compare the theoretical probability and experimental probability.

From the previous parts, we know that the experimental probability of both coins landing on head equals 20%, while in theory, there should be a 25% chance that both coins lands on head. Therefore, the theoretical probability is higher than the experimental probability.

Question 1d:

What can we do to reduce the difference between the experimental probability and theoretical probability? We can simply continue the experimental by flipping the coin for many more times —say, 20,000 times. When more trials are performed, the difference between experimental probability and theoretical probability will diminish. The experimental probability will gradually get closer to the value of the theoretical probability. In this case, the experimental probability will get closer to 25% as the coins is tossed over more times.

If you're looking for more experimental vs.theoretical probability examples, feel free to try out this question . It'll require you to do some hands-on experimentation!

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Experimental Data for Model Validation

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This chapter is concerned with experimental modelling techniques and the use of experimental test data for the purposes of model evaluation. It includes an overview of system identification and parameter estimation methods and gives emphasis to the importance of issues associated with the optimisation of the model structure. In the context of model validation, the potential “generalisation” capabilities of an identified model are considered in terms of model predictions for experimental situations which are not exactly the same as those used in the identification process. Issues of over-fitting and under-fitting are also discussed and procedures for the estimation of parameters of physically-based nonlinear models are considered, including evolutionary computing approaches, such as Genetic Algorithms and Genetic Programming. Issues of identifiability are discussed in some detail, as are questions of experimental design, the selection of the most appropriate test-input signals for system identification and model validation, together with ways of assessing the accuracy of parameter estimates.

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Murray-Smith, D.J. (2015). Experimental Data for Model Validation. In: Testing and Validation of Computer Simulation Models. Simulation Foundations, Methods and Applications. Springer, Cham. https://doi.org/10.1007/978-3-319-15099-4_5

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How to calculate theoretical and experimental data in general physics´experiments?

enter image description here

Im struggling how to calculate theoretical and experimental data with the added formulas and second Newton law. I did a free body diagram but it doesnt clarify how to calculate it. Any suggestion will be welcome. thank you.

Charlie Van Basten Øydne's user avatar

The experimental data is just the measurement of the time to reach each sensor, so the two lines above the chart. You should copy the times into the second row of the chart. From the inclination of the plane you should be able to calculate a predicted acceleration due to gravity. Presumably you start with the ball at rest, so $v_0=0$ . You can then predict the velocity as a function of time from your equation, the time the ball should have passed each sensor, and compare that with the measured data. I am not sure how your professor expects you to come up with the experimental values of velocity and acceleration. It might be an overall fit to get the acceleration. It might be computing the change in distance divided by the change in time, but that has the problem that the velocity is constantly changing.

Ross Millikan's user avatar

  • $\begingroup$ Thanks. So I think that my teacher wants to complete the chart with the added formulas. I can do it but, I need to clarify what is theoretical and what experimental. It seems confusing at first sight. $\endgroup$ –  Charlie Van Basten Øydne Commented Aug 13, 2020 at 1:35

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Estimating treatment effects using observational data and experimental data with non-overlapping support.

experimental data theoretical

1. Introduction

  • Regress Y P on Y S and X to obtain an estimate of μ , denoted as μ ^ .
  • Estimate the conditional average treatment effect τ ( x ) on the surrogate outcome Y S , obtaining an estimate τ ^ .
  • Define Y ^ i S ( 1 ) = Y i S if W i = 1 and Y ^ i S ( 1 ) = Y i S + τ ^ ( X i ) if W i = 0 .
  • Estimate E Y i P ( 1 ) by 1 N O ∑ i = 1 N O μ ^ ( X i , Y ^ i S ( 1 ) ) .
  • Define Y ^ i S ( 0 ) = Y i S if W i = 0 and Y ^ i S ( 0 ) = Y i S − τ ^ ( X i ) if W i = 1 .
  • Estimate E Y i P ( 0 ) by 1 N O ∑ i = 1 N O μ ^ ( X i , Y ^ i S ( 0 ) ) .
  • The final estimate is τ ^ P = 1 N O ∑ i = 1 N O μ ^ ( X i , Y ^ i S ( 1 ) ) − 1 N O ∑ i = 1 N O μ ^ ( X i , Y ^ i S ( 0 ) ) .

4. Applications

4.1. covariate support mismatch between samples.

  • Apply any CATE estimation algorithm on the observational sample to obtain an estimate ω ^ .
  • Solve the following optimization problem to obtain θ ^ : θ ^ = arg min θ ∑ i = 1 N E q E ( X i ) Y i − ω ^ ( X i ) − θ T X i 2 .
  • Define τ ^ ( x ) = θ ^ T x + ω ^ ( x ) .

4.2. Instrumental Variable (IV) Setting in the Experimental Sample

4.2.1. constant effect, 4.2.2. non-parametric iv.

  • Flexibility: GRF is capable of modeling complex, non-linear relationships between the covariates and the treatment effect, which is often essential in practical applications where such relationships are not adequately captured by parametric models.
  • Generalizability: One notable advantage of GRF is its ability to generalize beyond binary treatment variables. As discussed in Athey et al. ( 2019 ), GRF can be extended to settings where the treatment variable W is a real-valued continuous variable.

4.3. Instrumental Variable Setting with Different Support of Pre-Treatment Covariates

  • Apply any conditional average treatment effect (CATE) estimation algorithm, denoted by Q , to the set { X i , W i , Y i S } i = 1 m to obtain an initial estimate ω ^ ( x ) .
  • Solve the following optimization problem on the experimental sample to refine the estimate: θ ^ = arg min θ ∑ i = 1 n m ^ ( x i ) − μ ^ ( x i ) π ^ ( x i ) − θ T x i + ω ^ ( x i ) γ ^ ( x i ) − e ^ ( x i ) π ^ ( x i ) 2 .
  • Use the combined estimate ω ^ ( x ) + θ ^ T x as the final estimate of the CATE on the surrogate.

5. Simulations

  • Presence of Confounding: We vary ω to be either 0 or 1. If ω = 0 , there is no confounding; otherwise, there is confounding, and we are in the non-parametric instrumental variable (IV) model.
  • Sparsity of the Signal: We set κ τ to be either 2 or 4 to vary the sparsity of the signal.
  • Additivity of the Signal: When true, τ ( x ) = ∑ j = 1 κ τ max { 0 , x j } ; when false, τ ( x ) = max { 0 , ∑ j = 1 κ τ x j } .
  • Presence of Nuisance Terms: When true, μ ( x ) = 3 max { 0 , x 5 } + 3 max { 0 , x 6 } or μ ( x ) = 3 max { 0 , x 5 + x 6 } depending on the additive signal condition; when false, μ ( x ) = 0 .
  • Identical Support: When true, we assume the distribution of the covariates in the experimental sample and that in the observational sample are the same; when false, X i ∼ N ( [ 1 , ⋯ , 1 ] T , I p × p ) in the observational sample.

6. A Real Data Example

  • Use D g t to calculate the average treatment effect of average grade in year 3. This estimate τ g t will be viewed as the ground truth.
  • Repeat the following steps 500 times.
  • Sample n exp rural or inner-city students together with all the covariates except the student location covariate, treatment variable and average grade in year 1. This is our experimental sample D E .
  • Sample n obs / 4 rural or inner-city students in control group that are not sampled in experimental sample, sample n obs / 4 rural or inner-city students in treatment group whose year 1 average grade is in the lower half among treated rural or inner-city students, sample n obs / 4 urban or suburban students in control group, and finally sample n obs / 4 urban or suburban students in treatment group whose year 1 average grade is in the lower half among treated urban or suburban students. This is our observational sample (which is confounded because we remove students with higher scores selectively from the population) D O .
  • Use different methods to estimate τ g t based on D E and D O .
  • Compare based on mean squared error (MSE).

7. Conclusions

Author contributions, data availability statement, conflicts of interest.

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AdditivityNuisanceIdentical SupportMC EstimateGRFImputationKallusWinner
02YesYesYes1.620.191.020.34GRF
02YesNoYes1.580.120.220.24GRF
04NoYesYes2.100.221.130.55GRF
04NoNoYes2.100.140.260.41GRF
02YesYesNo8.7330.9143.3872.83GRF
02YesNoNo8.6727.2836.006.45Kallus
04NoYesNo8.1118.5629.0751.25GRF
04NoNoNo8.1115.9823.297.05Kallus
AdditivityNuisanceIdentical SupportMC EstimateGRFKallus IVWinner
12YesYesYes1.630.460.65GRF
12YesNoYes1.550.260.80GRF
14NoYesYes2.120.490.64GRF
14NoNoYes2.110.300.51GRF
12YesYesNo8.7331.6028.27Kallus IV
12YesNoNo8.7227.8410.80Kallus IV
12NoYesNo6.3515.0031.79GRF
12NoNoNo6.3312.6411.01Kallus IV
14NoYesNo8.1117.9332.65GRF
14NoNoNo8.0915.3516.72GRF
14YesNoNo17.30109.7828.89Kallus IV
14YesYesNo17.38114.7442.00Kallus IV
AdditivityNuisanceIdentical SupportMC EstimateGRFKallus/Kallus IVWinner
02YesYesNo1.610.600.30Kallus
02YesNoNo1.600.580.29Kallus
04NoYesNo2.111.120.54Kallus
04NoNoNo2.101.160.45Kallus
12YesYesNo1.600.770.71Kallus IV
12YesNoNo1.600.700.68Kallus IV
12NoYesNo1.340.610.83GRF
12NoNoNo1.350.580.71GRF
14NoYesNo2.101.210.66Kallus IV
14NoNoNo2.081.240.57Kallus IV
14YesNoNo3.212.370.60Kallus IV
14YesYesNo3.232.260.54Kallus IV
GRFImputationAIPW
30010007.0813.19167.52
20015009.3612.76167.43
50020004.547.43166.08
GRFImputationAIPW
30010006.647.90−5.217.62
20015006.898.21−5.247.62
50020006.708.06−5.217.62
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Share and Cite

Han, K.; Wu, H.; Wu, L.; Shi, Y.; Liu, C. Estimating Treatment Effects Using Observational Data and Experimental Data with Non-Overlapping Support. Econometrics 2024 , 12 , 26. https://doi.org/10.3390/econometrics12030026

Han K, Wu H, Wu L, Shi Y, Liu C. Estimating Treatment Effects Using Observational Data and Experimental Data with Non-Overlapping Support. Econometrics . 2024; 12(3):26. https://doi.org/10.3390/econometrics12030026

Han, Kevin, Han Wu, Linjia Wu, Yu Shi, and Canyao Liu. 2024. "Estimating Treatment Effects Using Observational Data and Experimental Data with Non-Overlapping Support" Econometrics 12, no. 3: 26. https://doi.org/10.3390/econometrics12030026

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Quantitative Finance > Computational Finance

Title: theoretical and empirical validation of heston model.

Abstract: This study focuses on the application of the Heston model to option pricing, employing both theoretical derivations and empirical validations. The Heston model, known for its ability to incorporate stochastic volatility, is derived and analyzed to evaluate its effectiveness in pricing options. For practical application, we utilize Monte Carlo simulations alongside market data from the Crude Oil WTI market to test the model's accuracy. Machine learning based optimization methods are also applied for the estimation of the five Heston parameters. By calibrating the model with real-world data, we assess its robustness and relevance in current financial markets, aiming to bridge the gap between theoretical finance models and their practical implementations.
Comments: 32 pages, 18 figures, 3 tables
Subjects: Computational Finance (q-fin.CP); Probability (math.PR)
classes: 60H15
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Novo Nordisk's Experimental Oral Drug Reports 'Remarkable' Weight Loss, Early Data Shows

Bloomberg / Getty Images

Key Takeaways

  • In a phase 1 trial, Novo Nordisk's experimental obesity drug amycretin led to up to 13% weight loss in just three months.
  • Amycretin targets GLP-1 receptors and a second hormone called amylin.
  • Amylin appears to act in the brain, rather than in the gut. It’s possible that amylin can control appetite with fewer gastrointestinal side effects.

An experimental new pill from Novo Nordisk, called amycretin, could cause substantial weight loss in people with obesity.

The once-daily oral medication is in the same class as the blockbuster obesity and diabetes medications, Ozempic and Mounjaro. It targets GLP-1 receptors and stimulates levels of a second hormone called amylin.

In a phase 1 clinical trial, researchers tested if the drug was safe for humans at different doses. Although regulatory approval is still years away, early data suggests that the drug could lead to rapid weight loss. Participants taking amycretin at the highest doses lost up to 13% of their body weight in just three months.

That outcome is “remarkable,” said David Lau, MD, PhD , professor emeritus and director of the Julia McFarlane Diabetes Research Centre at the University of Calgary, who was not involved with the study. "This adds to the current and future investigations and development of weight loss medications to help people to achieve better body weight and, of course, overall health."

How Amycretin Works

Amycretin targets amylin, a hormone secreted by the pancreas. After eating, amylin signals fullness, slows the rate at which food moves through the stomach and limits the release of glucagon, a hormone that increases blood sugar levels.

In a presentation at EASD, Kirsten Raun, DVM , Scientific Vice President at Novo Nordisk, said that amylin could benefit people with obesity by reducing appetite, improving fat-to-lean mass ratio, supporting bone formation, lowering blood pressure, improving lipid profile, and more.

Combining amylin and GLP-1 receptor agonists into one medication could stimulate weight loss in more ways than semaglutide, which targets GLP-1 alone.

“The data are very consistent that amylin agonists actually affect appetite centrally in the brain. But what we don’t know is the exact location in the brain where amylin works,” Lau said. “If amylin acts differently from the GLP-1 receptor agonists, there may be an additive effect on appetite regulation. If they act on different parts of the brain, they may have better effect.”

What We Know From the Clinical Trial

The trial included 144 participants between the ages of 18 and 55 years who had a BMI of 25 to 40 and were otherwise considered healthy.

Novo Nordisk used the same technology to create an oral form of amycretin as it uses for Rybelsus, the oral version of semaglutide.

The researchers tested multiple dosing regimens. In a presentation of the data, Agnes Gasiorek, PhD , senior clinical pharmacology specialist at Novo Nordisk, highlighted a portion of the study in which the dosage for some participants about doubled every two to three weeks for three months.

One group ended with a dose of 50 milligrams. They saw an average 10.4% body weight loss by the end of the trial. A group that took twice that dose lost 13.1% of their body weight during that time. The placebo group, meanwhile, lost 1.2% of their body weight.

That outcome “really is remarkable for an orally delivered biologic,” Gasiorek said.

Gasiorek said it’s too early to compare the benefits of amycretin with semaglutide or other obesity medications. Future studies will test how amycretin affects the body over a longer period.

One challenge of developing an oral version is making the drug effective at the lowest dose possible. About 1% of oral semaglutide is bioavailable, so people need to take a much higher dose of the medication to receive the same effect as an injectable dose. Novo Nordisk hasn’t yet studied what percentage of amycretin is absorbed orally. 

Striving for Weight Loss With Fewer GI Side Effects

A common complaint among people who take GLP-1-based drugs is the discomfort of gastrointestinal side effects. Research by Lau and his team suggests that targeting amylin can increase feelings of satiety and fullness while reducing the risk of gastrointestinal side effects.

In the trial data presented last week, Novo Nordisk reported that most people experienced mild to moderate gastrointestinal side effects, such as nausea, vomiting, and abdominal pain. The likelihood of those side effects increased as participants started taking higher doses of amycretin.

Amylin appears to act in the brain, rather than in the gut. Scientists are still learning about which parts of the brain are responsible for nausea and which parts amylin stimulates, but it’s possible that amylin helps control appetite while signaling less gastrointestinal discomfort.

“The effect of nausea and the effect of weight loss are completely separate, so nausea in and by itself does not necessarily lead to weight loss. Some people can lose weight without experiencing nausea, and some people experiencing weight loss also can experience nausea,” Lau said.

For companies competing to create the most tolerable and effective obesity and diabetes medications, Lau said a primary goal is to understand how to target certain hormones to induce weight loss without nausea.

Where Amycretin Could Fit Into Obesity Care

Novo Nordisk will advance the once-daily oral tablet to phase 2 clinical trials. The company is also testing a subcutaneous injection version of the drug.

Lau said that GLP-1 receptor agonists will continue to be the “major ingredient” for future anti-obesity medications. Drugs that also target another hormone or two have the potential to be more potent.

For instance, Eli Lilly’s tirzepatide stimulates GLP-1 and GIP receptors and causes greater average weight loss in clinical trials than semaglutide, which targets GLP-1 alone. A drug in phase 3 clinical trials, called retatrutide, targets three different hormones with promising effects.

“Obesity, as a condition, is actually very heterogeneous. Some people respond tremendously, other people don’t,” Lau said.

Someone who is a “super responder” to GLP-1 drugs may lose sufficient weight when taking a drug that contains amylin with even fewer side effects than they may experience on semaglutide, for instance.

What This Means For You

If you're interested in obesity management options, talk to a health provider about your treatment options. You can use this tool from the Obesity Medicine Association to find an obesity medicine provider.

Gasiorek A, Kirkeby K, Toubro S, et al. Safety, tolerability and weight reduction findings of oral amycretin: a novel amylin and glucagon-like peptide-1 receptor co-agonist, in a first-in-human study . Paper presented at: 60th Annual Meeting of the European Association for the Study of Diabetes; September 9-13, 2024, Madrid, Spain.

Brayden DJ, Hill TA, Fairlie DP, Maher S, Mrsny RJ. Systemic delivery of peptides by the oral route: formulation and medicinal chemistry approaches . Adv Drug Deliv Rev . 2020;157:2-36. doi:10.1016/j.addr.2020.05.007

Enebo LB, Berthelsen KK, Kankam M, et al. Safety, tolerability, pharmacokinetics, and pharmacodynamics of concomitant administration of multiple doses of cagrilintide with semaglutide 2·4 mg for weight management: a randomised, controlled, phase 1b trial . Lancet . 2021;397(10286):1736-1748. doi:10.1016/S0140-6736(21)00845-X

Sanyal AJ, Kaplan LM, Frias JP, et al. Triple hormone receptor agonist retatrutide for metabolic dysfunction-associated steatotic liver disease: a randomized phase 2a trial . Nat Med . 2024;30(7):2037-2048. doi:10.1038/s41591-024-03018-2

By Claire Bugos Bugos is a senior news reporter at Verywell Health. She holds a bachelor's degree in journalism from Northwestern University.

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  2. Experimental data and theoretical

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  3. Student results showing experimental and theoretical data for the

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  4. Theoretical And Experimental Probability Worksheet

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  5. Comparison of the experimental data with the theoretical results

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  6. Comparison between theoretical and experimental data

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  1. A Guide to Analyzing Experimental Data

    Step 0: Import and Inspect data. The data we will use in this tutorial are generated with Qualtrics, a popular website used for designing questionnaires and experimental surveys. We developed an experimental survey based on the flow we described earlier. Then, we generated 500 automated ("test") responses for the purpose of our analysis.

  2. Data, measurement and empirical methods in the science of science

    Here we review three quasi-experimental methods: difference-in-differences, instrumental variables and regression discontinuity (Fig. 3). Fig. 3: Quasi-experiment methods. a - c, This figure ...

  3. Theoretical vs. Experimental Probability: How do they differ?

    Theoretical and experimental probabilities are two ways of calculating the likelihood of an event occurring. Theoretical probability uses mathematical formulas, while experimental probability uses data from experiments. Both types of probability are useful in different situations. I believe that both theoretical and experimental probabilities ...

  4. Lecture 9: Understanding Experimental Data

    Lecture 9: Understanding Experimental Data Description: Prof. Grimson talks about how to model experimental data in a way that gives a sense of the underlying mechanism and to predict behaviour in new settings.

  5. PDF Theory versus Experiment: Analysis and Measurements of Allocation Costs

    Introduction. This handout illustrates techniques you can use to compare experimental data with theoretical predictions. We have chosen units so that theoretical and experimental results can be compared directly, with no "curve fitting.". We present theoretical and experimental results on the same graph.

  6. Experimental data

    Experimental data. Experimental data in science and engineering is data produced by a measurement, test method, experimental design or quasi-experimental design. In clinical research any data produced are the result of a clinical trial. Experimental data may be qualitative or quantitative, each being appropriate for different investigations.

  7. Experimental Data Analysis

    By their insistence on the decision-theoretic elements of the Bayesian approach, many authors have obscured the contribution of Bayesian inference to experimental data analysis and scientific reporting. Within this context, many Bayesians place emphasis on a subjective perspective. This can be the reasons why until now scientists have been reluctant to use Bayesian inferential procedures in ...

  8. Statistics and the Treatment of Experimental Data

    The first refers to the theoretical mean, as calculated from the theoretical distribution, while the latter is an experimental mean taken from a sample. As we shall see in Sect. 4.2, the sample mean is an estimate of the theoretical mean. Throughout the remainder of this chapter, we shall always use the Greek letter µ todesignate the ...

  9. 5: Experimental Design

    In a broad stoke view, data are obtained from two kinds of studies: observational studies and experimental (manipulative) studies. what a correctly designed experiment can tell you about the world, and how a poorly designed experiment works against you. At the end of the semester, you should be familiar with the issues of Randomization, Control ...

  10. Integration of theory and experiment in the modelling of ...

    Moreover, design rules for new materials and molecules are often difficult to derive based only on experimental data. Theoretical and computational studies are playing an increasingly important ...

  11. Khan Academy

    Khan Academy. If you're seeing this message, it means we're having trouble loading external resources on our website. If you're behind a web filter, please make sure that the domains *.kastatic.org and *.kasandbox.org are unblocked. Explore. Search. AI for Teachers Donate Log in Sign up.

  12. Comparing Theoretical and Experimental Probability: Key Insights

    Question 1c: Compare the theoretical probability and experimental probability. From the previous parts, we know that the experimental probability of both coins landing on head equals 20%, while in theory, there should be a 25% chance that both coins lands on head. Therefore, the theoretical probability is higher than the experimental probability.

  13. 7.3: Theoretical and Experimental Spinners

    Theoretical and Experimental Spinners. The 2 types of probability are theoretical probability and experimental probability. Theoretical probability is defined as the number of desired outcomes divided by the total number of outcomes. Theoretical Probability. Experimental probability is, just as the name suggests, dependent on some form of data ...

  14. Statistics and the Treatment of Experimental Data

    2.4 The Chi-Square Distribution. As we will see in Section 7, the chi-square distribution is particularly useful for testing the goodness-of-fit of theoretical formulae to experimental data. Mathematically, the chi-square is defined in the following manner. Suppose we have a set of n independent random variables, x i, distributed as Gaussian densities with theoretical means µ i and standard ...

  15. PDF Fitting Experimental Data

    an equation like the above for every (x;y) data point we have. So we need to collect enough (x;y) data points to fit the model to the data. If our model is an n-th degree polynomial, we need n+1 data points (hence equations). Here the model is "an n-th order polynomial", the data is the (x;y) pairs from the exper-

  16. Comparison of Theoretical and Experimental Data

    The dashed lines are the linear least-squares fits to the experimental data. In the following, we first determine experimental \ ( {\Phi }_ {bp}^ {p}\) values from barrier heights of p -type Schottky contacts and then compare these with corresponding theoretical p -type branch point energies. Experimental barrier heights of p -type diamond, Si ...

  17. Comparison between experimental data and theoretical calculations of

    To provide temperature data accurate to 0.1C, the electromotive force of each thermocouple is amplified, detected, and recorded, by a standard computer on-line-interface whose exhaustive descriptions Experimental Data and Theoretical Calculations 111 Figure 2. A complete experiment of free convection in water.

  18. Theoretical vs. Experimental Probability

    Theoretical probability is what we expect to happen, where experimental probability is what actually happens when we try it out. The probability is still calculated the same way, using the number of possible ways an outcome can occur divided by the total number of outcomes. As more trials are conducted, the experimental probability generally ...

  19. Experimental Data for Model Validation

    Abstract. This chapter is concerned with experimental modelling techniques and the use of experimental test data for the purposes of model evaluation. It includes an overview of system identification and parameter estimation methods and gives emphasis to the importance of issues associated with the optimisation of the model structure.

  20. How to analyze the differences between experimental and theoretical data

    $\begingroup$ @vb628 Well, I am not sure whether I understand you, but the theoretical data points are computed using potential energy curve. Now, I just mean very basic statistics, like variance, mean, median. How much the data points diverge from zero ( in case the theoretical and measured data points agree completely). $\endgroup$ -

  21. How to calculate theoretical and experimental data in general physics

    I need to calculate theoretical and experimental data in general physics´experiment laboratory. I have an inclined plane with a particle called ball. Just let the ball free to go from one point to another-the ball slides down with the angle 15 degrees and the plane is 56 centimeters long. As a result after the experiment,I obtained time and ...

  22. Theoretical and Experimental Data for a Number of NACA 6A-Series

    Theoretical data are presented for NACA 6A-series basic thickness forms having the position of minimum pressure at 30-, 40-, and 50-percent chord and with thickness ratios varying from 6 percent to 15 percent. ... The experimental results of a two dimensional wind tunnel investigation of the aerodynamic characteristics of five NACA 64A-series ...

  23. Estimating Treatment Effects Using Observational Data and Experimental

    When estimating treatment effects, the gold standard is to conduct a randomized experiment and then contrast outcomes associated with the treatment group and the control group. However, in many cases, randomized experiments are either conducted with a much smaller scale compared to the size of the target population or accompanied with certain ethical issues and thus hard to implement ...

  24. Generative neural networks for experimental manipulation: Examining

    To this end we develop a version of recent 'deep models of face impressions' better suited for data-efficient experimental manipulation. ... it may be possible to postulate a novel explanation of the observed quadratic pattern that has a theoretical basis in the functional interpretation of these traits and the evolutionary origin of their ...

  25. Exploring Spectral and Electrochemical Behavior of Hydroxy-N

    The geometry optimization of unsubstituted and (o/p)-OH-substituted analogs revealed the coplanarity of the molecules. The vibrational spectra of the compounds were computed using density functional theory (DFT) and compared with the experimental data. The observed bands were assigned based on total energy distribution (TED).

  26. Understanding the compaction behavior of uncured thermoset prepreg

    The deformation behavior of uncured thermoset prepreg during hot compaction process was investigated by dividing the whole compaction process into an initial compression stage and the subsequent creep stage.

  27. H-shift and cyclization reactions in unsaturated alkylperoxy radicals

    These H-shift reactions have been the subject of numerous experimental and theoretical studies, especially for alkyl and oxygenated RO 2. 3 Structure activity relationships (SAR) have been proposed to predict the rate coefficients for the H-shift reactions of RO 2 with a wide range of molecular structures. 4-6 This included unsaturated RO 2 that are especially relevant for the atmospheric ...

  28. Theoretical and Empirical Validation of Heston Model

    This study focuses on the application of the Heston model to option pricing, employing both theoretical derivations and empirical validations. The Heston model, known for its ability to incorporate stochastic volatility, is derived and analyzed to evaluate its effectiveness in pricing options. For practical application, we utilize Monte Carlo simulations alongside market data from the Crude ...

  29. Moleculin Announces Positive In Vivo Efficacy Data of ...

    Moleculin Announces Positive In Vivo Efficacy Data of Annamycin in Orthotopic and Experimental Lung Metastatic Models of Sarcoma Published Sep 23, 2024 8:00am EDT

  30. Experimental Oral Drug Shows 'Remarkable' Weight Loss, Novo Nordisk Says

    In a phase 1 trial, Novo Nordisk's experimental obesity drug amycretin led to up to 13% weight loss in just three months. Amycretin targets GLP-1 receptors and a second hormone called amylin. Amylin appears to act in the brain, rather than in the gut. It's possible that amylin can control appetite with fewer gastrointestinal side effects.