Evidence map›Paper›PMID 39192091›Full record

ArticleJournal of pharmacokinetics and pharmacodynamics2024

Generative models for synthetic data generation: application to pharmacokinetic/pharmacodynamic data.

Yulun Jiang, Alberto García-Durán, Idris Bachali Losada, Pascal Girard, Nadia Terranova

Abstract read
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In one paragraph

Article in Journal of pharmacokinetics and pharmacodynamics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Diffusion models for virtual populations and pharmacometric simulations.Journal of pharmacokinetics and pharmacodynamics · 2026
    Article
  3. Article
  4. Review
  5. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Yulun JiangSchool of Computer and Communication Science, Ecole Polytechnique Federale de Lausanne (EPFL), Lausanne, Switzerland.
Alberto García-DuránMerck Quantitative Pharmacology, Ares Trading SA (an affiliate of Merck KGaA, Darmstadt, Germany), Lausanne, Switzerland.
Idris Bachali LosadaMerck Quantitative Pharmacology, Ares Trading SA (an affiliate of Merck KGaA, Darmstadt, Germany), Lausanne, Switzerland.
Pascal GirardMerck Quantitative Pharmacology, Ares Trading SA (an affiliate of Merck KGaA, Darmstadt, Germany), Lausanne, Switzerland.
Nadia TerranovaMerck Quantitative Pharmacology, Ares Trading SA (an affiliate of Merck KGaA, Darmstadt, Germany), Lausanne, Switzerland. nadia.terranova@merckgroup.com.ORCID 0000-0002-0033-3695

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The generation of synthetic patient data that reflect the statistical properties of real data plays a fundamental role in today's world because of its potential to (i) be enable proprietary data access for statistical and research purposes and (ii) increase available data (e.g., in low-density regions-i.e., for patients with under-represented characteristics). Generative methods employ a family of solutions for generating synthetic data. The objective of this research is to benchmark numerous state-of-the-art deep-learning generative methods across different scenarios and clinical datasets comprising patient covariates and several pharmacokinetic/pharmacodynamic endpoints. We did this by implementing various probabilistic models aimed at generating synthetic data, such as the Multi-layer Perceptron Conditioning Generative Adversarial Neural Network (MLP cGAN), Time-series Generative Adversarial Networks (TimeGAN), and a more traditional approach like Probabilistic Autoregressive (PAR). We evaluated their performance by calculating discriminative and predictive scores. Furthermore, we conducted comparisons between the distributions of real and synthetic data using Kolmogorov-Smirnov and Chi-square statistical tests, focusing respectively on covariate and output variables of the models. Lastly, we employed pharmacometrics-related metric to enhance interpretation of our results specific to our investigated scenarios. Results indicate that multi-layer perceptron-based conditional generative adversarial networks (MLP cGAN) exhibit the best overall performance for most of the considered metrics. This work highlights the opportunities to employ synthetic data generation in the field of clinical pharmacology for augmentation and sharing of proprietary data across institutions.

Indexed as

Neural Networks, ComputerDeep LearningHumansModels, StatisticalPharmacokineticsDeep learningGenerative methodsNeural networksSynthetic pharmacokinetic/Pharmacodynamic dataVirtual patients

Identifiers

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.