Evidence map›Paper›PMID 42560888›Full record

ArticleToxicological sciences : an official journal of the Society of Toxicology2026

GanCtrl: a generative AI approach to derive study-aligned synthetic controls for reducing concurrent control animal use.

Mansi Chandra, Xi Chen, Ting Li, Weida Tong

Abstract read
In one paragraph

Article in Toxicological sciences : an official journal of the Society of Toxicology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Mansi ChandraNational Center for Toxicological Research, Food and Drug Administration, Jefferson, AR 72079, United States.ORCID 0009-0006-9308-3037
Xi ChenNational Center for Toxicological Research, Food and Drug Administration, Jefferson, AR 72079, United States.ORCID 0000-0003-3459-4217
Ting LiNational Center for Toxicological Research, Food and Drug Administration, Jefferson, AR 72079, United States.ORCID 0000-0003-2280-8433
Weida TongNational Center for Toxicological Research, Food and Drug Administration, Jefferson, AR 72079, United States.ORCID 0000-0003-3488-6148

Funding

National Center for Toxicological Research (NCTR) of the US FDAOak Ridge Institute for Science and Education (ORISE)US Food and Drug Administration
6 · The paper itself

Abstract

Minimizing the use of animals as concurrent controls in in vivo studies directly supports the 3Rs principles of Replacement, Reduction, and Refinement. Current virtual control group (VCG) approaches primarily rely on historical control data, but their utility may be limited by cross-study variability from differences in study design, laboratory practices, and data heterogeneity. We propose GanCtrl, a generative AI approach to infer study-specific control data directly from time-matched treatment data. By generating synthetic controls analogous to concurrent controls, GanCtrl aims to mitigate biological, temporal, and technical biases inherent in VCG approaches based on historical control data. GanCtrl was applied to rat repeat-dose toxicity studies to simulate 38 clinical pathology endpoints under control conditions using corresponding treatment data. Synthetic controls closely approximated real concurrent controls, with differences smaller than intra- and inter-laboratory baseline variation and comparable to biological replicate variability, while also preserving the typical magnitude and distribution of control responses across studies. Importantly, synthetic controls enabled detection of drug-induced clinical pathology signals and maintained biologically relevant endpoint relationships, such as ALT-AST. For practical utility, toxicity assessments using GanCtrl-derived synthetic controls were compared with those using real concurrent controls and benchmarked against VCGs constructed from single-laboratory or combined multi-laboratory historical data. Although both approaches performed comparably in the single-laboratory setting, GanCtrl outperformed VCGs when data from multiple laboratories were combined. These findings suggest that GanCtrl offers a potential approach for generating VCGs that may reduce the use of concurrent control animals and advance the 3Rs.

Indexed as

Control GroupsToxicity TestsAnimalsDose-Response Relationship, DrugGenerative Adversarial NetworksGenerative Artificial IntelligenceRats3Rsconcurrent control groups (CCGs)generative adversarial networks (GANs)generative AItoxicologyvirtual control groups (VCGs)

Identifiers

PMID42560888
PMCPMC13505625

What OpenQuestion holds

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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 OpenQuestion graph.