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Cardio-Tox TEEM Model for Cardiotoxicity and Arrhythmia Risk Assessment

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Summary

The USPTO has published a patent application detailing the Cardio-Tox Tissue Engineered Model (TEEM). This in vitro model uses 3D human heart microtissues to assess cardiotoxicity and arrhythmia risk from test compounds, aiming to establish safe human exposure levels for environmental and pharmaceutical substances.

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What changed

The United States Patent and Trademark Office (USPTO) has published patent application US20260086083A1, which describes the Cardio-Tox Tissue Engineered Model (TEEM). This invention provides an in vitro system utilizing 3D human heart microtissues to quantify dose-dependent changes in electromechanical activity, thereby enabling a comprehensive assessment of cardiotoxicity and arrhythmia risk for various compounds.

This patent application is relevant to drug manufacturers and other entities involved in chemical and toxicological screening. While this is a patent application and not a regulatory rule, it signifies innovation in methods for predicting potential adverse effects of compounds on human cardiac health. Companies in the pharmaceutical and chemical sectors may find this technology useful for developing predictive in vitro screening platforms to establish safe exposure levels for their products.

Archived snapshot

Mar 27, 2026

GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.

← USPTO Patent Applications

Human In Vitro Cardiotoxicity Model

Application US20260086083A1 Kind: A1 Mar 26, 2026

Inventors

Kareen L. K. Coulombe, Cassady E. Rupert, Celinda M. Kofron, Bum-Rak Choi, Taeyun Kim, Ulrike Mende

Abstract

The Cardio-Tox Tissue Engineered Model (TEEM) invention provides a robust in vitro model for cardiotoxicity evaluation using three-dimensional (3D) human heart microtissues to quantify dose-dependent changes in electromechanical activity, resulting in a comprehensive cardiotoxicity and arrhythmia risk assessment of test compounds. The invention also provides a predictive in vitro screening platform for pro-arrhythmic toxicity testing using human three-dimensional cardiac microtissues. The invention enables the screening of environmental and pharmaceutical compounds, chemicals, and toxicants to establish safe human exposure levels.

CPC Classifications

G01N 33/5088 C12N 5/0697 G01N 1/30 G01N 21/6428 G01N 21/6456 G01N 33/5014 G06T 7/0012 G01N 2021/6439 G01N 2800/32 G06T 2207/10064 G06T 2207/30024 G06T 2207/30048

Filing Date

2025-09-24

Application No.

19338399

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Named provisions

Human In Vitro Cardiotoxicity Model

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Classification

Agency
USPTO
Instrument
Notice
Legal weight
Non-binding
Stage
Final
Change scope
Minor
Document ID
US20260086083A1

Who this affects

Applies to
Drug manufacturers Medical device makers Pharmaceutical companies
Industry sector
3254 Pharmaceutical Manufacturing 3345 Medical Device Manufacturing
Activity scope
Drug Testing Toxicological Screening
Geographic scope
United States US

Taxonomy

Primary area
Pharmaceuticals
Operational domain
Research & Development
Compliance frameworks
GxP
Topics
Medical Devices Product Safety

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