Nearly 90% of drugs under development fail to reach the market. Many of these failures occur due to cardiotoxicity, usually when the candidate molecule induces cardiac arrhythmias. In a few notable cases, some drugs pass pre-clinical screens and clinical trials, only to be removed from the market once toxic effects are discovered in large patient populations. These failures represent a tremendous source of waste and constitute a significant part of the ~$2 billion cost of bringing a single drug to market. Consequently, the FDA now mandates that all drugs undergo in vitro cardiotoxicity testing before being tested in humans. This has led to a significant and growing market for tools and technologies that enable earlier detection of toxic effects before exposure to patients. However, current screening methods fall short of predicting how a drug will behave in the body; indeed there is a pressing need for more predictive model systems. Human induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs) are an attractive model for in vitro preclinical toxicity screening; they are relatively easy to maintain, are derived from human tissue, and have the potential to reduce the need for animal experimentation. However, at present, iPSC-CM based assays do not properly replicate the function of the human heart. These cells exhibit phenotypes similar to that of fetal tissue and do not respond as expected to drugs of known effect; in some cases, known bad-actor drugs fail to induce arrhythmias, while others only show in vivo cardiotoxicity when exposed to supra-physiological doses of the drug in question. The drug discovery industry and its regulators realize the potential of iPSC-CMs for early cardiotoxicity screening, but also understand that?at present?there are significant limitations to their use in the drug development process. Thus, it is clear that the production of mature cardiac tissues that accurately recapitulate in vivo drug responses represents a significant opportunity for reducing cost and waste in drug development. NanoSurface Biomedical, Inc., aims to develop an enhanced iPSC-CM cell line that has been optimized for highly predictive drug-induced cardiotoxicity screening. We hypothesize that iPSC-CMs that give more predictive results in in vitro cardiotoxicity detection can be made by combining nanoscale extracellular cues with biochemical and molecular biological stimuli that drive their maturation. We will first focus on demonstrating that these enhanced iPSC-CMs can correctly classify drugs that are currently improperly screened (Phase 1, Aim 1). After validation, we will generate a stable cell line that encompasses the maturation factors determined in Phase 1 in preparation for scaling and commercial production (Phase 2, Aim 1). Commercialization efforts will further be facilitated by characterizing transcriptomic, structural, and functional phenotypes of the predictive cell line and in identifying a set of key physiological metrics that will be used for in-line quality control (Phase 2, Aim 2). Last, we will validate and generate data for market release with our research partners in the drug development industry and regulatory bodies (Phase 2, Aim 3).

Public Health Relevance

In this project, the company will optimize, validate, and scale methods to produce engineered cardiac tissues which can be used to pre-clinically assess how the human heart will react to drugs. We anticipate that the combination of various cues (mechanical, electrical, biomolecular, and biochemical) will greatly enhance the utility of cardiac tissues in providing more predictive toxicity data than currently available using existing technologies. This product has great potential to dramatically reduce the cost of drug development, improve clinical outcomes, and save lives across a wide spectrum of diseases and conditions.

National Institute of Health (NIH)
National Heart, Lung, and Blood Institute (NHLBI)
Small Business Innovation Research Grants (SBIR) - Phase II (R44)
Project #
Application #
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Lundberg, Martha
Project Start
Project End
Budget Start
Budget End
Support Year
Fiscal Year
Total Cost
Indirect Cost
Nanosurface Biomedical, Inc.
United States
Zip Code