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Using Human Induced Pluripotent Stem Cell-derived Hepatocyte-like Cells for Drug Discovery
Published on: May 19, 2018
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hiPSC-Derived Cells as Models for Drug Discovery
1BGU-iPSC Core Facility, The Regenerative Medicine & Stem Cell (RMSC) Research Center, Ben Gurion University of the Negev, Be'er Sheva 84105, Israel.
International Journal of Molecular Sciences
|August 27, 2021
Summary
Most drugs fail in clinical trials because animal models do not accurately predict human biology. This high failure rate highlights the need for better preclinical testing methods to improve drug development efficiency.
Area of Science:
- Pharmacology
- Translational Medicine
- Drug Discovery
Background:
- Over 85% of drugs fail during clinical trials.
- Current preclinical animal models often poorly predict human biological responses.
- This inefficiency leads to significant delays and increased costs in drug development.
Discussion:
- The high attrition rate of drug candidates suggests a fundamental disconnect between animal model efficacy and human outcomes.
- Investigating the biological and physiological differences between species is crucial.
- Rethinking the reliance on traditional animal models for predicting human drug response is necessary.
Key Insights:
- Animal models are frequently inadequate predictors of human drug efficacy and safety.
- The limitations of animal models contribute significantly to the high cost and low success rate of pharmaceutical development.
- A paradigm shift in preclinical testing is required to enhance predictive accuracy.
Outlook:
- Developing novel in vitro or in silico models that better mimic human physiology.
- Exploring alternative preclinical testing strategies to improve the success rate of drug candidates.
- Enhancing the translational validity of preclinical research to accelerate the delivery of effective therapies.
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