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Updated: Jul 18, 2025

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Nutrient Regulation by Continuous Feeding for Large-scale Expansion of Mammalian Cells in Spheroids
Published on: September 25, 2016
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Special Issue "Stem Cell Biology & Regenerative Medicine"
1BGU-iPSC Core Facility, The Regenerative Medicine & Stem Cell (RMSC) Research Center, Ben Gurion University of the Negev, Israel and Desert & Dead Sea R&D, Central Arava Branch, Be'er Sheva 84105, Israel.
International Journal of Molecular Sciences
|August 26, 2023
Summary
Most pre-clinical drug discovery studies fail, wasting resources. Improving animal models is crucial for successful drug development and reducing costs.
Area of Science:
- Pharmacology and Toxicology
- Pre-clinical Research Methodologies
Background:
- The drug discovery pipeline is lengthy and costly.
- Over 50% of pre-clinical studies fail to translate to clinical success.
- Animal models are extensively used but have limitations in predicting human responses.
Discussion:
- High failure rates in pre-clinical studies indicate a need for better predictive models.
- Current animal models may not accurately recapitulate human disease complexity.
- Investigating alternative or refined pre-clinical models is essential for efficiency.
Key Insights:
- The significant failure rate highlights inefficiencies in current drug discovery paradigms.
- Animal models, while valuable, present challenges in translational accuracy.
- Optimizing pre-clinical study design is critical for resource optimization.
Outlook:
- Future research should focus on developing more translatable pre-clinical models.
- Enhancing the predictive power of early-stage drug testing is a key goal.
- Reducing attrition rates will accelerate the delivery of effective therapeutics.
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