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FDA Launches Immediate Plan to Replace Animal Testing with Human-Relevant Methods

The agency's new strategy leverages advanced technologies like AI and organoids to improve drug safety, reduce costs, and expedite approvals.

PETA commends the Trump administration's efforts to phase out animal testing in federal research, with the FDA moving to adopt more ethical methods like organoids.
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Activists of the People for the Ethical Treatment of Animals (PETA) hold placards which read "Sanofi: Stop the mad scientists, Stop the forced swimming tests" as they protest against animal testing by French multinational pharmaceutical and healthcare company Sanofi on the sidelines of the company's general assembly at the Palais des Congres in Paris, on April 30, 2024. (Photo by Antonin UTZ / AFP) (Photo by ANTONIN UTZ/AFP via Getty Images)
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Overview

  • The FDA has announced the immediate implementation of a plan to phase out animal testing for monoclonal antibody therapies and other drugs.
  • The new strategy incorporates cutting-edge technologies, including AI-based computational modeling, lab-grown organoids, and organ-on-a-chip systems, to test drug safety and efficacy.
  • Real-world human safety data from countries with established regulatory standards will now be used to streamline drug approvals and reduce reliance on animal testing.
  • The initiative aims to enhance drug safety, accelerate treatment availability, lower research costs, and reduce drug prices while addressing ethical concerns.
  • The move has garnered bipartisan support and praise from animal rights groups, with PETA and the Physicians Committee for Responsible Medicine highlighting its potential to save both human and animal lives.