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The events at ARDD2025 have sparked urgent discussions among R&D leaders, all grappling with the same fundamental questions: What is the best way to discover and develop longevity therapeutics that will follow the GLP-1 story

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Watch reporters Jeanne Lenzer and Shannon Brownlee explain what they found: how the FDA approved 73 % of new drugs without solid proof they work and how drug-company money now funds two-thirds of the agencys budget

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Under this framework, dietary supplements do not undergo pre-market FDA approval