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Why did dihexa never enter clinical trials if the animal data was promising? Pharmaceutical companies evaluate preclinical compounds based on risk-benefit calculus, intellectual property landscape, competitive market positioning, and probability of regulatory approval many promising animal compounds are abandoned before human trials because the investment required for Phase 13 studies (often $50$100 million) cannot be justified

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It was found that the cells adhered and spread from tendon tissues (Fig

Clinical characteristics and pathophysiological mechanisms of focal and diffuse traumatic brain injury

The current study aimed to investigate the therapeutic effects of Iva against scopolamine (Sco) induced dementia

This may unintentionally exaggerate perceived effectiveness