When talking about Drug Repurposing, the practice of finding new therapeutic uses for already approved medicines. Also known as drug repositioning, it bridges the gap between existing pharmacology and emerging health challenges. Off‑label use, prescribing a drug for an unapproved condition is a common entry point, but true repurposing moves beyond anecdote to systematic investigation. It requires rigorous Clinical trials, controlled studies that test safety and efficacy in the new indication and often navigates the FDA approval, the regulatory process that validates the new use for market entry. The underlying Pharmacology, how a drug interacts with biological targets informs which compounds have the best chance of success, making repurposing a cost‑effective shortcut in drug development.
Because existing drugs already have known safety profiles, the time and money saved can be huge. Researchers use big‑data screens, AI models, and patient registries to spot hidden potentials—think anti‑viral properties in an old cancer pill or anti‑inflammatory effects in a cholesterol drug. These discoveries often arise from the same therapeutic classes highlighted in our articles, such as the cardiovascular insights in the Cardizem vs alternatives piece or the epilepsy focus in phenytoin monitoring. By understanding how each medication works, you can see the logical steps that lead from one indication to another. Below, you’ll find practical guides, side‑effect alerts, and comparison charts that illustrate real‑world repurposing examples and help you stay ahead of the curve.
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