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Alzheimer's disease affects more than five million Americans, but the disease is still a mystery to scientists and doctors. There’s no cure. But some…
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There’s a new treatment now for thousands of patients in the U.S. who live with a rare disorder where blood doesn’t clot. The Food and Drug Administration…
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One of the first uses for the buzzy gene-editing tool CRISPR could be a treatment for patients with sickle-cell disease. But the Black community’s…
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Reporting the results of trials on humans to the federal government's public-access website ClinicalTrials.gov has been mandatory since 2008. But…
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Twenty-two years after Congress ordered the National Institutes of Health to include women in the clinical trials it funds to test medical treatments,…
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Kim Hudak was a young mother who was done having children when she volunteered for a clinical trial to an experimental birth control implant designed to…
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Federal law requires publicly funded medical researchers to promptly report the results of many experimental treatments. But few are doing so, a review shows, and patients may be hurt.
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There is no effective treatment for the rare genetic disorder fragile X syndrome, so two parents created a foundation to fund research. But they found there's no easy road to a cure.