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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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When a child falls ill with cancer, many of the drugs that might help are either experimental or unapproved for use in kids.
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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.
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While several states have approved so-called right-to-try measures that aim to give patients with life-threatening illnesses access to unapproved drugs, drugmakers don't have to comply.
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Future outbreaks of superbugs that resist treatment will test the American health care system's ability to respond. A prominent patient advocate says we need to be ready.