As is often the case with cancer treatments, many patients are able to benefit from therapy for a time. Tumor activity ...
A closely watched clinical trial in Britain that screened blood for early detection of cancer did not show a reduction in ...
As Candel Therapeutics gears up for a planned U.S. approval push for its prostate cancer drug later this year, RTW ...
Regenerative Medicine Advanced Therapy (RMAT) designation requests update submitted to FDA with recent biomarker data ...
Pharmalittle: We’re reading about an FDA official’s speech, a Grail cancer blood test, and much more
The FDA's top drug regulator indicated in her first address to staff that she will scrutinize antidepressants and shots used to protect babies from RSV ...
Some six years after the FDA approved Eli Lilly’s Retevmo to treat lung a | Six years after the FDA approved Eli Lilly’s ...
The agency could by late December approve a therapy that Roche sees as potentially becoming a new treatment standard for ...
Filing acceptance based on phase III data showing giredestrant plus everolimus reduced the risk of disease progression or ...
Shares in the company lost about half their value in Friday trading after use of the test wasn’t associated with a statistically significant reduction in late-stage cancer diagnoses.
On Friday, the U.S. Food and Drug Administration (FDA) approved AbbVie Inc.'s ABBV combination treatment for chronic ...
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Distinct gut toxicity patterns emerge with targeted cancer treatments
A new paper was published in Volume 13 of Oncoscience on February 6, 2026, titled "Gastrointestinal toxicity of targeted cancer therapies in the United States: Clinicopathologic patterns, FDA safety ...
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