Researchers worked with two labs to identify 16 consensus lower-risk pathogenic variants and are pushing for greater ...

NEW YORK – The US Food and Drug Administration on Friday approved Syndax Pharmaceuticals' Revuforj (revumenib) as a treatment for adult and pediatric patients one year and older with relapsed or ...

Patients with MSI-high/dMMR advanced colorectal cancers had a 79 percent lower risk of disease progression or death on Opdivo-Yervoy compared to chemo.

The US Food and Drug Administration approved Augtyro in 2023 for the treatment of ROS1-positive advanced NSCLC. Earlier this year, the FDA also approved the drug for adult and pediatric patients 12 ...

The FDA has cleared the research organization's investigational new drug application, allowing it to start clinical tests of the experimental treatment DT2-SCT.

January, come a year after the drugmaker slashed 7 percent of the workforce at Kite Pharma, its cell therapy business.

As drugmakers take lessons from oncology in developing CAR T cells for other diseases, they must contend with risks that ...

The pharmaceutical distributor has launched InspiroGene, a business unit offering logistics and other support for ...

A 31-year-old woman with stage IV breast cancer learns a test ordered more than a year before her diagnosis detected a TP53 ...

The agency had previously recommended against marketing authorization for the Alzheimer's disease but reconsidered after a review.

The panels assess genes with strong disease links and clinical management guidelines, but the firm offers limited-evidence genes as an add-on option.

The bill would establish the right of cancer patients to access advanced care, including precision medicine and genomic testing, in their communities.