Only 13% of oncology trial press releases from major pharma companies include precise data — raising concerns about ...

The U.S. Food and Drug Administration has approved AbbVie's drug to treat adults with a type of lung cancer who have received ...

The U.S. Food and Drug Administration said on Wednesday it has approved the expanded use of Merck's cancer drug to treat two ...

The U.S. Food and Drug Administration (FDA) on Wednesday approved Merck & Co. Inc.’s (NYSE:MRK) Welireg (belzutifan) for ...

The cells targeted the cancer and eradicated it. Thirteen years later, Whitehead is still cancer-free. Since then, however, ...

Biotech company AbbVie (ABBV) said on Wednesday that the U.S. Food and Drug Administration has approved Emrelis medicine for ...

The popular California-based fast food burger chain is giving some of its drinks and ketchup a new taste after the FDA banned ...

The FDA has granted accelerated approval to Avmapki (avutometinib) plus Fakzynja (defactinib) for the treatment of KRAS-mutated, recurrent low-grade serous ovarian cancer.

May 9 (UPI) --The U.S. Food and Drug Administration on Friday approved Teal Health to provide the nation's first at-home test kit to screen for cervical cancer. The Teal Wand, which will be ...

The Food and Drug Administration (FDA) has approved the first at-home screening test for cervical cancer, the product’s maker announced on Friday. The DIY test could serve as an alternative to ...

A study of more than 100 patients found that immunotherapy can cure a rare type of cancer in various tumor sites without ...

Verastem Oncology said the Food and Drug Administration approved the combination of avutometinib capsules and defactinib tablets for certain patients with KRAS-mutated recurrent low-grade serous ...