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A new study reported by Reuters suggests that GLP-1 receptor agonists, a widely used class of diabetes and weight-loss drugs, may be associated with a lower risk of developing 10 cancers tied to…
A new study published on Sunday suggests that an AI-powered wearable device could help detect early signs of diabetes with high accuracy. Researchers say the tool identified indicators of the…
The U.S. Food and Drug Administration has approved a new gene therapy for adults living with transfusion-dependent beta-thalassemia, a rare inherited blood disorder that often requires frequent…
The U.S. Food and Drug Administration has approved the first gene-editing treatment for adults with severe sickle cell disease, a milestone that could change care for patients with limited options.…
Researchers have reported encouraging results from a new blood test that may help identify Alzheimer’s disease years before symptoms become obvious. The test was evaluated in a large clinical trial…
A large analysis of electronic health records suggests that GLP-1 receptor agonists, a class of drugs widely used for diabetes and weight loss, may be associated with lower rates of several cancers…
A major U.S. hospital network has been hit by a ransomware attack that may have exposed patient records and medical information, according to a Reuters report citing the incident and the group that…
A major U.S. hospital network said a ransomware attack exposed personal information tied to about 1.5 million patients, underscoring the growing security risks facing the healthcare sector. The…
A new gene-editing treatment has shown encouraging early results for people living with severe sickle cell disease, according to interim findings published in The New England Journal of Medicine.…
Interim data from an early-stage clinical trial suggest a CRISPR-based gene-editing treatment may offer meaningful relief for people living with severe sickle cell disease. Researchers said 92% of…
The U.S. Food and Drug Administration has approved a new gene therapy for a rare inherited disorder, giving patients and families a fresh treatment option in a field where choices are often limited.…
