HealthDay News — Among individuals eligible for lung cancer screening (LCS), use of breast cancer screening (BCS) and colorectal cancer screening (CCS) is much higher than use of LCS, according to a ...

The Food and Drug Administration (FDA) has granted Fast Track designation to PBGENE-HBV, an investigational gene editing therapy for adults with chronic hepatitis B.

The software-based intervention aims to reduce brain hypersensitivity in patients with migraine by modulating responses to environmental and internal stimuli through a 12-week program.

To achieve these ends, the FDA will use computer modeling and artificial intelligence (AI) to predict a drug’s behavior and promote the use of lab-grown human organoids (tiny, self-organized ...

The randomized, double-blind, placebo-controlled ODYSSEY-HCM trial included 580 adult patients with symptomatic nonobstructive HCM.

When used with the companion app, the smart belt automatically alerts caregivers when a fall or impact is detected.

CJD is caused by infectious proteins called prions. These proteins damage the brain and lead to fast-moving dementia.

The Food and Drug Administration (FDA) has approved Opdivo ® (nivolumab) in combination with Yervoy ® (ipilimumab) for the first-line treatment of adult patients with unresectable or metastatic ...

Seventy-four percent of respondents unaware of FDA-approved treatments; 56% said these options had not been discussed by clinician.

After proper training on subcutaneous injection technique, the prefilled syringe may be administered by the patient or caregiver.

In the past, experts from the CDC’s EpiAid program have provided short-term help to local agencies dealing with urgent public health issues.

The recall involves the "Brunch & Go" stroller toy, a set of make-believe breakfast items including avocado toast, bacon, a tomato and an egg.