Credit: BrainsWay. The outpatient procedure provides noninvasive magnetic stimulation through a cushioned helmet to targeted areas of the brain. The Food and Drug Administration (FDA) has expanded the ...
The availability of these generics is still unclear as the patent for Entresto does not expire until July 15, 2025. The Food and Drug Administration (FDA) has approved the first generics of Entresto ® ...
The program automatically reduces the cost of the inhaler at the pharmacy for eligible patients with commercial insurance. Out-of-pocket costs for Boehringer Ingelheim asthma and chronic obstructive ...
Authors found that BMI of 27 or greater shows excellent diagnostic performance. HealthDay News — The optimal body mass index (BMI) cutoff point appears to be 27kg/m 2 for detecting obesity in ...
Greater use of weight management treatments seen with WNP, including bariatric surgery, low-calorie meal replacement. HealthDay News — A primary care-based weight navigation program (WNP) is feasible ...
Findings showed patients treated with plozasiran 25mg and 50mg had median triglyceride reductions of -80% and -78%, respectively, compared with -17% for placebo. Plozasiran significantly reduced ...
Results showed 30.4% of patients treated with mitapivat achieved a transfusion reduction response vs 12.6% of patients who received placebo. Mitapivat was associated with a significant reduction in ...
Credit: Moderna. The approval was based on data from the phase 3 ConquerRSV trial, which included approximately 37,000 adults 60 years of age and older. The Food and Drug Administration (FDA) has ...
Results from LIBRETTO-121 showed a confirmed overall response rate of 48% (95% CI, 28-69). The Food and Drug Administration (FDA) has granted accelerated approval to Retevmo (selpercatinib) for the ...
The CDC is monitoring influenza activity closely in states affected by the H5N1 outbreak and said there's been "no sign of unusual influenza activity." HealthDay News — Amid an ongoing outbreak of ...
Insmed plans to file a New Drug Application with the Food and Drug Administration in the fourth quarter of 2024. Treatment with brensocatib reduced the frequency of pulmonary exacerbations in patients ...
The additional information provided by Regeneron and Sanofi was considered a major amendment to the application. The Food and Drug Administration (FDA) has extended the review period for the ...