CagriSema is a fixed-dose combination of cagrilintide, a long-acting amylin analogue, and semaglutide, a glucagon-like peptide-1 receptor agonist.
The Food and Drug Administration (FDA) has approved Alyftrek â„¢ (vanzacaftor/tezacaftor/deutivacaftor) for the treatment of cystic fibrosis (CF) in patients aged 6 years and olde ...
The Food and Drug Administration (FDA) has approved Zepbound ® (tirzepatide) for the treatment of moderate to severe obstructive sleep apnea (OSA) in adults with obesity.
The Food and Drug Administration (FDA) has approved Steqeyma ® (ustekinumab-stba), a biosimilar to Stelara ® (ustekinumab), for the treatment of various chronic inflammatory diseases in adults and ...
GSK has made the decision to withdraw Jesduvroq (daprodustat) from the US market. Approved in 2023, Jesduvroq, (HIF-PHI), is ...
Significant changes from previous guideline include recommendation that only FSH >25 IU required for POI diagnosis.
The prescribing information for Veozah (fezolinetant) has been updated to include a boxed warning regarding the risk of hepatotoxicity, following the Food and Drug Administration’s review of a ...
Black mothers are faced with a disproportionate number of barriers to breastfeeding compared to other racial and ethnic groups.
Black mothers are faced with a disproportionate number of barriers to breastfeeding compared to other racial and ethnic groups.
The newly approved regimen is expected to simplify administration and potentially reduce medication errors and dose-related reactions.