Dasiglucagon Reduces Glucose Requirements in Congenital Hyperinsulinism Trial
The phase 3 trial evaluated dasiglucagon administered as a continuous IV infusion via a pump in 12 children with persistent CHI.
The phase 3 trial evaluated dasiglucagon administered as a continuous IV infusion via a pump in 12 children with persistent CHI.
Tasquinimod is an investigational oral small molecule immune modulator with anti-angiogenic properties.
The test includes the Weavr Velvet blood collection device, which separates the sample into its red blood cell and plasma components.
The totality of the evidence led the FDA to determine that the criteria for issuing an EUA had not been met.
The test is the first non-prescription multi-analyte COVID-19 test that allows individuals to test nasal swab samples self-collected at home.
The Pfizer-BioNTech COVID-19 vaccine can be administered as a single booster dose to individuals 5 to 11 years of age at least 5 months after completion of the primary series.
The FDA has accepted for Priority Review the New Drug Application for sparsentan for the treatment of IgA nephropathy.
Furoscix is a wearable, pre-programmed on-body furosemide delivery system for outpatient self-administration.
Mounjaro is a first-in-class once-weekly, dual glucose-dependent insulinotropic polypeptide and glucagon-like peptide-1 receptor agonist.
Bimekizumab is an investigational humanized monoclonal IgG1 antibody that selectively inhibits both interleukin (IL)-17A and IL-17F.