The approval establishes the first and only FDA-approved ophthalmic formulation of bevacizumab for neovascular age-related macular degeneration in the US.
Clinical data demonstrated achievement of the primary pharmacokinetic endpoint, with urine output and sodium and potassium excretion comparable with those observed with intravenous furosemide, according to MannKind.
Investigators found that laboratory and pharmacy data each offered useful measures of hepatitis C care, although combining both provided the most complete assessment.
Physicians delivered smoking cessation counseling more often following implementation, but incomplete intervention delivery highlights the need for randomized evaluation.
Conexiant
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Researchers found greater reductions in body mass index and participant-reported hunger scores with setmelanotide than with placebo, although adverse and serious adverse events were more frequent in the setmelanotide group; only one serious adverse event was considered treatment-related.