The US Food and Drug
Administration (FDA) has
approved Sylvant (siltuximab) to
treat patients with multicentric
Castleman’s disease.
It was the first FDA approved
treatment for patients with the
disease and demonstrated its
commitment to approving drugs for
rare diseases, FDA Centre for Drug
Evaluation and Research Office of
Hematology and Oncology Products
director Richard Pazdur said.The above article was sent to subscribers in Pharmacy Daily's issue from 24 Apr 14 To see the full newsletter, see the embedded issue below or CLICK HERE to download Pharmacy Daily from 24 Apr 14
THE Senate’s Community Affairs Legislation Committee is holding a two-day inquiry into the Therapeutic Goods and Other Legislation Amendment (Vaping Reforms) Bill 2024, which is currently under discussion in Federal Parliament.
A NEW study from the University of South Australia has discovered that an increased cardio-fitness level will reduce risk of death from any cause by nearly 20%.
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