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The FDA has approved Gammagard Liquid ERC as a replacement therapy for PI in adult and pediatric patients 2 years of age and older.
The FDA has approved Benlysta for SC administration using an autoinjector in patients 5 years of age and older with active LN.
The US Food and Drug Administration (FDA) has granted accelerated approval to Zegfrovy (sunvozertinib) for the treatment of adults with locally advanced or metastatic non-small cell lung cancer (NSCLC ...
In a primary efficacy population of 85 patients, the confirmed overall response rate was 46%.
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