Why it matters
The approval gives eligible U.S. adults a new treatment option for a rare condition. The supplied announcement does not describe the treatment’s availability, cost, or how many patients may use it.
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The FDA granted accelerated approval to Voceryq for adults with recurrent respiratory papillomatosis, a disease that causes growths in the respiratory tract. The agency described it as the first approved plasmid DNA-based immunotherapy.
HOW THIS BRIEF WAS MADE 1 outlet: 1 official. Automated sourcing and summaries by the BLUF engine. Corrections
The approval gives eligible U.S. adults a new treatment option for a rare condition. The supplied announcement does not describe the treatment’s availability, cost, or how many patients may use it.