FDA Regulatory Friday, October 30, 2026 0.00 Neutral

FDA Approves First Plasmid DNA Immunotherapy for RRP

The FDA granted accelerated approval to Voceryq for treating adults with recurrent respiratory papillomatosis, marking the first plasmid DNA-based immunotherapy for this indication.

View original filing at SEC.gov →
AI-generated summary for informational purposes only. Always verify against the original filing. Not investment advice. BriefTape is not a registered investment adviser.

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