FDA approves first immunotherapy for recurrent respiratory papillomatosis

FDA

14 August 2025 - Today, the US FDA approved Papzimeos (zopapogene imadenovec-drba), a first of its kind non-replicating adenoviral vector-based immunotherapy for the treatment of adult patients with recurrent respiratory papillomatosis.

The approval is based on results from a single-arm, open-label trial evaluating Papzimeos in adult patients with recurrent respiratory papillomatosis who required three or more surgeries per year.

Read FDA press release

Michael Wonder

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Michael Wonder

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Outcome , US , Registration , Gene therapy