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medcelerator · clinician one-pager

First FDA-Approved Treatment for Adults With Recurrent Respiratory Papillomatosis

Papzimeos (zopapogene imadenovec-drba) — four subcutaneous shots over 12 weeks for adults with recurrent respiratory papillomatosis

FDA Approved · United States · September 18, 2026

Condition: Recurrent Respiratory Papillomatosis

Who this is for

This is for adults living with recurrent respiratory papillomatosis who still need repeated airway surgeries and may be candidates for labelled US Papzimeos — four under-the-skin shots over about 12 weeks after surgical debulking — through an ENT / laryngology clinician and Papzimeos SUPPORT. It explains the first FDA-approved RRP therapy, the 12- and 24-month surgery-free results, injection-site and clotting-watch cautions, how to start the prescription conversation, and why authorised is not funded — without treating complete response as a forever cure guarantee, dosing children off-label from this pack, or importing a US vial. Authorized is not funded.

Next clinical step

The US Food and Drug Administration (FDA) has approved this medicine. In the United States, ask your doctor or a specialist whether it suits you. They can write a prescription. Insurance or public drug plan coverage is not guaranteed.

Ways to access this treatment

See 1 trial on ClinicalTrials.gov: https://clinicaltrials.gov/search?cond=recurrent%20respiratory%20papillomatosis&intr=zopapogene%20imadenovec&aggFilters=status:rec

Possible routes (not confirmed)

General resources for further research

AI-produced discussion aid; not prescribing instructions. Approval does not establish coverage. Full article: https://medcelerator.com/articles/papzimeos-zopapogene-imadenovec