Precigen presents new long-term durability data for PAPZIMEOS
83% of complete responders maintained response for at least 36 months, with five beyond four years, and the drug received seven-year market exclusivity.
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Gene and cell therapy biopharmaceutical company
precigen.comLast updated
In short: Precigen achieved a historic milestone with the FDA approval and successful commercial launch of PAPZIMEOS for recurrent respiratory papillomatosis.
83% of complete responders maintained response for at least 36 months, with five beyond four years, and the drug received seven-year market exclusivity.
The data shows complete responses and reduced surgical debulking in recurrent respiratory papillomatosis patients.
The FDA granted seven-year market exclusivity for the RRP treatment, effective through August 2032.
PAPZIMEOS generated $21.6M in net product revenue, with 400 patients enrolled and strong payer coverage.
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