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INO-3107 DNA

Updated ยทnext FDA decision on the calendar

INO-3107 DNA is a Inovio Pharmaceuticals program in Recurrent respiratory papillomatosis (RRP) BLA. Its PDUFA date is Oct 30, 2026, the FDA's goal date to complete review of the application. Every date links its source.

INO catalyst hub

All upcoming FDA decision dates on the 2026 PDUFA calendar

About this program

Indication under review: Recurrent respiratory papillomatosis (RRP) BLA. Sponsor: Inovio Pharmaceuticals (INO). Market-cap tier at the time we tracked it: Micro. We track 1 catalyst event for this program: 1 upcoming and 0 in the record. A PDUFA date is the FDA's target date to complete review of a marketing application; a readout is the sponsor's expected date for clinical trial results. What a PDUFA date is · why we do not compare trial results across drugs.

Catalyst history

PDUFA · Oct 30, 2026INO

Questions

When is INO-3107 DNA's next FDA decision or readout?

INO-3107 DNA's PDUFA date is Oct 30, 2026. That is the FDA's goal date to complete review of the application; the agency can act earlier or extend it.

What happened at INO-3107 DNA's most recent FDA decision?

No FDA decision for INO-3107 DNA is in our archive yet.

What is INO-3107 DNA used for?

In our records INO-3107 DNA is under review or in development for Recurrent respiratory papillomatosis (RRP) BLA.

Who makes INO-3107 DNA?

Inovio Pharmaceuticals (INO).

Where does this data come from?

FDA announcements, sponsor press releases and SEC filings; every date on this page links its source.