FDA accepts for review Inovio's BLA for INO-3107 for the treatment of adults with recurrent respiratory papillomatosis

Inovio

29 December 2025 - Inovio today announced that the US FDA accepted the company's niologics license application for INO-3107 for review as a potential treatment for adults with recurrent respiratory papillomatosis.

The review classification designated by FDA is standard. The FDA assigned INO-3107 a PDUFA review goal date of 30 October 2026.

Read Inovio press release

Michael Wonder

Posted by:

Michael Wonder

Posted in:

Medicine , US , Dossier , Registration