Inovio Gets Accelerated FDA Approval of Voceryq; Shares More Than Triple After Hours

By Josh Beckerman


Inovio Pharmaceuticals said the Food and Drug Administration granted accelerated approval of Voceryq to reduce the frequency of surgery in adults with recurrent respiratory papillomatosis.

Shares more than tripled after hours to $2.17.

The drug was previously known as INO-3107.

Inovio expects Voceryq will be available to order and ship in about 60 days, with full commercial launch in the first quarter of 2027.


Write to Josh Beckerman at josh.beckerman@wsj.com


(END) Dow Jones Newswires

October 30, 2026 18:38 ET (22:38 GMT)

Copyright (c) 2026 Dow Jones & Company, Inc.

The articles, information, and content displayed on this webpage may include materials prepared and provided by third parties. Such third-party content is offered for informational purposes only and is not endorsed, reviewed, or verified by Morningstar.

Morningstar makes no representations or warranties regarding the accuracy, completeness, timeliness, or reliability of any third-party content displayed on this site. The views and opinions expressed in third-party content are those of the respective authors and do not necessarily reflect the views of Morningstar, its affiliates, or employees.

Morningstar is not responsible for any errors, omissions, or delays in this content, nor for any actions taken in reliance thereon. Users are advised to exercise their own judgment and seek independent financial advice before making any decisions based on such content. The third-party providers of this content are not affiliated with Morningstar, and their inclusion on this site does not imply any form of partnership, agency, or endorsement.

Popular

Sponsor Center