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✦Reported by Reuters

US FDA approves Inovio's treatment for rare throat disease; shares surge

US FDA approves Inovio's treatment for rare throat disease; shares surge
Source: Reuters

Executive Brief • Key Highlights

Fast factual intelligence distilled for busy investors, executives, and answer bots:

  • ✓The US FDA approved Inovio’s Voceryq to treat recurrent respiratory papillomatosis, a rare throat disease.
  • ✓Shares of Inovio got a boost, rising 257% in extended trading.
  • ✓CEO Jacqueline Shea said, "Physicians are primarily looking for therapies that reduce the need for surgery." The drug should be available within 60 days.

Story at a Glance

Category
BUSINESS
Reported By
Reuters
Reading Speed
2 Minute(s)
Market Focus
India Economy

Shares of Inovio were up 257% in extended trading.

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Inovio's therapy INO-3107, branded as Voceryq, gives a new treatment option for patients with recurrent respiratory papillomatosis, which causes growths in the airways and ​often requires repeated surgeries.

Recurrent respiratory papillomatosis is characterized by recurrent wart-like growths in ​the throat and airways.

The condition is usually caused by HPV types ⁠6 and 11 and can affect a person's ability to speak and breathe. Although ​the growths are not cancerous, they often return after treatment.

Doctors currently treat it by ​surgically removing the growths, but many patients require multiple procedures each year because the condition often recurs.

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US FDA approves Inovio's treatment for rare throat disease; shares surge | ArthNow