INOVIO wins FDA accelerated approval for RRP immunotherapy
The plasmid DNA-based treatment reduces the frequency of surgery in adults with recurrent respiratory papillomatosis, a rare HPV-related disease. A webcast is set for Monday, November 2.
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Biotechnology company developing DNA-based medicines
inovio.comLast updated
In short: INOVIO secured FDA accelerated approval for VOCERYQ and expected to begin shipping in about 60 days.
The plasmid DNA-based treatment reduces the frequency of surgery in adults with recurrent respiratory papillomatosis, a rare HPV-related disease. A webcast is set for Monday, November 2.
The company joins global experts on October 12th to discuss drug discovery and next-generation DNA medicine for rare disease.
Researchers are testing whether an INOVIO DNA medicine can help people with BRCA1 and BRCA2 mutations by detecting early disease signs and stopping breast cancer before it develops.
The company also shares operational highlights for the quarter.
Inovio Pharmaceuticals is focusing on the commercialization of VOCERYQ following the accelerated approval granted yesterday. The company expects orders and shipments in approximately 60...
The US Food and Drug Administration on Friday approved Inovio Pharmaceuticals' treatment for a rare...
Inovio Pharmaceuticals was awarded $80 million in a breach of contract lawsuit tied to its unsuccessful Covid-19 vaccine effort.
Inovio Pharmaceuticals is approaching a key regulatory milestone as the U.S. FDA is scheduled to decide on the company's Biologics License Application for INO-3107 by...
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