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INOVIO Pharmaceuticals announced that it has received accelerated approval from the FDA for its plasmid DNA-based immunotherapy. The newly approved therapy is designed to reduce the frequency of surgery in adults suffering from recurrent respiratory papillomatosis, a rare and debilitating HPV-related disease.
This regulatory milestone represents a significant development for patients with this condition, offering a new treatment option that may decrease the need for repeated surgical interventions. INOVIO Pharmaceuticals highlighted the innovation as a major achievement in advancing care for RRP patients.
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