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Ionis partner GSK announces bepirovirsen NDA accepted for priority review

Ionis Pharmaceuticals (IONS) partner GSK (GSK) announced the FDA has accepted for priority review the new drug application, or NDA, for bepirovirsen, an investigational antisense oligonucleotide, or ASO, for the treatment of adults with chronic hepatitis B. The FDA has granted bepirovirsen breakthrough therapy designation and set a Prescription Drug User Fee Act target action date of October 26.

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