Innoviva reported strong Q3 2024 financial results, driven by solid performance from core GSK royalty assets and accelerating sales from IST commercial products. The company is on track to submit an NDA for zoliflodacin to the U.S. FDA in early 2025.
Core royalty platform continued strong performance, receiving GSK royalties of $60.5 million with 6% year-over-year growth.
Innoviva Specialty Therapeutics’ (IST) marketed portfolio achieved U.S. net product sales of $19.7 million, reflecting 68% year-over-year growth
XACDURO® was nominated for the Best Biotechnology Product by The Galien Foundation USA
Company is on track to submit a New Drug Application (“NDA”) for zoliflodacin to the U.S. FDA in early 2025.
Company remains focused on prudent capital allocation in quest to maximize shareholder value and see multiple opportunities for continued value creation.
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