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Harmony’s lead product, WAKIX (pitolisant), is FDA approved and widely prescribed for narcolepsy (excessive daytime sleepiness and cataplexy). Pipeline candidates are in Phase 3 (ZYN002 for Fragile X Syndrome, pitolisant label expansion), with multiple late-stage programs expected to produce topline data in 2025. The company demonstrates continued revenue growth, with WAKIX reaching 7,300 patients in Q1 2025 and robust Phase 3 clinical activity in rare neurological conditions.
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