ALKS · Company research
3 upcoming catalysts · 0 phase 2+ trials on file
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Alkermes expects to report results from its Phase 3 study of Alixorexton (ALKS 2680) for Idiopathic hypersomnia in Q4 2026 (Oct–Dec) (no exact date yet). Phase 3 is the last stage before a drug can be approved, so this result usually decides the program’s future.
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sNDA submission for LUMRYZ in idiopathic hypersomnia by year-end 2026, expected in Q4 2026 (Oct–Dec) (no exact date yet). A company milestone for Alkermes (LUMRYZ (sodium oxybate ER) for idiopathic hypersomnia): a step in the program rather than a decision or a data readout.
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Alkermes expects to report results from its Phase 3 study of Alixorexton (ALKS 2680) for Narcolepsy type 1 and type 2 during 2027 (no exact date yet). Phase 3 is the last stage before a drug can be approved, so this result usually decides the program’s future.
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Alkermes reported results from its Phase 1b study of ALKS 7290 for ADHD in Q3 2026 (Jul–Sep). The linked source has what the numbers showed.
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Alkermes reported results from its Phase 2 study of alixorexton (ALKS 2680) for Narcolepsy type 1 and type 2 on Jul 13, 2026. The study met its main goal.
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Alkermes presented data on alixorexton (ALKS 2680) for Narcolepsy type 2 (NT2) at a medical meeting on Jun 17, 2026. The linked source has the details.
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Alkermes reported results from its Phase 3 study of LUMRYZ (sodium oxybate) extended-release for Idiopathic hypersomnia (IH) on May 12, 2026. The study met its main goal.
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