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Phase 3

Development Phase

1

Upcoming Catalysts

0

Historical Events

1

Regulatory Approvals

Upcoming Catalysts
What are catalysts?
Dec '26
AXSMPhase 3

Solriamfetol 150 mg Phase 3 Est. Readout

Solriamfetol 150 mg
Dec 2026~
CT.gov
00%
Competitive Landscape

1 competitor in Excessive Sleepiness

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Drug Information

Target Indication

Excessive Sleepiness

Clinical Trial

NCT06568367

Last updated: 12/4/2025

Patent & Exclusivity

No patent data available. Pre-approval drugs may not have Orange Book listings.

Regulatory Approvals
EMA1/16/2020

Sunosi

Sunosi is indicated to improve wakefulness and reduce excessive daytime sleepiness in adult patients with narcolepsy (with or without cataplexy). Sunosi is indicated to improve wakefulness and reduce excessive daytime sleepiness (EDS) in adult patients with obstructive sleep apnoea (OSA) whose EDS has not been satisfactorily treated by primary OSA therapy, such as continuous positive airway pressure (CPAP).

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Drug Science
Mechanism of action & safety profile
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