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AXSM

NASDAQNEW YORK, NY
Axsome Therapeutics, Inc.

Axsome Therapeutics is a fully integrated biopharmaceutical company focused on central nervous system conditions with three FDA-approved commercial products: AUVELITY for major depressive disorder, SUNOSI for excessive daytime sleepiness associated with obstructive sleep apnea or narcolepsy, and SYMBRAVO for acute migraine treatment. The company develops small molecules targeting novel mechanisms of action to address unmet needs in CNS indications.

$207.75+85.01%1Y
AXSM · daily close · illustrative · 0 catalysts marked
1Y high$207.751Y low$100.39range$107.36(107%)past catalysts

Pipeline6

Phase 3Fibromyalgia
small-molecule
Phase 3Binge-Eating Disorder
Phase 3Major Depressive Disorder With Excessive Daytime Sleepiness Symptoms
Phase 3Excessive Sleepiness
Phase 3Shift-work Disorder
small-molecule
Phase 3Binge-Eating Disorder
Phase 3Excessive Sleepiness
Phase 3Shift-work Disorder
small-molecule
UnknownIndication pending review
Unknownnarcolepsy
UnknownIndication pending review

Catalyst Calendar4

DEC
2026
170d
ReadoutSolriamfetol 150 mg
A Multi-center, Randomized, Double-blind, Placebo-controlled Trial to Assess the Efficacy and Safety of Solriamfetol in Excessive Sleepiness Associated With Shift Work Disorder — primary completion 2026-12
CT.gov
MAR
2028
626d
ReadoutAXS-14 (Esreboxetine)
A Double-Blind, Placebo-Controlled, Randomized Withdrawal Study to Assess the Efficacy and Safety of AXS-14 in the Management of Fibromyalgia — primary completion 2028-03
CT.gov
DEC
2028
901d
ReadoutSolriamfetol 150 mg
A Multicenter, Double-blind, Placebo-controlled, Randomized Withdrawal Study of Solriamfetol in Subjects With Major Depressive Disorder With Excessive Daytime Sleepiness Symptoms — primary completion 2028-12
CT.gov
Past (1)
DEC 31
2025
NDAAXS-12
the Company issued a press release announcing that it had received formal pre-New Drug Application ("NDA") meeting minutes from the FDA for its planned NDA submission for AXS-12 in narcolepsy
8-K

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