Clinical trials

6

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Clinical Assessment of Response in the Treatment of Depression With Daytime Sleepiness Using Solriamfetol

CLARITY (Clinical Assessment of Response in the Treatment of Depression with Daytime Sleepiness Using Solriamfetol) is a Phase 3, double-blind, placebo-controlled, multicenter randomized withdrawal trial in patients with major depressive disorder (MDD) with excessive daytime sleepiness (EDS) symptoms consisting of an open-label solriamfetol treatment period and a randomized, double-blind treatment period.

Participants needed: 508
Trial details
Phase: Phase 3Age: 18-65Biological sex: AllType: InterventionalSponsor: Axsome Therapeutics, Inc.Updated: Mar 20, 2026Locations: 13
Eligibility criteria

Currently meets the DSM-5 criteria for MDD without psychotic features, based on... [+3]

Any clinically significant medical (e.g., OSA, narcolepsy), behavioral, or psych... [+2]

Status: Recruiting

Fibromyalgia Response With Esreboxetine Evaluated Using a Randomized Withdrawal Research Design

The study is a Phase 3, double-blind, placebo-controlled, randomized withdrawal study to assess the efficacy and safety of AXS-14 in the management of fibromyalgia.

Participants needed: 620
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Axsome Therapeutics, Inc.Updated: Feb 9, 2026Locations: 16
Eligibility criteria

Has a primary diagnosis of fibromyalgia based on the 2016 ACR diagnostic criteri... [+2]

Previous participation in a clinical trial with reboxetine or esreboxetine or cu... [+2]

Status: Recruiting

Studying Solriamfetol Modulation of TAAR-1, Dopamine, and Norepinephrine in Shift Work Disorder (SUSTAIN)

SUSTAIN (Studying Solriamfetol Modulation of TAAR-1, Dopamine, and Norepinephrine in Shift Work Disorder) is a Phase 3, multi-center, randomized, double-blind, placebo-controlled, parallel- group trial to assess the efficacy and safety of solriamfetol in adults with excessive sleepiness associated with shift work disorder (SWD).

Participants needed: 520
Trial details
Phase: Phase 3Age: 18-65Biological sex: AllType: InterventionalSponsor: Axsome Therapeutics, Inc.Updated: Nov 25, 2025Locations: 40
Eligibility criteria

Meets International Classification of Sleep Disorders, Third Edition (ICSD-3) cr... [+2]

Prior exposure to solriamfetol/Sunosi, through either a clinical study or prescr... [+2]

Status: Recruiting

Elucidating TAAR-1, Dopamine, and Norepinephrine in Binge Eating Disorder Using Solriamfetol

ENGAGE (Elucidating TAAR-1, Dopamine, and Norepinephrine in Binge Eating Disorder Using Solriamfetol) is a Phase 3, randomized, double-blind, placebo-controlled, multicenter trial to assess the efficacy and safety of solriamfetol for the treatment of binge eating disorder (BED) in adults.

Participants needed: 450
Trial details
Phase: Phase 3Age: 18-55Biological sex: AllType: InterventionalSponsor: Axsome Therapeutics, Inc.Updated: Nov 21, 2025Locations: 45
Eligibility criteria

Primary diagnosis of BED according to DSM-5 criteria. [+2]

Prior exposure to solriamfetol/Sunosi, through either a clinical study or prescr... [+2]

Status: Recruiting

A Study to Evaluate the Efficacy of AXS-05 Compared to Bupropion in Preventing the Relapse of Depressive Symptoms

This is a randomized, double-blind, active-controlled, multi-center study to evaluate the efficacy of AXS-05, compared to bupropion, in preventing the relapse of depressive symptoms in subjects with major depressive disorder (MDD) who have responded to treatment with AXS-05.

Participants needed: 350
Trial details
Phase: Phase 4Age: 18-65Biological sex: AllType: InterventionalSponsor: Axsome Therapeutics, Inc.Updated: Jan 23, 2025Locations: 40
Eligibility criteria

Currently meets DSM-5 criteria for diagnosis of MDD without psychotic features [+1]

Previously participated in another clinical study of AXS-05; received any invest... [+2]

Status: Recruiting

SUNOSI® (Solriamfetol) Pregnancy Registry

The SUNOSI (solriamfetol) Pregnancy Registry is a prospective, multi-country, observational study to evaluate the safety of solriamfetol exposure during pregnancy in women with a diagnosis of narcolepsy or obstructive sleep apnea (OSA).

Participants needed: 1,731
Trial details
Biological sex: FemaleType: ObservationalSponsor: Axsome Therapeutics, Inc.Updated: May 14, 2024Locations: 2Duration: 12 Months
Eligibility criteria

Pregnant women of any age [+4]

Occurrence of pregnancy outcome prior to first contact with the registry coordin... [+1]