Clinical Assessment of Response in the Treatment of Depression With Daytime Sleepiness Using Solriamfetol
Axsome Therapeutics, Inc. · NCT07484217
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18–65 · All sexes
- Healthy volunteers
- Not accepted (a condition is required)
- Study type
- Interventional · Phase 3
- Target enrollment
- 508
- US sites recruiting
- 40
- Study start
- February 23, 2026
- Record last updated
- October 13, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
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.
Being studied: Solriamfetol 150 MG; Placebo
Conditions: Major Depressive Disorder With Excessive Daytime Sleepiness Symptoms
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Currently meets the DSM-5 criteria for MDD without psychotic features, based on the SCID-5-CT
- Excessive daytime sleepiness symptoms
- Able to comply with study procedures
- Male or female, aged 18 to 65 years inclusive
Exclusion Criteria
- Any clinically significant medical (e.g., OSA, narcolepsy), behavioral, or psychiatric disorder, other than MDD with EDS symptoms
- Unable to comply with study procedures
- Medically inappropriate for study participation in the opinion of the investigator
Recruiting US locations
Clinical Research Site
Tucson, AZ 85704
Clinical Research Site
Bellflower, CA 90706
Clinical Research Site
Chino, CA 91710
Clinical Research Site
Glendale, CA 91206
Clinical Research Site
Imperial, CA 92251
Clinical Research Site
Los Angeles, CA 90015
Clinical Research Site
Oceanside, CA 92056
Clinical Research Site
Redlands, CA 92374
Clinical Research Site
San Diego, CA 92123
Clinical Research Site
Sherman Oaks, CA 91403
Clinical Research Site
Walnut Creek, CA 94596
Clinical Research Site
Jacksonville, FL 32256
Clinical Research Site
Miami, FL 33122
Clinical Research Site
Miami, FL 33176
Clinical Research Site
Atlanta, GA 30331
Clinical Research Site
Norcross, GA 30092
Clinical Research Site
Snellville, GA 30078
Clinical Research Site
Chicago, IL 60634
Clinical Research Site
Pikesville, MD 21208
Clinical Research Site
Springfield, MA 01103
Clinical Research Site
Las Vegas, NV 89102
Clinical Research Site
Las Vegas, NV 89119
Clinical Research Site
Cherry Hill, NJ 08002
Clinical Research Site
Toms River, NJ 08755
Clinical Research Site
Brooklyn, NY 11235
Clinical Research Site
New York, NY 10036
Clinical Research Site
New York, NY 10128
Clinical Research Site
Staten Island, NY 10314
Clinical Research Site
The Bronx, NY 10464
Clinical Research Site
Cincinnati, OH 45215
Clinical Research Site
Cincinnati, OH 45245
Clinical Research Site
Edmond, OK 73013
Clinical Research Site
Oklahoma City, OK 73116
Clinical Research Site
Portland, OR 97210
Clinical Research Site
Memphis, TN 38119
Clinical Research Site
Austin, TX 78759
Clinical Research Site
Bellaire, TX 77401
Clinical Research Site
Dallas, TX 75243
Clinical Research Site
Houston, TX 77007
Clinical Research Site
San Antonio, TX 78240
Study contacts (from the official record)
- Study Director · 2123325061 · sol-mdd-302@axsome.com
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