Purpose

PARADIGM (Progressing TAAR-1, Dopamine, and Norepinephrine in Depression Using Solriamfetol) is a Phase 3, randomized, double-blind, placebo-controlled, multicenter trial to assess the safety and efficacy of solriamfetol for the treatment of major depressive disorder (MDD) in adults.

Condition

Eligibility

Eligible Ages
Between 18 Years and 65 Years
Eligible Genders
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Currently meets the DSM-5 criteria for MDD without psychotic features, based on the SCID-5-CT - Current major depressive episode - Male or female, aged 18 to 65 inclusive

Exclusion Criteria

  • Prior exposure to solriamfetol/Sunosi, through either a clinical study or prescription - Unable to comply with study procedures - Medically inappropriate for study participation in the opinion of the investigator

Study Design

Phase
Phase 3
Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel Assignment
Primary Purpose
Treatment
Masking
Triple (Participant, Care Provider, Investigator)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Solriamfetol 300 mg
Up to 6 weeks
  • Drug: Solriamfetol 300 mg
    Solriamfetol tablets, taken once daily
Placebo Comparator
Placebo
Up to 6 weeks
  • Drug: Placebo
    Placebo tablets, taken once daily

Recruiting Locations

More Details

Status
Recruiting
Sponsor
Axsome Therapeutics, Inc.

Study Contact

Study Director
212-332-5061
SOL-MDD-301@axsome.com

Detailed Description

Eligible subjects must have a primary diagnosis of MDD without psychotic features based on the Diagnostic and Statistical Manual of Mental Disorders Fifth Edition (DSM-5) criteria. Subjects will be randomized in a 1:1 ratio to receive either solriamfetol (300 mg) or placebo for 6 weeks.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.