Phase
Condition
Neurologic Disorders
Pain (Pediatric)
Memory Loss
Treatment
Solriamfetol
Placebo
Clinical Study ID
Ages 18-60 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Male or female, 18 to 60 years of age, inclusive.
Medically stable on the basis of physical examination, medical history, and vitalsigns
Must meet McDonald 2017 diagnostic criteria for multiple sclerosis based on the PIreview of the medical records
Must complain from fatigue as one of their main symptoms and have a screening MFISscore of 33 or more
A screening ESS score of 10 or more
Must be ambulatory (able to walk at least 20 feet using bilateral assistance)
Must have internet and email access and the ability to use a computer or tablet, orsmartphone
Own an android smartphone or an iphone
Consent to use a medically acceptable method of contraception for the duration ofthe study
Willing and able to comply with the study design schedule and other requirements
Willing and able to provide written informed consent
Exclusion
Exclusion Criteria:
History of coronary artery disease or congestive heart failure
Uncontrolled hypertension at Screening (history of high blood pressure and screeningsystolic blood pressure >160 or diastolic blood pressure>100)
A known history of uncontrolled diabetes (the last known hemoglobin A1c level above 7.0%), high BMI (>35), or hyperlipidemia (last known total cholesterol >240 mg/dl,or LDL cholesterol level >160 mg/dl)
Receiving drugs/treatments that increase blood pressure or heart rate (based on thePI review of the medications/treatments)
A history of cerebrovascular disease or stroke
A medical or neurological disorder other than MS, that was associated with excessivesleepiness.
A history of phenylketonuria or hypersensitivity to the phenylalanine-derivedproduct
A history of alcohol or drug abuse within the past two years
A history of psychosis, or bipolar disorder
A history of cardiac arrythmias
The use of any product with stimulating or sedating properties, unless they havebeen on a steady dose for at least a month prior to the screening visit and agree tostay on the same dose over the course of the study
Use within 14 days of a monoamine oxidase (MAO) inhibitor drug
Pregnant or lactating
Use of medications used for the treatment of fatigue (including amantadine,modafinil, armodafinil, and amphetamine-like stimulants) in the past two weeks ofthe screening visit
A known history of moderate or severe kidney dysfunction (estimated Glomerularfiltration rate of less than 60 mL/min)
Study Design
Connect with a study center
Johns Hopkins University
Baltimore, Maryland 21287
United StatesActive - Recruiting
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