Safety and Efficacy of ADS-5102 in Multiple Sclerosis Patients With Walking Impairment



Status:Recruiting
Conditions:Neurology, Neurology, Multiple Sclerosis
Therapuetic Areas:Neurology, Other
Healthy:No
Age Range:18 - 70
Updated:8/4/2018
Start Date:March 29, 2018
End Date:September 1, 2019
Contact:Clinical Trials Administrator
Email:clinicaltrials@adamaspharma.com
Phone:5104503500

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A 3-arm, Multicenter, Double-blind, Placebo-controlled, Randomized Study to Assess the Efficacy and Safety of ADS-5102 Amantadine Extended Release Capsules in Multiple Sclerosis Patients With Walking Impairment

This is a multicenter, 3-arm, randomized, placebo-controlled, double-blind, parallel-group
study of ADS-5102 (amantadine extended release [ER] capsules) in MS patients with walking
impairment. ADS-5102 will be administered once daily at bed time.


Inclusion Criteria:

- Signed a current IRB-approved informed consent form

- Male or female subjects between 18 and 70 years of age, inclusive, at the time of
Screening

- Confirmed diagnosis of MS according to the 2017 McDonald criteria

- Current medication regimen must be stable for at least 30 days prior to screening, and
subject must be willing to continue the same dosing regimen for the duration of study
participation

- Maximum Expanded Disability Status Scale (EDSS) score during screening of 6.5

- Stable physical activity level (inclusive of prescribed physical therapy) for at least
30 days prior to screening and willing to continue without change for the duration of
study participation

- A score on each of two completed screening T25FW tests between 8 and 45 seconds,
inclusive

Exclusion Criteria:

- Documented inability to tolerate amantadine

- Clinically significant MS relapse with onset less than 30 days prior to screening

- Receipt of dalfampridine (or any 4-aminopyridine or 2,4-diaminopyridine preparation)
or amantadine within 30 days prior to screening

- History of seizures within 3 years prior to screening

- History of hallucinations (visual, auditory, or any other type) within 3 years prior
to screening

- History of bipolar disorder, schizophrenia, or psychosis, regardless of treatment

- For subjects with a history of major depressive disorder, the presence of active
depressive symptoms that, in the opinion of the investigator, would affect the
subject's ability to complete study assessments, or which would not be in the
subject's best interest to participate in the study

- Presence of orthostatic hypotension at screening: a decrease in systolic blood
pressure (at least 20 mm Hg) or diastolic blood pressure (at least 10 mm Hg) within 3
minutes of the subject standing up, compared to pressures obtained while sitting

- If female, is pregnant or lactating

- If a sexually active female, is not surgically sterile or at least 2 years
post-menopausal, or does not agree to utilize a highly effective hormonal method of
contraception (an IUD, or vasectomized male partner is also acceptable), in
combination with a barrier method, from screening through at least 4 weeks after the
completion of study treatment. If a sexually active male, does not agree to utilize
condoms from screening through at least 4 weeks after the completion of study
treatment.

- Treatment with an investigational drug or device within 30 days prior to screening

- Treatment with an investigational biologic within 6 months or 5 half-lives, whichever
is longer, prior to screening
We found this trial at
48
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Atlanta, Georgia 30309
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Charleston, South Carolina 29406
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Charlotte, North Carolina 28207
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Cleveland, Ohio 44195
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Colorado Springs, Colorado 80907
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Columbus, Ohio 43214
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Cullman, Alabama 35058
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Denver, Colorado 80209
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Fairfield, Connecticut 06824
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Farmington Hills, Michigan 48334
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Fort Collins, Colorado 80528
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Franklin, Tennessee 37064
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Fresno, California 93710
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Fullerton, California 92835
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Golden Valley, Minnesota 55422
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Greer, South Carolina 29650
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Houston, Texas 77074
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Indian Land, South Carolina 29707
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Indianapolis, Indiana 46256
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Johnson City, Tennessee 37604
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12039 Northeast 128th Street
Kirkland, Washington 98034
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Lake Success, New York 11042
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Lenexa, Kansas 66214
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Lincoln, Nebraska 68506
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Maitland, Florida 32751
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Naples, Florida 34105
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New London, Connecticut 06320
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Newport Beach, California 92663
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Newport News, Virginia 23601
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Norfolk, Virginia 23502
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Orlando, Florida 32806
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Ormond Beach, Florida 32174
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Overland Park, Kansas 66212
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Palm Coast, Florida 32164
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Patchogue, New York 11772
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Phoenix, Arizona 85032
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Port Charlotte, Florida 33952
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Raleigh, North Carolina 27607
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Rochester, New York 14642
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Round Rock, Texas 78681
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Sacramento, California 95817
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Saint Louis, Missouri 63110
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Salt Lake City, Utah 84103
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Savannah, Georgia 31406
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Scottsdale, Arizona 85251
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Tucson, Arizona 85704
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Vero Beach, Florida 32960
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