Study to Assess the Efficacy of VLY-686 in Relieving Symptoms of Gastroparesis



Status:Recruiting
Conditions:Gastrointestinal
Therapuetic Areas:Gastroenterology
Healthy:No
Age Range:18 - 70
Updated:4/29/2018
Start Date:November 2016
End Date:December 2018
Contact:Vanda Pharmaceuticals
Phone:202-734-3400

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A Multicenter, Randomized, Double-Blind, Placebo-Controlled Proof of Concept Study to Assess the Efficacy of VLY-686 (Tradipitant) in Relieving Symptoms of Gastroparesis

This is a multicenter, randomized, double-blind, placebo-controlled study to be conducted in
the United States. One hundred fifty (150) subjects diagnosed with gastroparesis, who satisfy
the selection criteria for the study, will be randomized to one of two treatment groups,
active or placebo.

This is a multicenter, randomized, double-blind, placebo-controlled study to be conducted in
the United States. One hundred fifty (150) subjects diagnosed with gastroparesis, who satisfy
the selection criteria for the study, will be randomized to one of two treatment groups,
active or placebo.

The study is divided into two phases: the screening phase and the evaluation phase. The
screening phase includes a screening visit to evaluate subjects' preliminary eligibility for
the study. During the screening phase, subjects will collect diary data for at least 4 weeks.
The evaluation phase includes 4 weeks of randomized double-blind treatment.

Inclusion Criteria:

1. Diagnosed with gastroparesis;

2. Subjects must agree to the use of contraception

3. Ability and acceptance to provide written informed consent;

4. Willing to participate in the pharmacogenomics sample collection;

5. Willing and able to comply with all study requirements and restrictions

6. Willing to not participate in any other interventional trial for the duration of their
participation.

Exclusion Criteria:

1. Another active disorder or treatment which could explain or contribute to symptoms in
the opinion of the Investigator (including but not limited to gastric malignancy,
neurological disorder, or heavy doses of strong anticholinergics);

2. Pregnancy or nursing;

3. History of intolerance and/or hypersensitivity to medications similar to VLY-686
(Tradipitant) and its accompanying excipients;

4. Use of another NK1 antagonist or palonosetron;

5. Exposure to any investigational medication, including placebo, within 60 days of the
Baseline Visit;

6. Any other reason as determined by the Investigator which may lead to an unfavorable
risk-benefit of study participation, may interfere with study compliance, or may
confound study results.
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Minneapolis, Minnesota 55114
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Athens, Georgia 30607
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Boston, Massachusetts 02135
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Chattanooga, Tennessee 37421
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Chevy Chase, Maryland 20815
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Chula Vista, California 91910
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Dothan, Alabama 36305
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El Paso, Texas 79905
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Elgin, Illinois 60123
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Great Neck, New York 11023
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Houston, Texas 77063
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Huber Heights, Ohio 45424
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Huntsville, Alabama 35801
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Indianapolis, Indiana 46202
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Jackson, Tennessee 38305
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Little Rock, Arkansas 72211
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Mentor, Ohio 44060
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Norfolk, Virginia 23502
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Raleigh, North Carolina 27612
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