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Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 4 weeks
Awards & highlights
Study Summary
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.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 4 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~4 weeks
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in gastroparesis associated symptoms as assessed by patient reported diary
Trial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: Study DrugExperimental Treatment1 Intervention
VLY-686 (Tradipitant) oral capsule for 4 weeks.
Group II: PlaceboPlacebo Group1 Intervention
Placebo oral capsule for 4 weeks.
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Who is running the clinical trial?
Vanda PharmaceuticalsLead Sponsor
61 Previous Clinical Trials
19,254 Total Patients Enrolled
2 Trials studying Gastroparesis
250 Patients Enrolled for Gastroparesis
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Who else is applying?
What state do they live in?
Indiana
Arizona
How old are they?
18 - 65
What site did they apply to?
Vanda Investigational Site
What portion of applicants met pre-screening criteria?
Met criteria
Recent research and studies
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