Gastroparesis Clinical Trial
Official title:
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.
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