Vanda Investigational Site
Springfield, Missouri, 65802, United States
NCT Number: NCT06803290
A single center, two-period, randomized study to evaluate the food effect of VHX-896 tablets in healthy volunteers
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Notify Me18 year–55 year
All sexes
Interventional
Phase 1
Springfield, Missouri, 65802, United States
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Oral tablet
Time frame: 96 Hours
As measured by plasma concentrations
Time frame: 17 Days
As measured by the incidence of adverse events and clinically significant changes in laboratory values, ECG parameters, and vital signs.
Vanda Pharmaceuticals
Industry
An Open-Label, Two-Period, Two-Sequence, Two-Treatment Randomized, Single Oral Dose, Crossover Study to Evaluate the Effect of Food on the Pharmacokinetic Profile of VHX-896 in Healthy Volunteers
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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