ICON, plc.
Salt Lake City, Utah, 84124, United States
NCT Number: NCT05594615
A Drug-Drug Interaction study to assess the effects of EDP-235 on the Pharmacokinetics and Safety of midazolam, caffeine and rosuvastatin.
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Notify Me18 year–55 year
All sexes
Interventional
Phase 1
Salt Lake City, Utah, 84124, United States
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Subjects will receive EDP-235 once daily on Days 5-15
Subjects will receive midazolam once daily on Days 1 and 12
Subjects will receive rosuvastatin once daily on Days 2 and 13
Subjects will receive caffeine once daily on Days 1 and 12
Time frame: Up to 17 Days
Time frame: Up to 17 Days
Time frame: Up to 22 days
Enanta Pharmaceuticals, Inc
Industry
A NON-RANDOMIZED, MULTIPLE-DOSE, OPEN-LABEL, SINGLE SEQUENCE STUDY TO EVALUATE THE EFFECT OF CONCOMITANT ADMINISTRATION OF EDP-235 ON THE PHARMACOKINETICS AND SAFETY OF MIDAZOLAM, CAFFEINE, AND ROSUVASTATIN IN HEALTHY PARTICIPANTS
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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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