ICON, plc
San Antonio, Texas, 78209, United States
NCT Number: NCT06917508
The primary aim of this study is to assess the effect of EDP-323 on the pharmacokinetics and safety of midazolam, caffeine, and rosuvastatin in healthy adult participants.
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Notify Me18 year–65 year
All sexes
Interventional
Phase 1
San Antonio, Texas, 78209, 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-323 once daily on Days 5-15
Subjects will receive midazolam once daily on Days 1 and 12
Subjects will receive caffeine once daily on Days 1 and 12
Subjects will receive rosuvastatin once daily on Days 2 and 13
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-323 on the Pharmacokinetics and Safety of Midazolam, Caffeine, and Rosuvastatin in Healthy Participants
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
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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