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The objective of this study is to evaluate the tolerability, safety, and pharmacokinetics after multiple-dose administration of aprocitentan (25 mg) in healthy Japanese and Caucasian subjects.
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Lead Sponsor
Idorsia Pharmaceuticals Ltd.
Collaborators
NCT06342713 · Healthy Participants, Healthy Subjects, and more
NCT06014515 · Healthy Subjects, Cardiovascular Disease
NCT07181369 · Healthy Subjects, Cold Urticaria, and more
NCT07364149 · Healthy, Healthy Participants, and more
NCT07219940 · Healthy Subjects, Exosome, and more
Anaheim Clinical Trials
Anaheim, California
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Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
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