Zanubrutinib
DrugA single oral dose of 80 mg Zanubrutinib will be administered.
NCT Number: NCT03465059
This study is designed to evaluate the safety and pharmacokinetics of zanubrutinib in subjects with impaired liver function in comparison with healthy subjects
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Notify Me18 year–75 year
All sexes
Interventional
Phase 1
University of Miami, Miami, Florida, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Additional Inclusion Criteria for Healthy Subjects Only:
Additional Inclusion Criteria for Hepatic Impaired Subjects Only:
Exclusion criteria
Additional Exclusion Criteria for Hepatic Impaired Subjects Only:
A single oral dose of 80 mg Zanubrutinib will be administered.
Time frame: Days 1, 2 & 3
Plasma concentration of Zanubrutinib (BGB-3111) to evaluate Area Under the Plasma Concentration-Time Curve (AUC) of Zanubrutinib
Time frame: Days 1, 2 & 3
Plasma concentration of Zanubrutinib (BGB-3111) to evaluate Maximum Observed Plasma Concentration (Cmax) of Zanubrutinib
Time frame: up to Day 17
Percentage of Participants with Treatment-Emergent Adverse Events (AE)
BeiGene
Industry
A Phase 1, Open-label, Single-dose Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Zanubrutinib (BGB-3111) in Subjects With Varying Degrees of Hepatic Impairment
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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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