The First Affiliated Hospital of Jilin University
Changchun, Jilin, China
NCT Number: NCT04293029
Study to Evaluate Pharmacokinetics and Safety of SHR0302 in Patients With Mild, Moderate Hepatic Impairment and Normal Liver Function in Phase I Clinical Study
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Notify Me18 year–65 year
All sexes
Interventional
Phase 1
Changchun, Jilin, China
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
All subjects::
Normal liver function:
Hepatic impaired subjects:
Exclusion criteria
All subjects:
Normal liver function:
Hepatic impaired subjects:
SHR0302
Time frame: 72 hours after dosing
Peak Plasma Concentration (Cmax) will be compared between normal hepatic function patients and mild or moderate hepatic dysfunction patients
Time frame: 72 hours after dosing
Area under the plasma concentration versus time curve from single dosing time extrapolated to infinity(AUC0-∞) will be compared between normal hepatic function patients and mild or moderate hepatic dysfunction patients
Time frame: 72 hours after dosing
Area under the plasma concentration versus time curve from the last time of dosing to the last measurable concentration (AUC0-t) will be compared between normal hepatic function patients and mild or moderate hepatic dysfunction patients
Time frame: 72 hours after dosing
Number of Participants With Adverse Events and Serious Adverse Events
Jiangsu HengRui Medicine Co., Ltd.
Industry
Pharmacokinetics and Safety of SHR0302 in Patients With Mild, Moderate Hepatic Impairment and Normal Liver Function in Phase I Clinical Study
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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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