Pharmacokinetics of ZSP1273 in Participants With Hepatic Impairment
Study Details
Study Description
Brief Summary
This study will assess the effect of hepatic impairment on the pharmacokinetics (PK), safety and tolerability of ZSP1273.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
| Phase 1 |
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Cohort 1 8 participants with mild hepatic impairment (Child-Pugh A) will be given 600mg of ZSP1273. |
Drug: ZSP1273
Participants receive ZSP1273 orally.
|
| Experimental: Cohort 2 8 participants with moderate hepatic impairment (Child-Pugh B) will be given 600mg of ZSP1273. |
Drug: ZSP1273
Participants receive ZSP1273 orally.
|
| Experimental: Cohort 3 8 participants with normal hepatic function will be given 600mg of ZSP1273. |
Drug: ZSP1273
Participants receive ZSP1273 orally.
|
Outcome Measures
Primary Outcome Measures
- Maximum observed plasma concentration (Cmax) [Day 1 to Day 6]
The Cmax of a single dose of ZSP1273 in participants with impaired hepatic function and controls with normal hepatic function will be evaluated and compared.
- Area under the concentration-time curve from time zero to infinity (AUCinf) [Day 1 to Day 6]
The AUCinf of a single dose of ZSP1273 in participants with impaired hepatic function and controls with normal hepatic function will be evaluated and compared.
- Area under the concentration-time curve from time zero to last time of quantifiable concentration (AUClast) [Day 1 to Day 6]
The AUClast of a single dose of ZSP1273 in participants with impaired hepatic function and controls with normal hepatic function will be evaluated and compared.
Secondary Outcome Measures
- Number of participants with drug-related adverse events as assessed by CTCAE v5.0 [Day 1 to Day12]
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Participant must be ≥ 18 to ≤ 68 years, at the time of signing the informed consent.
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BMI ≥ 18 kg/m2 up to ≤ 32 kg/m2.
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Participates (including partners) must use reliable methods of contraception during the study and until 3 months following the last dose of investigational product.
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Signature of a dated Informed Consent Form (ICF) indicating that the participates has been informed of all the relevant aspects(including adverse events) of the trial prior to enrollment.
Participants with hepatic impairment only:
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Supporting documents confirming that the participant has liver cirrhosis with hepatic impairment must be available.
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Unless otherwise stated, participants must have been on stable doses and regimens of the concomitant medication for at least 4 weeks before screening, or treatment-naïve participants
Exclusion Criteria:
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Participates with an allergic disposition (multiple drug and food allergies) or who, as determined by the investigator, are likely to be allergic to the investigational drug product or any component of the investigational drug product.
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QTcF (male) > 470ms，QTcF (female) > 480ms
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Participates with serious infections, trauma, gastrointestinal surgery or other major surgical procedures within 4 weeks
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Participates who donated blood or bleeding profusely (> 400 mL) in the 3 months.
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Pregnant or lactating women, or women of childbearing age with a positive pregnancy test
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Smoking averaged more than 10 cigarettes per day in the 3 months prior to screening
Participants with Normal Hepatic Function Only:
- Any history of hepatic impairment, or potential presence of liver function impairment by physical examination and laboratory examination at screening.
Participants with Hepatic Impairment Only:
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Any history of clinically serious illness or disease or condition except for primary liver disease that the investigator believes may affect the results of the trial, including but not limited to a history of circulatory, endocrine, nervous, digestive, urinary, respiratoryor hematological, immune, psychiatric, and metabolic disorders.
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Participates with drug-induced liver injury; history of liver transplantation; cirrhosis in combination with the following complications: including but not limited to liver failure, hepatic encephalopathy, hepatocellular carcinoma, esophageal bleeding from ruptured fundic varices
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | The First Hospital of Jilin University | Jilin | China |
Sponsors and Collaborators
- Guangdong Raynovent Biotech Co., Ltd
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- ZSP1273-23-12