A Pharmacokinetic Study of HS-10504 in Participants With Hepatic Impairment and Normal Hepatic Function.

NCT07836504 | Not Yet Recruiting Phase 1 FDA Drug

• 1 other identifier: HS-10504-116
• Study Type: interventional
• Target: 32
• Locations: 0 countries
• Sites: N/A

Brief Summary

This is a two-part single-center, open-label, parallel, single-dose pharmacokinetic study of HS-10504 in participants with hepatic impairment and normal hepatic function.

Conditions

To Compare the Pharmacokinetic (PK) Differences of HS-10504 Between Participants With Hepatic Impairment and Participants With Normal Hepatic Function

Keywords

Phase I; Hepatic impairment; HS-10504

Outcome Measures

Primary Outcomes (3)

• Evaluation of PK parameters of HS-10504: Cmax

  To evaluate the Cmax of HS-10504 in participants with hepatic impairment and normal hepatic function

  216 hours after administration of HS-10504

• Evaluation of PK parameters of HS-10504: AUC0-t

  To evaluate the AUC0-t of HS-10504 in participants with hepatic impairment and normal hepatic function

  216 hours after administration of HS-10504

• Evaluation of PK parameters of HS-10504: AUC0-∞

  To evaluate the AUC0-∞ of HS-10504 in participants with hepatic impairment and normal hepatic function

  216 hours after administration of HS-10504

Secondary Outcomes (35)

• Evaluation of PK parameters of HS-10504 and metabolite M6-2: Cmax.

  216 hours after administration of HS-10504

• Evaluation of PK parameters of HS-10504 and metabolite M6-2: AUC0-t.

  216 hours after administration of HS-10504

• Evaluation of PK parameters of HS-10504 and metabolite M6-2: AUC0-∞.

  216 hours after administration of HS-10504

• Evaluation of PK parameters of HS-10504 and metabolite M6-2: Tmax.

  216 hours after administration of HS-10504

• Evaluation of PK parameters of HS-10504 and metabolite M6-2: t1/2z.

  216 hours after administration of HS-10504

Study Arms (2)

Participants with hepatic impairment

EXPERIMENTAL

Drug: HS-10504

Participants with normal hepatic function

EXPERIMENTAL

Drug: HS-10504

Interventions

HS-10504 DRUG

HS-10504:On Day 1, a single oral dose of 400 mg HS-10504 tablet was administered in the fasting state.

Participants with hepatic impairment; Participants with normal hepatic function

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• All participants must meet ALL of the following criteria to be eligible for this study:
• Provide written informed consent before any study related procedures, have a full understanding of the study, its procedures, and possible adverse events, and express a willingness and ability to comply with the protocol requirements.
• Be male or female adults.
• Agree to practice highly effective contraception from the time of signing the informed consent form until 6 months after the last dose of study drug (only non pharmacological contraceptive measures are allowed during the study), and refrain from attempting to conceive or donate sperm/eggs during this period.
• Participants with normal hepatic function must meet the following criterion to be eligible for this study:
• \. Participants in the normal hepatic function group should be matched with those in the hepatic impairment group for body mass index (BMI), age, and sex.
• Participants with hepatic impairment must meet the following criteria to be eligible for this study:
• Chronic liver injury caused by primary liver disease;
• The investigator judges that the participant's hepatic function status is stable based on the participant's clinical symptoms and other available examination results at screening;
• Have had a stable medication regimen for the treatment of hepatic impairment, complications, and other concomitant diseases for at least 14 days prior to administration of the investigational product, with no need for dose adjustment; or have not been on any such medication.

You may not qualify if:

• Participants who meet any of the following criteria will not be enrolled in this study:
• Have participated in any other clinical trial and used any investigational drug/device within 3 months prior to screening;
• Have a history of surgery within 3 months prior to screening, or have planned surgery during the study period, or have undergone surgery that may affect drug absorption, distribution, metabolism, or excretion;
• Have experienced significant blood loss or blood donation within 3 months prior to screening, or blood loss ≥200 mL within 1 month, or have planned blood donation during the study period;
• Have used strong or moderate inhibitors or inducers of CYP3A4/5, CYP2C8, and CYP2D6 within 30 days prior to the first dose of the investigational product, or have used albumin within 14 days prior to the first dose;
• Have a history of, or currently have, severe diseases of the nervous, psychiatric, digestive, circulatory, respiratory, urinary systems, etc., or have developed a new illness before administration of the investigational product, which is assessed by the investigator as unsuitable for participation in this study;
• Have a history of severe allergy, are prone to allergic reactions, or have an allergic constitution, or are known to be allergic to any component of the investigational product;
• Have regularly consumed alcohol within 3 months prior to screening or are unable to refrain from alcohol consumption during the study period, or have a positive alcohol breath test at screening;
• Have smoked an average of \>5 cigarettes per day within 3 months prior to screening, or are unable to refrain from using any tobacco products during the study period;
• Have consumed excessive amounts of tea, coffee, and/or caffeinated beverages within 3 months prior to screening;
• Have a history of drug abuse, drug dependence, or illicit drug use within 5 years prior to screening, or have a positive drug abuse screening test;
• Are lactating women within 1 month prior to screening or during the study period, or have a positive pregnancy test;
• Have had unprotected sexual intercourse within 14 days prior to screening;
• Have special dietary requirements, are unable to comply with a uniform diet, or have difficulty swallowing;
• Are unable to tolerate venipuncture or indwelling needle blood sampling, or have a history of needle phobia or blood phobia;

Sponsors & Collaborators

• Jiangsu Hansoh Pharmaceutical Co., Ltd.: lead

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NON RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: September 11, 2026
• First Posted: September 23, 2026
• Study Start: September 30, 2026
• Primary Completion (Estimated): September 25, 2027
• Study Completion (Estimated): October 30, 2027
• Last Updated: September 23, 2026

Record last verified: 2026-07