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The objectives of this study is to access the pharmacokinetics and safety of HMS5552 in single dose in mild and moderate hepatic impaired subjects and matched healthy adult subjects.
This is an open-label and paralleled study with single oral dose of HMS5552 given to hepatic impaired subjects and matched healthy volunteers.
The primary objective is to access the pharmacokinetic profiles of HMS5552 in 25 mg dose in hepatic impaired subjects and (gender, age and BMI) matched healthy adult subjects.
The secondary objective is to characterize the safety profiles of HMS5552 in single dose in hepatic impaired subjects.
The subjects include mild hepatic impaired subjects (A group), moderate hepatic impaired subjects (B group), and healthy subjects (C Group) matched with hepatic impaired subjects in gender, age and BMI. The number of subjects in each group was no less than 8, and no less than 3 subjects in each gender.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Mild hepatic impaired subjects (A) | Experimental | Mild hepatic impaired subjects: to receive a single dose of HMS5552 ( 25mg ) tablet orally |
|
| Moderate hepatic impaired subjects (B) | Experimental | Moderate hepatic impaired subjects: to receive a single dose of HMS5552 ( 25mg ) tablet orally |
|
| Healthy volunteers (C) | Experimental | Matched healthy volunteers: to receive a single dose of HMS5552 ( 25mg ) tablet orally |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| HMS5552 | Drug | single dose of HMS5552 25mg |
|
| Measure | Description | Time Frame |
|---|---|---|
| The single dose pharmacokinetics of HMS5552 will be described by estimating parameters of Cmax; | Plasma will be collected at predose, 0.25, 0.5, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 24, 36, 48 and 72 hour post-dose. | Up to 72 hours post-dose |
| The single dose pharmacokinetics of HMS5552 will be described by estimating parameters of AUClast; | Plasma will be collected at predose, 0.25, 0.5, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 24, 36, 48 and 72 hour post-dose. | Up to 72 hours post-dose |
| The single dose pharmacokinetics of HMS5552 will be described by estimating parameters of AUCinf; | Plasma will be collected at predose, 0.25, 0.5, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 24, 36, 48 and 72 hour post-dose. | Up to 72 hours post-dose |
| Measure | Description | Time Frame |
|---|---|---|
| The single dose pharmacokinetics of HMS5552 will be described by estimating parameters of Cmax,u | Plasma will be collected at predose, 0.25, 0.5, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 24, 36, 48 and 72 hour post-dose. | Up to 72 hours post-dose |
| The single dose pharmacokinetics of HMS5552 will be described by estimating parameters of AUClast,u |
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Inclusion Criteria:
For hepatic impaired subjects:
Male and female subjects between ages of 18 and 65 years, no less than 3 subjects in each gender.
Body weight≥50kg for male and ≥45kg for female; BMI: 18.5~30 kg/m2
ALT>2×normal upper limit (ULN), or TBiL>1.5×ULN, or diagnosed cirrhosis. The related clinical manifestations have been stable for 4-12 weeks, and Child-Pugh score is in grade A or B:
A= mild liver damage (Group A): Child-Pugh 5-6; B= moderate liver damage (Group B): Child-Pugh 7-9;
Willing to sign the informed consent form (ICF) and take reliable contraceptive measures within 6 months after taking the last dose of study drug;
Willing to adhere to the protocol requirement.
For healthy volunteers:
Exclusion Criteria:
Subjects with impaired hepatic function cannot be enrolled if they meet one of the following criteria:
Healthy subjects cannot be enrolled if they meet one of the following criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| West China Hospital of Sichuan University | Chengdu | Sichuan | 610000 | China |
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| ID | Term |
|---|---|
| D003924 | Diabetes Mellitus, Type 2 |
| ID | Term |
|---|---|
| D003920 | Diabetes Mellitus |
| D044882 | Glucose Metabolism Disorders |
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |
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| ID | Term |
|---|---|
| C000629807 | Dorzagliatin |
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Plasma will be collected at predose, 0.25, 0.5, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 24, 36, 48 and 72 hour post-dose. |
| Up to 72 hours post-dose |
| The single dose pharmacokinetics of HMS5552 will be described by estimating parameters of AUCinf,u | Plasma will be collected at predose, 0.25, 0.5, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 24, 36, 48 and 72 hour post-dose. | Up to 72 hours post-dose |
| The single dose pharmacokinetics of HMS5552 will be described by estimating parameters of Tmax ; | Plasma will be collected at predose, 0.25, 0.5, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 24, 36, 48 and 72 hour post-dose. | Up to 72 hours post-dose |
| The single dose pharmacokinetics of HMS5552 will be described by estimating parameters of T1/2; | Plasma will be collected at predose, 0.25, 0.5, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 24, 36, 48 and 72 hour post-dose. | Up to 72 hours post-dose |
| The single dose pharmacokinetics of HMS5552 will be described by estimating parameters of CL/F; | Plasma will be collected at predose, 0.25, 0.5, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 24, 36, 48 and 72 hour post-dose. | Up to 72 hours post-dose |
| The single dose pharmacokinetics of HMS5552 will be described by estimating parameters of Vz/F; | Plasma will be collected at predose, 0.25, 0.5, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 24, 36, 48 and 72 hour post-dose. | Up to 72 hours post-dose |
| The single dose pharmacokinetics of HMS5552 will be described by estimating parameters of fu; | Plasma will be collected at predose, 0.25, 0.5, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 24, 36, 48 and 72 hour post-dose. | Up to 72 hours post-dose |
| D004700 | Endocrine System Diseases |