Relative Bioavailability and Pharmacodynamics of HSK7653 in Healthy Volunteers

Healthy Clinical Trial

Official title:

A Randomized, Open-label, Two-Way Crossover Study to Evaluate Relative Bioavailability and Pharmacodynamics of Two Doses of HSK7653 in Healthy Volunteers

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT06003088
• Other study ID #: HSK7653-105
• Status: Completed
• Phase: Phase 1
• Start date: June 15, 2022
• Est. completion date: September 9, 2022

Study information

• Verified date: August 2023
• Source: Haisco Pharmaceutical Group Co., Ltd.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

To investigate the relative bioavailability of HSK7653(5mg) given as formulation A versus formulation B.

To investigate the relative bioavailability of HSK7653(25mg) given as formulation A versus formulation B.

To investigate safety and pharmacodynamics of two doses of HSK7653 in healthy male subjects.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 48
• Est. completion date: September 9, 2022
• Est. primary completion date: August 12, 2022
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Healthy male and female subjects, age =18 years old,with appropriate sex ratio;

2. A total body weight =40 kg for females and =50 kg for males;BMI of 19 to 26 kg/m^2(inclusive);

3. Subjects(and their partners) volunteered to use effective physical contraception, had no plans to have children or donate sperm/eggs from 14 days before the first dose to 6 months after the last dose;

4. Evidence of a personally signed and dated informed consent document indicating that the subject has been informed of all pertinent aspects of the study.

Exclusion Criteria:

1. Subjects who are allergic to two or more medicine, foods or pollens or have a history of allergy to the investigational product and the related compounds;

2. Have a history of severe unconscious hypoglycemia;

3. Clinical evidence or history of any of the following diseases:

• Inflammatory bowel disease, gastritis, ulcers, bile duct stones, or gastrointestinal bleeding

• Major gastrointestinal surgery (e.g., gastrectomy, gastrostomy, or enterectomy)

• Pancreatic injury or pancreatitis

• Abnormal liver function tests (such as ALT, AST, serum bilirubin) , indicating liver disease or liver injury

• Renal insufficiency

• Urinary tract obstruction or difficulty in bladder emptying;

4. Evidence or history of chronic or serious diseases of the blood system, circulatory system, digestive system, urinary system, respiratory system, nervous system, immune system, endocrine system, mental disorders, metabolic disorders, or any other diseases that may affect the results of the study;

5. Serious trauma and surgery within 3 month prior to Screening;

6. Use of vaccines within 1 month prior to dosing;

7. Use of prescription within 1 month prior to dosing,or use of nonprescription drugs(i.e. vitamins and herbal medicines)within 14 days prior to dosing;

8. Participation in another trial with an investigational drug or instrument within 3 months prior to dosing and for the duration of the study;

9. History of regular alcohol consumption exceeding 14 drinks/week (1 drink = 150 mL of wine or 360 mL of beer or 45 mL of hard liquor) within 6 months of Screening.

10. Use of alcohol during the trial,or have a positive result for alcohol breath test;

11. Smoking =5 cigarettes per day within 3 months prior to Screening;

12. Blood donation or loss of blood for= 400 mL or received blood transfusion or use of blood products within 3 months prior to Screening, or blood donation program for the duration of the study and for 1 month after the trial;

13. Drinking excessive amounts of tea, coffee, and/or caffeinated beverages daily (average more than 8 cups per day,1 cup =250 mL) within 3 months prior to Screening;

14. Use of grapefruit, pomelo, dragon fruit, mango and other fruits or related products that may affect metabolic enzymes within 7 days prior to dosing;

15. Use of products containing alcohol within 48 hours prior to dosing and for the duration of the study;

16. Smoking or using any tobacco product within 48 hours prior to dosing and for the duration of the study;

17. Strenuous activities within 48 hours prior to dosing;

18. Use of chocolate, food or beverages containing caffeine or xanthine within 48 hours prior to dosing;

19. History of drug abuse or drug dependence;

20. Human immunodeficiency virus (HIV) antibody, hepatitis B surface antigen (HBsAg), hepatitis C virus (HCV) antibody, or Treponema pallidum antibody (TPPA) has a positive result;

21. Any clinically significant physical examination, vital signs, electrocardiogram or clinical laboratory measurement abnormalities during screening, or Screening 12-lead ECG demonstrating QT interval >440 msec for males and >420 msec for females,or FPG< 3.9mmol/L or > 6.1mmol/L;

22. Pregnant or lactating women, or female subjects whose pregnancy test results are positive;

23. Lactose intolerant;

24. Subjects who have a history of fainting needles and blood, or who cannot tolerate venipuncture blood sampling;

25. Difficulty in swallowing tablets and capsules;

26. Special dietary requirements (e.g. vegetarians) or cannot follow a uniform diet during the trial;

27. Unable to cooperate to complete the study due to other reasons, or in the judgment of the investigator, would make the subject inappropriate for entry into this study.

Related Conditions & MeSH terms

• Healthy

Intervention

Drug:
• HSK7653(5mg)
Participants will receive a single oral dose of HSK7653(5mg) Formulation A Or a single oral dose of HSK7653(5mg) Formulation B on Day 1 Period 1. Depending on what Formulation was received on Day 1 Period 1, participants will receive either a single oral dose of HSK7653(5mg) Formulation A Or a single oral dose of HSK7653(5mg) Formulation B on Day 1 of Period 2. Each period lasts for 15 days.
• HSK7653(25mg)
Participants will receive a single oral dose of HSK7653(25mg) Formulation A Or a single oral dose of HSK7653(25mg) Formulation B on Day 1 Period 1. Depending on what Formulation was received on Day 1 Period 1, participants will receive either a single oral dose of HSK7653(25mg) Formulation A Or a single oral dose of HSK7653(25mg) Formulation B on Day 1 of Period 2. Each period lasts for 15 days.

Locations

Country	Name	City	State
China	The First Affiliated Hospital of Liaoning University of Traditional Chinese Medicine	Shenyang	Liaoning

Sponsors (1)

Lead Sponsor	Collaborator
Haisco Pharmaceutical Group Co., Ltd.

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Relative bioavailability (F)	To Evaluate Relative Bioavailability (F) of Two Doses of HSK7653 in Healthy Volunteers.; Relative bioavailability of HSK7653(5mg) given as formulation A versus formulation B=AUC(0-t)(HSK7653(5mg) Formulation A)/AUC(0-t)(HSK7653(5mg) Formulation B).; Relative bioavailability of HSK7653(25mg) given as formulation A versus formulation B=AUC(0-t)(HSK7653(25mg) Formulation A)/AUC(0-t)(HSK7653(25mg) Formulation B).	Pre-dose,0.25, 0.5, 1, 1.5, 2, 4, 6, 8, 10, 12, 24, 48, 72, 120, 168 and 336 hours post-dose.
Primary	AUC(0-t)	The pharmacokinetic parameters of HSK7653 in plasma	Pre-dose,0.25, 0.5, 1, 1.5, 2, 4, 6, 8, 10, 12, 24, 48, 72, 120, 168 and 336 hours post-dose.
Primary	AUC(0-8)	The pharmacokinetic parameters of HSK7653 in plasma	Pre-dose,0.25, 0.5, 1, 1.5, 2, 4, 6, 8, 10, 12, 24, 48, 72, 120, 168 and 336 hours post-dose.
Primary	Cmax	The pharmacokinetic parameters of HSK7653 in plasma	Pre-dose,0.25, 0.5, 1, 1.5, 2, 4, 6, 8, 10, 12, 24, 48, 72, 120, 168 and 336 hours post-dose.
Primary	Tmax	The pharmacokinetic parameters of HSK7653 in plasma	Pre-dose,0.25, 0.5, 1, 1.5, 2, 4, 6, 8, 10, 12, 24, 48, 72, 120, 168 and 336 hours post-dose.
Primary	t1/2	The pharmacokinetic parameters of HSK7653 in plasma	Pre-dose,0.25, 0.5, 1, 1.5, 2, 4, 6, 8, 10, 12, 24, 48, 72, 120, 168 and 336 hours post-dose.
Primary	?z	The pharmacokinetic parameters of HSK7653 in plasma	Pre-dose,0.25, 0.5, 1, 1.5, 2, 4, 6, 8, 10, 12, 24, 48, 72, 120, 168 and 336 hours post-dose.
Primary	Vd/F	The pharmacokinetic parameters of HSK7653 in plasma	Pre-dose,0.25, 0.5, 1, 1.5, 2, 4, 6, 8, 10, 12, 24, 48, 72, 120, 168 and 336 hours post-dose.
Primary	CL/F	The pharmacokinetic parameters of HSK7653 in plasma	Pre-dose,0.25, 0.5, 1, 1.5, 2, 4, 6, 8, 10, 12, 24, 48, 72, 120, 168 and 336 hours post-dose.
Secondary	The Safety of HSK7653	Number of participants with treatment-related adverse events as assessed by CTCAE v5.0.	From First dose until Follow up visit, assessed up to 3 months.
Secondary	AUEC(0-last)	The pharmacodynamic parameters of HSK7653 in plasma	Pre-dose,0.25, 0.5, 1, 1.5, 2, 4, 6, 8, 10, 12, 24, 48, 72, 120, 168 and 336 hours post-dose.
Secondary	ECmax	The pharmacodynamic parameters of HSK7653 in plasma	Pre-dose,0.25, 0.5, 1, 1.5, 2, 4, 6, 8, 10, 12, 24, 48, 72, 120, 168 and 336 hours post-dose.
Secondary	ETmax	The pharmacodynamic parameters of HSK7653 in plasma	Pre-dose,0.25, 0.5, 1, 1.5, 2, 4, 6, 8, 10, 12, 24, 48, 72, 120, 168 and 336 hours post-dose.
Secondary	DPP-4(WAI-2W)	The pharmacodynamic parameters of HSK7653 in plasma	Pre-dose,0.25, 0.5, 1, 1.5, 2, 4, 6, 8, 10, 12, 24, 48, 72, 120, 168 and 336 hours post-dose.