Drug-Drug Interaction Study of Itraconazole With GST-HG171/Ritonavir in Healthy Participants

NCT ID: NCT06087055

Last Updated: 2023-10-17

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 12 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-05-12
• Study Completion Date: 2023-08-07

Brief Summary

The purpose of this study is to estimate the effect of a strong inhibitor of CYP3A4 (itraconazole) on the pharmacokinetics (PK) of GST-HG171/ritonavir in healthy participants.

Conditions

Healthy Participant

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: BASIC_SCIENCE
• Blinding Strategy: NONE

Study Groups

Period 1

GST-HG171/ritonavir orally

Group Type: EXPERIMENTAL

GST-HG171/Ritonavir

Intervention Type: DRUG

Administered orally every 12 hours for days for a total of 5 doses from Day 1 through Day 3

Period 2

Itraconazole+GST-HG171/ritonavir orally

Group Type: EXPERIMENTAL

Itraconazole

Intervention Type: DRUG

Administered orally once daily for 9 days from Days 8 through 16

GST-HG171/Ritonavir

Intervention Type: DRUG

Administered orally BID for 3 day for a total on 5 doses starting on Day 12 through Day 14

Interventions

GST-HG171/Ritonavir

Administered orally every 12 hours for days for a total of 5 doses from Day 1 through Day 3

Intervention Type: DRUG

Itraconazole

Administered orally once daily for 9 days from Days 8 through 16

Intervention Type: DRUG

GST-HG171/Ritonavir

Administered orally BID for 3 day for a total on 5 doses starting on Day 12 through Day 14

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Sign the informed consent before the trial and fully understand the content, process and possible adverse reactions of the trial;

2. Ability to complete research in accordance with test plan requirements;

3. Subjects (including partners) are willing to take effective pregnancy avoidance measures within 6 months after screening to the last study drug administration;

4. Male and female healthy subjects aged 18 to 50 years (including 18 and 50 years old);

5. Male subjects weigh no less than 50 kg, and female subjects weigh no less than 45 kg. Body mass index (BMI) = body weight (kg) / height 2 (m2), body mass index is in the range of 18 ~ 28 kg / m2 (including critical value);

6. Physical examination, normal or abnormal vital signs have no clinical significance.

Exclusion Criteria

1. Allergies (multiple drugs and food allergies);

2. Those who smoked more than 5 cigarettes per day in the 3 months before the trial;

3. Have a history of drug abuse and / or alcoholism (drink 14 units of alcohol per week: 1 unit = 285 mL of beer, or 25 mL of spirits, or 100 mL of wine);

4. Blood donation or massive blood loss (> 400 mL) within three months before screening;

5. Have a history of dysphagia or any gastrointestinal disease that affects drug absorption, including a history of frequent nausea or vomiting caused by any cause;

6. Have any disease that increases the risk of bleeding, such as hemorrhoids, acute gastritis, or gastric and duodenal ulcers;

7. Have taken the study drug or participated in the drug clinical trial within three months before taking the study drug;

8. Have Intended to take any drug that changes the activity of drug metabolizing enzyme 28 days before screening or during the study, including strong inhibitors and inducers that affect the metabolizing enzyme;

9. Took any prescription drugs or herbs within 14 days before screening, or took over-the-counter drugs or any vitamin products within 7 days before screening;

10. Vaccinated within 14 days before screening or planned to be vaccinated during the study;

11. Those who have taken special diets (including dragon fruit, mango, grapefruit, etc.) or have vigorous exercise or other factors affecting drug absorption, distribution, metabolism, excretion, etc. within 2 weeks before screening;

12. Abnormal ECG has clinical significance;

13. Female subjects were breastfeeding or had a positive serum pregnancy result during the screening period or during the study;

14. Clinical laboratory examinations are abnormal and clinically significant, or find the following diseases with clinical significance (including but not limited to gastrointestinal tract, kidney, liver, nerve, blood, endocrine, tumor, lung, Immune, mental or cardiovascular disease) within 6 months before screening;

15. Positive screening for viral hepatitis (including hepatitis B and C), AIDS antigen / antibody, and Treponema pallidum antibody;

16. Acute disease or concomitant medication occurs from the screening stage to before study medication;

17. Ingested chocolate, any caffeinated or xanthine-rich food or drink 24 hours before taking the study drug;

18. People who have a positive urine drug screen or have a history of drug abuse or have used drugs within the past five years;

19. The investigator believes that there are other subjects who are not suitable for participating in this trial.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 50 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Fujian Akeylink Biotechnology Co., Ltd.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

The first hospital of Jilin University

Changchun, Jilin, China

Countries

China

Other Identifiers

GST-HG171-I-04

Identifier Type: -

Identifier Source: org_study_id