Efficacy and Safety After Multiple Doses of TNP-2198 Capsules, Rabeprazole Sodium Enteric-coated Tablets and Amoxicillin Capsules in Helicobacter Pylori Infected-positive Participants

• Status: Completed
• Trial end date: 2022-09-20
• Target enrollment: 0
• Participant gender: All

Summary

This is a single-center, randomized, open-label phase Ic/IIb clinical study to evaluate the efficacy and safety of TNP-2198 capsules, rabeprazole sodium enteric-coated tablets and amoxicillin capsules combined with multiple doses of rabeprazole sodium enteric-coated tablets and amoxicillin capsules compared with multiple doses of rabeprazole sodium enteric-coated tablets and amoxicillin capsules combined with multiple doses in Helicobacter pylori infection-positive population.

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: TenNor Therapeutics (Suzhou) Limited
• Treatments: Amoxicillin; Rabeprazole

Criteria

Inclusion Criteria:

• Signing the informed consent form (ICF);

• Male and female subjects aged 18 to 65 years (inclusive);

• Health condition: no clinically significant history of heart, liver, kidney, digestive tract, nervous system, respiratory system diseases, mental disorders or metabolic abnormalities;

• Normal results or clinically insignificant abnormal results in physical examinations and vital signs;

• Positive result of 14C urea breath test (UBT);

• The subject (including the partner) is willing to take effective contraceptive measures voluntarily without pregnancy plan in the next 6 months;

• Willing to follow and able to complete all trial procedures.

Exclusion Criteria:

• History of Helicobacter Pylori eradication therapy (including participation in other clinical studies of Helicobacter Pylori eradication);

• Average daily consumption of more than 5 cigarettes within 3 months prior to the start of the study;

• History of hypersensitivity to study drug or its excipients, or allergic constitution (allergy to multiple drugs and food);

• History of drug and/or alcohol abuse (mean consumption of ≥ 14 units of alcohol per week: 1 unit = 285 mL of beer, or 25 mL of liquor, or 100 mL of wine);

• Blood donation or massive blood loss (> 450 mL) within 3 months prior to screening;

• Using any drug that changes liver enzyme activity within 28 days prior to screening;

• Taking orally any prescription drug, over-the-counter drug, any vitamin product, or herbal medicine within 14 days prior to screening;

• Taking special diet (including dragon fruit, mango, grapefruit, etc.) or strenuous exercise, or having other factors that affect drug absorption, distribution, metabolism, excretion, etc., within 2 weeks prior to screening;

• Significant changes in diet or exercise habits recently;

• Those who have participated in, or are still participating in clinical studies within 1 months before taking the study drug;

• With difficulty in swallowing or history of any gastrointestinal diseases that affect drug absorption;

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

• With clinically significant ECG abnormalities;

• Female subjects who are lactating during the screening period or during the study, or have positive serum pregnancy test results;

• With symptoms or previous history of cardiovascular, digestive, respiratory, urinary, neurological, hematologic, immunological, endocrine system diseases or tumor, or psychiatric diseases;

• Clinically significant abnormalities in clinical laboratory tests, or other clinically significant findings (including but not limited to gastrointestinal, renal, hepatic, neurological, hematological, endocrine, neoplastic, pulmonary, immunological, psychiatric, or cardiovascular disease);

• Those who have positive tests results of viral hepatitis (including hepatitis B and C), HIV antibody, treponema pallidum antibody (additional Rapid Plasma Reagin（RPR）test is required for those with positive treponema pallidum antibody);

• Acute illness occurs or concomitant medication is used from the date of signing the informed consent to the date prior to study medication;

• Consumption of chocolate, any caffeine- or xanthine-containing food or drink within 48 hours prior to taking the study drug;

• Consumption of any alcoholic product within 48 hours prior to taking the study drug;

• Those who have positive test result of urine drug screening or history of drug abuse or drug addiction within the past 5 years;

• Those who have other conditions that, in the opinion of the investigator, make participation in this study inappropriate.