CompletedPhase 1

Investigation of Drug-drug Interaction of HRS-5965 With Clopidogrel and Clarithromycin in Healthy Subjects

China36 participantsStarted 2025-07-08

Plain-language summary

The study is being conducted to compare the drug-drug interaction of HRS-5965 with clopidogrel and clarithromycin in healthy subjects.

Age range18 Years – 45 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

✓. Ability to understand the study procedures and methods, participate voluntarily and be able to complete the study according to the protocol requirements, and sign the informed consent form (ICF) in writing.
✓. Aged 18-45 years old on the date of signing the ICF (including the threshold), both male and female.
✓. At the time of screening, male subjects weighing no less than 50 kg and female subjects weighing no less than 45 kg; body mass index (BMI): 19\~26 kg/m2 (including the threshold).
✓. During the screening period, human immunodeficiency virus antibody (HIV-Ab), treponema pallidum antibody, hepatitis B surface antigen (HBsAg) and hepatitis C virus antibody (HCV-Ab) were all negative.
✓. Female subjects with reproductive capacity or male subjects whose partners are female subjects with reproductive capacity need to have no plans for fertility or sperm/egg donation within 3 months +1 week for male subjects and 6 months +1 week for female subjects from the date of signing the informed consent form until the last medication use, and voluntarily take efficient contraceptive measures (including partners).

✕. Allergic to two or more allergens, or in the judgment of the investigator, may be allergic to the study drug or its components.
✕. Disease or medical condition that, in the judgment of the investigator, may interfere with the absorption, distribution, metabolism, and excretion of the drug or that may reduce compliance.
✕. Patients with a previous history of coronary artery disease, severe cardiac insufficiency, conduction disorders or clinically significant bradycardia.
✕. Patients with a history of electrolyte disorders (such as hypomagnesemia).
✕. Patients with a history of congenital or acquired QT interval prolongation or ventricular arrhythmia.
✕. Those with a history of meningococcal infection and streptococcus pneumoniae infection.
✕. Those with a history of neuromuscular diseases (such as myotonic dystrophy, poliomyelitis, myasthenia gravis, botulism poisoning) and poliomyelitis.
✕. Subjects who have had or are currently suffering from active pathological bleeding.

The maximum plasma concentration (Cmax)

Timeframe: Day 1 to day 12.

Area under the concentration curve from time 0 to the last quantifiable concentration (AUClast)

Timeframe: Day 1 to day 12.

NCT IDNCT07040787

SponsorChengdu Suncadia Medicine Co., Ltd.

Sponsor typeINDUSTRY

Study typeINTERVENTIONAL

Primary completion2025-08-17

Who can participate

Age range18 Years – 45 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

✓. Ability to understand the study procedures and methods, participate voluntarily and be able to complete the study according to the protocol requirements, and sign the informed consent form (ICF) in writing.
✓. Aged 18-45 years old on the date of signing the ICF (including the threshold), both male and female.
✓. At the time of screening, male subjects weighing no less than 50 kg and female subjects weighing no less than 45 kg; body mass index (BMI): 19\~26 kg/m2 (including the threshold).
✓. During the screening period, human immunodeficiency virus antibody (HIV-Ab), treponema pallidum antibody, hepatitis B surface antigen (HBsAg) and hepatitis C virus antibody (HCV-Ab) were all negative.
✓. Female subjects with reproductive capacity or male subjects whose partners are female subjects with reproductive capacity need to have no plans for fertility or sperm/egg donation within 3 months +1 week for male subjects and 6 months +1 week for female subjects from the date of signing the informed consent form until the last medication use, and voluntarily take efficient contraceptive measures (including partners).

✕. Allergic to two or more allergens, or in the judgment of the investigator, may be allergic to the study drug or its components.
✕. Disease or medical condition that, in the judgment of the investigator, may interfere with the absorption, distribution, metabolism, and excretion of the drug or that may reduce compliance.
✕. Patients with a previous history of coronary artery disease, severe cardiac insufficiency, conduction disorders or clinically significant bradycardia.
✕. Patients with a history of electrolyte disorders (such as hypomagnesemia).
✕. Patients with a history of congenital or acquired QT interval prolongation or ventricular arrhythmia.
✕. Those with a history of meningococcal infection and streptococcus pneumoniae infection.
✕. Those with a history of neuromuscular diseases (such as myotonic dystrophy, poliomyelitis, myasthenia gravis, botulism poisoning) and poliomyelitis.
✕. Subjects who have had or are currently suffering from active pathological bleeding.